G J Snipes|W Orfali - JoVE Visualize

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Neurology|November 18, 1998

Trigeminal nerve hypertrophy in chronic inflammatory demyelinating polyradiculoneuropathyN Guibord, C Chalk, F Wein, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 15, 1991

A myelin protein is encoded by the homologue of a growth arrest-specific geneA A Welcher, U Suter, M De Leon, et al.

The Journal of Biological Chemistry|May 15, 1993

Detection and processing of peripheral myelin protein PMP22 in cultured Schwann cellsS Pareek, U Suter, G J Snipes, et al.

Journal of Neuropathology and Experimental Neurology|March 1, 1996

Ultrastructural distribution of PMP22 in Charcot-Marie-Tooth disease type 1AC Haney, G J Snipes, E M Shooter, et al.

Science (New York, N.Y.)|August 15, 1986

A protein induced during nerve growth (GAP-43) is a major component of growth-cone membranesJ H Skene, R D Jacobson, G J Snipes, et al.

Neurology|December 31, 1997

Progressive myoclonus epilepsy in young adults with neuropathologic features of Alzheimer's diseaseM Melanson, J Nalbantoglu, S Berkovic, et al.

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 1, 1987

Evidence for the coidentification of GAP-43, a growth-associated protein, and F1, a plasticity-associated proteinG J Snipes, S Y Chan, C B McGuire, et al.

Journal of Neuroscience Research|January 1, 1985

Steady growth cone currents revealed by a novel circularly vibrating probe: a possible mechanism underlying neurite growthJ A Freeman, P B Manis, G J Snipes, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 18, 2002

Association of calnexin with mutant peripheral myelin protein-22 ex vivo: a basis for "gain-of-function" ER diseasesK M Dickson, J J M Bergeron, I Shames, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 15, 1992

A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouseU Suter, J J Moskow, A A Welcher, et al.

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Showing results (21-30 of 38) with videos related to

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Pageof 4

Neurology|November 18, 1998

Trigeminal nerve hypertrophy in chronic inflammatory demyelinating polyradiculoneuropathyN Guibord, C Chalk, F Wein, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 15, 1991

A myelin protein is encoded by the homologue of a growth arrest-specific geneA A Welcher, U Suter, M De Leon, et al.

The Journal of Biological Chemistry|May 15, 1993

Detection and processing of peripheral myelin protein PMP22 in cultured Schwann cellsS Pareek, U Suter, G J Snipes, et al.

Journal of Neuropathology and Experimental Neurology|March 1, 1996

Ultrastructural distribution of PMP22 in Charcot-Marie-Tooth disease type 1AC Haney, G J Snipes, E M Shooter, et al.

Science (New York, N.Y.)|August 15, 1986

A protein induced during nerve growth (GAP-43) is a major component of growth-cone membranesJ H Skene, R D Jacobson, G J Snipes, et al.

Neurology|December 31, 1997

Progressive myoclonus epilepsy in young adults with neuropathologic features of Alzheimer's diseaseM Melanson, J Nalbantoglu, S Berkovic, et al.

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 1, 1987

Evidence for the coidentification of GAP-43, a growth-associated protein, and F1, a plasticity-associated proteinG J Snipes, S Y Chan, C B McGuire, et al.

Journal of Neuroscience Research|January 1, 1985

Steady growth cone currents revealed by a novel circularly vibrating probe: a possible mechanism underlying neurite growthJ A Freeman, P B Manis, G J Snipes, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 18, 2002

Association of calnexin with mutant peripheral myelin protein-22 ex vivo: a basis for "gain-of-function" ER diseasesK M Dickson, J J M Bergeron, I Shames, et al.

Proceedings of the National Academy of Sciences of the United States of America|May 15, 1992

A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouseU Suter, J J Moskow, A A Welcher, et al.

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