\\n\\n
More than half of the publishers listed alongside IntechOpen (18 out of 30) are Social Science and Humanities publishers. IntechOpen is an exception to this as a leader in not only Open Access content but Open Access content across all scientific disciplines, including Physical Sciences, Engineering and Technology, Health Sciences, Life Science, and Social Sciences and Humanities.
\\n\\nOur breakdown of titles published demonstrates this with 47% PET, 31% HS, 18% LS, and 4% SSH books published.
\\n\\n“Even though ItechOpen has shown the potential of sci-tech books using an OA approach,” other publishers “have shown little interest in OA books.”
\\n\\nAdditionally, each book published by IntechOpen contains original content and research findings.
\\n\\nWe are honored to be among such prestigious publishers and we hope to continue to spearhead that growth in our quest to promote Open Access as a true pioneer in OA book publishing.
\\n\\n\\n\\n
\\n"}]',published:!0,mainMedia:null},components:[{type:"htmlEditorComponent",content:'
Simba Information has released its Open Access Book Publishing 2020 - 2024 report and has again identified IntechOpen as the world’s largest Open Access book publisher by title count.
\n\nSimba Information is a leading provider for market intelligence and forecasts in the media and publishing industry. The report, published every year, provides an overview and financial outlook for the global professional e-book publishing market.
\n\nIntechOpen, De Gruyter, and Frontiers are the largest OA book publishers by title count, with IntechOpen coming in at first place with 5,101 OA books published, a good 1,782 titles ahead of the nearest competitor.
\n\nSince the first Open Access Book Publishing report published in 2016, IntechOpen has held the top stop each year.
\n\n\n\nMore than half of the publishers listed alongside IntechOpen (18 out of 30) are Social Science and Humanities publishers. IntechOpen is an exception to this as a leader in not only Open Access content but Open Access content across all scientific disciplines, including Physical Sciences, Engineering and Technology, Health Sciences, Life Science, and Social Sciences and Humanities.
\n\nOur breakdown of titles published demonstrates this with 47% PET, 31% HS, 18% LS, and 4% SSH books published.
\n\n“Even though ItechOpen has shown the potential of sci-tech books using an OA approach,” other publishers “have shown little interest in OA books.”
\n\nAdditionally, each book published by IntechOpen contains original content and research findings.
\n\nWe are honored to be among such prestigious publishers and we hope to continue to spearhead that growth in our quest to promote Open Access as a true pioneer in OA book publishing.
\n\n\n\n
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\r\n\tThis book will focus on the wide specter of mucosal inflammation intending to provide the reader with a comprehensive overview of the current knowledge on the topic. More and more studies are focused on finding different aspects of mucosal inflammation since it is involved in the pathogenesis of many diseases - from gut to lungs, urogenital system, etc. To better understand the causes of its occurrence as well as the search for therapeutic strategies, many resources are invested in scientific developments in this field.
\r\n\r\n\tFacts about the role of calprotectin and other biomarkers were accumulated. Participation of neutrophils appears an attractive way to explain the involvement of different subpopulations of immunocompetent cells and cytokines in mucosal inflammation. Over the last five years, scientific developments in the field have discovered more genes involved in the pathogenesis of mucosal inflammation elucidating the interaction of innate immune mechanisms with the microorganisms in the gut and their role in maintaining intestinal homeostasis. Besides, the science aims at identifying and characterizing immune and non-immune cells involved in the emergence and maintenance of chronic inflammation.
\r\n\r\n\tThe book aims to cover the developing diagnostic methods for identifying the mucosal inflammation, towards a better analysis of the inflammation, understanding of the relationship between genetic and proteomic markers and response to therapy; and improving therapeutic options for patients who have mucosal inflammation.
