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Neurology|April 11, 2001
Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate geneH Haravuori, A Vihola, V Straub, et al.Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.Oncogene|May 8, 2009
The Wnt receptor FZD1 mediates chemoresistance in neuroblastoma through activation of the Wnt/beta-catenin pathwayM Flahaut, R Meier, A Coulon, et al.Human Molecular Genetics|December 23, 1999
Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genesF Fougerousse, P Bullen, M Herasse, et al.Journal of Medical Genetics|May 12, 2000
A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 familiesP Dinçer, Z Akçören, E Demir, et al.Circulation Research|June 13, 2000
Series of exon-skipping events in the elastic spring region of titin as the structural basis for myofibrillar elastic diversityA Freiburg, K Trombitas, W Hell, et al.Proceedings of the National Academy of Sciences of the United States of America|September 15, 1999
A homeobox gene, vax2, controls the patterning of the eye dorsoventral axisA M Barbieri, G Lupo, A Bulfone, et al.Genomics|October 1, 1992
Exclusion of linkage between hypokalemic periodic paralysis (HOKPP) and three candidate lociW L Casley, M Allon, H K Cousin, et al.Poultry Science|February 9, 2006
Microsatellite markers associated with resistance to Marek's disease in commercial layer chickensJ P McElroy, J C M Dekkers, J E Fulton, et al.American Journal of Human Genetics|December 5, 1998
Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31H Feit, A Silbergleit, L B Schneider, et al.Pageof 22