\\n\\n
Dr. Pletser’s experience includes 30 years of working with the European Space Agency as a Senior Physicist/Engineer and coordinating their parabolic flight campaigns, and he is the Guinness World Record holder for the most number of aircraft flown (12) in parabolas, personally logging more than 7,300 parabolas.
\\n\\nSeeing the 5,000th book published makes us at the same time proud, happy, humble, and grateful. This is a great opportunity to stop and celebrate what we have done so far, but is also an opportunity to engage even more, grow, and succeed. It wouldn't be possible to get here without the synergy of team members’ hard work and authors and editors who devote time and their expertise into Open Access book publishing with us.
\\n\\nOver these years, we have gone from pioneering the scientific Open Access book publishing field to being the world’s largest Open Access book publisher. Nonetheless, our vision has remained the same: to meet the challenges of making relevant knowledge available to the worldwide community under the Open Access model.
\\n\\nWe are excited about the present, and we look forward to sharing many more successes in the future.
\\n\\nThank you all for being part of the journey. 5,000 times thank you!
\\n\\nNow with 5,000 titles available Open Access, which one will you read next?
\\n\\nRead, share and download for free: https://www.intechopen.com/books
\\n\\n\\n\\n
\\n"}]',published:!0,mainMedia:null},components:[{type:"htmlEditorComponent",content:'
Preparation of Space Experiments edited by international leading expert Dr. Vladimir Pletser, Director of Space Training Operations at Blue Abyss is the 5,000th Open Access book published by IntechOpen and our milestone publication!
\n\n"This book presents some of the current trends in space microgravity research. The eleven chapters introduce various facets of space research in physical sciences, human physiology and technology developed using the microgravity environment not only to improve our fundamental understanding in these domains but also to adapt this new knowledge for application on earth." says the editor. Listen what else Dr. Pletser has to say...
\n\n\n\nDr. Pletser’s experience includes 30 years of working with the European Space Agency as a Senior Physicist/Engineer and coordinating their parabolic flight campaigns, and he is the Guinness World Record holder for the most number of aircraft flown (12) in parabolas, personally logging more than 7,300 parabolas.
\n\nSeeing the 5,000th book published makes us at the same time proud, happy, humble, and grateful. This is a great opportunity to stop and celebrate what we have done so far, but is also an opportunity to engage even more, grow, and succeed. It wouldn't be possible to get here without the synergy of team members’ hard work and authors and editors who devote time and their expertise into Open Access book publishing with us.
\n\nOver these years, we have gone from pioneering the scientific Open Access book publishing field to being the world’s largest Open Access book publisher. Nonetheless, our vision has remained the same: to meet the challenges of making relevant knowledge available to the worldwide community under the Open Access model.
\n\nWe are excited about the present, and we look forward to sharing many more successes in the future.
\n\nThank you all for being part of the journey. 5,000 times thank you!
\n\nNow with 5,000 titles available Open Access, which one will you read next?
\n\nRead, share and download for free: https://www.intechopen.com/books
\n\n\n\n
\n'}],latestNews:[{slug:"webinar-introduction-to-open-science-wednesday-18-may-1-pm-cest-20220518",title:"Webinar: Introduction to Open Science | Wednesday 18 May, 1 PM CEST"},{slug:"step-in-the-right-direction-intechopen-launches-a-portfolio-of-open-science-journals-20220414",title:"Step in the Right Direction: IntechOpen Launches a Portfolio of Open Science Journals"},{slug:"let-s-meet-at-london-book-fair-5-7-april-2022-olympia-london-20220321",title:"Let’s meet at London Book Fair, 5-7 April 2022, Olympia London"},{slug:"50-books-published-as-part-of-intechopen-and-knowledge-unlatched-ku-collaboration-20220316",title:"50 Books published as part of IntechOpen and Knowledge Unlatched (KU) Collaboration"},{slug:"intechopen-joins-the-united-nations-sustainable-development-goals-publishers-compact-20221702",title:"IntechOpen joins the United Nations Sustainable Development Goals Publishers Compact"},{slug:"intechopen-signs-exclusive-representation-agreement-with-lsr-libros-servicios-y-representaciones-s-a-de-c-v-20211123",title:"IntechOpen Signs Exclusive Representation Agreement with LSR Libros Servicios y Representaciones S.A. de C.V"},{slug:"intechopen-expands-partnership-with-research4life-20211110",title:"IntechOpen Expands Partnership with Research4Life"},{slug:"introducing-intechopen-book-series-a-new-publishing-format-for-oa-books-20210915",title:"Introducing IntechOpen Book Series - A New Publishing Format for OA Books"}]},book:{item:{type:"book",id:"8821",leadTitle:null,fullTitle:"New Frontiers in Brain - Computer Interfaces",title:"New Frontiers in Brain",subtitle:"Computer Interfaces",reviewType:"peer-reviewed",abstract:"Brain-Computer Interface (BCI) sounds comparable to plugging a USB cable into a human brain with a laptop and accessing brain information. However, it is not as simple as it sounds. BCI is a multidisciplinary discipline with an exponential progress parallel to and with Artificial Intelligence for the past decades. Initially started with the Electroencephalography (EEG) analysis, BCI offers practical applications for cortical physiology today. Although BCI outcomes are more perceptible in medicine such as cognitive assessment, neurofeedback, and neuroprosthetic implants, it opens up amazing avenues for the business community through machine learning and robotics. Thought-to-text is one example of a hot topic in BCI. So, it is quite predictable to see BCI for individual usage given the current affordability of platforms for less technologically savvy users as well as BCI integrated within office automation productivity tools. The current trend is towards vulgarization for businesses benefits, by extension to the society at large. Thus, the interest in preparing a book on BCI. This book aims to compile and disseminate the latest research findings and best practices on how BCI is expanding the frontiers of knowledge in clinical practices, on the brain itself, and the underlying technologies.",isbn:"978-1-83880-508-1",printIsbn:"978-1-83880-499-2",pdfIsbn:"978-1-83880-509-8",doi:"10.5772/intechopen.80912",price:119,priceEur:129,priceUsd:155,slug:"new-frontiers-in-brain-computer-interfaces",numberOfPages:142,isOpenForSubmission:!1,isInWos:null,isInBkci:!1,hash:"58effd86e005fc9a6416c380f19e5f42",bookSignature:"Nawaz Mohamudally, Manish Putteeraj and Seyyed Abed Hosseini",publishedDate:"February 26th 2020",coverURL:"https://cdn.intechopen.com/books/images_new/8821.jpg",numberOfDownloads:5159,numberOfWosCitations:1,numberOfCrossrefCitations:1,numberOfCrossrefCitationsByBook:0,numberOfDimensionsCitations:5,numberOfDimensionsCitationsByBook:0,hasAltmetrics:0,numberOfTotalCitations:7,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"August 28th 2018",dateEndSecondStepPublish:"October 16th 2018",dateEndThirdStepPublish:"December 15th 2018",dateEndFourthStepPublish:"March 5th 2019",dateEndFifthStepPublish:"May 4th 2019",currentStepOfPublishingProcess:5,indexedIn:"1,2,3,4,5,6",editedByType:"Edited by",kuFlag:!1,featuredMarkup:null,editors:[{id:"119486",title:"Dr.",name:"Nawaz",middleName:null,surname:"Mohamudally",slug:"nawaz-mohamudally",fullName:"Nawaz Mohamudally",profilePictureURL:"https://mts.intechopen.com/storage/users/119486/images/system/119486.jpeg",biography:"Dr. Nawaz Mohamudally graduated in telecommunications from the University of Science and Technology of Lille I in France. He is presently an Associate Professor at the University of Technology, Mauritius, where he has occupied the posts of Head of School of Business Informatics and Software Engineering and recently the Chairman of the Research Degrees Committee. He was formerly the Chairman of the Internet Management Committee at the national level and a member of the Mauritius Academy of Science and Technology. He is an academic researcher and practitioner in the fields of pervasive computing and data science. His latest ongoing research and development work with the industry is on customers behaviors insights. He is the recipient of the Outstanding Contribution in Education award from Stars of The Industry-Indo-African Forum and Best Professor in Industrial Systems Engineering from Africa Leadership Awards.",institutionString:"University of Technology",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"4",totalChapterViews:"0",totalEditedBooks:"4",institution:{name:"University of Technology, Mauritius",institutionURL:null,country:{name:"Mauritius"}}}],equalEditorOne:null,equalEditorTwo:null,equalEditorThree:null,coeditorOne:{id:"270591",title:"Dr.",name:"Manish",middleName:null,surname:"Putteeraj",slug:"manish-putteeraj",fullName:"Manish Putteeraj",profilePictureURL:"https://mts.intechopen.com/storage/users/270591/images/7830_n.jpg",biography:"Dr.Manish Putteeraj is a fellow graduate from Monash University where he has been awarded a doctoral degree in Neuroscience. His field of research encompasses neurobiology, neuro-endocrinology and has a special interest in circadian biology investigating both molecular mechanisms of timed-regulatory systems as well as behavioural responses to external determinants. He is also working in close collaboration with external contributors from national and international platforms to further his research and bridging the gap between social sciences and behavioural neuroscience. Presently working as a lecturer at the University of Technology, Mauritius, he also looks into the expansion of programmes offered at a post-graduate level such as the MSc. Mental Health.",institutionString:"University of Technology",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"1",totalChapterViews:"0",totalEditedBooks:"0",institution:null},coeditorTwo:{id:"86475",title:"Dr.",name:"Seyyed Abed",middleName:null,surname:"Hosseini",slug:"seyyed-abed-hosseini",fullName:"Seyyed Abed Hosseini",profilePictureURL:"https://mts.intechopen.com/storage/users/86475/images/system/86475.jpg",biography:"Dr. Seyyed Abed Hosseini received his B.Sc. and M.Sc. in Electrical Engineering and Biomedical Engineering in 2006 and 2009, respectively. He received his Ph.D. in Electrical Engineering from Ferdowsi University of Mashhad, Iran in 2016. He has a multidisciplinary background, 15 years of teaching experience, and a 1-year industry experience. He is currently an assistant professor at the Department of Electrical Engineering and Research Center of Biomedical Engineering, Mashhad Branch, Islamic Azad University, Mashhad, Iran. He is currently the Dean of Laboratory and Research Services at Khorasan Razavi, Islamic Azad University, Iran and the Director of Laboratories and Workshops at Mashhad Branch, Islamic Azad University. He is a senior researcher at the Center of Excellence on Soft Computing and Intelligent Information Processing, Iran. He has received 10 national and international awards and has published over 70 peer-reviewed papers and book chapters. 