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Congenital Heart Disease|October 21, 2011
Combined mutation screening of NKX2-5, GATA4, and TBX5 in congenital heart disease: multiple heterozygosity and novel mutationsJavier T Granados-Riveron, Mark Pope, Frances A Bu'lock, et al.Human Molecular Genetics|July 27, 2010
Alpha-cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defectsJavier T Granados-Riveron, Tushar K Ghosh, Mark Pope, et al.Journal of Molecular and Cellular Cardiology|April 1, 2017
Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defectsJennifer England, Javier Granados-Riveron, Luis Polo-Parada, et al.European Archives of Psychiatry and Clinical Neuroscience|April 7, 2005
Polymorphisms in the NMDA subunit 2B are not associated with alcohol dependence and alcohol withdrawal-induced seizures and delirium tremensAndre Tadic, Norbert Dahmen, Armin Szegedi, et al.BMC Genetics|June 21, 2013
Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of FallotJulian Palomino Doza, Ana Topf, Jamie Bentham, et al.Vaccine|September 15, 2014
Evaluation of safety and efficacy as an adjuvant for the chitosan-based vaccine delivery vehicle ViscoGel in a single-blind randomised Phase I/IIa clinical trialTheresa Neimert-Andersson, Jonas Binnmyr, Mattias Enoksson, et al.Human Molecular Genetics|December 19, 2018
Transcriptome alterations in myotonic dystrophy skeletal muscle and heartEric T Wang, Daniel Treacy, Katy Eichinger, et al.Human Molecular Genetics|November 2, 2013
High-content screening identifies small molecules that remove nuclear foci, affect MBNL distribution and CELF1 protein levels via a PKC-independent pathway in myotonic dystrophy cell linesAmi Ketley, Catherine Z Chen, Xin Li, et al.Genome Medicine|August 30, 2020
Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart diseaseJose M G Izarzugaza, Sabrina G Ellesøe, Canan Doganli, et al.Circulation. Cardiovascular Genetics|April 17, 2012
A common variant in the PTPN11 gene contributes to the risk of tetralogy of FallotJudith A Goodship, Darroch Hall, Ana Topf, et al.Pageof 9