",isbn:null,printIsbn:"979-953-307-X-X",pdfIsbn:null,doi:null,price:0,priceEur:0,priceUsd:0,slug:null,numberOfPages:0,isOpenForSubmission:!1,hash:"2e7bde3621cdf64518356b76e3132542",bookSignature:"Dr. Tsvetelina Velikova",publishedDate:null,coverURL:"https://cdn.intechopen.com/books/images_new/8843.jpg",keywords:"Inflammation, Neutrophils, Cytokines, Mucosal Biomarkers, Gut Tolerance, Antigen Tolerance, Mayo Score, Lesions, Acute Inflammation, Chronic Inflammation, Gut Permeability, Asthma",numberOfDownloads:null,numberOfWosCitations:0,numberOfCrossrefCitations:null,numberOfDimensionsCitations:null,numberOfTotalCitations:null,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"June 16th 2020",dateEndSecondStepPublish:"July 7th 2020",dateEndThirdStepPublish:"September 5th 2020",dateEndFourthStepPublish:"November 24th 2020",dateEndFifthStepPublish:"January 23rd 2021",remainingDaysToSecondStep:"8 months",secondStepPassed:!0,currentStepOfPublishingProcess:5,editedByType:null,kuFlag:!1,biosketch:"Dr. Velikova research focuses on autoimmune disorders, such as celiac disease, IBD, diabetes, asthma, as well as on the delicate autoimmunity mechanisms involving Th17 and Treg cells, cytokines, biomarkers, novel biologic therapies. She has been engaged in fifteen projects in the field of immunology and internal medicine. She is an editorial board member and reviewer for several medical journals and has publications in eminent journals and book chapters in the field of gastrointestinal immunology.",coeditorOneBiosketch:null,coeditorTwoBiosketch:null,coeditorThreeBiosketch:null,coeditorFourBiosketch:null,coeditorFiveBiosketch:null,editors:[{id:"180979",title:"Dr.",name:"Tsvetelina",middleName:null,surname:"Velikova",slug:"tsvetelina-velikova",fullName:"Tsvetelina Velikova",profilePictureURL:"https://mts.intechopen.com/storage/users/180979/images/system/180979.jpg",biography:"Dr. Tsvetelina Velikova received her MD and Ph.D. degrees, both with honors, from the Medical University of Sofia, Bulgaria. Subsequently, she became involved in active immunology research and teaching. Dr. Velikova also received advanced training in Clinical Immunology at University Hospital St. Ivan Rilski, Sofia, Bulgaria. \r\nShe is currently an assistant professor of Clinical immunology affiliated to the Sofia University and University Hospital Lozenetz, Bulgaria. \r\nHer research focuses on autoimmune disorders, such as celiac disease, IBD, diabetes, asthma, as well as on the delicate autoimmunity mechanisms involving Th17 and Treg cells, cytokines, biomarkers, novel biologic therapies and their implication in clinical practice.\r\nDr. Velikova has been engaged in fifteen projects in the field of immunology and internal medicine. 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This requires extensive analysis of developing trends in scientific research in order to offer our readers relevant content. Creating the book catalogue is also based on keeping track of the most read, downloaded and highly cited chapters and books and relaunching similar topics. I am also responsible for consulting with our Scientific Advisors on which book topics to add to our catalogue and sending possible book proposal topics to them for evaluation. Once the catalogue is complete, I contact leading researchers in their respective fields and ask them to become possible Academic Editors for each book project. Once an editor is appointed, I prepare all necessary information required for them to begin their work, as well as guide them through the editorship process. I also assist editors in inviting suitable authors to contribute to a specific book project and each year, I identify and invite exceptional editors to join IntechOpen as Scientific Advisors. 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Venkateswarlu",coverURL:"https://cdn.intechopen.com/books/images_new/371.jpg",editedByType:"Edited by",editors:[{id:"58592",title:"Dr.",name:"Arun",surname:"Shanker",slug:"arun-shanker",fullName:"Arun Shanker"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"878",title:"Phytochemicals",subtitle:"A Global Perspective of Their Role in Nutrition and Health",isOpenForSubmission:!1,hash:"ec77671f63975ef2d16192897deb6835",slug:"phytochemicals-a-global-perspective-of-their-role-in-nutrition-and-health",bookSignature:"Venketeshwer Rao",coverURL:"https://cdn.intechopen.com/books/images_new/878.jpg",editedByType:"Edited by",editors:[{id:"82663",title:"Dr.",name:"Venketeshwer",surname:"Rao",slug:"venketeshwer-rao",fullName:"Venketeshwer Rao"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}},{type:"book",id:"4816",title:"Face Recognition",subtitle:null,isOpenForSubmission:!1,hash:"146063b5359146b7718ea86bad47c8eb",slug:"face_recognition",bookSignature:"Kresimir Delac and Mislav Grgic",coverURL:"https://cdn.intechopen.com/books/images_new/4816.jpg",editedByType:"Edited by",editors:[{id:"528",title:"Dr.",name:"Kresimir",surname:"Delac",slug:"kresimir-delac",fullName:"Kresimir