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Basic physical principles of such devices are described. Reviews supply readers with summary of recent development in dynamics and perspectives of the field in question. Examples of NIRS usage in BCI systems are provided and different experimental paradigms are described. Review not only deals mainly with noninvasive NIRS-BCIs but also covers some instances of usage of neighboring fields methods (such as EEG, for instance) for the sake of their importance in so-called hybrid BCI systems and/or in fundamental research, which may be less relevant in case of separate application of different encephalographic methods. As potentially beneficial for NIRS-BCIs, the phenomena of fast optical signals (FOS) are described, and some research on connectivity, including those based on NIRS, is covered. Some attention is paid to the perspective for future BCI’s construction using optogenetics.",signatures:"Korshakov Alexei Vyacheslavovich",downloadPdfUrl:"/chapter/pdf-download/65098",previewPdfUrl:"/chapter/pdf-preview/65098",authors:[{id:"275489",title:"Dr.",name:"Alexei",surname:"Korshakov",slug:"alexei-korshakov",fullName:"Alexei Korshakov"}],corrections:null},{id:"67368",title:"Speech Enhancement Using an Iterative Posterior NMF",doi:"10.5772/intechopen.84976",slug:"speech-enhancement-using-an-iterative-posterior-nmf",totalDownloads:838,totalCrossrefCites:1,totalDimensionsCites:2,hasAltmetrics:0,abstract:"Over the years, miscellaneous methods for speech enhancement have been proposed, such as spectral subtraction (SS) and minimum mean square error (MMSE) estimators. These methods do not require any prior knowledge about the speech and noise signals nor any training stage beforehand, so they are highly flexible and allow implementation in various situations. However, these algorithms usually assume that the noise is stationary and are thus not good at dealing with nonstationary noise types, especially under low signal-to-noise (SNR) conditions. To overcome the drawbacks of the above methods, nonnegative matrix factorization (NMF) is introduced. NMF approach is more robust to nonstationary noise. In this chapter, we are actually interested in the application of speech enhancement using NMF approach. A speech enhancement method based on regularized nonnegative matrix factorization (NMF) for nonstationary Gaussian noise is proposed. The spectral components of speech and noise are modeled as Gamma and Rayleigh, respectively. We propose to adaptively estimate the sufficient statistics of these distributions to obtain a natural regularization of the NMF criterion.",signatures:"Sunnydayal Vanambathina",downloadPdfUrl:"/chapter/pdf-download/67368",previewPdfUrl:"/chapter/pdf-preview/67368",authors:[{id:"279891",title:"Dr.",name:"Sunnydayal",surname:"Vanambathina",slug:"sunnydayal-vanambathina",fullName:"Sunnydayal Vanambathina"}],corrections:null},{id:"65241",title:"A Self-Paced Two-State Mental Task-Based Brain-Computer Interface with Few EEG Channels",doi:"10.5772/intechopen.83425",slug:"a-self-paced-two-state-mental-task-based-brain-computer-interface-with-few-eeg-channels",totalDownloads:745,totalCrossrefCites:0,totalDimensionsCites:2,hasAltmetrics:0,abstract:"A self-paced brain-computer interface (BCI) system that is activated by mental tasks is introduced. The BCI’s output has two operational states, the active state and the inactive state, and is activated by designated mental tasks performed by the user. The BCI could be operated using several EEG brain electrodes (channels) or only few (i.e., five or seven channels) at a small loss in performance. The performance is evaluated on a dataset we have collected from four subjects while performing one of the four different mental tasks. The dataset contains the signals of 29 EEG electrodes distributed over the scalp. The five and seven highly discriminatory channels are selected using two different methods proposed in the paper. The signal processing structure of the interface is computationally simple. The features used are the scalar autoregressive coefficients. Classification is based on the quadratic discriminant analysis. Model selection and testing procedures are accomplished via cross-validation. The results are highly promising in terms of the rates of false and true positives. The false-positive rates reach zero, while the true-positive rates are sufficiently high, i.e., 54.60 and 59.98% for the 5-channel and 7-channel systems, respectively.",signatures:"Farhad Faradji, Rabab K. Ward and Gary E. Birch",downloadPdfUrl:"/chapter/pdf-download/65241",previewPdfUrl:"/chapter/pdf-preview/65241",authors:[{id:"113410",title:"Prof.",name:"Rabab",surname:"Ward",slug:"rabab-ward",fullName:"Rabab Ward"},{id:"164366",title:"Dr.",name:"Farhad",surname:"Faradji",slug:"farhad-faradji",fullName:"Farhad Faradji"},{id:"272118",title:"Dr.",name:"Gary E.",surname:"Birch",slug:"gary-e.-birch",fullName:"Gary E. Birch"}],corrections:null},{id:"67166",title:"Neural Signaling and Communication",doi:"10.5772/intechopen.86318",slug:"neural-signaling-and-communication",totalDownloads:650,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"To understand the complex nature of the human brain, network science approaches have played an important role. Neural signaling and communication form the basis for studying the dynamics of brain activity and functions. The neuroscientific community is interested in the network architecture of the human brain its simulation and for prediction of emergent network states. In this chapter we focus on how neurosignaling and communication is playing its part in medical psychology, furthermore, we have also reviewed how the interaction of network topology and dynamic models of a brain network.",signatures:"Syeda Huma Jabeen, Nadeem Ahmed, Muhammad Ejaz Sandhu, Nauman Riaz Chaudhry and Reeha Raza",downloadPdfUrl:"/chapter/pdf-download/67166",previewPdfUrl:"/chapter/pdf-preview/67166",authors:[{id:"263857",title:"Dr.",name:"Nadeem",surname:"Ahmed",slug:"nadeem-ahmed",fullName:"Nadeem Ahmed"},{id:"283476",title:"Ms.",name:"Huma",surname:"Jabeen",slug:"huma-jabeen",fullName:"Huma Jabeen"},{id:"283480",title:"Prof.",name:"Muhammad Ejaz",surname:"Sandhu",slug:"muhammad-ejaz-sandhu",fullName:"Muhammad Ejaz Sandhu"},{id:"291428",title:"Dr.",name:"Nauman",surname:"Riaz",slug:"nauman-riaz",fullName:"Nauman Riaz"}],corrections:null},{id:"69776",title:"Integration of Spiking Neural Networks for Understanding Interval Timing",doi:"10.5772/intechopen.89781",slug:"integration-of-spiking-neural-networks-for-understanding-interval-timing",totalDownloads:762,totalCrossrefCites:0,totalDimensionsCites:0,hasAltmetrics:0,abstract:"The ability to perceive the passage of time in the seconds-to-minutes range is a vital and ubiquitous characteristic of life. This ability allows organisms to make behavioral changes based on the temporal contingencies between stimuli and the potential rewards they predict. While the psychophysical manifestations of time perception have been well-characterized, many aspects of its underlying biology are still poorly understood. A major contributor to this is limitations of current in vivo techniques that do not allow for proper assessment of the di signaling over micro-, meso- and macroscopic spatial scales. Alternatively, the integration of biologically inspired artificial neural networks (ANNs) based on the dynamics and cyto-architecture of brain regions associated with time perception can help mitigate these limitations and, in conjunction, provide a powerful tool for progressing research in the field. To this end, this chapter aims to: (1) provide insight into the biological complexity of interval timing, (2) outline limitations in our ability to accurately assess these neural mechanisms in vivo, and (3) demonstrate potential application of ANNs for better understanding the biological underpinnings of temporal processing.",signatures:"Nicholas A. 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Then an applied memory model that could serve as a framework to study the memory function was also introduced. Therefore, the memory unit was introduced as a basic information structure. Also, a structured platform for the memory unit was determined for encoding the information and data in the brain. Then a pattern of information coding was detected. Thus, a basic framework to study the memory function was conceived. The results of this thesis pave the way for the discovery of a basic algorithm to understand the memory function in the human. Also, this study introduces a simple way to overcome Alzheimer disease (AD). 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\r\n\tWe are living in a society where automation in each electrical appliance/instrument is a great demand. We wish to have automatic devices/gadgets/instruments with no or minimal intervention from humans in their daily operation. Then only, these devices can qualify to call it is smart instruments. To fulfill this, one of the major requirements is to come up with highly sensitive, long-lasting, low-cost smart sensors. On the other hand, the healthcare industry demands low-cost, Lab-on-chip type biosensors for simple and rapid detection of various biomolecules or biogases. A sensor is an analytical device that detects the change in the environment and responds to some output in terms of a measurable analog resistance/voltage/current converted into a human-readable display or transmitted for further processing. In the last two decades, a significant amount of research has been devoted to the development of various types of gas sensors using different nanomaterials in the electronic and healthcare industry.
\r\n\r\n\tThis book aims to provide the reader (research scholars, scientists, and engineers working in the field of sensors) an overview of the recent advances made in the development of various gas sensors for the electronic and healthcare industries for the betterment of the human lifestyle. Also, this book will intend to address existing challenges and a few future directions of research for easy integration and cost-effective fast sensing of such
\r\n\tgas sensors.
Now, as we move into the third decade of the twenty-first century, it is time to examine some of the current research in autism, for example, microbiome and other research, which is described in this book. Therapies for children with autism continue to be challenging, with no one therapy has been shown to be superior to all other forms of therapy. Indeed, the treatment situation echoes what Lewis Carroll wrote, “
Diagnosis is still a problem with some diagnosticians still holding on to outdated concepts like Kanner’s autism. Kanner’s autism is very real but an extremely rare form of autism, and only a small minority of children meet the criteria for Kanner’s autism. Fitzgerald et al. [1] showed that there were different prevalences of diagnosis, depending on which criteria were used:
There were 309 with a possible autism diagnosis, of which 285 (85%) met DSM III-R criteria.
