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M F Peters

Showing results (11-20 of 23) with videos related to

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The Journal of Biological Chemistry|February 12, 1998
beta-dystrobrevin, a new member of the dystrophin family. Identification, cloning, and protein associationsM F Peters, K F O'Brien, H M Sadoulet-Puccio, et al.
American Journal of Medical Genetics|May 8, 2000
Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophinP Rocco, M Vainzof, S C Froehner, et al.
The Journal of Cell Biology|September 10, 1998
Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscleM F Peters, H M Sadoulet-Puccio, M R Grady, et al.
Neuromuscular Disorders : NMD|August 6, 2003
Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathyK J Jones, A G Compton, N Yang, et al.
Molecular Psychiatry|July 27, 2005
Alternative transcripts and evidence of imprinting of GNAL on 18p11.2J P Corradi, V Ravyn, A K Robbins, et al.
Molecular and Cellular Neurosciences|September 10, 1999
Nuclear targeting of mutant Huntingtin increases toxicityM F Peters, F C Nucifora, J Kushi, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 6, 1999
Polyglutamine pathogenesisC A Ross, J D Wood, G Schilling, et al.
The Journal of Experimental Medicine|August 1, 1996
Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophyD S Chao, J R Gorospe, J E Brenman, et al.
Science (New York, N.Y.)|March 27, 2001
Interference by huntingtin and atrophin-1 with cbp-mediated transcription leading to cellular toxicityF C Nucifora, M Sasaki, M F Peters, et al.
Cell|March 8, 1996
Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alpha1-syntrophin mediated by PDZ domainsJ E Brenman, D S Chao, S H Gee, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
The Journal of Biological Chemistry|February 12, 1998
beta-dystrobrevin, a new member of the dystrophin family. Identification, cloning, and protein associationsM F Peters, K F O'Brien, H M Sadoulet-Puccio, et al.
American Journal of Medical Genetics|May 8, 2000
Brazilian family with pure autosomal dominant spastic paraplegia maps to 8q: analysis of muscle beta 1 syntrophinP Rocco, M Vainzof, S C Froehner, et al.
The Journal of Cell Biology|September 10, 1998
Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscleM F Peters, H M Sadoulet-Puccio, M R Grady, et al.
Neuromuscular Disorders : NMD|August 6, 2003
Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathyK J Jones, A G Compton, N Yang, et al.
Molecular Psychiatry|July 27, 2005
Alternative transcripts and evidence of imprinting of GNAL on 18p11.2J P Corradi, V Ravyn, A K Robbins, et al.
Molecular and Cellular Neurosciences|September 10, 1999
Nuclear targeting of mutant Huntingtin increases toxicityM F Peters, F C Nucifora, J Kushi, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 6, 1999
Polyglutamine pathogenesisC A Ross, J D Wood, G Schilling, et al.
The Journal of Experimental Medicine|August 1, 1996
Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophyD S Chao, J R Gorospe, J E Brenman, et al.
Science (New York, N.Y.)|March 27, 2001
Interference by huntingtin and atrophin-1 with cbp-mediated transcription leading to cellular toxicityF C Nucifora, M Sasaki, M F Peters, et al.
Cell|March 8, 1996
Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alpha1-syntrophin mediated by PDZ domainsJ E Brenman, D S Chao, S H Gee, et al.
Pageof 3