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Science

Volumn 282, Issue 5391, 1998, Pages 1079-1083

Genetic neurodegenerative diseases: The human illness and transgenic models

(3) Price, Donald L a Sisodia, Sangram S b Borchelt, David R a

a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE (United States)

b UNIVERSITY OF CHICAGO (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALZHEIMER DISEASE; AMYOTROPHIC LATERAL SCLEROSIS; CEREBELLAR ATAXIA; GENE MUTATION; GENETIC SUSCEPTIBILITY; HUMAN; HUNTINGTON CHOREA; MOTOR NEURON DISEASE; NEUROPATHOLOGY; NONHUMAN; PARKINSON DISEASE; PATHOPHYSIOLOGY; PRION DISEASE; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVIEW; TRANSGENIC MOUSE;

ATAXIA; MUS MUSCULUS;

EID: 0032491494 PISSN: 00368075 EISSN: None Source Type: Journal
DOI: 10.1126/science.282.5391.1079 Document Type: Review

Times cited : (234)

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- note
- We thank T. Siddique (for tissue samples from the human cases of FALS described in Fig. 1), M. Lee, P. Wong, A. Markowska, G. Thinakaran, N. Jenkins, N. Copeland, D. Cleveland, C. Ross, G. Schilling, C. Pardo, and J. Rothstein for their contributions to some of the work mentioned in this text. Supported by grants from the U.S. Public Health Service (NIH NS 20471, NS 10580, NS 37145, AG 05146, AG 07914, AG 14248), as well as the Metropolitan Life Foundation, the Adler Foundation, the Alzheimer's Association (Temple Award, Zenith Award), the DeVelbiss fund, the American Health Assistance Foundation, the Amyotrophic Lateral Sclerosis Association, the Hereditary Disease Foundation, and the Huntington's Disease Society of America.

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