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Volumn 5, Issue 4, 1999, Pages 383-384

Variation on a trinucleotide theme

Author keywords

[No Author keywords available]

Indexed keywords

TRINUCLEOTIDE;

EID: 0032928358     PISSN: 10788956     EISSN: None     Source Type: Journal    
DOI: 10.1038/7381     Document Type: Short Survey
Times cited : (5)

References (10)
  • 2
    • 0030669689 scopus 로고    scopus 로고
    • Polyglutamines, nuclear inclusions and neurodegeneration
    • Lunkes, A. & Mandel, J-L. Polyglutamines, nuclear inclusions and neurodegeneration. Nature Med. 3, 1201-1202 (1997).
    • (1997) Nature Med. , vol.3 , pp. 1201-1202
    • Lunkes, A.1    Mandel, J.-L.2
  • 3
    • 0032191848 scopus 로고    scopus 로고
    • Neuronal intranuclear inclusions in polyglutamine diseases: Nuclear weapons or nuclear fallout?
    • Kim, T-W. & Tanzi, R.E. Neuronal Intranuclear inclusions in polyglutamine diseases: Nuclear Weapons or Nuclear Fallout? Neuron 21, 657-659 (1998).
    • (1998) Neuron , vol.21 , pp. 657-659
    • Kim, T.-W.1    Tanzi, R.E.2
  • 4
    • 6844254538 scopus 로고    scopus 로고
    • Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)
    • David, C. et al. Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7). Hum. Mol. Genet. 7, 165-170 (1998).
    • (1998) Hum. Mol. Genet. , vol.7 , pp. 165-170
    • David, C.1
  • 5
    • 9844263366 scopus 로고    scopus 로고
    • Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p
    • Jodice, C. et al. Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p. Hum. Mol. Genet. 6, 1973-1978 (1997).
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 1973-1978
    • Jodice, C.1
  • 6
    • 0032900772 scopus 로고    scopus 로고
    • An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
    • Koob, M.D. et al. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8). Nature Genet. 21, 379-384 (1999).
    • (1999) Nature Genet. , vol.21 , pp. 379-384
    • Koob, M.D.1
  • 7
    • 0027256423 scopus 로고
    • Direct detection of novel expanded trinucleotide repeats in the human genome
    • Schalling, M. et al. Direct detection of novel expanded trinucleotide repeats in the human genome. Nature. Genet. 4, 135-139 (1993).
    • (1993) Nature. Genet. , vol.4 , pp. 135-139
    • Schalling, M.1
  • 8
    • 0031712686 scopus 로고    scopus 로고
    • Two commonly expanded CAG/CTG repeat loci: Involvement in affective disorders?
    • Lindblad, K. et al. Two commonly expanded CAG/CTG repeat loci: involvement in affective disorders? Mol. Psychiatry 3, 405-410 (1998).
    • (1998) Mol. Psychiatry , vol.3 , pp. 405-410
    • Lindblad, K.1
  • 9
    • 0032231668 scopus 로고    scopus 로고
    • Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations
    • Takano, H. et al. Close Associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations. Am. J. Hum. Genet. 63, 1060-1066 (1998).
    • (1998) Am. J. Hum. Genet. , vol.63 , pp. 1060-1066
    • Takano, H.1
  • 10
    • 0031647246 scopus 로고    scopus 로고
    • Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families
    • Moseley, M.L. et al. Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families. Neurology 51, 1666-1671 (1998).
    • (1998) Neurology , vol.51 , pp. 1666-1671
    • Moseley, M.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.