المؤلفون: Agnès Linglart, Deborah J G Mackay, Eamonn R. Maher, Karen Grønskov, Irene Netchine, Guiomar Perez de Nanclares, Andrea Riccio, I. Karen Temple, Zeynep Tümer, Thomas Eggermann, Dave Nicholas Monk

المساهمون: Service de néphrologie et pédiatrie générale [CHU Trousseau], Université Pierre et Marie Curie - Paris 6 (UPMC)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU), Rheinisch-Westfälische Technische Hochschule Aachen (RWTH), Centre de Recherche Saint-Antoine (UMRS893), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Molecular (Epi)Genetics Laboratory, Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Center, University of Cambridge [UK] (CAM), Wessex Clinical Genetics Service, School of Medicine, University of Southampton, Princess Anne Hospital, Human Genetics and Genomic Medicine group, Faculty of Medicine, Clinical genetic clinic, Copenhagen University Hospital, Cancer Epigenetics and Biology Program-PEBC, Institut d'Investigació Biomèdica de Bellvitge [Barcelone] (IDIBELL), DISTABiF, Seconda Universita di Napoli, Institute of Genetics and Biophysics—ABT, Service d'endocrinologie et diabétologie pédiatriques - Le Kremlin-Bicêtre, HAL-UPMC, Gestionnaire, Rheinisch-Westfälische Technische Hochschule Aachen University (RWTH), Maher, Eamonn [0000-0002-6226-6918], Apollo - University of Cambridge Repository, CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Eggermann, Thoma, Perez de Nanclares, Guiomar, Maher, Eamonn R, Temple, I. Karen, Tümer, Zeynep, Monk, David, Mackay, Deborah J. G, Grønskov, Karen, Riccio, Andrea, Linglart, Agnè, Netchine, Irène

المصدر: Clinical epigenetics 7, 123 (2015). doi:10.1186/s13148-015-0143-8
Clinical Epigenetics
Clinical Epigenetics, BioMed Central, 2015, 7 (1), pp.123. ⟨10.1186/s13148-015-0143-8⟩
Clinical Epigenetics, 2015, 7 (1), pp.123. ⟨10.1186/s13148-015-0143-8⟩
Clinical epigenetics
7 (2015): 123. doi:10.1186/s13148-015-0143-8
info:cnr-pdr/source/autori:Eggermann T.; Perez de Nanclares G.; Maher E.R.; Temple I.K.; Tumer Z.; Monk D.; Mackay D.J.G.; Gronskov K.; Riccio A.; Linglart A.; Netchine I./titolo:Imprinting disorders: A group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci/doi:10.1186%2Fs13148-015-0143-8/rivista:Clinical epigenetics (Print)/anno:2015/pagina_da:123/pagina_a:/intervallo_pagine:123/volume:7
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona

مصطلحات موضوعية: Imprinted genes, ADN, Review, Disease, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, Biology, DNA sequencing, Imprinting disorder, Imprinted gene, Malalties hereditàries, Genetics, medicine, Epimutation, Epigenetics, Imprinting (psychology), Molecular Biology, Gene, Genetics (clinical), [SDV.MHEP] Life Sciences [q-bio]/Human health and pathology, Uniparental disomy, DNA, medicine.disease, Human genetics, 3. Good health, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Erratum, Genomic imprinting, Genetic disorders, Imprinting disorders, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, Developmental Biology

وصف الملف: text; applicaton/octet-stream; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92c3bad2093372061da365807915ca8e
https://doi.org/10.1186/s13148-015-0143-8

المؤلفون: Wenbin Wei, Paul Nathan, Michael D Brown, Eamonn R. Maher, Christopher J. Ricketts, Salwati Shuib, Dean Gentle, Noel W. Clarke, Farida Latif, Mark R. Morris

المصدر: Clinical Epigenetics
Ricketts, C J, Morris, M R, Gentle, D, Shuib, S, Brown, M, Clarke, N, Wei, W, Nathan, P, Latif, F & Maher, E R 2013, ' Methylation profiling and evaluation of demethylating therapy in renal cell carcinoma ', Clinical Epigenetics, vol. 5, no. 1, 16 . https://doi.org/10.1186/1868-7083-5-16

مصطلحات موضوعية: medicine.medical_treatment, Azacitidine, Bioinformatics, urologic and male genital diseases, Methylation, Targeted therapy, Pathogenesis, Renal cell carcinoma, VHL, Genetics, medicine, Genetics(clinical), Epigenetics, Molecular Biology, Genetics (clinical), business.industry, Research, Chromosome, medicine.disease, Human genetics, female genital diseases and pregnancy complications, Demethylation, Renal cancer, Cancer research, Therapy, business, Developmental Biology, medicine.drug

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::566571ce1837e8f3032f73bcafb06f96