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Neurobiology of Disease|January 1, 1997

Connexin32 and X-linked Charcot-Marie-Tooth diseaseL J Bone, S M Deschênes, R J Balice-Gordon, et al.

Novartis Foundation Symposium|April 20, 1999

The role of the gap junction protein connexin32 in the pathogenesis of X-linked Charcot-Marie-Tooth diseaseS S Scherer, L J Bone, S M Deschênes, et al.

Circulation|December 13, 1997

In utero cardiac gene transfer via intraplacental delivery of recombinant adenovirusY J Woo, G P Raju, J L Swain, et al.

Neuron|December 14, 1999

Disruption of Trkb-mediated signaling induces disassembly of postsynaptic receptor clusters at neuromuscular junctionsM Gonzalez, F P Ruggiero, Q Chang, et al.

Annals of Neurology|May 11, 2000

Functional motor unit failure precedes neuromuscular degeneration in canine motor neuron diseaseR J Balice-Gordon, D B Smith, J Goldman, et al.

Human Gene Therapy|October 1, 1996

In vivo expression of full-length human dystrophin from adenoviral vectors deleted of all viral genesS E Haecker, H H Stedman, R J Balice-Gordon, et al.

Nature Genetics|July 1, 1996

Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathyS Reddy, D B Smith, M M Rich, et al.

Nature Medicine|April 15, 1999

Stable restoration of the sarcoglycan complex in dystrophic muscle perfused with histamine and a recombinant adeno-associated viral vectorJ P Greelish, L T Su, E B Lankford, et al.

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Showing results (21-30 of 28) with videos related to

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You have reached the last page of results.This site can display upto 28 results.

Neurobiology of Disease|January 1, 1997

Connexin32 and X-linked Charcot-Marie-Tooth diseaseL J Bone, S M Deschênes, R J Balice-Gordon, et al.

Novartis Foundation Symposium|April 20, 1999

The role of the gap junction protein connexin32 in the pathogenesis of X-linked Charcot-Marie-Tooth diseaseS S Scherer, L J Bone, S M Deschênes, et al.

Circulation|December 13, 1997

In utero cardiac gene transfer via intraplacental delivery of recombinant adenovirusY J Woo, G P Raju, J L Swain, et al.

Neuron|December 14, 1999

Disruption of Trkb-mediated signaling induces disassembly of postsynaptic receptor clusters at neuromuscular junctionsM Gonzalez, F P Ruggiero, Q Chang, et al.

Annals of Neurology|May 11, 2000

Functional motor unit failure precedes neuromuscular degeneration in canine motor neuron diseaseR J Balice-Gordon, D B Smith, J Goldman, et al.

Human Gene Therapy|October 1, 1996

In vivo expression of full-length human dystrophin from adenoviral vectors deleted of all viral genesS E Haecker, H H Stedman, R J Balice-Gordon, et al.

Nature Genetics|July 1, 1996

Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathyS Reddy, D B Smith, M M Rich, et al.

Nature Medicine|April 15, 1999

Stable restoration of the sarcoglycan complex in dystrophic muscle perfused with histamine and a recombinant adeno-associated viral vectorJ P Greelish, L T Su, E B Lankford, et al.

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