One hundred forty-four (47%) met ICD-10 criteria.
Twenty-four (8%) met Kanner’s five criteria.
Two-hundred twenty (71%) met Kanner and Eisenberg’s two criteria, and nobody met criteria for Asperger’s syndrome.
This remains a problem, and it remains to be seen what the final diagnostic criteria for autism spectrum disorder will be. Currently, we use DSM 5 [2]. According to Baird et al. [3], about 25 per 10,000 met criteria for autism diagnosis based on the autism diagnostic interview/autism diagnostic observation scale (ADI-ADOS), while the rate for current diagnosis which would be the autism spectrum disorder gave a rate of about 116 per 10,000. This means ADI-ADOS is missing over three-quarters of patients who would now be described as having an autism spectrum disorder. It is commonly missed by professionals that the diagnosis of autism is a clinical diagnosis by an expert in the diagnosis of autism [4]. Missing autism spectrum disorder has catastrophic effects on the child themselves, the family and school.
Clearly, only those with higher IQ , the standard IQ necessary for university, will move on to a university. One of the most damaging aspects of the school life, which is almost pervasive and long lasting, is bullying. This leads to anxiety, PTSD, and depression in these children, as well as suicidal behaviour.
It is critical that the quality of training that teachers and classroom assistants have is good. It is almost impossible for those in the classroom to work with children with autism without the clinical autism gestalt. Staff who have this correct sense of the world as seen by a child with autism do extremely good work, become fascinated with the topic and spend the rest of their professional life working with children with autism. Many of the children with autism are the most interesting children a teacher can have the privilege to work with. Many have special talents, and there is a need to build on these special talents and use them in the context of social interaction and building social skills. This will increase the chances of the child living independently and having occupational success later, sometimes which is something that is extremely challenging for persons on the autism spectrum, including those with a high IQ on the autism spectrum. The issues of parent and school relations are very challenging. Because of the nature of autism, both sides can have extreme difficulty seeing things from the others’ point of view. Parent/staff meetings will have to be twice as long, when the child has autism because of the difficulties of communication. It is not surprising that staff can feel persecuted and misunderstood because they are speaking on a different level to the parents. The child with autism requires special understanding on the part of the school to understand their difficulties. It is not surprising because of these difficulties that there are often threats of litigation or actual litigation, because of these interpersonal communicational problems.
Of course, it is very easy in these situations for both sides to feel misunderstood. It is sometimes helpful for an outside professional child psychiatrist/child psychologist to be engaged to deal with these difficulties. Children with autism and their autistic friends live in a culture in an autistic culture, and it is necessary for teachers to understand them. Teachers have to be aware of the family’s and particularly the child with autism difficulty understanding emotions. It is not rare for more than one member of a family to have autism because it has such a high genetic loading. It is critical that teachers make reference to special autism services when the child is depressed, is very anxious or is making threats of killing themselves, which are far from uncommon. The relationship between the teacher and the outside autism professional will be critical to the child’s success in school. Severe depression of psychotic proportions may need to be treated with antidepressants, and attention deficit hyperactivity disorder, which is so often co-morbid with autism, is often missed by child psychologists and child psychiatrists, and this needs to be diagnosed and treated, if the child is to have a successful school outcome. Indeed, untreated children with autism who have also ADHD may be unmanageable in the classroom. They are then excluded, which unfortunately is a very common outcome. There are excellent behavioural strategies for dealing with ADHD, and medications like Ritalin are sometimes necessary as well.
They were drawn to this by previous hypothesis about the opioid excess theory of autism and clinical experience by some of the authors. They observed improvements in autistic behaviour in children on gluten- and casein-free diets. These treatments have been around for over 30 years, have always been controversial, but are now becoming far more central to the treatment and understanding of autism or at least autism subgroups. These theories have not gone away because there was always a kernel of truth in them. I myself have observed a subgroup of patients with autism who have benefitted significantly from gluten- and casein-free diets. Other patients in my experience got no benefit from the diets. The reason is that there is such massive heterogeneity in autism, both at the etiological, clinical presentation and response to treatment level. Someday, we may have biomarkers which will allow us to subtype autism spectrum disorders in a meaningful way. There is no available at this time, but this chapter is working on the possibility of a biomarker. This lack of biomarkers is a central problem in all psychiatry, and we have no biomarkers that can be used clinically in psychiatry, as of now. The scientific study by Ann-Mari Knivsberg and colleagues in 1995 [5] is of critical importance for understanding the relationship between diet and clinical improvement in patients with autism.
Hepatitis B virus (HBV) is a partially double-stranded viral agent with a circular deoxyribose nucleic acid (DNA) that replicates by reverse transcription. HBV infection is a hepatocyte infection that is globally considered as a public health concern [1, 2, 3]. There are more than 2 billion persons infected with HBV living today worldwide with 260 million estimated to be chronically infected with the infection and having a carrier rate varying from 9 to 20% in Sub-Saharan Africa (SSA) [4, 5, 6]. Annually, there are close to 900,000 HBV-related deaths, mainly due to cirrhosis or hepatocellular carcinoma (HCC). The viral infection is the fourth most common vaccine preventable infection among travelers returning home ill after enteric fever, acute hepatitis A, and influenza [7, 8]. This viral agent can cause both acute and chronic infections. Many infected persons show no symptoms during the initial stage of the infection. Typically, the viral agent has an incubation period of 90 days (range, 60–150 days). The acute HBV infection that is acquired newly only shows symptoms rarely. Signs and symptoms of the viral infection differs with age; most children aged under 5 years old and newly infected immunosuppressed adults often show no symptoms, while about 30–50% of people that are more than 5 years of age are usually symptomatic [7]. When present, the typical signs and symptoms of acute infection include malaise, fatigue, poor appetite, nausea, vomiting, abdominal pain, fever, dark urine, light color (clay-colored) stool, joint pain, and jaundice [8]. The overall case fatality ratio of acute infection due to HBV is approximately 1% [9]. People infected with HBV are susceptible to infection with hepatitis D virus; coinfection increases the risk of fulminant hepatitis and rapidly progressive liver disease [10]. Transmission of HBV is mainly through percutaneous or mucosal exposure to HBV-infected blood or bodily fluids including saliva or semen [2]. There are reports of transmission via sexual contact and contaminated medical equipment and through sharing of infected needles and injecting apparatus [11].
The prevalence of chronic HBV infection is ≥2%, such as in the western Pacific and African regions; expatriates, missionaries, and long-term development workers may be at increased risk for HBV infection in such countries [7, 8]. Serologic markers specific for the viral agent are necessary to diagnose HBV infection and for appropriate clinical management [12]. These markers can differentiate between acute, resolving, and chronic infections. Polymerase chain reaction (PCR) method can further be use to qualitatively or quantitatively detect the amount of HBV DNA in patients’ specimen after checking the markers of the virus [13]. All travelers should be screened for HBV infection markers, so that they would not be at risk of acquiring the virus during their stay [7].
Hepatitis B virus belongs to the family of
Morphology of hepatitis B virus [
The cardinal feature of HBV replication cycle is the replication of the DNA genome by reverse transcription, when virions bind susceptible cell-surface receptors and IgA receptors on liver cells following of RNA intermediate [18, 20]. The viral genome is transported into the nucleus, and it is then converted into a covalently closed circular double-stranded HBV DNA (cccDNA) molecule which acts as the transcriptional template for the host RNA polymerase II machinery that synthesizes polyadenylated and four capped mRNAs which encode the envelope structural proteins, viral core and the precore; polymerase; and X non-structural viral proteins [20]. A 3.5-kb genome length RNA is one of the major HBV transcripts which is translated to synthesize the viral core and polymerase proteins and also plays role as a pregenomic RNA that is encapsidated with the polymerase by the core protein in the cytoplasm of the liver cells. The replication of the viral agent usually happens entirely within these capsids by reverse transcription of the pregenomic RNA to synthesize a single-strand DNA copy that serves as the template for the second strand DNA produced, synthesizing a circular double-stranded DNA [21]. The viral capsids that contain the double-stranded DNA traffic either to the nucleus where amplification occurs or the viral cccDNA genome to stabilize intranuclear pool of transcriptional templates or to the endoplasmic reticulum, where they acquire the viral envelope proteins, bud into the lumen, and exit the cell as virions that can infect other cells [22, 23].
Hepatitis B virus gets entry into the bloodstream and targets the liver cells [24]. The hepatocytes which are infected are distended, and the cytoplasm assumes a ground appearance that is glassy. The virus is not cytopathic, and injury of the liver in HBV chronic infection is due to immunological responses [8, 25]. Although, the virus has a long incubation period of 45–180 days, replication starts few days after infection. The infection can be acute, an unexpected sickness with a mild-to-severe course followed by comprehensive resolve [26]. On the other hand, if the cell-mediated immune reaction is feeble, the infection does not resolve, and chronic hepatitis arises with an extended course of active disease or silent asymptomatic infection [27].
About 30–80% adults of acute HBV infection shows symptoms (1% fulminant hepatitis), whereas less than 1 year old children shows no symptoms [28]. Symptoms of HBV infection include malaise, dark urine, fever, nausea, jaundice, pale stools, right upper quadrant pain, and anorexia. The risk of chronic infection of HBV is hinged on the duration of acquisition [26]. About 90% of infected neonates, 30–50% of children aged 1–4 years, and 1–10% of acutely infected adults result to persistent infection. There are approximately 15–40% with persistent infection that leads to advanced liver disease, cirrhosis, and/or HCC [8, 29].
Transmission of HBV in travelers is through percutaneous or mucosal exposure to HBV-infected blood or bodily fluids including saliva or semen [30, 31]. There are reports of transmission via sexual contact, contaminated blood and its products, and contaminated medical equipment and through sharing of infected needles and injecting apparatus [31, 32].
