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Biology Open|February 18, 2016
Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defectsBrian C Gibbs, Rama Rao Damerla, Eszter K Vladar, et al.Development (Cambridge, England)|September 6, 2021
Gene-teratogen interactions influence the penetrance of birth defects by altering Hedgehog signaling strengthJennifer H Kong, Cullen B Young, Ganesh V Pusapati, et al.Human Molecular Genetics|April 17, 2015
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomaliesRama Rao Damerla, Cheng Cui, George C Gabriel, et al.Frontiers in Neuroscience|December 5, 2022
Clinical factors associated with microstructural connectome related brain dysmaturation in term neonates with congenital heart diseaseJodie K Votava-Smith, Jenna Gaesser, Anna Lonyai Harbison, et al.Nature Communications|January 21, 2015
ANKS6 is the critical activator of NEK8 kinase in embryonic situs determination and organ patterningPeter G Czarnecki, George C Gabriel, Danielle K Manning, et al.Nature|March 26, 2015
Global genetic analysis in mice unveils central role for cilia in congenital heart diseaseYou Li, Nikolai T Klena, George C Gabriel, et al.Nature Genetics|May 23, 2017
The complex genetics of hypoplastic left heart syndromeXiaoqin Liu, Hisato Yagi, Shazina Saeed, et al.American Journal of Human Genetics|September 6, 2014
CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formationRim Hjeij, Alexandros Onoufriadis, Christopher M Watson, et al.Nature Genetics|October 6, 2015
MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebratesAnne Guimier, George C Gabriel, Fanny Bajolle, et al.Cell Reports. Medicine|March 4, 2022
Genetic resiliency associated with dominant lethal TPM1 mutation causing atrial septal defect with high heritabilityPolakit Teekakirikul, Wenjuan Zhu, Xinxiu Xu, et al.Pageof 4