Delac"}],productType:{id:"1",chapterContentType:"chapter",authoredCaption:"Edited by"}}]},chapter:{item:{type:"chapter",id:"66581",title:"Introduction to Recent Advances in Cannabinoid Research",doi:"10.5772/intechopen.85814",slug:"introduction-to-recent-advances-in-cannabinoid-research",body:'\nCannabis sativa has been used medicinally and recreationally for millennia by societies around the world, but our comprehension of Cannabis and cannabinoids from a modern perspective is still very much in its infancy [1]. The field of cannabinoid research has evolved from a curiosity following the first report of the medicinal properties of Cannabis in 1840 [2] to becoming a controlled product in 1925 following the signing of an international treaty controlling its trade [3] to ultimately becoming a highly active basic and clinical research discipline. The psychoactive and intoxicating constituent of Cannabis sativa, ∆9-tetrahydrocannabinol (THC), was first isolated and described by Dr. Raphael Mechoulam in 1964 [4]. Following this discovery, it was not until 1991 that a human cannabinoid receptor—later named the type 1 cannabinoid receptor (CB1R)—was identified, isolated, and cloned [5]. Other components of the endogenous cannabinoid system (ECS) were subsequently identified in rapid succession, including the endogenous cannabinoid anandamide (AEA) and 2-arachidonoylglycerol (2-AG), the type 2 cannabinoid receptor (CB2R), and the anabolic and catabolic enzymes that synthesize and degrade the endogenous cannabinoids, respectively [6]. During this period there was also a rapid growth in tool compounds (synthetic cannabinoids) to study the ECS and a race to understand the physiological and behavioral effects cannabinoids evoke in vivo [7]. With this rapid growth came some of the first modern preclinical and clinical data to suggest clinical efficacy of cannabinoid-based medicines in the treatment of pain, anxiety, addiction, and metabolic disorders [8], as well as preclinical and clinical data that indicated the potential harms associated with Cannabis use, in particular the long-term use of THC in the context of the developing brain [9]. Our understanding of Cannabis sativa itself was also growing during the 1990s and 2000s, with the draft sequence of the genome published in 2011 [10] and more than 220 identified constituents (>100 cannabinoids and >120 terpenes) now identified in the plant [11, 12]. Most recently, several crystal structures of CB1R were solved in 2016 and 2017 by large interdisciplinary research groups [13, 14, 15]. These crystal structures will allow for rational drug design and comprehension of drug-receptor relationships for the first time in the cannabinoid field.
\nAlthough the field of cannabinoid research has seen incredible growth during the past three decades, many questions remain unanswered. As a demonstration of the cannabinoid field’s infancy, the clinically relevant pharmacological effects of morphine have been documented since 1817 [16], and the crystal structure of the μ-opioid receptor was solved in 2012 [17]. The illegal status of Cannabis in most constituencies has represented a significant barrier to basic, epidemiological, and clinical research. However, interest in the potential applications of cannabinoids and their biology has grown tremendously since the discovery of the ECS. What was once a field with a single manuscript in 1964 has now grown to an area averaging 1500 studies per year in a veritable gold rush into a relatively poorly characterized system. With this book, our goal is to highlight the impressive work of some researchers in this field as they address what will become the critical scientific questions of our time concerning Cannabis.
\nThis book presents a collection of chapters addressing important preclinical topics, including the utility of the zebrafish model in cannabinoid research (Chapter 1), insights derived from the structural analysis of CB1R crystal structures (Chapter 2), and the analysis of medical Cannabis quality traits (Chapter 3). Dr. Ellis describes the historical usage of the zebrafish model and its applicability to studies of various aspects of vertebrate and mammalian biology, including neurobiology and neurological disorders, while focusing on the role of the endocannabinoid system. Dr. Al-Zoubi et al. provide an in-depth analysis of the unique aspects of cannabinoid receptors gleaned from studies of hCB1R crystal structures. These authors present an extensive review of studies using mutation and labeling of CB1R to characterize the orthostatic binding site and identify issues with crystal structures that could impact their utility in rational drug design. Dr. Calvi et al. provide a description of state-of-the-art analytical methods used to assess the quality attributes of medical Cannabis products. This is a particularly timely topic as the necessity to characterize Cannabis chemotypes has increased with the recent legalization and regulation of medicinal Cannabis in major markets around the world.