In SSA, the viral infection, is often disseminated through perinatal and horizontal route, while in the developed regions, most infections occur in adults of younger ages through injecting drug use or high-risk sexual behavior (e.g., bisexuals and homosexuals) [8, 33]. HBV infection is known to be transmitted from the mother to child and it is a thing of worry [34, 35]. Every year, about 25,000 infants are born to HBV-diagnosed mothers in the United States, and approximately 1000 mothers transmit HBV to their infants. This means that about 90% of HBV-infected newborns will eventually develop to chronic infection, and up to 25% of those infected at birth will eventually die prematurely due to HBV-related complications. Therefore, the standard care for pregnant women includes an HBV testing during each pregnancy, to prevent HBV-positive pregnant women from transmitting the viral agent to her unborn child [34, 35].
Inadequate infection control in healthcare settings also constitutes to a significant mode of HBV transmission. That is why immigrants from many countries are recommended to be tested for HBV [12]. Transmission by blood transfusion is now rare, whereas before screening of donor blood, it was not uncommon [32]. Cord blood is usually negative for the serological markers of HBV, but occasionally intrauterine infection might happen. Fetal blood sampling might enhance this risk, but amniocentesis does not appear to increase the chances of intrauterine transmission [36]. Infection presumably occurs at or soon after birth. It perhaps occurs through breast (feeding) milk, as it is known to carry the virus. Transmission could occur if there was an in apparent breach in the mucosa of the mouth or during teething [37]. Among adults, high-risk sexual activity is one of the most frequent routes of transmission for HBV [38]. Historically, male homosexual contacts have been associated with a high risk for the viral infection [38]. Sexual transmission accounts for a majority of the transmission occurring in adult life [38]. More recently, heterosexual transmission is reported to be the most common cause of acute HBV infection in adults [39]. Transmission may also continue to occur in healthcare settings. It is a result of nonadherence to isolation guidelines in a hemodialysis unit, or direct person-person exposure (e.g., surgeon-to-patient or dentist-to-patient) may transmit the virus [40]. Sharing of clothes and bed spaces could pose jeopardy because the virus could be found in saliva, tears, urine, breast milk, and any other body fluid [13]. Other possible means of transmission include an infected parent kissing the cut finger or scraped knee of his child and sharing of personal items of personal hygiene such as toothbrushes between parents and children [3].
There is insufficient information that depicts predisposing factors to travelers; however, there is scarcity of public reports of HBV infection in travelers, and there is low risk for travelers who are not engaged in high-risk behaviors [7]. The risk of the viral infection might increase in countries/regions that have a 2% prevalence of chronic HBV infection, such as in the African and Western Pacific regions; missionaries, long-term community development workers, and expatriates might be at high risk for the viral agent in such areas [41]. Travelers should take note on how the virus is acquired and take precautionary measures to mitigate transmission. The risk of injury due to accident is much higher for travelers than for people in their own environment. These injuries may involve medical attention that will require injections, IVs, or blood transfusions, thereby enhancing the risk of HBV exposure [7]. Older aged travelers, especially those with heart problems, may also require medical treatments that will require the same risks of exposure.
The global prevalence of HBV indicated by the proportion of chronic HBV carriers in the population that is seropositive for the hepatitis B surface antigen (HBsAg) varies strongly between different geographical regions [12]. The virus endemicity level is different from one nation to another. The level is mostly lowered in the Western Europe, the United States, Canada, and some South American and Northern African countries (with an HBsAg chronic carrier rate < 2%); intermediate (i.e., 2–8%) in Eastern Europe, Central Asia, and some Eastern Asian countries; and high (above 8%) in Alaska, Sub-Saharan African countries, and some Asian countries [12, 42]. Infection with HBV is considered among the commonest immunization preventable infections among immigrants [12, 43]. The prevalence of the virus in travelers is associated with the status of the traveler’s immunity, the duration of travel, and the level of HBV endemicity in the destination country. More so, there are peculiar populations of travelers that might be of higher risk of HBV acquisition which includes those visiting relatives and friends, the expatriates, dental surgery and medical procedure travelers, and those casual sex engagers [7]. Empirical information posited that travelers seeking urgent, unforeseen medical attention are common which makes travelers at risk of the viral agent [44]. There is paucity of empirical evidence to quantify the risk travelers might also be exposed to HBV through activities that involve tattooing, piercings, and acupuncturing [7].
Coppola et al. [42] reported HBsAg seropositivity of 9.6% among undocumented refugees and immigrants in Southern Italy. The study showed that male sex, SSA origin, low level of schooling, and minor parenteral risks for acquiring HBV infection (acupuncture, tattoo, piercing, or tribal practices) were independently associated with ongoing or past HBV infection [42]. A study in Thailand among international backpackers reported that 25% of its population had engaged in casual sex, while traveling and about half of the population did not often use condom [45]. The risk of HBV infection from sex without protection increase with the number of sex partners, and the incidence of unprotected sex was higher among the singles based on a study carried out on Dutch travelers to tropical and subtropical regions [46]. A study among Australian travelers reported that about half of them had indulged in at least one activity with an HBV risk during their last overseas trip to Southeast or East Asia [47]. Travelers without immunity for the virus traveling to high HBV prevalence countries like Nigeria might be at risk of acquiring the infection due to the many potential accidental and uncontrollable exposures during travel. A Netherlands study reported that 9% of all HBV cases between 1992 and 2003 were travel-related with an estimated incidence of HBV infection of 4.5 per 100,000 travelers [48]. In a study carried out between 1997 and 2007, HBV infection was reported in 51 cases of a cohort of ill travelers presenting to GeoSentinel clinics [49]. The study also found out that male sex and older age are associated with HBV acquisition statistically. Findings among travelers have shown that new sexual partners and unprotected sex are common, especially where there is excessive alcohol intake environment [44, 50, 51]. In countries with high HBV endemicity, the monthly estimated incidence of the infection ranges from 25 per 100,000 for symptomatic infections to 80–420 per 100,000 for all HBV infections in susceptible expatriates residing in such country [52]. Development/aid workers, volunteers, and missionaries pose greater risk of the infection due to extension of travel stay and local community close contact [7]. The prevalence of anti-HBc antibody was 5%, doubling that of the general population in a Swedish expatriate’s population. Short duration of travel stay will obviously lower the risk of the infection [53]. Nielsen et al. reported that the incidence per month of HBV infection was 10.2 per 100,000 with 62% of cases traveling for less than 4 weeks [54]. Most research is hinged on travelers becoming sick after travel before testing to occur, so this tends to underestimate the incidence of the viral infection [7, 49].
Many cross-sectional research have find out that travelers have reduced baseline understanding on infections related to travels and put themselves in jeopardy to HBV infection through their actions while in foreign land [47, 55]. Nielsen et al. reported that 5% of short-term and 5% nonimmune travelers were under a great risk of getting infected with HBV via tattooing, injections, and operation activities [44]. About 41% high-risk endeavors were reported among travelers in more than 6 months with most of the endeavors being unintentional and involuntary [44]. In a retrospective study among Australian travelers, 281 (56%) had visited a country with medium to high prevalence of HBV, of whom only 43% had been vaccinated and 162 (33%) undertook activities associated with potential HBV exposure [55]. Medical tourism and transplantation of organs have been identified several times as predictors for the viral agent, which highlights that checking for transmissible infection cannot be guaranteed universally [56, 57]. A study among Australian patients finds out that 2 of 16 who traveled overseas for commercial kidney transplantation developed fulminant hepatitis related to HBV infection and died [58]. Significantly high-incidence rate of HBV infection was reported among patients receiving renal transplantations in India than in Saudi Arabia [59].
Hepatitis B virus until now has been reported to have 10 genotypes (A–J) with identified peculiar distribution based on regions to its high degree of genetic heterogeneity [5, 60, 61, 62]. HBV genotyping is significant in diverse ways. First, it provides global data on the genotypic distribution of the virus including phylogenetic and phylogeographic evidence. Second, it justifies the relationship between the viral strain and course of disease. It makes us understand the role of human migration on the evolution of the virus [63, 64].
One of the three genotypes A, D, and E is predominantly circulating in Africa depending on the country. Genotype A is found in the Southern and Eastern regions, and genotype D is predominantly circulating in the Northern Africa region. Genotype E is more in most of SSA regions including Nigeria; this report excludes Uganda and Cameroon which are predominant with the A genotype [5, 60, 64, 65]. Genotype A is prevalent in Europe and Southeast Asia, including the Philippines [43, 66]. Genotypes B and C are predominant in Asia [67]; genotype D is common in the Mediterranean area, the Middle East, and India; genotype F is common in Central and South America [66]. Genotype G has been identified in Germany and France [67]. Genotype I has been detected in Laos, Vietnam, and China [68, 69], while the newest genotype J was identified in the Ryukyu Island in Japan [70, 71].
HBsAg is the standard diagnostic marker used to screen for HBV infection in travelers. A positive test depicts an acute or chronic infection [2]. Quantifying HBsAg (qHBsAg) is also an essential tool in staging of HBV infection and predicting responses to HBV treatment. This tool depend on both viral and host factors, such as genotype, preS/S gene variability, and hepatic disease stage [72]. The presence of hepatitis B envelope antigen (HBeAg) indicates that the virus is actively replicating and typically correlates with higher levels of HBV DNA. Immunoglobulin (Ig) G and IgM to hepatitis B core antigen indicates either that the individual has previously been infected or has an ongoing infection. IgG anti hepatitis B core (IgG anti-HBc) will often persists for life. The presence of anti-HBs shows that the individual has obtained immunity either from infection or vaccination [3, 6].
Touching upon the technical procedures behind the tests, tests for serological markers are carried out using different techniques, based on resources availability. Chemiluminescent microparticle immunoassay (CMIA) is one of those qualitative tests that detect the viral antigen in blood or serum. The technique has a high specificity and sensitivity and is based on the antigenic features (e.g., HBsAg or HBeAg) binding to commercially synthesized antibodies (anti-HB) with chemiluminescence [73]. The light produced in a chemiluminescent reaction can be measured. This method is more sensitive than the enzyme-linked immunosorbent assay (ELISA) [73].
