المؤلفون: Jenny van Dongen, Joost H.A. Martens, James E. Barrett, Lee M. Butcher, Edo Vellenga, Ian Dunham, Mattia Frontini, Andrew E. Teschendorff, John Ambrose, Robert Lowe, Dirk S. Paul, Guillaume Bourque, Sadia Saeed, Charles E. Breeze, Jonathan Laperle, Vardhman K. Rakyan, Willem H. Ouwehand, Ewan Birney, Filomena Matarese, Anke K. Bergmann, Hendrik G. Stunnenberg, Pierre-Étienne Jacques, Reiner Siebert, Javier Herrero, Stephan Beck, Kate Downes, Valentina Iotchkova

المساهمون: Paul, Dirk [0000-0002-8230-0116], Frontini, Mattia [0000-0001-8074-6299], Downes, Kate [0000-0003-0366-1579], Ouwehand, Willem [0000-0002-7744-1790], Apollo - University of Cambridge Repository, Biological Psychology, Guided Treatment in Optimal Selected Cancer Patients (GUTS), Stem Cell Aging Leukemia and Lymphoma (SALL)

المصدر: Breeze, C E, Paul, D S, van Dongen, J, Butcher, L M, Ambrose, J C, Barrett, J E, Lowe, R, Rakyan, V K, Iotchkova, V, Frontini, M, Downes, K, Ouwehand, W H, Laperle, J, Jacques, P E, Bourque, G, Bergmann, A K, Siebert, R, Vellenga, E, Saeed, S, Matarese, F, Martens, J H, Stunnenberg, H G, Teschendorff, A E, Herrero, J L, Birney, E, Dunham, I & Beck, S 2016, ' eFORGE: A Tool for Identifying Cell Type-Specific Signal in Epigenomic Data ', Cell Reports, vol. 17, no. 8, pp. 2137-2150 . https://doi.org/10.1016/j.celrep.2016.10.059Test
Cell Reports, 17(8), 2137-2150. Cell Press
Cell Reports
Cell Reports, 17, 2137-2150
Cell Reports, 17, 8, pp. 2137-2150
Cell reports, 17(8), 2137-2150. CELL PRESS

مصطلحات موضوعية: Resource, Epigenomics, 0301 basic medicine, False discovery rate, Multiple Sclerosis, BLOOD, Statistics as Topic, Cell type specific, DNase I hypersensitive sites, Genome-wide association study, Computational biology, Biology, ENCODE, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Humans, REGULATORY DNA, Epigenetics, EPIGENETIC SIGNATURE, Molecular Biology, GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries), Genetics, SJOGRENS-SYNDROME, epigenetics, histone marks, Stem Cells, ASSOCIATION, bioinformatics, DNA Methylation, epigenome-wide association study, CANCER, Disease etiology, FALSE DISCOVERY RATE, RHEUMATOID-ARTHRITIS, 030104 developmental biology, Organ Specificity, Karyotyping, DNA methylation, WIDE DNA METHYLATION, NAIVE CD4+T CELLS, Software, Genome-Wide Association Study, Signal Transduction

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1a1e52e2c2614a6946bb8c084d45ecdTest

المؤلفون: Anke K. Bergmann, Núria Verdaguer-Dot, José I. Martín-Subero, Christiane Pott, Hendrik G. Stunnenberg, Eva Giné, Wolfram Klapper, Itziar Salaverria, Roser Vilarrasa-Blasi, Joost H.A. Martens, Ivo Gut, Paul Flicek, Avik Datta, Giancarlo Castellano, Ana C. Queirós, Marta Kulis, Alba Navarro, Wyndham H. Wilson, María José Calasanz, Reiner Siebert, Armando López-Guillermo, Nuria Russiñol, Pedro Jares, Elias Campo, Anna Enjuanes, Emanuele Raineri, Renée Beekman, Angelika Merkel, Guillem Clot, Inga Vater, Harmen J.G. van de Werken, Simon Heath, Sílvia Beà, Romina Royo, Martí Duran-Ferrer

المساهمون: Cell biology, Urology

المصدر: Cancer Cell, 30, 5, pp. 806-821
Cancer Cell, 30(5), 806-821. Cell Press
Cancer Cell, 30, 806-821

مصطلحات موضوعية: Epigenomics, 0301 basic medicine, Cancer Research, mantle cell lymphoma, lymphoma, Lymphoma, Mantle-Cell, Biology, Article, Epigenesis, Genetic, SOXC Transcription Factors, 03 medical and health sciences, 0302 clinical medicine, Cell Line, Tumor, hemic and lymphatic diseases, SOX11, Humans, Cell Lineage, Computer Simulation, Epigenetics, DNA looping, GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries), RNA-Directed DNA Methylation, Molecular Biology, B-Lymphocytes, High-Throughput Nucleotide Sequencing, Methylation, Cell Biology, DNA Methylation, Molecular biology, Chromatin, ChIP-seq, Gene Expression Regulation, Neoplastic, Enhancer Elements, Genetic, 030104 developmental biology, Differentially methylated regions, Oncology, 030220 oncology & carcinogenesis, DNA methylation, Disease Progression, chromatin, Illumina Methylation Assay, enhancer, whole-genome bisulfite sequencing

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47009c6206375c77f9c779e79533b226Test

المؤلفون: Arturo Borzutzky, Anke K. Bergmann, Brian D. Crompton, Silvia Giliani, Sachin N. Baxi, Madelena Martin, Luigi D. Notarangelo, Ellis J. Neufeld

المصدر: Clinical Immunology. 133:287-294

مصطلحات موضوعية: Male, Cellular immunity, Anemia, T-Lymphocytes, Lymphocyte, Immunology, Leucovorin, Biology, Polymerase Chain Reaction, Article, Immunophenotyping, Hypogammaglobulinemia, Folic Acid, medicine, Humans, Point Mutation, Immunology and Allergy, Immunodeficiency, Severe combined immunodeficiency, Base Sequence, Genetic Variation, Infant, Membrane Transport Proteins, DNA, Normocytic anemia, Flow Cytometry, medicine.disease, medicine.anatomical_structure, Intestinal Absorption, Inborn error of metabolism, Female, Severe Combined Immunodeficiency, Proton-Coupled Folate Transporter

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b927e832b9101dc4a602fe0c80e520aTest
https://doi.org/10.1016/j.clim.2009.08.006Test

المؤلفون: Adam Bagg, Robin Casey, Jill F. Falcone, Inderneel Sahai, Elizabeth O. Hexner, Lulu Mathews, Anke K. Bergmann, Klaas J. Wierenga, Caterina Borgna-Pignati, Luca Fabris, Maria Leticia Ribeiro, Judy Fleming, Ellis J. Neufeld

المصدر: The Journal of Pediatrics. 155:888-892.e1

مصطلحات موضوعية: Adult, Male, Heterozygote, thiamine, megaloblastic anemia, Anemia, Megaloblastic, Deafness, Biology, medicine.disease_cause, Compound heterozygosity, Article, Cohort Studies, Diabetes Mellitus, OMIM : Online Mendelian Inheritance in Man, medicine, Thiamine transporter, Humans, Missense mutation, Allele, Child, Megaloblastic anemia, Genetics, Mutation, Infant, Membrane Transport Proteins, medicine.disease, Phenotype, Child, Preschool, Vitamin B Complex, Pediatrics, Perinatology and Child Health, biology.protein, SLC19A2, Female

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f8d23913e93cac91499dce0d83dc155Test
https://doi.org/10.1016/j.jpeds.2009.06.017Test