\nThe clinical research described in this book focuses on the clinical effects of Cannabis and cannabinoids on cognition (Chapter 4), the treatment of pain (Chapter 5), Tourette’s syndrome (Chapter 6), Cannabis use disorder and Cannabis withdrawal (Chapters 7 and 8), cannabinoid dosing considerations in pediatric populations (Chapter 9), and Cannabis use for treating pediatric and adult epilepsy (Chapter 10). Dr. Weston-Green provides a comprehensive overview of cannabinoid-dependent effects on cognition, including discussions about (1) the many “lesser-known” plant cannabinoids beyond THC and cannabidiol that have been under-assessed to date and (2) the potential “entourage effects” of cannabinoid combinations occurring in Cannabis products. Dr. Uhelski et al. review the anti-nociceptive properties of cannabinoids and the preclinical as well as clinical evidence for the use of cannabinoids as analgesics for peripheral pain. Cannabis-based medicines (CBM) are presently being examined for a wide array of psychiatric conditions for which the evidence base is small yet growing. Dr. Szejko provides a review of the clinical evidence for CBM in Tourette’s syndrome and the potential mechanisms of action at work for cannabinoids in this disorder. Cannabis and the ECS are now recognized for their potential to treat substance abuse disorders, including opioid addiction and Cannabis use disorder itself. Dr. Balodis et al. provide a comprehensive review of Cannabis use disorder, its epidemiology, potential harms, and other important considerations. Dr. Ferreira et al. review the potential of cannabinoids—including novel bioligands—to treat substance use disorders. At long last, cannabidiol is now recognized and accepted as an anticonvulsant medication for the treatment of refractory pediatric epilepsies, such as Dravet and Lennox-Gastaut syndromes, with the recent FDA approval of Epidiolex® for these conditions. In the final chapters of this book, Dr. Huntsman et al. review the clinical evidence for high-cannabidiol Cannabis herbal extracts for the treatment of pediatric and adult epilepsies, while Dr. Alcorn et al. review critical dosing considerations and pharmacokinetic parameters for Cannabis in the pediatric population.
\nBasic and clinical cannabinoid research has recently become a greater priority due to the increasing number of jurisdictions where legalization of Cannabis use for both medical and recreational purposes has occurred. There have been numerous health claims attributed to Cannabis, and the evidence supporting some of the claims remains inconclusive. According to the conclusion of a report by a Committee On The Health Effects Of Marijuana, the therapeutic benefit of Cannabis on chronic pain, chemotherapy-induced nausea and vomiting, and multiple sclerosis spasticity has been deemed effective, whereas insufficient evidence was available to support a similar conclusion in the treatment of cancer, anorexia and weight loss, irritable bowel syndrome, epilepsy, spinal cord injury-induced spasticity, Tourette’s syndrome, amyotrophic lateral sclerosis, Huntington’s disease, Parkinson’s disease, dystonia, dementia, glaucoma, traumatic brain injury or intracranial hemorrhage, addiction, anxiety, depression, sleep disorders, posttraumatic stress disorder, schizophrenia, and other psychoses [8]. Thus, while tremendous advances have been made in understanding the biology of the ECS and of Cannabis sativa, it is clear that many aspects of the medical use of Cannabis require further clarification. Additionally, there has been a marked increase in the generation of novel synthetic cannabinoids over the last decade [18], the general availability of which has prompted concern among regulatory agencies due to their unknown safety profiles [19, 20]. This is highlighted by the rapidly increasing number of case reports detailing the effects of acute synthetic cannabinoid intoxication [21, 22, 23]. The potential dangers of synthetic cannabinoid use are attributable to the intrinsic properties of these substances and their metabolites. The potential for harm is further exacerbated by the poor pharmacological and toxicological characterization of synthetic cannabinoids. Thus, intensified research efforts into the health benefits and harms of Cannabis and cannabinoids will hasten the positive exploitation of Cannabis and reduce the drawbacks of Cannabis and synthetic cannabinoids.
