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V Allamand

Showing results (11-20 of 33) with videos related to

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Magnetic Resonance in Medicine|October 12, 2000
Contrast agent-enhanced magnetic resonance imaging of skeletal muscle damage in animal models of muscular dystrophyV Straub, K M Donahue, V Allamand, et al.
Nucleic Acids Research|November 21, 2007
Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codonM Rederstorff, V Allamand, P Guicheney, et al.
Genomics|January 15, 1994
Targeted development of microsatellite markers from inter-Alu amplification of YAC clonesA P de Souza, V Allamand, I Richard, et al.
Neuropediatrics|May 6, 2004
Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 lociE Demir, A Ferreiro, P Sabatelli, et al.
Cell|April 7, 1995
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2AI Richard, O Broux, V Allamand, et al.
Genomics|October 1, 1994
Regional localization of human chromosome 15 lociI Richard, O Broux, N Chiannilkulchai, et al.
Nature Genetics|November 1, 1995
Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12L E Lim, F Duclos, O Broux, et al.
American Journal of Human Genetics|March 1, 1992
Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish originS A Jordan, G J Farrar, R Kumar-Singh, et al.
Genomics|December 1, 1991
Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6G J Farrar, S A Jordan, P Kenna, et al.
Molecular Cell|March 11, 2000
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2EM Durbeej, R D Cohn, R F Hrstka, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Magnetic Resonance in Medicine|October 12, 2000
Contrast agent-enhanced magnetic resonance imaging of skeletal muscle damage in animal models of muscular dystrophyV Straub, K M Donahue, V Allamand, et al.
Nucleic Acids Research|November 21, 2007
Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codonM Rederstorff, V Allamand, P Guicheney, et al.
Genomics|January 15, 1994
Targeted development of microsatellite markers from inter-Alu amplification of YAC clonesA P de Souza, V Allamand, I Richard, et al.
Neuropediatrics|May 6, 2004
Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 lociE Demir, A Ferreiro, P Sabatelli, et al.
Cell|April 7, 1995
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2AI Richard, O Broux, V Allamand, et al.
Genomics|October 1, 1994
Regional localization of human chromosome 15 lociI Richard, O Broux, N Chiannilkulchai, et al.
Nature Genetics|November 1, 1995
Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12L E Lim, F Duclos, O Broux, et al.
American Journal of Human Genetics|March 1, 1992
Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish originS A Jordan, G J Farrar, R Kumar-Singh, et al.
Genomics|December 1, 1991
Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6G J Farrar, S A Jordan, P Kenna, et al.
Molecular Cell|March 11, 2000
Disruption of the beta-sarcoglycan gene reveals pathogenetic complexity of limb-girdle muscular dystrophy type 2EM Durbeej, R D Cohn, R F Hrstka, et al.
Pageof 4