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Volumn 285, Issue 24, 2010, Pages 18627-18639

The Legs at odd angles (Loa) mutation in cytoplasmic dynein ameliorates mitochondrial function in SOD1G93A mouse model for motor neuron disease

Author keywords

[No Author keywords available]

Indexed keywords

AMYOTROPHIC LATERAL SCLEROSIS; AUTOSOMAL DOMINANTS; CYTOPLASMIC DYNEIN; DIRECT INTERACTIONS; HEAVY CHAIN; LIFE SPAN; MEMBRANE POTENTIALS; MITOCHONDRIAL FUNCTION; MITOCHONDRIAL MATRIX; MITOCHONDRIAL RESPIRATION; MOTOR NEURON DISEASE; MOTOR NEURONS; MOUSE MODELS; NEURODEGENERATIVE DISEASE; SPINAL CORDS; SUPER OXIDE DISMUTASE; TOXIC EFFECT; TRANSGENIC MICE; WILD TYPES;

EID: 77953309202     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M110.129320     Document Type: Article
Times cited : (23)

References (60)
  • 5
    • 0033599646 scopus 로고    scopus 로고
    • Shaw, P. J. (1999) BMJ 318, 1118-1121
    • (1999) BMJ , vol.318 , pp. 1118-1121
    • Shaw, P.J.1
  • 26
    • 0037459061 scopus 로고    scopus 로고
    • Vale, R. D. (2003) Cell 112, 467-480
    • (2003) Cell , vol.112 , pp. 467-480
    • Vale, R.D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.