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Neurology|November 1, 1995
Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalitiesY Sunada, T S Edgar, B P Lotz, et al.Pediatric Neurology|May 1, 1995
Congenital myopathy with ringlike distribution of myonuclei and mitochondria and accumulation of nemaline rods. A variant of centronuclear myopathy?A J Waclawik, T S Edgar, B P Lotz, et al.Current Opinion in Neurology|October 1, 1995
Dystrophin-glycoprotein complex: molecular organization and critical roles in skeletal muscleY Sunada, K P CampbellNature Genetics|December 1, 1994
Dp71 can restore the dystrophin-associated glycoprotein complex in muscle but fails to prevent dystrophyG A Cox, Y Sunada, K P Campbell, et al.Human Molecular Genetics|June 1, 1995
Identification of a novel mutant transcript of laminin alpha 2 chain gene responsible for muscular dystrophy and dysmyelination in dy2J miceY Sunada, S M Bernier, A Utani, et al.Nature Genetics|December 1, 1994
Exogenous Dp71 restores the levels of dystrophin associated proteins but does not alleviate muscle damage in mdx miceD S Greenberg, Y Sunada, K P Campbell, et al.The Journal of Biological Chemistry|May 13, 1994
Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locusY Sunada, S M Bernier, C A Kozak, et al.Neuropediatrics|December 1, 1996
Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome?M Z Seidahmed, Y Sunada, C O Ozo, et al.Human Molecular Genetics|October 1, 1994
Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoformJ A Rafael, Y Sunada, N M Cole, et al.Gene Therapy|November 1, 1996
In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genesP R Clemens, S Kochanek, Y Sunada, et al.Pageof 32