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NICHTS NEUES SCHAFFEN. Perspektiven auf die treue Kopie 1300–1900

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ISBN: 9783110431148 Year: Pages: 316 DOI: 10.1515/9783110431148 Language: German / English
Publisher: De Gruyter
Subject: Arts in general
Added to DOAB on : 2019-11-06 16:06:17
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Faithfulness as a genuine quality of copies

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Copy

The Transformative Power of the Copy. A Transcultural and Interdisciplinary Approach

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Book Series: Heidelberg Studies on Transculturality ISSN: 23657987/eISSN 23657995 ISBN: 9783946054153 9783946054146 9783946054160 Year: Pages: 414 DOI: 10.17885/heiup.195.260 Language: English
Publisher: Heidelberg University Publishing (heiUP)
Subject: Sociology --- History of arts --- Archaeology
Added to DOAB on : 2018-08-06 11:58:34
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This volume offers a fresh perspective on the copy and the practice of copying, two topics that, while the focus of much academic discussion in recent decades, have been underrepresented in the discourse on transculturality. Here, experts from a wide range of academic disciplines present their views on the copy from a transcultural perspective, seeking not to define the copy uniformly, but to reveal its dynamic and transformative power. The copy and the practice of copying are thus presented as constituents of transculturality via thought-provoking contributions on topics spanning time periods from antiquity to the present, and regions from Asia to Europe. In so doing, these contributions aim to create the basis for a novel, interdisciplinary discourse on the copy and its transcultural impact throughout history.

Les spectacles du patrimoine : Sources, exposition, usages

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ISBN: 9791035103064 DOI: 10.4000/books.psorbonne.16647 Language: French
Publisher: Éditions de la Sorbonne
Subject: Arts in general
Added to DOAB on : 2019-12-06 13:15:41
License: OpenEdition Licence for Books

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Ce volume est divisé en deux grandes parties, regroupant sept études approfondies en sciences humaines et sociales. Les auteurs, jeunes chercheurs de haut niveau, ont mené leurs enquêtes de Londres aux pays Baltes, de la Polynésie française au Congo et au Panama, en questionnant les archives et leurs multiples usages, les processus d’exposition et de réception dans les domaines des arts plastiques, du cinéma et du théâtre. Dans le questionnement des dispositifs d’exposition et de leurs versants discursifs, à travers quelques exemples relevant de champs différents (histoire de l’art, histoire du cinéma, histoire sociale), une importance centrale est accordée aux sources et à leurs utilisations. Comment articuler concrètement l’analyse d’une image ou d’une œuvre avec l’examen de la manière dont les acteurs sociaux façonnent le regard pour les futurs spectateurs ? À l’encontre d'une idée reçue qui voudrait que le patrimoine constitue un ensemble donné de biens qu’il s’agirait d’entretenir (ou non), les sujets abordés dans ce volume mettent au contraire en évidence la dimension vivante, active, mouvante des patrimoines concernés – tout en rappelant que cette dimension mouvante n’est ni univoque, ni positive. L’intérêt porté aux processus de fabrication et d’emploi de différents types de patrimoine permettra de mettre en lumière les dynamiques internes à ces ensembles.

The Identification of the Genetic Components of Autism Spectrum Disorders 2017

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ISBN: 9783038425205 9783038425212 Year: Pages: X, 462 Language: English
Publisher: MDPI - Multidisciplinary Digital Publishing Institute
Subject: Biology
Added to DOAB on : 2017-10-27 12:54:46
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This textbook is dedicated to the study of genetic factors contributing to autism and includes a collection of original research and review articles related to this topic. Autism spectrum disorders (ASD) include a collection of neurodevelopmental disorders characterized by three recognized behavioral domains involving difficulties in communication, social interaction and repetitive behavior. ASD affects 1 to 2 percent of children and is on the increase worldwide. Significant genetic contributions and mechanisms underlie the causation of ASD. Advances in genetic technology and better awareness have led to a diagnosis of 50 to 70 percent of individuals with ASD primarily due to chromosomal abnormalities, submicroscopic deletions or duplications now identified with high-resolution microarray analysis, next-generation DNA (exome) sequencing of gene variants or mutations, recognized single gene disorders or metabolic disturbances. Through discovery by searching genomic databases and peer-reviewed research articles, nearly 800 genes have been identified to contribute to ASD. Highlights in the field of autism research, discovery and identification of genetic components with characterization will be addressed. Furthermore, reviews of current understanding of the causes and diagnostic approaches for ASD and related syndromes will be presented along with discussion of psychiatric/behavior comorbidities and related features, environmental risk factors, parental attitudes and treatment.

