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European Journal of Human Genetics : EJHG|November 26, 1999
A common disease haplotype segregating in spinocerebellar ataxia 2 (SCA2) pedigrees of diverse ethnic originJ Pang, R Allotey, N Wadia, et al.Brain : a Journal of Neurology|January 5, 1999
A clinicogenetic analysis of six Indian spinocerebellar ataxia (SCA2) pedigrees. The significance of slow saccades in diagnosisN Wadia, J Pang, J Desai, et al.Human Molecular Genetics|October 13, 2000
Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophyA Ahmad, M Brinson, B L Hodges, et al.Journal of Clinical Gastroenterology|September 19, 2000
Current surgical therapy for carcinoma of the pancreasA M Cooperman, S Kini, H Snady, et al.Nucleic Acids Research|March 4, 2020
TimeMeter assesses temporal gene expression similarity and identifies differentially progressing genesPeng Jiang, Connie S Chamberlain, Ray Vanderby, et al.Nature Genetics|May 1, 1993
New mdx mutation disrupts expression of muscle and nonmuscle isoforms of dystrophinG A Cox, S F Phelps, V M Chapman, et al.Genomics|May 15, 1997
Exon-intron structure of a 2.7-kb transcript of the STM7 gene with phosphatidylinositol-4-phosphate 5-kinase activityM A Pook, J J Carvajal, K Doudney, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|November 6, 2009
Dystrophin delivery to muscles of mdx mice using lentiviral vectors leads to myogenic progenitor targeting and stable gene expressionEn Kimura, Sheng Li, Paul Gregorevic, et al.The West Indian Medical Journal|October 11, 2014
St George's University's Medical Student Research Institute: A Novel, Virtual Programme for Medical Research CollaborationR S Chamberlain, Z Klaassen, M C Meadows, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|April 17, 2008
Emergent dilated cardiomyopathy caused by targeted repair of dystrophic skeletal muscleDeWayne Townsend, Soichiro Yasuda, Sheng Li, et al.Pageof 45