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Human Molecular Genetics|September 11, 2004
Positive selection on the human genomeEric J Vallender, Bruce T LahnHuman Molecular Genetics|September 11, 2004
RNA interference: from model organisms towards therapy for neural and neuromuscular disordersSteven D Buckingham, Behrooz Esmaeili, Matthew Wood, et al.Human Molecular Genetics|November 13, 2004
Urogenital and caudal dysgenesis in adrenocortical dysplasia (acd) mice is caused by a splicing mutation in a novel telomeric regulatorCatherine E Keegan, Janna E Hutz, Tobias Else, et al.Human Molecular Genetics|November 13, 2004
Distinct patterns of abnormal GNAS imprinting in familial and sporadic pseudohypoparathyroidism type IBJie Liu, Julie G Nealon, Lee S WeinsteinHuman Molecular Genetics|November 19, 2004
Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13Dalila Pinto, Birgit Westland, Gerrit-Jan de Haan, et al.Human Molecular Genetics|November 19, 2004
Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathiesTakuro Arimura, Anne Helbling-Leclerc, Catherine Massart, et al.Human Molecular Genetics|November 5, 2004
Orexin loss in Huntington's diseaseAsa Petersén, Joana Gil, Marion L C Maat-Schieman, et al.Human Molecular Genetics|October 22, 2004
Somatic deletion events occur during early embryonic development and modify the extent of CAG expansion in subsequent generationsI V Kovtun, A R Thornhill, C T McMurrayHuman Molecular Genetics|October 22, 2004
Branch site haplotypes that control alternative splicingJana Královicová, Sophie Houngninou-Molango, Angela Krämer, et al.Human Molecular Genetics|October 22, 2004
The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathwayHsien-Yang Lee, Ying Xu, Yong Huang, et al.Pageof 1,196