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L V Anderson

Showing results (31-40 of 45) with videos related to

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Journal of Neurochemistry|April 1, 1996
Characterization of dp6troglycan-laminin interaction in peripheral nerveH Yamada, A Chiba, T Endo, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophiesR Pogue, L V Anderson, A Pyle, et al.
Journal of Molecular Neuroscience : MN|October 23, 2001
Dysferlin protein analysis in limb-girdle muscular dystrophiesM Vainzof, L V Anderson, E M McNally, et al.
Human Molecular Genetics|April 10, 1999
Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)T Weiler, R Bashir, L V Anderson, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD familyI B Ginjaar, A L Kneppers, J D v d Meulen, et al.
Brain : a Journal of Neurology|October 6, 1997
Utrophin abundance is reduced at neuromuscular junctions of patients with both inherited and acquired acetylcholine receptor deficienciesC R Slater, C Young, S J Wood, et al.
Human Molecular Genetics|December 1, 1996
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophiesM Vainzof, M R Passos-Bueno, M Canovas, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Molecular analysis of a spontaneous dystrophin 'knockout' dogS J Schatzberg, N J Olby, M Breen, et al.
Human Molecular Genetics|April 10, 1999
Dysferlin is a plasma membrane protein and is expressed early in human developmentL V Anderson, K Davison, J A Moss, et al.
Nature Medicine|May 6, 1999
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2AS Baghdiguian, M Martin, I Richard, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Journal of Neurochemistry|April 1, 1996
Characterization of dp6troglycan-laminin interaction in peripheral nerveH Yamada, A Chiba, T Endo, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophiesR Pogue, L V Anderson, A Pyle, et al.
Journal of Molecular Neuroscience : MN|October 23, 2001
Dysferlin protein analysis in limb-girdle muscular dystrophiesM Vainzof, L V Anderson, E M McNally, et al.
Human Molecular Genetics|April 10, 1999
Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)T Weiler, R Bashir, L V Anderson, et al.
European Journal of Human Genetics : EJHG|October 20, 2000
Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD familyI B Ginjaar, A L Kneppers, J D v d Meulen, et al.
Brain : a Journal of Neurology|October 6, 1997
Utrophin abundance is reduced at neuromuscular junctions of patients with both inherited and acquired acetylcholine receptor deficienciesC R Slater, C Young, S J Wood, et al.
Human Molecular Genetics|December 1, 1996
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophiesM Vainzof, M R Passos-Bueno, M Canovas, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Molecular analysis of a spontaneous dystrophin 'knockout' dogS J Schatzberg, N J Olby, M Breen, et al.
Human Molecular Genetics|April 10, 1999
Dysferlin is a plasma membrane protein and is expressed early in human developmentL V Anderson, K Davison, J A Moss, et al.
Nature Medicine|May 6, 1999
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2AS Baghdiguian, M Martin, I Richard, et al.
Pageof 5