Polymerase chain reaction (PCR) is an advanced technique to detect HBV. It amplifies the nucleic acid and greatly enhances the amount of DNA [3]. This method can qualitatively or quantitatively detect the amount of HBV DNA in patients’ specimen, which reflects the replicative condition of the virus. To monitor and manage HBV infection, then a quantitative detection method is the technique of choice [73]. ALT levels are measured to help determine liver inflammation. ALT is an enzyme that is normally found in the liver, but also present in other body tissue, that is discharged into the circulation system as a consequence to hepatocellular injury [26]. ALT plays a role in characterization of HBV infection phases in synergy with HBV DNA [74]. Different noninvasive diagnoses such as aspartate aminotransferase (AST), platelet ratio index (APRI), and transient elastography (FibroScan) still exist. APRI is an index to determine the hepatic fibrosis based on a formula derived from platelet and AST concentrations [3]. FibroScan measures grade of liver fibroses through the detection of liver stiffness. Both methods are recommended by WHO to evaluate cirrhosis presence, but while FibroScan is preferred in a context where availability and cost is not an issue, APRI is used in settings with limited resources. Liver biopsy has been used to assess degree of necroinflammation and fibrosis degrees. However, the method has diverse demerits and constraints [6, 75].
All travelers should be screened for HBV infection markers, so that they will not be at risk of acquiring the virus during stay [74]. Recently updated guidelines also recommend that pregnant women with chronic HBV be referred to a specialist and considered for HBV treatment to further reduce the chance of transmitting the virus [3]. In infants born to HBsAg-positive mothers, the risk of mother-to-child transmission is significantly greater if the mother is positive for HBeAg, has a high viral load, and/or is infected with HIV [33]. Such infants should be given both vaccine and HBIgG (0.5 ml) within 12 hours of delivery. The infants should be evaluated for HBsAg, anti-HBs, and anti-HBc at age 12 months. The presence of anti-HBs depicts vaccine-induced immunity, and detection of both anti-HBs and anti-HBc shows immunoprophylaxis-modified infection, whereas the presence of HBsAg indicates prophylaxis failure [15, 76, 77].
Individuals who have not received the HBV vaccination and are exposed to the virus (through needle stick injury, splashing, or sexual exposure to partners infected with the viral agent) should be vaccinated with HBIG (0.04–0.07 ml/kg) as soon as possible after exposure. Immunization for the newborn babies should start immediately with the initial shot given at a site that is not similar with that for HBIG; an accelerated four dose immunization schedule (0, 1, 2, and 12 months) is required in the maternal-fetal transmission scenario [8, 77]. HBV can also be prevented by avoiding contact with contaminated blood and blood products and unprotected sexual exposure. Using condoms has also been shown to reduce the chance of sexually transmitted infections [8].
Several reasons why people did not opt for pre-travel vaccinations include traveler’s pre-knowledge regarding the prevention of diseases during overseas travel, the limited number of healthcare settings that gives immunization, and that some countries have not yet approved the number of vaccines a traveler needs [9, 31].
There are commercially hepatitis B vaccines available currently, for example, recombinant HBV vaccine (Engerix-B®, GlaxoSmithKline, and Recombivax HB®, Merck & Co., Inc.) and the HAV and HBV combined vaccine (Twinrix®, GlaxoSmithKline) [78]. The complete HBV vaccination requires three shots of vaccine. The normal timeline of the three intramuscular injections is to have the second and third injections given 1 and 6 months after the first dose. An accelerated schedule (doses on days 0, 7, and 21 and then a post-travel dose at 12 months) might be required if there is an inadequate time for immunization prior to travel [79, 80]. An HBV vaccine can also be used to treat persons who have been exposed to the virus, in order to prevent disease development [31].
The prevalence of HBV differs between countries and regions, and therefore the number of persons acquiring protective immunity from a previous HBV infection also changes. Therefore, the recommendation of its vaccination should be hinged on likelihood of infection during travel and evidence of previous immunization or recovery from previous infection [74]. In those travelers without evidence of previous HBV immunity, HBV vaccination is recommended in those with HBV exposure risks and traveling to HBV endemic regions [78]. The CDC has recommend HBV vaccination to all persons without evidence of immunization before traveling to areas with intermediate and high prevalence of chronic hepatitis B and, irrespective of the traveler’s destination, and based on the traveler’s potential risky activities and exposures [11, 81]. High-risk activities might include unprotected sex with a new partner, getting a tattoo or piercing, or having any medical procedures like surgery [11, 81]. Studies have reported that only 19% of all American travelers and 30% of American travelers planning high-risk activities had received a completed HBV vaccination before departure irrespective of the recommendation made by the CDC [79]. This finding is in consonance with information from Europe that only 15% of international travelers to HBV endemic regions receive a completed HBV vaccination before travel [79]. There is often a very low immunity of HBV to travelers from low endemic regions and those born before the EPI schedules [82, 83]. Obviously, there are no recommendations for HBV serologic examination of international travelers currently. This might be because of the large population of international travelers, thus making it impossible to screen all for the virus. Reports have it that only 3.4–3.9% of the population in low endemic countries will have evidence of the HBV serologic markers prior infection [82, 83]. Vaccination of those populations should be considered when long-term travel is arranged to countries where HBV prevalence is intermediate or hyperendemic [31].
There are several antiviral treatments available for chronic HBV infection, and everyone with chronic HBV should be linked to care, considered for treatment, and checked for liver damage and liver cancer regularly [84]. Therapy of HBV reduces the amount of virus in the system and lowers the chance of developing to serious liver disease and liver cancer. However, most people cannot be cured of the viral agent, and as such therapy is recommended to continue for life [85, 86].
Worthy of note is the fact that there are currently two main antiviral drugs for the treatment of chronic HBV infection [87]. They are nucleos(t)ide analogues (NA) and interferon (IFN) including normal IFNs and pegylated IFNs (Peg-IFNs). NA gives a direct antiviral effect by stopping DNA polymerase. It is usually given orally. There are six types of NAs as approved for treatment of HBV by the WHO: Lamivudine (LAM), Adefovir (ADV), Telbivudine (TBV), Entecavir (ETV), Tenofovir disoproxil fumarate (TDF), and Tenofovir alafenamide (TAF). IFNs, especially the Peg-IFNs, have a suppressed antiviral effect than the NA therapy, but its persistent effect can be achieved with a finite therapy. It is usually given via subcutaneous injection. There are reports of combination therapy of NA + NA and Peg-IFN + NA [86, 87].
There are serious ongoing clinical trials for the development of more effective treatments and a cure for HBV infection [3, 6].
Early screening and treatment will help mitigate frequent transmission of the viral agent and curb morbidities and mortalities in infected persons [85]. The first line should be to give the exact medical advice and start antiviral treatment, if available. Sadly, undergoing this step is often a problem in developing regions where there is lack of access to good healthcare facilities, and antiviral treatment is often exorbitant [6, 86].
Advocacy of immunization exercise for HBV infection should be key in eliminating the viral agent worldwide which is central to WHO’s agenda [6, 10]. To maximize implementation of the WHO agenda, provision of technical guidance and support to reduce transmission of the disease such as adhering to safer blood transfusion and disposable needles among others. The virus vaccine is very effective in preventing disease progression. It has been reported that only 27% of newborn babies had receive a birth dose of hepatitis B vaccine globally [86]. Birth dose vaccination of the viral agent is fundamental to halting mother-to-child transmission as late immunization is not fully effective in destroying the chain of mother-to-child transmission. Coordination between maternal health services and immunization should be effectively established [88].
Self-protection measures are one of the pre-travel counseling given to potential travelers to HBV and other blood-borne pathogen endemic regions [7, 8, 43]. Persons should be guided from contaminated items or equipment used in medical or cosmetic procedures, blood products, injection drug use or any exercise that involve piercing the skin or mucosa, or unprotected sexual activity. Travelers should be advised properly against the use of equipment that is not properly sterilized or disinfected on medical or beautification tourism (such as tattooing or piercing) [8]. The viral agent can be disseminated to others if tools are not sterile or if personnel do not follow proper infection control protocols [89].
Educational awareness and programs that will be targeted towards HBV awareness lowers transmission of the infection [90, 91]. There is a large pool of persons suffering from chronic HBV infection in Sub-Saharan Africa that are not aware of their situation. Educational awareness and implementation of local health measures are pertinent in eradicating the scourge of the infection [2]. These should include training local communities on how to perform safe blood transfusion and establishing efficient screening methods for transfusion of donated bloods. Health education programs should include administration of safe injections (intravenous drug users and healthcare settings) and implementation of safer sex practices (especially the use of condoms). More so, occupational safety trainings should be advocated for health workers [92]. It is also worthy to note that effective communication and emphasizing the role of the virus testing, follow-up visits, and monitoring therapy will help eliminate HBV infection [43].
Enhancing the socioeconomic conditions of a particular population has shown reduction in the rate of HBV infection. Government and non-governmental organization (NGO) bodies should ensure that there is a universal access to portable water and encourage food handling that is safe and hygienic [92]. They should also implement good sanitation systems. Safe disposal practice of medical waste should be advocated in the health settings [43].
There are ongoing development of two novel anti-HBV drugs, namely, Besifovir and Myrcludex-B that will soon be in the market [3]. The infection is one of those preventable infections by immunization in travelers. Therefore, travelers should often be screened and immunized for HBV infection before traveling to endemic countries because immigrants and/or travelers who have the viral infection pose a great risk of HCC and death. They as well serve as transmitters of the viral agent to those not infected when returned from travel. Continuous health surveillance and strict checking of migrants to ascertain previous vaccination evidence will go a long way in mitigating the infection across travelers. There is no single measure strong enough to curb viral hepatitis epidemics, but having a global vision and implementing multiple strategies will go a long way towards eliminating HBV infection and other global disease burden in 2030.
