-
1
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 PRESSمصطلحات 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
-
2
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