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The Journal of Clinical Investigation|August 1, 1993
Deficiency of dystrophin-associated proteins in Duchenne muscular dystrophy patients lacking COOH-terminal domains of dystrophinK Matsumura, F M Tomé, V Ionasescu, et al.Neuromuscular Disorders : NMD|September 1, 1993
The role of the dystrophin-glycoprotein complex in the molecular pathogenesis of muscular dystrophiesK Matsumura, K Ohlendieck, V V Ionasescu, et al.Annales De Genetique|January 1, 1997
Molecular diagnosis of congenital bilateral absence of the vas deferens: analyses of the CFTR gene in 64 French patientsT Bienvenu, M Adjiman, N Thiounn, et al.Nucleic Acids Research|February 25, 1983
Lambda Ig constant region genes are translocated to chromosome 8 in Burkitt's lymphoma with t(8;22)A de la Chapelle, G Lenoir, J Boué, et al.Neuromuscular Disorders : NMD|June 19, 2001
Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with 'de novo' duplication of dystrophin geneN B Romero, P De Lonlay, S Llense, et al.Proceedings of the National Academy of Sciences of the United States of America|August 15, 1992
Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissuesJ P Hugnot, H Gilgenkrantz, N Vincent, et al.American Journal of Human Genetics|May 1, 1982
Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridizationC Junien, D Weil, J C Myers, et al.Nature|July 23, 1987
HIV-specific cytotoxic T lymphocytes in seropositive individualsB D Walker, S Chakrabarti, B Moss, et al.Journal of Medical Genetics|March 1, 1997
Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22V des Portes, J M Pinard, D Smadja, et al.AIDS Research and Human Retroviruses|June 1, 1993
Interactions between HIV-1 and cytomegalovirus in human osteosarcoma cells carrying both virusesM Margalith, D J Medina, G D Hsiung, et al.Pageof 19