Faking, Forging, Counterfeiting

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Book Series: Edition Kulturwissenschaft ISBN: 9783837637625 9783839437629 Year: Language: English
Publisher: transcript Verlag Grant: Knowledge Unlatched - 101227
Subject: History
Added to DOAB on : 2018-03-16 11:02:30
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Forgeries are an omnipresent part of our culture. They are closely related to historically and culturally informed ideas of authenticity, legality, authorship, creativity, tradition and innovation. Based on the concept of mimesis, the volume illustrates that forgeries are thus not to be understood as a negative copy or disgraced rip-off of an original – but as an autonomous aesthetic practice, a creative act in itself. The contributions focus on such different implementations such as faked traditions, pseudotranslations, imposters, identity theft, and hoaxes in different arts and historic contexts. Most importantly, they scrutinize the bonds and borders between original and forgery, and turn out their epistemic capability.

Middleware Solutions for Wireless Internet of Things

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ISBN: 9783039210367 / 9783039210374 Year: Pages: 262 DOI: 10.3390/books978-3-03921-037-4 Language: eng
Publisher: MDPI - Multidisciplinary Digital Publishing Institute
Subject: Technology (General) --- General and Civil Engineering
Added to DOAB on : 2019-08-28 11:21:27
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The proliferation of powerful but cheap devices, together with the availability of a plethora of wireless technologies, has pushed for the spread of the Wireless Internet of Things (WIoT), which is typically much more heterogeneous, dynamic, and general-purpose if compared with the traditional IoT. The WIoT is characterized by the dynamic interaction of traditional infrastructure-side devices, e.g., sensors and actuators, provided by municipalities in Smart City infrastructures, and other portable and more opportunistic ones, such as mobile smartphones, opportunistically integrated to dynamically extend and enhance the WIoT environment. A key enabler of this vision is the advancement of software and middleware technologies in various mobile-related sectors, ranging from the effective synergic management of wireless communications to mobility/adaptivity support in operating systems and differentiated integration and management of devices with heterogeneous capabilities in middleware, from horizontal support to crowdsourcing in different application domains to dynamic offloading to cloud resources, only to mention a few. The book presents state-of-the-art contributions in the articulated WIoT area by providing novel insights about the development and adoption of middleware solutions to enable the WIoT vision in a wide spectrum of heterogeneous scenarios, ranging from industrial environments to educational devices. The presented solutions provide readers with differentiated point of views, by demonstrating how the WIoT vision can be applied to several aspects of our daily life in a pervasive manner.

Application of Bioinformatics in Cancers

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ISBN: 9783039217885 / 9783039217892 Year: Pages: 418 DOI: 10.3390/books978-3-03921-789-2 Language: eng
Publisher: MDPI - Multidisciplinary Digital Publishing Institute
Subject: Technology (General) --- Biotechnology
Added to DOAB on : 2019-12-09 11:49:16
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This collection of 25 research papers comprised of 22 original articles and 3 reviews is brought together from international leaders in bioinformatics and biostatistics. The collection highlights recent computational advances that improve the ability to analyze highly complex data sets to identify factors critical to cancer biology. Novel deep learning algorithms represent an emerging and highly valuable approach for collecting, characterizing and predicting clinical outcomes data. The collection highlights several of these approaches that are likely to become the foundation of research and clinical practice in the future. In fact, many of these technologies reveal new insights about basic cancer mechanisms by integrating data sets and structures that were previously immiscible.

