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Genome Research|December 1, 1996
Structure of the human alpha 2 subunit gene of the glycine receptor--use of vectorette and Alu-exon PCRU Monani, A H BurghesCurrent Opinion in Neurology|October 1, 1994
Gene therapy for muscle diseasesD D Coovert, A H BurghesJournal of the Neurological Sciences|May 1, 1980
Erythrocyte ghost Na+,K+-adenosine triphosphatase in Duchenne muscular dystrophyM J Dunn, A H Burghes, V DubowitzThe Biochemical Journal|March 1, 1982
Erythrocyte-ghost Ca2+-stimulated Mg2+-dependent adenosine triphosphatase in Duchenne muscular dystrophyM J Dunn, A H Burghes, V DubowitzBiochimica Et Biophysica Acta|June 15, 1999
Promoter analysis of the human centromeric and telomeric survival motor neuron genes (SMNC and SMNT)U R Monani, J D McPherson, A H BurghesHuman Molecular Genetics|September 27, 2000
Animal models of spinal muscular atrophyU R Monani, D D Coovert, A H BurghesBrain Research|March 19, 1993
Gene delivery to spinal motor neuronsZ Sahenk, J Seharaseyon, J R Mendell, et al.The Journal of Clinical Investigation|July 1, 1983
Isolation and characterization of a mutant liver aldolase in adult hereditary fructose intolerance. Identification of the enzyme variant by radioassay in tissue biopsy specimensT M Cox, M W O'Donnell, M Camilleri, et al.Genomics|January 1, 1989
Mapping of four translocation breakpoints within the Duchenne muscular dystrophy geneS E Bodrug, A H Burghes, P M Ray, et al.Brain Research. Molecular Brain Research|May 29, 1998
Identification and characterization of RPTP rho, a novel RPTP mu/kappa-like receptor protein tyrosine phosphatase whose expression is restricted to the central nervous systemP E McAndrew, A Frostholm, R A White, et al.Pageof 6