IntechOpen implements a robust policy to minimize and deal with instances of fraud or misconduct. As part of our general commitment to transparency and openness, and in order to maintain high scientific standards, we have a well-defined editorial policy regarding Retractions and Corrections.
",metaTitle:"Retraction and Correction Policy",metaDescription:"Retraction and Correction Policy",metaKeywords:null,canonicalURL:"/page/retraction-and-correction-policy",contentRaw:'[{"type":"htmlEditorComponent","content":"IntechOpen’s Retraction and Correction Policy has been developed in accordance with the Committee on Publication Ethics (COPE) publication guidelines relating to scientific misconduct and research ethics:
\\n\\n1. RETRACTIONS
\\n\\nA Retraction of a Chapter will be issued by the Academic Editor, either following an Author’s request to do so or when there is a 3rd party report of scientific misconduct. Upon receipt of a report by a 3rd party, the Academic Editor will investigate any allegations of scientific misconduct, working in cooperation with the Author(s) and their institution(s).
\\n\\nA formal Retraction will be issued when there is clear and conclusive evidence of any of the following:
\\n\\nPublishing of a Retraction Notice will adhere to the following guidelines:
\\n\\n1.2. REMOVALS AND CANCELLATIONS
\\n\\n2. STATEMENTS OF CONCERN
\\n\\nA Statement of Concern detailing alleged misconduct will be issued by the Academic Editor or publisher following a 3rd party report of scientific misconduct when:
\\n\\nIntechOpen believes that the number of occasions on which a Statement of Concern is issued will be very few in number. In all cases when such a decision has been taken by the Academic Editor the decision will be reviewed by another editor to whom the author can make representations.
\\n\\n3. CORRECTIONS
\\n\\nA Correction will be issued by the Academic Editor when:
\\n\\n3.1. ERRATUM
\\n\\nAn Erratum will be issued by the Academic Editor when it is determined that a mistake in a Chapter originates from the production process handled by the publisher.
\\n\\nA published Erratum will adhere to the Retraction Notice publishing guidelines outlined above.
\\n\\n3.2. CORRIGENDUM
\\n\\nA Corrigendum will be issued by the Academic Editor when it is determined that a mistake in a Chapter is a result of an Author’s miscalculation or oversight. A published Corrigendum will adhere to the Retraction Notice publishing guidelines outlined above.
\\n\\n4. FINAL REMARKS
\\n\\nIntechOpen wishes to emphasize that the final decision on whether a Retraction, Statement of Concern, or a Correction will be issued rests with the Academic Editor. The publisher is obliged to act upon any reports of scientific misconduct in its publications and to make a reasonable effort to facilitate any subsequent investigation of such claims.
\\n\\nIn the case of Retraction or removal of the Work, the publisher will be under no obligation to refund the APC.
\\n\\nThe general principles set out above apply to Retractions and Corrections issued in all IntechOpen publications.
\\n\\nAny suggestions or comments on this Policy are welcome and may be sent to permissions@intechopen.com.
\\n\\nPolicy last updated: 2017-09-11
\\n"}]'},components:[{type:"htmlEditorComponent",content:'IntechOpen’s Retraction and Correction Policy has been developed in accordance with the Committee on Publication Ethics (COPE) publication guidelines relating to scientific misconduct and research ethics:
\n\n1. RETRACTIONS
\n\nA Retraction of a Chapter will be issued by the Academic Editor, either following an Author’s request to do so or when there is a 3rd party report of scientific misconduct. Upon receipt of a report by a 3rd party, the Academic Editor will investigate any allegations of scientific misconduct, working in cooperation with the Author(s) and their institution(s).
\n\nA formal Retraction will be issued when there is clear and conclusive evidence of any of the following:
\n\nPublishing of a Retraction Notice will adhere to the following guidelines:
\n\n1.2. REMOVALS AND CANCELLATIONS
\n\n2. STATEMENTS OF CONCERN
\n\nA Statement of Concern detailing alleged misconduct will be issued by the Academic Editor or publisher following a 3rd party report of scientific misconduct when:
\n\nIntechOpen believes that the number of occasions on which a Statement of Concern is issued will be very few in number. In all cases when such a decision has been taken by the Academic Editor the decision will be reviewed by another editor to whom the author can make representations.
\n\n3. CORRECTIONS
\n\nA Correction will be issued by the Academic Editor when:
\n\n3.1. ERRATUM
\n\nAn Erratum will be issued by the Academic Editor when it is determined that a mistake in a Chapter originates from the production process handled by the publisher.
\n\nA published Erratum will adhere to the Retraction Notice publishing guidelines outlined above.
\n\n3.2. CORRIGENDUM
\n\nA Corrigendum will be issued by the Academic Editor when it is determined that a mistake in a Chapter is a result of an Author’s miscalculation or oversight. A published Corrigendum will adhere to the Retraction Notice publishing guidelines outlined above.
\n\n4. FINAL REMARKS
\n\nIntechOpen wishes to emphasize that the final decision on whether a Retraction, Statement of Concern, or a Correction will be issued rests with the Academic Editor. The publisher is obliged to act upon any reports of scientific misconduct in its publications and to make a reasonable effort to facilitate any subsequent investigation of such claims.
\n\nIn the case of Retraction or removal of the Work, the publisher will be under no obligation to refund the APC.
\n\nThe general principles set out above apply to Retractions and Corrections issued in all IntechOpen publications.
\n\nAny suggestions or comments on this Policy are welcome and may be sent to permissions@intechopen.com.
\n\nPolicy last updated: 2017-09-11
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I am also a member of the team in charge for the supervision of Ph.D. students in the fields of development of silicon based planar waveguide sensor devices, study of inelastic electron tunnelling in planar tunnelling nanostructures for sensing applications and development of organotellurium(IV) compounds for semiconductor applications. I am a specialist in data analysis techniques and nanosurface structure. I have served as the editor for many books, been a member of the editorial board in science journals, have published many papers and hold many patents.",institutionString:null,institution:{name:"Sheffield Hallam University",country:{name:"United Kingdom"}}},{id:"12392",title:"Mr.",name:"Alex",middleName:null,surname:"Lazinica",slug:"alex-lazinica",fullName:"Alex Lazinica",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/12392/images/7282_n.png",biography:"Alex Lazinica is the founder and CEO of IntechOpen. 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Čepička",authors:[{id:"103948",title:"Dr.",name:"Ivan",middleName:null,surname:"Cepicka",slug:"ivan-cepicka",fullName:"Ivan Cepicka"},{id:"103954",title:"MSc.",name:"Tomas",middleName:null,surname:"Panek",slug:"tomas-panek",fullName:"Tomas Panek"}]},{id:"28888",doi:"10.5772/35101",title:"Genotyping Techniques for Determining the Diversity of Microorganisms",slug:"genotyping-techniques-for-determining-the-diversity-of-microorganisms",totalDownloads:6449,totalCrossrefCites:3,totalDimensionsCites:13,abstract:null,book:{id:"2253",slug:"genetic-diversity-in-microorganisms",title:"Genetic Diversity in Microorganisms",fullTitle:"Genetic Diversity in Microorganisms"},signatures:"Katarzyna Wolska and Piotr Szweda",authors:[{id:"102977",title:"Dr.",name:"Katarzyna",middleName:null,surname:"Wolska",slug:"katarzyna-wolska",fullName:"Katarzyna Wolska"},{id:"117528",title:"Dr.",name:"Szweda",middleName:null,surname:"Piotr",slug:"szweda-piotr",fullName:"Szweda Piotr"}]},{id:"71577",doi:"10.5772/intechopen.91886",title:"Single Nucleotide Polymorphisms (SNPs) in Plant Genetics and Breeding",slug:"single-nucleotide-polymorphisms-snps-in-plant-genetics-and-breeding",totalDownloads:1488,totalCrossrefCites:8,totalDimensionsCites:10,abstract:"Recent advances in genome technology revealed various single nucleotide polymorphisms (SNPs), the most common form of DNA sequence variation between alleles, in several plant species. The discovery and application of SNPs increased our knowledge about genetic diversity and a better understanding on crop improvement. Natural breeding process which takes an agelong time during collecting, cultivating, and domestication has been accelerated by detecting dozens of SNPs on various species using advanced biotechnological techniques such as next-generation sequencing. This will result in the improvement of economically important traits. Therefore, we would like to focus on the discovery, current technologies, and applications of SNPs in breeding. The chapter covers the following topics: (1) introduction, (2) application of SNPs, (3) techniques to detect SNPs, (4) importance of SNPs for crop improvement, and (5) conclusion.",book:{id:"7947",slug:"the-recent-topics-in-genetic-polymorphisms",title:"The Recent Topics in Genetic Polymorphisms",fullTitle:"The Recent Topics in Genetic Polymorphisms"},signatures:"Hande Morgil, Yusuf Can Gercek and Isil Tulum",authors:null}],mostDownloadedChaptersLast30Days:[{id:"75504",title:"Introductory Chapter: Genetic Variation - The Source of Biological Diversity",slug:"introductory-chapter-genetic-variation-the-source-of-biological-diversity",totalDownloads:420,totalCrossrefCites:0,totalDimensionsCites:0,abstract:null,book:{id:"9743",slug:"genetic-variation",title:"Genetic Variation",fullTitle:"Genetic Variation"},signatures:"Rafael Trindade Maia and Magnólia de Araújo Campos",authors:[{id:"212393",title:"Prof.",name:"Rafael",middleName:"Trindade",surname:"Trindade Maia",slug:"rafael-trindade-maia",fullName:"Rafael Trindade Maia"},{id:"344747",title:"Associate Prof.",name:"Magnólia",middleName:"De Araújo",surname:"de Araújo Campos",slug:"magnolia-de-araujo-campos",fullName:"Magnólia de Araújo Campos"}]},{id:"73657",title:"Potential of Mutation Breeding