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Y Sunada

Showing results (71-80 of 77) with videos related to

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Annals of Neurology|February 1, 1996
Clinical heterogeneity of adhalin deficiencyL Morandi, R Barresi, C Di Blasi, et al.
Neuromuscular Disorders : NMD|December 1, 1996
From adhalinopathies to alpha-sarcoglycanopathies: an overviewM Jeanpierre, A Carrié, F Piccolo, et al.
Human Molecular Genetics|May 1, 1997
Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chainV Allamand, Y Sunada, M A Salih, et al.
The Journal of Biological Chemistry|December 13, 1996
Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophyD Jung, F Duclos, B Apostol, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateF Duclos, O Broux, N Bourg, et al.
Journal of Medical Genetics|June 1, 1997
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A Carrié, F Piccolo, F Leturcq, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophiesJ S Beckmann, I Richard, O Broux, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
Annals of Neurology|February 1, 1996
Clinical heterogeneity of adhalin deficiencyL Morandi, R Barresi, C Di Blasi, et al.
Neuromuscular Disorders : NMD|December 1, 1996
From adhalinopathies to alpha-sarcoglycanopathies: an overviewM Jeanpierre, A Carrié, F Piccolo, et al.
Human Molecular Genetics|May 1, 1997
Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chainV Allamand, Y Sunada, M A Salih, et al.
The Journal of Biological Chemistry|December 13, 1996
Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophyD Jung, F Duclos, B Apostol, et al.
Neuromuscular Disorders : NMD|May 5, 1998
Beta-sarcoglycan: genomic analysis and identification of a novel missense mutation in the LGMD2E Amish isolateF Duclos, O Broux, N Bourg, et al.
Journal of Medical Genetics|June 1, 1997
Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)A Carrié, F Piccolo, F Leturcq, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophiesJ S Beckmann, I Richard, O Broux, et al.
Pageof 8