Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Magdalena Jagla"'
Autor:
Constance A. Mitchell, Natalie Burden, Mark Bonnell, Markus Hecker, Thomas H. Hutchinson, Magdalena Jagla, Carlie A. LaLone, Laurent Lagadic, Scott G. Lynn, Bryon Shore, You Song, Sara M. Vliet, James R. Wheeler, Michelle R. Embry
Publikováno v:
Environmental Toxicology and Chemistry
Multiple in vivo test guidelines focusing on the estrogen, androgen, thyroid, and steroidogenesis pathways have been developed and validated for mammals, amphibians, or fish. However, these tests are resource-intensive and often use a large number of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3fe71b43572cb1eb48029a65c51c0f3
https://hdl.handle.net/11250/3063129
https://hdl.handle.net/11250/3063129
Autor:
Nathalie G. Bérubé, Marie Mangelsdorf, Magdalena Jagla, Jackie Vanderluit, David Garrick, Richard J. Gibbons, Douglas R. Higgs, Ruth S. Slack, David J. Picketts
Mutations in genes encoding chromatin-remodeling proteins, such as the ATRX gene, underlie a number of genetic disorders including several X-linked mental retardation syndromes; however, the role of these proteins in normal CNS development is unknown
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca5379c62d793fb5778669ce31c5de0e
https://ora.ox.ac.uk/objects/uuid:3ebc12e6-e4d0-482f-87e5-780bf2114882
https://ora.ox.ac.uk/objects/uuid:3ebc12e6-e4d0-482f-87e5-780bf2114882
Publikováno v:
Environmental Pollution. 158:2733-2737
Herring gulls (Larus argentatus) bioaccumulate mercury (Hg) but it is unknown whether they are exposed at levels of neurological concern. Here we studied brain tissues from gulls at five Great Lakes colonies and one non-Great Lakes colony during spri
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
Autor:
Cecelia Smeenk, Nathalie G. Bérubé, Magdalena Jagla, Yves De Repentigny, Rashmi Kothary, David J. Picketts
Publikováno v:
Scopus-Elsevier
Several X-linked mental retardation syndromes are caused by mutations in the ATRX gene. Common clinical features associated with ATRX mutations include severe mental retardation, characteristic facial anomalies and variable degrees of urogenital defe