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L V Anderson

Showing results (21-30 of 45) with videos related to

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Neuromuscular Disorders : NMD|December 1, 1996
Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophyC A Sewry, J Taylor, L V Anderson, et al.
Muscle & Nerve|July 9, 1998
Alternative dystrophin gene transcripts in golden retriever muscular dystrophyS J Schatzberg, L V Anderson, S D Wilton, et al.
Human Molecular Genetics|July 1, 1997
Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophyL Metzinger, D J Blake, M V Squier, et al.
Neuromuscular Disorders : NMD|March 11, 2000
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain diseaseM Auranen, J Rapola, H Pihko, et al.
The American Journal of Pathology|October 20, 1998
Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2AL V Anderson, K Davison, J A Moss, et al.
Neuroreport|March 10, 2001
Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutationE Vafiadaki, A Reis, S Keers, et al.
The Journal of Biological Chemistry|September 20, 1996
Dystroglycan is a dual receptor for agrin and laminin-2 in Schwann cell membraneH Yamada, A J Denzer, H Hori, et al.
Neuromuscular Disorders : NMD|April 9, 2008
Late onset in dysferlinopathy widens the clinical spectrumL Klinge, A F Dean, W Kress, et al.
Journal of the Neurological Sciences|March 10, 1997
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)M J Spencer, J G Tidball, L V Anderson, et al.
The Journal of Biological Chemistry|May 23, 1997
A role of dystroglycan in schwannoma cell adhesion to lamininK Matsumura, A Chiba, H Yamada, et al.
Pageof 5

Showing results (21-30 of 45) with videos related to

Sort By:
Pageof 5
Neuromuscular Disorders : NMD|December 1, 1996
Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophyC A Sewry, J Taylor, L V Anderson, et al.
Muscle & Nerve|July 9, 1998
Alternative dystrophin gene transcripts in golden retriever muscular dystrophyS J Schatzberg, L V Anderson, S D Wilton, et al.
Human Molecular Genetics|July 1, 1997
Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophyL Metzinger, D J Blake, M V Squier, et al.
Neuromuscular Disorders : NMD|March 11, 2000
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain diseaseM Auranen, J Rapola, H Pihko, et al.
The American Journal of Pathology|October 20, 1998
Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2AL V Anderson, K Davison, J A Moss, et al.
Neuroreport|March 10, 2001
Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutationE Vafiadaki, A Reis, S Keers, et al.
The Journal of Biological Chemistry|September 20, 1996
Dystroglycan is a dual receptor for agrin and laminin-2 in Schwann cell membraneH Yamada, A J Denzer, H Hori, et al.
Neuromuscular Disorders : NMD|April 9, 2008
Late onset in dysferlinopathy widens the clinical spectrumL Klinge, A F Dean, W Kress, et al.
Journal of the Neurological Sciences|March 10, 1997
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)M J Spencer, J G Tidball, L V Anderson, et al.
The Journal of Biological Chemistry|May 23, 1997
A role of dystroglycan in schwannoma cell adhesion to lamininK Matsumura, A Chiba, H Yamada, et al.
Pageof 5