Heather McDermid
Affiliations: | Biological Sciences | University of Alberta, Edmonton, Alberta, Canada |
Area:
Molecular Biology, Genetics, Evolution and Development BiologyGoogle:
"Heather McDermid"Children
Sign in to add trainee| Graham S. Banting | grad student | 2003 | University of Alberta |
| Nicholas A. Fairbridge | grad student | 2013 | University of Alberta |
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Publications
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| Norton KA, Humphreys R, Weatherill C, et al. (2021) Subfertility in young male mice mutant for chromatin remodeler CECR2. Reproduction (Cambridge, England) |
| Niri F, Terpstra A, Lim KRQ, et al. (2021) Chromatin remodeling factor CECR2 forms tissue-specific complexes with CCAR2 and LUZP1. Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire |
| Dicipulo R, Norton KA, Fairbridge NA, et al. (2021) Cecr2 mutant mice as a model for human cat eye syndrome. Scientific Reports. 11: 3111 |
| Leduc RY, Singh P, McDermid HE. (2016) Genetic backgrounds and modifier genes of NTD mouse models: An opportunity for greater understanding of the multifactorial etiology of neural tube defects. Birth Defects Research. Part a, Clinical and Molecular Teratology |
| Thompson PJ, Norton KA, Niri FH, et al. (2012) CECR2 is involved in spermatogenesis and forms a complex with SNF2H in the testis. Journal of Molecular Biology. 415: 793-806 |
| Kooistra MK, Leduc RY, Dawe CE, et al. (2012) Strain-specific modifier genes of Cecr2-associated exencephaly in mice: genetic analysis and identification of differentially expressed candidate genes. Physiological Genomics. 44: 35-46 |
| Phelan K, McDermid HE. (2012) The 22q13.3 deletion syndrome (Phelan-McDermid syndrome) Molecular Syndromology. 2: 186-201 |
| Dawe CE, Kooistra MK, Fairbridge NA, et al. (2011) Role of chromatin remodeling gene Cecr2 in neurulation and inner ear development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 240: 372-83 |
| Fairbridge NA, Dawe CE, Niri FH, et al. (2010) Cecr2 mutations causing exencephaly trigger misregulation of mesenchymal/ectodermal transcription factors. Birth Defects Research. Part a, Clinical and Molecular Teratology. 88: 619-25 |
| Wilson HL, Crolla JA, Walker D, et al. (2008) Interstitial 22q13 deletions: genes other than SHANK3 have major effects on cognitive and language development. European Journal of Human Genetics : Ejhg. 16: 1301-10 |