Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Christine E. Dawe"'
Publikováno v:
Journal of Molecular Biology. 415:793-806
The regulation of nucleosome positioning and composition by ATP-dependent chromatin remodeling enzymes and their associated binding partners plays important biological roles in mammals. CECR2 is a binding partner to the ISWI (imitation switch) ATPase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::964a23578231ff3c4f769e07de53eb20
https://doi.org/10.1016/j.jmb.2011.11.041
https://doi.org/10.1016/j.jmb.2011.11.041
Autor:
Christine E. Dawe, Heather E. McDermid, Megan K. Kooistra, Amanda C. Pisio, Nicholas A. Fairbridge
Publikováno v:
Developmental Dynamics. 240:372-383
The loss of Cecr2, which encodes a chromatin remodeling protein, has been associated with the neural tube defect (NTD) exencephaly and open eyelids in mice. Here, we show that two independent mutations of Cecr2 are also associated with specific inner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::670aa612fc0209bdab24c8d458ab371f
https://doi.org/10.1002/dvdy.22547
https://doi.org/10.1002/dvdy.22547
Autor:
Heather E. McDermid, Kirst King-Jones, Farshad H. Niri, Christine E. Dawe, Nicholas A. Fairbridge, Megan K. Kooistra
Publikováno v:
Birth Defects Research Part A: Clinical and Molecular Teratology. 88:619-625
BACKGROUND: Over 200 mouse genes are associated with neural tube defects (NTDs), including Cecr2, the bromodomain-containing subunit of the CERF chromatin remodeling complex. METHODS: Gene-trap mutation Cecr2Gt45Bic results in 74% exencephaly (equiva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7c33100bd937fc45a2ad88faf97f924
https://doi.org/10.1002/bdra.20695
https://doi.org/10.1002/bdra.20695
Autor:
Christine E. Dawe, Diana M. Juriloff, Megan K. Kooistra, Renee Y.M. Leduc, Mattea Bujold, Nicholas A. Fairbridge, Jay Rasmussen, Kirst King-Jones, Julie H.Y. Man, Heather E. McDermid
Publikováno v:
Physiological genomics. 44(1)
Although neural tube defects (NTDs) are common in humans, little is known about their multifactorial genetic causes. While most mouse models involve NTDs caused by a single mutated gene, we have previously described a multigenic system involving susc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bbe75eb03ba4d3e8ddf50a1ba5973c6
https://pubmed.ncbi.nlm.nih.gov/22045912
https://pubmed.ncbi.nlm.nih.gov/22045912