to Sustain Food Security",slug:"potential-of-mutation-breeding-to-sustain-food-security",totalDownloads:741,totalCrossrefCites:1,totalDimensionsCites:1,abstract:"Mutation is a sudden heritable change in the genetic material of living organism. Spontaneous mutation, the natural process that develops new allele copies of a gene was the only source of genetic diversity until the 20th century. Besides, mutations can also be induced artificially using physical or chemical mutagens. Chemical mutations received popularity due to its efficiency in creating gene mutations contrary to chromosomal changes. Mutation has played a vital role in the improvement of crop productivity and quality, resultantly > 3,000 varieties of 175 plant species have been developed either through direct or indirect induced mutation breeding approaches worldwide. The advances in plant breeding also achieved through molecular marker technology. The in vitro mutagenesis, heavy-ion beam, and space mutation breeding are being efficiently used to create genetic variability to improve various complicated traits in crop plants. In mutation breeding, TILLING (Targeting Induced Local Lesions in Genomes), a more advanced molecular technique is being used to identify specific sequential genomic changes in mutant plants. Therefore, the mutation breeding in combination with molecular techniques could be an efficient tool in plant breeding programs. This chapter will discuss and review the mutation breeding application for the improvement of crop productivity and environmental stresses.",book:{id:"9743",slug:"genetic-variation",title:"Genetic Variation",fullTitle:"Genetic Variation"},signatures:"Arain Saima Mir, Meer Maria, Sajjad Muhammad and Sial Mahboob Ali",authors:[{id:"329068",title:"Dr.",name:"Arain Saima Mir",middleName:null,surname:"Saima Mir",slug:"arain-saima-mir-saima-mir",fullName:"Arain Saima Mir Saima Mir"},{id:"330046",title:"Ms.",name:"Meer",middleName:null,surname:"Maria",slug:"meer-maria",fullName:"Meer Maria"},{id:"330047",title:"Dr.",name:"Sajjad",middleName:null,surname:"Muhammad",slug:"sajjad-muhammad",fullName:"Sajjad Muhammad"},{id:"330048",title:"Dr.",name:"Sial",middleName:null,surname:"Mahboob Ali",slug:"sial-mahboob-ali",fullName:"Sial Mahboob Ali"}]},{id:"65713",title:"Introductory Chapter: Population Genetics - The Evolution Process as a Genetic Function",slug:"introductory-chapter-population-genetics-the-evolution-process-as-a-genetic-function",totalDownloads:2336,totalCrossrefCites:0,totalDimensionsCites:0,abstract:null,book:{id:"6974",slug:"integrated-view-of-population-genetics",title:"Integrated View of Population Genetics",fullTitle:"Integrated View of Population Genetics"},signatures:"Rafael Trindade Maia and Magnólia de Araújo Campos",authors:[{id:"212393",title:"Prof.",name:"Rafael",middleName:"Trindade",surname:"Trindade Maia",slug:"rafael-trindade-maia",fullName:"Rafael Trindade Maia"}]},{id:"71577",title:"Single Nucleotide Polymorphisms (SNPs) in Plant Genetics and Breeding",slug:"single-nucleotide-polymorphisms-snps-in-plant-genetics-and-breeding",totalDownloads:1492,totalCrossrefCites:8,totalDimensionsCites:10,abstract:"Recent advances in genome technology revealed various single nucleotide polymorphisms (SNPs), the most common form of DNA sequence variation between alleles, in several plant species. The discovery and application of SNPs increased our knowledge about genetic diversity and a better understanding on crop improvement. Natural breeding process which takes an agelong time during collecting, cultivating, and domestication has been accelerated by detecting dozens of SNPs on various species using advanced biotechnological techniques such as next-generation sequencing. This will result in the improvement of economically important traits. Therefore, we would like to focus on the discovery, current technologies, and applications of SNPs in breeding. The chapter covers the following topics: (1) introduction, (2) application of SNPs, (3) techniques to detect SNPs, (4) importance of SNPs for crop improvement, and (5) conclusion.",book:{id:"7947",slug:"the-recent-topics-in-genetic-polymorphisms",title:"The Recent Topics in Genetic Polymorphisms",fullTitle:"The Recent Topics in Genetic Polymorphisms"},signatures:"Hande Morgil, Yusuf Can Gercek and Isil Tulum",authors:null},{id:"71702",title:"Single-Nucleotide Polymorphisms in Inflammatory Bowel Disease",slug:"single-nucleotide-polymorphisms-in-inflammatory-bowel-disease",totalDownloads:975,totalCrossrefCites:0,totalDimensionsCites:0,abstract:"Inflammatory bowel disease (IBD) mainly includes ulcerative colitis (UC) and Crohn’s disease (CD). Both conditions are characterized by chronic inflammation of the gastrointestinal tract, with alternating periods of relapse and remission. Both forms of IBD involve an uncontrolled inflammatory process in the intestines, leading to worsening quality of life and requiring long-term medical and/or surgical intervention. Epidemiological and clinical studies suggest that the pathogenesis of inflammatory bowel disease is strongly linked to genetic predisposition. CD and UC are considered polygenic diseases in which familial clustering is observed in 5–10% of patients. Among genetic factors associated with IBD development, it has been found that many single nucleotide polymorphisms are associated with susceptibility to IBD progression. SNP can affect the production or function of a protein and thus affect the development of the disease. However, although the overall role of genes involved in the development of IBD is already in most cases known, as of today it is unclear how the SNPs in these genes affect cellular function, or how such changed cellular functions would contribute to the development of IBD. In the present work several selected polymorphisms in genes involved in IBD development are discussed.",book:{id:"7947",slug:"the-recent-topics-in-genetic-polymorphisms",title:"The Recent Topics in Genetic Polymorphisms",fullTitle:"The Recent Topics in Genetic Polymorphisms"},signatures:"Ewa Dudzińska",authors:null}],onlineFirstChaptersFilter:{topicId:"61",limit:6,offset:0},onlineFirstChaptersCollection:[],onlineFirstChaptersTotal:0},preDownload:{success:null,errors:{}},subscriptionForm:{success:null,errors:{}},aboutIntechopen:{},privacyPolicy:{},peerReviewing:{},howOpenAccessPublishingWithIntechopenWorks:{},sponsorshipBooks:{sponsorshipBooks:[],offset:8,limit:8,total:0},allSeries:{pteSeriesList:[{id:"14",title:"Artificial Intelligence",numberOfPublishedBooks:9,numberOfPublishedChapters:87,numberOfOpenTopics:6,numberOfUpcomingTopics:0,issn:"2633-1403",doi:"10.5772/intechopen.79920",isOpenForSubmission:!0},{id:"7",title:"Biomedical Engineering",numberOfPublishedBooks:12,numberOfPublishedChapters:99,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2631-5343",doi:"10.5772/intechopen.71985",isOpenForSubmission:!0}],lsSeriesList:[{id:"11",title:"Biochemistry",numberOfPublishedBooks:27,numberOfPublishedChapters:289,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2632-0983",doi:"10.5772/intechopen.72877",isOpenForSubmission:!0},{id:"25",title:"Environmental Sciences",numberOfPublishedBooks:1,numberOfPublishedChapters:9,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2754-6713",doi:"10.5772/intechopen.100362",isOpenForSubmission:!0},{id:"10",title:"Physiology",numberOfPublishedBooks:11,numberOfPublishedChapters:139,numberOfOpenTopics:4,numberOfUpcomingTopics:0,issn:"2631-8261",doi:"10.5772/intechopen.72796",isOpenForSubmission:!0}],hsSeriesList:[{id:"3",title:"Dentistry",numberOfPublishedBooks:8,numberOfPublishedChapters:129,numberOfOpenTopics:0,numberOfUpcomingTopics:2,issn:"2631-6218",doi:"10.5772/intechopen.71199",isOpenForSubmission:!1},{id:"6",title:"Infectious Diseases",numberOfPublishedBooks:13,numberOfPublishedChapters:108,numberOfOpenTopics:3,numberOfUpcomingTopics:1,issn:"2631-6188",doi:"10.5772/intechopen.71852",isOpenForSubmission:!0},{id:"13",title:"Veterinary Medicine and Science",numberOfPublishedBooks:11,numberOfPublishedChapters:104,numberOfOpenTopics:3,numberOfUpcomingTopics:0,issn:"2632-0517",doi:"10.5772/intechopen.73681",isOpenForSubmission:!0}],sshSeriesList:[{id:"22",title:"Business, Management and Economics",numberOfPublishedBooks:1,numberOfPublishedChapters:12,numberOfOpenTopics:2,numberOfUpcomingTopics:1,issn:"2753-894X",doi:"10.5772/intechopen.100359",isOpenForSubmission:!0},{id:"23",title:"Education and Human Development",numberOfPublishedBooks:0,numberOfPublishedChapters:0,numberOfOpenTopics:2,numberOfUpcomingTopics:0,issn:null,doi:"10.5772/intechopen.100360",isOpenForSubmission:!1},{id:"24",title:"Sustainable Development",numberOfPublishedBooks:0,numberOfPublishedChapters:12,numberOfOpenTopics:4,numberOfUpcomingTopics:1,issn:null,doi:"10.5772/intechopen.100361",isOpenForSubmission:!0}],testimonialsList:[{id:"6",text:"It is great to work with the IntechOpen to produce a worthwhile collection of research that also becomes a great educational resource and guide for future research endeavors.",author:{id:"259298",name:"Edward",surname:"Narayan",institutionString:null,profilePictureURL:"https://mts.intechopen.com/storage/users/259298/images/system/259298.jpeg",slug:"edward-narayan",institution:{id:"3",name:"University of Queensland",country:{id:null,name:"Australia"}}}},{id:"13",text:"The collaboration with and support of the technical staff of IntechOpen is fantastic. The whole process of submitting an article and editing of the submitted article goes extremely smooth and fast, the number of reads and downloads of chapters is high, and the contributions are also frequently cited.",author:{id:"55578",name:"Antonio",surname:"Jurado-Navas",institutionString:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRisIQAS/Profile_Picture_1626166543950",slug:"antonio-jurado-navas",institution:{id:"720",name:"University of Malaga",country:{id:null,name:"Spain"}}}}]},series:{item:{id:"10",title:"Physiology",doi:"10.5772/intechopen.72796",issn:"2631-8261",scope:"Modern physiology requires a comprehensive understanding of the integration of tissues and organs throughout the mammalian body, including the cooperation between structure and function at the cellular and molecular levels governed by gene and protein expression. While a daunting task, learning is facilitated by identifying common and effective signaling pathways mediated by a variety of factors employed by nature to preserve and sustain homeostatic life. \r\nAs a leading example, the cellular interaction between intracellular concentration of Ca+2 increases, and changes in plasma membrane potential is integral for coordinating blood flow, governing the exocytosis of neurotransmitters, and modulating gene expression and cell effector secretory functions. Furthermore, in this manner, understanding the systemic interaction between the cardiovascular and nervous systems has become more important than ever as human populations' life prolongation, aging and mechanisms of cellular oxidative signaling are utilised for sustaining life. \r\nAltogether, physiological research enables our identification of distinct and precise points of transition from health to the development of multimorbidity throughout the inevitable aging disorders (e.g., diabetes, hypertension, chronic kidney disease, heart failure, peptic ulcer, inflammatory bowel disease, age-related macular degeneration, cancer). 