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Nature Medicine|August 11, 2014
Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and miceNicolas Wein, Adeline Vulin, Maria S Falzarano, et al.Human Mutation|February 15, 2022
Intron mutations and early transcription termination in Duchenne and Becker muscular dystrophyMegan A Waldrop, Steven A Moore, Katherine D Mathews, et al.Neuromuscular Disorders : NMD|July 16, 2010
Clinical and genetic characterization of manifesting carriers of DMD mutationsPayam Soltanzadeh, Michael J Friez, Diane Dunn, et al.Brain : a Journal of Neurology|September 13, 2023
Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophyRichard J L F Lemmers, Russell Butterfield, Patrick J van der Vliet, et al.Human Mutation|November 26, 2009
Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohortKevin M Flanigan, Diane M Dunn, Andrew von Niederhausern, et al.Plos Genetics|August 12, 2010
Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPDNancy L Saccone, Robert C Culverhouse, Tae-Hwi Schwantes-An, et al.Behavior Genetics|September 23, 2015
Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry CohortsTae-Hwi Schwantes-An, Juan Zhang, Li-Shiun Chen, et al.Genetic Epidemiology|November 5, 2013
Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smokingSarah H Stephens, Sarah M Hartz, Nicole R Hoft, et al.Archives of General Psychiatry|August 8, 2012
Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokersSarah M Hartz, Susan E Short, Nancy L Saccone, et al.Nature|December 6, 2002
Initial sequencing and comparative analysis of the mouse genome, Robert H Waterston, Kerstin Lindblad-Toh, et al.Pageof 10