Keywords

comorbidity score --- mortality --- locoregionally advanced --- HNSCC --- curative surgery --- traditional Chinese medicine --- health strengthening herb --- cancer treatment --- network pharmacology --- network target --- high-throughput analysis --- brain metastases --- colorectal cancer --- KRAS mutation --- PD-L1 --- tumor infiltrating lymphocytes --- drug resistance --- gefitinib --- erlotinib --- biostatistics --- bioinformatics --- Bufadienolide-like chemicals --- molecular mechanism --- anti-cancer --- bioinformatics --- cancer --- brain --- pathophysiology --- imaging --- machine learning --- extreme learning --- deep learning --- neurological disorders --- pancreatic cancer --- TCGA --- curation --- DNA --- RNA --- protein --- single-biomarkers --- multiple-biomarkers --- cancer-related pathways --- colorectal cancer --- DNA sequence profile --- Monte Carlo --- mixture of normal distributions --- somatic mutation --- tumor --- mutable motif --- activation induced deaminase --- AID/APOBEC --- transcriptional signatures --- copy number variation --- copy number aberration --- TCGA mining --- cancer CRISPR --- firehose --- gene signature extraction --- gene loss biomarkers --- gene inactivation biomarkers --- biomarker discovery --- chemotherapy --- microarray --- ovarian cancer --- predictive model --- machine learning --- overall survival --- observed survival interval --- skin cutaneous melanoma --- The Cancer Genome Atlas --- omics --- breast cancer prognosis --- artificial intelligence --- machine learning --- decision support systems --- cancer prognosis --- independent prognostic power --- omics profiles --- histopathological imaging features --- cancer --- intratumor heterogeneity --- genomic instability --- epigenetics --- mitochondrial metabolism --- miRNAs --- cancer biomarkers --- breast cancer detection --- machine learning --- feature selection --- classification --- denoising autoencoders --- breast cancer --- feature extraction and interpretation --- concatenated deep feature --- cancer modeling --- interaction --- histopathological imaging --- clinical/environmental factors --- oral cancer --- miRNA --- bioinformatics --- datasets --- biomarkers --- TCGA --- GEO DataSets --- hormone sensitive cancers --- breast cancer --- StAR --- estrogen --- steroidogenic enzymes --- hTERT --- telomerase --- telomeres --- alternative splicing --- network analysis --- hierarchical clustering analysis --- differential gene expression analysis --- cancer biomarker --- diseases genes --- variable selection --- false discovery rate --- knockoffs --- bioinformatics --- copy number variation --- cell-free DNA --- methylation --- mutation --- next generation sequencing --- self-organizing map --- head and neck cancer --- treatment de-escalation --- HP --- molecular subtypes --- tumor microenvironment --- Bioinformatics tool --- R package --- machine learning --- meta-analysis --- biomarker signature --- gene expression analysis --- survival analysis --- functional analysis --- bioinformatics --- machine learning --- artificial intelligence --- Network Analysis --- single-cell sequencing --- circulating tumor DNA (ctDNA) --- Neoantigen Prediction --- precision medicine --- Computational Immunology

Evolution, Composition and Regulation of Supernumerary B Chromosomes

Authors: --- --- ---
ISBN: 9783038977865 / 9783038977872 Year: Pages: 254 DOI: 10.3390/books978-3-03897-787-2 Language: eng
Publisher: MDPI - Multidisciplinary Digital Publishing Institute
Subject: Science (General) --- Biology
Added to DOAB on : 2019-08-28 11:21:28
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Supernumerary B chromosomes (Bs) are dispensable genetic elements found in thousands of species of plants and animals, and some fungi. Since their discovery more than a century ago, they have been a source of puzzlement, as they only occur in some members of a population and are absent from others. When they do occur, they are often harmful, and in the absence of “selfishness”, based on mechanisms of mitotic and meiotic drive, there appears to be no obvious reason for their existence. Cytogeneticists have long wrestled with questions about the biological existence of these enigmatic elements, including their lack of any adaptive properties, apparent absence of functional genes, their origin, sequence organization, and co-evolution as nuclear parasites. Emerging new technologies are now enabling researchers to step up a gear, to look enthusiastically beyond the previous limits of the horizon, and to uncover the secrets of these “silent” chromosomes. This book provides a comprehensive guide to theoretical advancements in the field of B chromosome research in both animal and plant systems.

Keywords

repetitive elements --- RNA-Seq --- genomics --- evolution --- cytogenetics --- supernumerary elements --- extra chromosomes --- B chromosomes --- transmission --- drive --- host/parasite interaction --- supernumerary chromosomes --- karyotype evolution --- genome instability --- supernumerary chromosomes --- heterochromatin --- parent-of-origin effects --- paternal X chromosome --- maternal X chromosome --- controlling element --- teleost --- population analysis --- whole genome resequencing --- DNA copy number variation --- ribosomal DNA --- B chromosomes --- FISH (fluorescence in situ hybridisation) --- GISH (genomic in situ hybridisation) --- Prospero autumnale complex --- supernumerary chromosomal segments (SCS) evolution --- tandem repeats --- Drosophila --- supernumerary --- satellite DNA --- sSMC --- B chromosomes --- dot-like (micro) Bs --- karyotypic characteristics --- ?s --- B morphotypes --- Apodemus peninsulae --- maize B chromosome --- centromere --- inactivation --- reactivation --- de novo centromere formation --- epigenetics --- supernumerary chromosomes --- additional chromosomes --- chromosome polymorphism --- evolution --- B chromosomes --- karyotypes --- genome evolution --- interphase nucleus --- mammals --- genes --- repetitive DNA --- transcription of heterochromatin --- B chromosomes --- grasshoppers --- DNA composition --- repeat clusters --- euchromatin degradation --- microdissected DNA probes --- B chromosome --- satellite DNA --- mobile element --- organelle DNA --- chromosome evolution --- fluorescent in situ hybridization --- Orthoptera --- satellite DNA --- supernumerary chromosome --- RepeatExplorer --- supernumerary chromosomes --- B chromosomes --- next-generation sequencing --- coverage ratio analysis --- n/a --- B chromosome --- transmission --- origin --- drive --- n/a

