Showing results (91-100 of 116) with videos related to
Sort By:
Pageof 12
Genome Biology|December 23, 2008
A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in developmentAlyson Ashe, Daniel K Morgan, Nadia C Whitelaw, et al.Developmental Biology|August 4, 2015
Discovery and characterization of spontaneous mouse models of craniofacial dysmorphologyKristina Palmer, Heather Fairfield, Suhaib Borgeia, et al.International Journal of Molecular Sciences|April 17, 2025
Correction: Kularbkaew et al. Genetic Variants in the <i>TBC1D2B</i> Gene Are Associated with Ramon Syndrome and Hereditary Gingival Fibromatosis. <i>Int. J. Mol. Sci.</i> 2024, <i>25</i>, 8867Thatphicha Kularbkaew, Tipaporn Thongmak, Phan Sandeth, et al.Biorxiv : the Preprint Server for Biology|February 6, 2026
Ift43 Controls the Ciliary Levels of Gli2 and Gli3Michael W Stuck, Mohona Gupta, Luke N Knutson, et al.Proceedings of the National Academy of Sciences of the United States of America|November 7, 2013
X-linked microtubule-associated protein, Mid1, regulates axon developmentTingjia Lu, Renchao Chen, Timothy C Cox, et al.Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|April 20, 2010
Cyclin-dependent kinase-like 5 (CDKL5) mutation screening in Rett syndrome and related disordersRose White, Gladys Ho, Swetlana Schmidt, et al.Nature Communications|January 3, 2024
A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial developmentAndrea Wilderman, Eva D'haene, Machteld Baetens, et al.Brain : a Journal of Neurology|August 28, 2023
Hypomyelination, hypodontia and craniofacial abnormalities in a Polr3b mouse model of leukodystrophyMackenzie A Michell-Robinson, Kristin E N Watt, Vladimir Grouza, et al.Plos Genetics|March 24, 2015
Genome-wide association studies in dogs and humans identify ADAMTS20 as a risk variant for cleft lip and palateZena T Wolf, Harrison A Brand, John R Shaffer, et al.Nature Communications|May 17, 2025
Auricular malformations are driven by copy number variations in a hierarchical enhancer cluster and a dominant enhancer recapitulates human pathogenesisXiaopeng Xu, Qi Chen, Qingpei Huang, et al.Pageof 12