Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Chantal F. Medina"'
Autor:
Valerie A. Wallace, Nathalie G. Bérubé, Richard J. Gibbons, David J. Picketts, Stuart G Coupland, Chantal F. Medina, Yaping Wang, Chantal Mazerolle
Publikováno v:
Biochemistry Publications
ATRX is an SWI/SNF-like chromatin remodeling protein that is mutated in several X-linked mental retardation syndromes, including the ATR-X syndrome. In mice, Atrx expression is widespread and attempts to understand its function in brain development a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03cfca8c4af8e1d731bf124ddaa2eb3b
https://doi.org/10.1093/hmg/ddn424
https://doi.org/10.1093/hmg/ddn424
Autor:
Nathalie G. Bérubé, David J. Picketts, Chantal F. Medina, Jasmine Healy, Shaobo Wu, Magdalena Jagla, Todd Hodgson
Publikováno v:
European Journal of Human Genetics. 16:192-201
ATRX is a SWI/SNF-like chromatin remodeling protein mutated in several X-linked mental retardation syndromes. Gene inactivation studies in mice demonstrate that ATRX is an essential protein and suggest that patient mutations likely retain partial act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31f4274c3ce17f8d5d2dea77ca3129e2
https://doi.org/10.1038/sj.ejhg.5201943
https://doi.org/10.1038/sj.ejhg.5201943
Autor:
Brandon Y. H. Zhao, Keqin Yan, Stuart G Coupland, Adam N. Baker, Catherine Tsilfidis, Pamela S. Lagali, Chantal F. Medina, David J. Picketts, Valerie A. Wallace
Publikováno v:
Human Molecular Genetics. :ddw306
ATRX is a chromatin remodeling protein that is mutated in several intellectual disability disorders including alpha-thalassemia/mental retardation, X-linked (ATR-X) syndrome. We previously reported the prevalence of ophthalmological defects in ATR-X
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fead4530b7841f42b91c95438884b47c
https://doi.org/10.1093/hmg/ddw306
https://doi.org/10.1093/hmg/ddw306
Autor:
Chantal F Medina, Alan J. Mears, David J. Picketts, Pamela S Lagali, Valerie A. Wallace, Keqin Yan
Publikováno v:
Epigenetics & Chromatin
Background Atrx is a member of the SNF2 family of chromatin remodeling proteins that functions by remodeling or repositioning nucleosomes at specific target genes using the energy from ATP hydrolysis. Mutations in the gene encoding Atrx cause the hum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3beb1552b22be931a5ae2f59e01df578
http://europepmc.org/articles/PMC3600692
http://europepmc.org/articles/PMC3600692