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Dystrophin: The protein product of the duchenne muscular dystrophy locus
Eric P. Hoffman;Robert H. Brown;Louis M. Kunkel;Louis M. Kunkel.
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.
T. J. Kwiatkowski;D. A. Bosco;D. A. Bosco;A. L. LeClerc;A. L. LeClerc;E. Tamrazian.
Motor neurons in Cu/Zn superoxide dismutase-deficient mice develop normally but exhibit enhanced cell death after axonal injury.
Andrew. G. Reaume;Jeffrey L. Elliott;Eric K. Hoffman;Neil W. Kowall;Neil W. Kowall.
Nature Genetics (1996)
Decoding ALS: from genes to mechanism
J. Paul Taylor;Robert H. Brown;Don W. Cleveland;Don W. Cleveland.
Molecular biology of amyotrophic lateral sclerosis: insights from genetics.
Piera Pasinelli;Robert H. Brown.
Nature Reviews Neuroscience (2006)
Wild-type nonneuronal cells extend survival of SOD1 mutant motor neurons in ALS mice.
A. M. Clement;M. D. Nguyen;E. A. Roberts;E. A. Roberts;M. L. Garcia;M. L. Garcia.
Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy
Hoffman Ep;Fischbeck Kh;Brown Rh;Johnson M.
The New England Journal of Medicine (1988)
Mutant dynactin in motor neuron disease.
Imke Puls;Catherine Jonnakuty;Bernadette H. LaMonte;Erika L.F. Holzbaur.
Nature Genetics (2003)
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
Jing Liu;Masashi Aoki;Isabel Illa;Chenyan Wu.
Nature Genetics (1998)
Evidence of increased oxidative damage in both sporadic and familial amyotrophic lateral sclerosis.
Ferrante Rj;Browne Se;Shinobu La;Bowling Ac.
Journal of Neurochemistry (2002)
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