\nInflammation is a response of vascularized tissues to infections and tissue damage, and contributes to the beginning and progression of diseases such as Alzheimer, type 2 diabetes, obesity, stroke, and cancer [1, 2]. The symptomatology of inflammation is characterized by pain, redness, swelling, heat, and loss of function. Depending on the time of duration, inflammation might be categorized into acute and chronic. Acute inflammation is considered as a protective response and occurs within minutes, hours, or few days after exposure to infections and/or tissue damage. Acute inflammation is characterized by the exudation of fluid (edema), elevated blood flow, and migration of neutrophils [3]. Chronic inflammation occurs when the initial response fails to repair tissue damaged or when a noxious stimulus is persistent, and is characterized with more tissue destruction, fibrosis, long presence of lymphocytes [4]. Macrophages, dendritic cells, and mast cells initiate the inflammatory process secreting pro-inflammatory cytokines such as interleukin 6 (IL-6) and interleukin 8 (IL-8), tumor necrosis factor-α (TNF-α), and inducing the production of reactive oxygen species (ROS), which play an important role in the modulation of inflammation [5]. The long-term use of current drugs for the treatment of inflammation, including nonsteroidal anti-inflammatory drugs (NSAIDs), the disease-modifying anti-rheumatic drugs (DMARDs), and steroids display several undesirable side effects such as gastric ulcers, nephrotoxicity, and hepatotoxicity, among others [6]. The search of new anti-inflammatory agents with less side effects is highly desirable. Furthermore, the efficient treatment of inflammation may be an interesting and effective way to prevent chronic diseases like cancer.
\nNatural products are a good source of anti-inflammatory compounds [7]. Terpenes, containing a C5 isoprene unit, are the large group of natural compounds found mostly in higher plants, but also in lower invertebrates. There are approximately more than 50,000 terpenes that have been isolated from different plant species. Terpenes, composed of isoprene units (C5H8), play a variety of vital roles in plant species, including growth and development and defense against herbivores and environmental stress [8]. Terpenes possess a great variety of biological activities as antimicrobial, against cancer, malaria, and anti-inflammatory effects in acute and chronic inflammatory conditions like chronic obstructive pulmonary disease and osteoarthritis [9, 10].
\nCyperus rotundus, a perennial plant, has several pharmacological activities, including antibacterial [11], antimutagenic [12], and anti-inflammatory [13]. Isocyperol, a sesquiterpene isolated from the rhizomes of C. rotundus, inhibited the production of NO and PGE2, decreased the levels pro-inflammatory interleukins (IL-1β and IL-6) and the monocyte chemotactic protein-1 (MCP-1), and suppressed the gene expression of iNOS and COX-2 in RAW-264 murine macrophages stimulated with lipopolysaccharide (LPS). In addition, isocyperol reduced the serum levels of NO, PGE2, and IL-6 in LPS-induced septic shock in mice, via suppression of the NF-кB and STAT3 signaling pathways [14]. Dodonaea viscosa induces gastroprotective [15], antibacterial [16], analgesic, and anti-inflammatory activities [17, 18]. Hawtriwaic acid, an ent-clerodane diterpene, was isolated from D. viscosa and showed anti-inflammatory activity on the murine ear edema induced with 12-O-tetradecanoylphorbol-13-acetate (TPA) by one or multiple applications. In both models, the compound diminished the edema [19]. Hawtriwaic acid at doses of 5, 10, and 20 mg/kg decreased knee inflammation in a murine model of monoarthritis induced with kaolin/carrageenan, by the reduction of serum levels of the pro-inflammatory interleukins Il-1β, IL-6, and TNF-α, and the increase in the serum levels of the anti-inflammatory interleukin IL-10 [20]. Ursolic acid, a pentacyclic triterpene found in many plant species, was identified for the first time in 1920 in the epicuticular waxes of apples. Ursolic acid exerts cytotoxic effects in various cancer cells by the inhibition of the STAT3 signaling pathway [21] and the induction of apoptosis [22]. Ursolic acid has protective effects on lung, kidney, liver, and brain, exerts anabolic effects on skeletal muscle [23], and induces antinociceptive activity in abdominal constriction test induced by acetic acid and the formalin test in mice [24]. Ursolic acid decreased the paw edema induced with carrageenan in rats [25], decreased the ear edema induced with Croton oil in mice [26], reduced the levels of iNOS, COX-2, IL-1β, IL-6, and TNF-α, and increased the level of IL-10 in macrophages stimulated with LPS [27].
