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H R Horvitz

Showing results (151-160 of 169) with videos related to

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Science (New York, N.Y.)|February 26, 2000
Translocation of C. elegans CED-4 to nuclear membranes during programmed cell deathF Chen, B M Hersh, B Conradt, et al.
Development (Cambridge, England)|December 19, 2001
unc-83 encodes a novel component of the nuclear envelope and is essential for proper nuclear migrationD A Starr, G J Hermann, C J Malone, et al.
Journal of Neurochemistry|May 1, 1995
Superoxide dismutase concentration and activity in familial amyotrophic lateral sclerosisA C Bowling, E E Barkowski, D McKenna-Yasek, et al.
Nature|March 8, 2000
The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegansB J Reinhart, F J Slack, M Basson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 23, 1997
Caenorhabditis elegans rab-3 mutant synapses exhibit impaired function and are partially depleted of vesiclesM L Nonet, J E Staunton, M P Kilgard, et al.
Neuromuscular Disorders : NMD|September 1, 1995
Identification of three novel mutations in the gene for Cu/Zn superoxide dismutase in patients with familial amyotrophic lateral sclerosisP C Sapp, D R Rosen, B A Hosler, et al.
Annals of Neurology|May 19, 1998
Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosisM Aoki, C L Lin, J D Rothstein, et al.
American Journal of Medical Genetics|May 15, 1994
Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markersD R Rosen, P Sapp, J O'Regan, et al.
Advances in Neurology|January 11, 1991
Gene linkage in familial amyotrophic lateral sclerosis: a progress reportR H Brown, H R Horvitz, G A Rouleau, et al.
Human Molecular Genetics|June 1, 1994
Identification of two novel mutations and a new polymorphism in the gene for Cu/Zn superoxide dismutase in patients with amyotrophic lateral sclerosisJ Esteban, D R Rosen, A C Bowling, et al.
Pageof 17

Showing results (151-160 of 169) with videos related to

Sort By:
Pageof 17
Science (New York, N.Y.)|February 26, 2000
Translocation of C. elegans CED-4 to nuclear membranes during programmed cell deathF Chen, B M Hersh, B Conradt, et al.
Development (Cambridge, England)|December 19, 2001
unc-83 encodes a novel component of the nuclear envelope and is essential for proper nuclear migrationD A Starr, G J Hermann, C J Malone, et al.
Journal of Neurochemistry|May 1, 1995
Superoxide dismutase concentration and activity in familial amyotrophic lateral sclerosisA C Bowling, E E Barkowski, D McKenna-Yasek, et al.
Nature|March 8, 2000
The 21-nucleotide let-7 RNA regulates developmental timing in Caenorhabditis elegansB J Reinhart, F J Slack, M Basson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 23, 1997
Caenorhabditis elegans rab-3 mutant synapses exhibit impaired function and are partially depleted of vesiclesM L Nonet, J E Staunton, M P Kilgard, et al.
Neuromuscular Disorders : NMD|September 1, 1995
Identification of three novel mutations in the gene for Cu/Zn superoxide dismutase in patients with familial amyotrophic lateral sclerosisP C Sapp, D R Rosen, B A Hosler, et al.
Annals of Neurology|May 19, 1998
Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosisM Aoki, C L Lin, J D Rothstein, et al.
American Journal of Medical Genetics|May 15, 1994
Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markersD R Rosen, P Sapp, J O'Regan, et al.
Advances in Neurology|January 11, 1991
Gene linkage in familial amyotrophic lateral sclerosis: a progress reportR H Brown, H R Horvitz, G A Rouleau, et al.
Human Molecular Genetics|June 1, 1994
Identification of two novel mutations and a new polymorphism in the gene for Cu/Zn superoxide dismutase in patients with amyotrophic lateral sclerosisJ Esteban, D R Rosen, A C Bowling, et al.
Pageof 17