المؤلفون: Oliver A. Kent, Manipa Saha, Etienne Coyaud, Helen E. Burston, Napoleon Law, Keith Dadson, Sujun Chen, Estelle M. Laurent, Jonathan St-Germain, Ren X. Sun, Yoshinori Matsumoto, Justin Cowen, Aaryn Montgomery-Song, Kevin R. Brown, Charles Ishak, Jose La Rose, Daniel D. De Carvalho, Housheng Hansen He, Brian Raught, Filio Billia, Peter Kannu, Robert Rottapel

المصدر: Nature Communications, Vol 11, Iss 1, Pp 1-12 (2020)

مصطلحات موضوعية: Science

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2041-1723Test

الوصول الحر: https://doaj.org/article/7477dd54517347169cc4551af1667746Test

المؤلفون: Helen E. Burston, Oliver A. Kent, Ren X. Sun, Justin Cowen, Daniel D. De Carvalho, Sujun Chen, Jonathan St-Germain, Robert Rottapel, Aaryn Montgomery-Song, Manipa Saha, Yoshinori Matsumoto, Napoleon Law, Housheng Hansen He, Kevin R. Brown, Peter Kannu, Jose La Rose, Keith Dadson, Charles A. Ishak, Filio Billia, Etienne Coyaud, Brian Raught, Estelle M.N. Laurent

المساهمون: University Health Network, Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U 1192 (PRISM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille-Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Toronto General Hospital Research Institute [Canada] (TGHRI), Okayama University, The Hospital for sick children [Toronto] (SickKids), INSERM, Université de Lille, Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192, Toronto General Hospital Research Institute [Canada] [TGHRI], The Hospital for sick children [Toronto] [SickKids]

المصدر: Nature Communications, Vol 11, Iss 1, Pp 1-12 (2020)
Nature Communications
Nature Communications, 2020, Nature Communications, 11 (4673), ⟨10.1038/s41467-020-18483-9⟩

مصطلحات موضوعية: Male, 0301 basic medicine, MAPK/ERK pathway, [SDV]Life Sciences [q-bio], General Physics and Astronomy, Haploinsufficiency, 030105 genetics & heredity, Epigenesis, Genetic, Histones, Hypertelorism, lcsh:Science, Histone Demethylases, Mice, Knockout, Genetics, DNA methylation, Multidisciplinary, Noonan Syndrome, Functional genomics, DNA-Binding Proteins, Sin3 Histone Deacetylase and Corepressor Complex, Mechanisms of disease, Chromosomes, Human, Pair 6, Female, Chromosome Deletion, medicine.symptom, Reprogramming, Cell signalling, Cell signaling, MAP Kinase Signaling System, Science, Biology, RASopathy, Methylation, Article, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, Germline mutation, medicine, Animals, Humans, Abnormalities, Multiple, General Chemistry, medicine.disease, Fibroblast Growth Factors, Mice, Inbred C57BL, 030104 developmental biology, ras Proteins, lcsh:Q, Transcription Factors

وصف الملف: application/octet-stream; application/rdf+xml; charset=utf-8

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c26c38393f0bd745f6a39c677dc7ac5Test
https://doaj.org/article/7477dd54517347169cc4551af1667746Test