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Volumn 412, Issue 6843, 2001, Pages 143-144

Cause of neural death in neurodegenerative diseases attributable to expansion of glutamine repeats

Author keywords

[No Author keywords available]

Indexed keywords

CELLS; DISEASES; NUCLEATION; PATHOLOGY; PROBABILITY; PROTEINS;

EID: 0035849879     PISSN: 00280836     EISSN: None     Source Type: Journal    
DOI: 10.1038/35084141     Document Type: Article
Times cited : (170)

References (17)
  • 3
    • 18544410106 scopus 로고    scopus 로고
    • Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation
    • (1997) Cell , vol.90 , pp. 537-548
    • Davies, S.W.1
  • 4
    • 0030752709 scopus 로고
    • Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain
    • (1993) Science , vol.277 , pp. 1990-1993
    • DiFiglia, M.1
  • 5
    • 0034644203 scopus 로고    scopus 로고
    • A one-hit model of cell death in inherited neuronal degenerations
    • (2000) Nature , vol.406 , pp. 195-199
    • Clarke, G.1
  • 7
    • 0030666001 scopus 로고    scopus 로고
    • Ataxin-1 with an expanded glutamine tract alters nuclear matrix-associated structures
    • (1997) Nature , vol.389 , pp. 971-974
    • Skinner, P.J.1
  • 9
    • 0032590053 scopus 로고    scopus 로고
    • Huntingtin aggregates may not predict neuronal death in Huntington's disease
    • (1999) Neurology , vol.46 , pp. 842-849
    • Kuemmerle, S.1
  • 10
    • 0034662915 scopus 로고    scopus 로고
    • Bacterial and yeast chaperones reduce both aggregate formation and cell death in mammalian cell models of Huntington's disease
    • (2000) Proc. Natl Acad. Sci. USA , vol.97 , pp. 9701-9705
    • Carmichael, J.1
  • 12
    • 0035937523 scopus 로고    scopus 로고
    • Interference by huntingtin and atrophin-1 with CPB-mediated transcription leading to cellular toxicity
    • (2001) Science , vol.291 , pp. 2423-2428
    • Nucifora F.C., Jr.1
  • 14
    • 0004509007 scopus 로고    scopus 로고
    • A polypeptide inhibitor of aggregation suppresses pathogenesis in a Drosophila model of polyglutamine repeat disease
    • submitted
    • Cell
    • Kazantsev, A.1
  • 15
  • 16
    • 18544400323 scopus 로고    scopus 로고
    • Huntingtin-encoded polyglutamine expansions form amyloid-like protein aggregates in vivo and in vitro
    • (1997) Cell , vol.90 , pp. 549-558
    • Scherzinger, E.1
  • 17
    • 0032450856 scopus 로고    scopus 로고
    • Amyloid formation by mutant huntingtin: Threshold, progressivity and recruitment of normal polyglutamine proteins
    • (1998) Somat. Cell Mol. Genet. , vol.24 , pp. 217-233
    • Huang, C.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.