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His primary area of interest is physiology and pathophysiology of the gastrointestinal (GI) tract, with the major focus on the mechanism of GI mucosal defense, protection, and ulcer healing. He was a postdoctoral NIH fellow at the University of California and the Gastroenterology VA Medical Center, Irvine, Long Beach, CA, USA, and at the Gastroenterology Clinics Erlangen-Nuremberg and Munster in Germany. He has published 290 original articles in some of the most prestigious scientific journals and seven book chapters on the pathophysiology of the GI tract, gastroprotection, ulcer healing, drug therapy of peptic ulcers, hormonal regulation of the gut, and inflammatory bowel disease.",institutionString:null,institution:{name:"Jagiellonian University",institutionURL:null,country:{name:"Poland"}}},editorTwo:null,editorThree:null},subseries:{paginationCount:4,paginationItems:[{id:"10",title:"Animal Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/10.jpg",isOpenForSubmission:!0,annualVolume:11406,editor:{id:"202192",title:"Dr.",name:"Catrin",middleName:null,surname:"Rutland",slug:"catrin-rutland",fullName:"Catrin Rutland",profilePictureURL:"https://mts.intechopen.com/storage/users/202192/images/system/202192.png",biography:"Catrin Rutland is an Associate Professor of Anatomy and Developmental Genetics at the University of Nottingham, UK. She obtained a BSc from the University of Derby, England, a master’s degree from Technische Universität München, Germany, and a Ph.D. from the University of Nottingham. She undertook a post-doctoral research fellowship in the School of Medicine before accepting tenure in Veterinary Medicine and Science. Dr. Rutland also obtained an MMedSci (Medical Education) and a Postgraduate Certificate in Higher Education (PGCHE). She is the author of more than sixty peer-reviewed journal articles, twelve books/book chapters, and more than 100 research abstracts in cardiovascular biology and oncology. She is a board member of the European Association of Veterinary Anatomists, Fellow of the Anatomical Society, and Senior Fellow of the Higher Education Academy. 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From\r\n1964 to 1974, he worked as Assistant in Biochemistry at the School of MedicineUniversidad Nacional de La Plata, Argentina. From 1974 to 1976, he was a Fellowof the National Institutes of Health (NIH) at the University of Connecticut, Health Center, USA. From 1985 to 2004, he served as a Full Professor oBiochemistry at the Universidad Nacional de La Plata, Argentina. He is Member ofthe National Research Council (CONICET), Argentina, and Argentine Society foBiochemistry and Molecular Biology (SAIB). His laboratory has been interested for manyears in the lipid peroxidation of biological membranes from various tissues and different species. Professor Catalá has directed twelve doctoral theses, publishedover 100 papers in peer reviewed journals, several chapters in books andtwelve edited books. Angel Catalá received awards at the 40th InternationaConference Biochemistry of Lipids 1999: Dijon (France). W inner of the Bimbo PanAmerican Nutrition, Food Science and Technology Award 2006 and 2012, South AmericaHuman Nutrition, Professional Category. 2006 award in pharmacology, Bernardo\r\nHoussay, in recognition of his meritorious works of research. Angel Catalá belongto the Editorial Board of Journal of lipids, International Review of Biophysical ChemistryFrontiers in Membrane Physiology and Biophysics, World Journal oExperimental Medicine and Biochemistry Research International, W orld Journal oBiological Chemistry, Oxidative Medicine and Cellular Longevity, Diabetes and thePancreas, International Journal of Chronic Diseases & Therapy, International Journal oNutrition, Co-Editor of The Open Biology Journal.",institutionString:null,institution:{name:"National University of La Plata",institutionURL:null,country:{name:"Argentina"}}},editorTwo:null,editorThree:null},{id:"12",title:"Human Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/12.jpg",isOpenForSubmission:!0,annualVolume:11408,editor:{id:"195829",title:"Prof.",name:"Kunihiro",middleName:null,surname:"Sakuma",slug:"kunihiro-sakuma",fullName:"Kunihiro Sakuma",profilePictureURL:"https://mts.intechopen.com/storage/users/195829/images/system/195829.jpg",biography:"Professor Kunihiro Sakuma, Ph.D., currently works in the Institute for Liberal Arts at the Tokyo Institute of Technology. He is a physiologist working in the field of skeletal muscle. He was awarded his sports science diploma in 1995 by the University of Tsukuba and began his scientific work at the Department of Physiology, Aichi Human Service Center, focusing on the molecular mechanism of congenital muscular dystrophy and normal muscle regeneration. His interest later turned to the molecular mechanism and attenuating strategy of sarcopenia (age-related muscle atrophy). His opinion is to attenuate sarcopenia by improving autophagic defects using nutrient- and pharmaceutical-based treatments.",institutionString:null,institution:{name:"Tokyo Institute of Technology",institutionURL:null,country:{name:"Japan"}}},editorTwo:null,editorThree:{id:"331519",title:"Dr.",name:"Kotomi",middleName:null,surname:"Sakai",slug:"kotomi-sakai",fullName:"Kotomi Sakai",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000031QtFXQA0/Profile_Picture_1637053227318",biography:"Senior researcher Kotomi Sakai, Ph.D., MPH, works at the Research Organization of Science and Technology in Ritsumeikan University. She is a researcher in the geriatric rehabilitation and public health field. She received Ph.D. from Nihon University and MPH from St.Luke’s International University. Her main research interest is sarcopenia in older adults, especially its association with nutritional status. Additionally, to understand how to maintain and improve physical function in older adults, to conduct studies about the mechanism of sarcopenia and determine when possible interventions are needed.",institutionString:null,institution:{name:"Ritsumeikan University",institutionURL:null,country:{name:"Japan"}}}},{id:"13",title:"Plant Physiology",coverUrl:"https://cdn.intechopen.com/series_topics/covers/13.jpg",isOpenForSubmission:!0,annualVolume:11409,editor:{id:"332229",title:"Prof.",name:"Jen-Tsung",middleName:null,surname:"Chen",slug:"jen-tsung-chen",fullName:"Jen-Tsung Chen",profilePictureURL:"https://mts.intechopen.com/storage/users/332229/images/system/332229.png",biography:"Dr. Jen-Tsung Chen is currently a professor at the National University of Kaohsiung, Taiwan. He teaches cell biology, genomics, proteomics, medicinal plant biotechnology, and plant tissue culture. Dr. Chen\\'s research interests include bioactive compounds, chromatography techniques, in vitro culture, medicinal plants, phytochemicals, and plant biotechnology. He has published more than ninety scientific papers and serves as an editorial board member for Plant Methods, Biomolecules, and International Journal of Molecular Sciences.",institutionString:"National University of Kaohsiung",institution:{name:"National University of Kaohsiung",institutionURL:null,country:{name:"Taiwan"}}},editorTwo:null,editorThree:null}]},overviewPageOFChapters:{paginationCount:17,paginationItems:[{id:"81791",title:"Self-Supervised Contrastive Representation Learning in Computer Vision",doi:"10.5772/intechopen.104785",signatures:"Yalin Bastanlar and Semih Orhan",slug:"self-supervised-contrastive-representation-learning-in-computer-vision",totalDownloads:12,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Pattern Recognition - New Insights",coverURL:"https://cdn.intechopen.com/books/images_new/11442.jpg",subseries:{id:"26",title:"Machine Learning and Data Mining"}}},{id:"79345",title:"Application of Jump Diffusion Models in Insurance Claim Estimation",doi:"10.5772/intechopen.99853",signatures:"Leonard Mushunje, Chiedza Elvina Mashiri, Edina Chandiwana and Maxwell Mashasha",slug:"application-of-jump-diffusion-models-in-insurance-claim-estimation-1",totalDownloads:2,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Data Clustering",coverURL:"https://cdn.intechopen.com/books/images_new/10820.jpg",subseries:{id:"26",title:"Machine Learning and Data Mining"}}},{id:"81557",title:"Object Tracking Using Adapted Optical Flow",doi:"10.5772/intechopen.102863",signatures:"Ronaldo Ferreira, Joaquim José de Castro Ferreira and António José Ribeiro Neves",slug:"object-tracking-using-adapted-optical-flow",totalDownloads:10,totalCrossrefCites:0,totalDimensionsCites:0,authors:null,book:{title:"Information Extraction and Object Tracking in Digital Video",coverURL:"https://cdn.intechopen.com/books/images_new/10652.jpg",subseries:{id:"24",title:"Computer Vision"}}},{id:"81558",title:"Thresholding Image Techniques for Plant Segmentation",doi:"10.5772/intechopen.104587",signatures:"Miguel Ángel Castillo-Martínez, Francisco Javier Gallegos-Funes, Blanca E. Carvajal-Gámez, Guillermo Urriolagoitia-Sosa and Alberto J. 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