Cell-Free Nucleic Acids

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ISBN: 9783039280742 / 9783039280759 Year: Pages: 248 DOI: 10.3390/books978-3-03928-075-9 Language: eng
Publisher: MDPI - Multidisciplinary Digital Publishing Institute
Subject: Medicine (General)
Added to DOAB on : 2020-01-30 16:39:46
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The deficits of mammography and the potential of noninvasive diagnostic testing using circulating miRNA profiles are presented in our first review article. Exosomes are important in the transfer of genetic information. The current knowledge on exosome-associated DNAs and on vesicle-associated DNAs and their role in pregnancy-related complications is presented in the next article. The major obstacle is the lack of a standardized technique for the isolation and measurement of exosomes. One review has summarized the latest results on cell-free nucleic acids in inflammatory bowel disease (IBD). Despite the extensive research, the etiology and exact pathogenesis are still unclear, although similarity to the cell-free ribonucleic acids (cfRNAs) observed in other autoimmune diseases seems to be relevant in IBD. Liquid biopsy is a useful tool for the differentiation of leiomyomas and sarcomas in the corpus uteri. One manuscript has collected the most important knowledge of mesenchymal uterine tumors and shows the benefits of noninvasive sampling. Microchimerism has also recently become a hot topic. It is discussed in the context of various forms of transplantation and transplantation-related advanced therapies, the available cell-free nucleic acid (cfNA) markers, and the detection platforms that have been introduced. Ovarian cancer is one of the leading serious malignancies among women, with a high incidence of mortality; the introduction of new noninvasive diagnostic markers could help in its early detection and treatment monitoring. Epigenetic regulation is very important during the development of diseases and drug resistance. Methylation changes are important signs during ovarian cancer development, and it seems that the CDH1 gene is a potential candidate for being a noninvasive biomarker in the diagnosis of ovarian cancer. Preeclampsia is a mysterious disease—despite intensive research, the exact details of its development are unknown. It seems that cell-free nucleic acids could serve as biomarkers for the early detection of this disease. Three research papers deal with the prenatal application of cfDNA. Copy number variants (CNVs) are important subjects for the study of human genome variations, as CNVs can contribute to population diversity and human genetic diseases. These are useful in NIPT as a source of population specific data. The reliability of NIPT depends on the accurate estimation of fetal fraction. Improvement in the success rate of in vitro fertilization (IVF) and embryo transfer (ET) is an important goal. The measurement of embryo-specific small noncoding RNAs in culture media could improve the efficiency of ET.

Keywords

breast cancer --- screening --- liquid biopsy --- omics --- multi-level diagnostics --- individualized patient profile --- miRNA --- mammography --- predictive and preventive approach --- personalized medicine --- cell-free DNA --- exosomes --- extracellular vesicles --- fetal DNA --- preeclampsia --- growth retardation --- gestational diabetes mellitus --- miRNA --- piRNA --- NGS --- RT-PCR --- embryo culture medium --- C19MC microRNA --- expression --- exosomes --- fetal growth restriction --- gestational hypertension --- plasma --- prediction --- preeclampsia --- pregnancy-related complications --- screening --- non-invasive prenatal testing --- statistical models --- z-score --- cell-free nucleic acids --- circulating nucleic acids --- cell-free DNAs --- cell-free RNAs --- exosomes --- inflammatory bowel disease --- neutrophil extracellular traps --- NETosis --- liquid biopsy --- cell-free nucleic acids --- circulating tumor cells --- leiomyomas --- sarcomas --- leiomyosarcomas --- exosomes --- NIPT --- fetal fraction --- statistical methods --- DNA --- maternal serum screening --- fetal cells --- liquid biopsy --- pyrosequencing --- ovarian cancer --- CDH1 --- PTEN --- PAX1 --- RASSF1 --- cfDNA --- cell-free DNA --- nuclease activity --- aging --- obesity --- gender differences --- copy number variants --- next generation sequencing --- non-invasive prenatal testing --- population study --- microchimerism --- solid organ transplantation --- hematopoietic stem cell transplantation --- genetic marker --- single nucleotide polymorphism --- deletion/insertion polymorphism --- ovarian cancer --- circulating miRNA --- blood plasma --- NanoString --- network analysis --- biomarker --- n/a

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