\nThe sesquiterpenes, vernomelitensin and onopordopicrin, isolated from Onopordum illyricum and the triterpene, Sootepin F, obtained from Gardenia sootepensis, decreased each NF-κB activity with IC50 values of 3.6, 8.6, and 20.3 μM, respectively [28, 29].
\nThe pro-inflammatory enzymes: (1) inducible the nitric oxide synthase (iNOS), which is involved in the nitric oxide (NO) production, and the cyclooxygenase-2 (COX-2) involved in the prostaglandin production, are estimated in LPS-induced macrophages to evaluate the in vitro anti-inflammatory activity. IL-1 and TNF-α stimulate the production of NO. The inhibitory concentration 50 (IC50) for these two pro-inflammatory enzymes has only been reported in some studies. The sesquiterpenes hydroxycostunolide (IC50 = 0.68 μM), costunolide (IC50 0.3 μM), and artemorin (IC50 = 0.16 μM), obtained from Inula montana, showed similar or higher potency in the inhibition of NO, compared to that reported for the positive control dexamethasone (IC50 = 0.45–4.33 μM) [30]. Further studies are recommended to be performed with theses sesquiterpenes. Toxicological studies to guarantee their safety in long-term studies are also necessary. The in vivo studies evaluate swelling, redness, and pain mainly in rodents.
\nIn the table is show the structure of 62 sesquiterpenes, 34 diterpenes, and 22 triterpenes with anti-inflammatory activity, isolated from 44 plant species, 1 sponge, and 2 corals.
\nThis book chapter indicates that there has been an increase in the search of terpenes with anti-inflammatory activity in recent years. This fact indicates that terpenes are a topic of interest. The possible mechanisms involved in the anti-inflammatory effects of the terpenes are pointing out on the inhibition of NF-κB, TNF-α, PGE2, and pro-inflammatory cytokines such as IL-6. NF-κB is one of the current targets for the development of new anti-inflammatory drugs [71]. In addition, the molecular targets of terpenes are highly desirable to find target-specific anti-inflammatory drugs. The mechanism of action of many terpenes remains to be studied. The combination of terpenes with high anti-inflammatory activity and with studied mechanism of action and currently used drugs could be another strategy for further anti-inflammatory therapy.
\nGeneral requirements for Open Access to Horizon 2020 research project outputs are found within Guidelines on Open Access to Scientific Publication and Research Data in Horizon 2020. The guidelines, in their simplest form, state that if you are a Horizon 2020 recipient, you must ensure open access to your scientific publications by enabling them to be downloaded, printed and read online. Additionally, said publications must be peer reviewed.
',metaTitle:"Horizon 2020 Compliance",metaDescription:"General requirements for Open Access to Horizon 2020 research project outputs are found within Guidelines on Open Access to Scientific Publication and Research Data in Horizon 2020. The guidelines, in their simplest form, state that if you are a Horizon 2020 recipient, you must ensure open access to your scientific publications by enabling them to be downloaded, printed and read online. Additionally, said publications must be peer reviewed. ",metaKeywords:null,canonicalURL:null,contentRaw:'[{"type":"htmlEditorComponent","content":"Publishing with IntechOpen means that your scientific publications already meet these basic requirements. It also means that through our utilization of open licensing, our publications are also able to be copied, shared, searched, linked, crawled, and mined for text and data, optimizing our authors' compliance as suggested by the European Commission.
\\n\\nMetadata for all publications is also automatically deposited in IntechOpen's OAI repository, making them available through the Open Access Infrastructure for Research in Europe's (OpenAIRE) search interface further establishing our compliance.
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\n\nMetadata for all publications is also automatically deposited in IntechOpen's OAI repository, making them available through the Open Access Infrastructure for Research in Europe's (OpenAIRE) search interface further establishing our compliance.
\n\nIn other words, publishing with IntechOpen guarantees compliance.
\n\nRead more about Open Access in Horizon 2020 here.
\n\nWhich scientific publication to choose?
\n\nWhen choosing a publication, Horizon 2020 grant recipients are encouraged to provide open access to various types of scientific publications including monographs, edited books and conference proceedings.
\n\nIntechOpen publishes all of the aforementioned formats in compliance with the requirements and criteria established by the European Commission for the Horizon 2020 Program.
\n\nAuthors requiring additional information are welcome to send their inquiries to funders@intechopen.com
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