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Volumn 108, Issue 1, 2009, Pages 82-90

Allele-specific silencing of mutant Huntington's disease gene

Author keywords

Allele specific; Huntington's disease; Polymorphism; siRNA

Indexed keywords

CASPASE 3; HUNTINGTIN; SMALL INTERFERING RNA;

EID: 57249086448     PISSN: 00223042     EISSN: 14714159     Source Type: Journal    
DOI: 10.1111/j.1471-4159.2008.05734.x     Document Type: Article
Times cited : (64)

References (20)
  • 1
    • 0141886425 scopus 로고    scopus 로고
    • Allele-specific silencing of a pathogenic mutant acetylcholine receptor subunit by RNA interference
    • Abdelgany A., Wood M. Beeson D. (2003) Allele-specific silencing of a pathogenic mutant acetylcholine receptor subunit by RNA interference. Hum. Mol. Genet. 12, 2637 2644.
    • (2003) Hum. Mol. Genet. , vol.12 , pp. 2637-2644
    • Abdelgany, A.1    Wood, M.2    Beeson, D.3
  • 2
    • 12244266688 scopus 로고
    • Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: Insights into the genetic evolution of Huntington disease
    • Almqvist E., Spence N., Nichol K. et al. (1995) Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease. Hum. Mol. Genet. 4, 207 214.
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 207-214
    • Almqvist, E.1    Spence, N.2    Nichol, K.3
  • 3
    • 0028260436 scopus 로고
    • Structure and expression of the Huntington's disease gene: Evidence against simple inactivation due to an expanded CAG repeat
    • Ambrose C. M., Duyao M. P., Barnes G. et al. (1994) Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat. Somat. Cell Mol. Genet. 20, 27 38.
    • (1994) Somat. Cell Mol. Genet. , vol.20 , pp. 27-38
    • Ambrose, C.M.1    Duyao, M.P.2    Barnes, G.3
  • 4
    • 28644433087 scopus 로고    scopus 로고
    • Normal huntingtin function: An alternative approach to Huntington's disease
    • Cattaneo E., Zuccato C. Tartari M. (2005) Normal huntingtin function: an alternative approach to Huntington's disease. Nat. Rev. Neurosci. 6, 919 930.
    • (2005) Nat. Rev. Neurosci. , vol.6 , pp. 919-930
    • Cattaneo, E.1    Zuccato, C.2    Tartari, M.3
  • 5
    • 36749033738 scopus 로고    scopus 로고
    • Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits
    • Difiglia M., Sena-Esteves M., Chase K. et al. (2007) Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits. Proc. Natl Acad. Sci. USA 104, 17204 17209.
    • (2007) Proc. Natl Acad. Sci. USA , vol.104 , pp. 17204-17209
    • Difiglia, M.1    Sena-Esteves, M.2    Chase, K.3
  • 6
    • 0033757718 scopus 로고    scopus 로고
    • Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in mice
    • Dragatsis I., Levine M. S. Zeitlin S. (2000) Inactivation of Hdh in the brain and testis results in progressive neurodegeneration and sterility in mice. Nat. Genet. 26, 300 306.
    • (2000) Nat. Genet. , vol.26 , pp. 300-306
    • Dragatsis, I.1    Levine, M.S.2    Zeitlin, S.3
  • 11
    • 0028332346 scopus 로고
    • Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease
    • Novelletto A., Persichetti F., Sabbadini G. et al. (1994) Polymorphism analysis of the huntingtin gene in Italian families affected with Huntington disease. Hum. Mol. Genet. 3, 1129 1132.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1129-1132
    • Novelletto, A.1    Persichetti, F.2    Sabbadini, G.3
  • 12
    • 0034657112 scopus 로고    scopus 로고
    • Wild-type huntingtin protects from apoptosis upstream of caspase-3
    • Rigamonti D., Bauer J. H., De-Fraja C. et al. (2000) Wild-type huntingtin protects from apoptosis upstream of caspase-3. J. Neurosci. 20, 3705 3713.
    • (2000) J. Neurosci. , vol.20 , pp. 3705-3713
    • Rigamonti, D.1    Bauer, J.H.2    De-Fraja, C.3
  • 13
    • 0028986598 scopus 로고
    • Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotype
    • Rubinsztein D. C., Leggo J., Goodburn S., Barton D. E. Ferguson-Smith M. A. (1995) Haplotype analysis of the delta 2642 and (CAG)n polymorphisms in the Huntington's disease (HD) gene provides an explanation for an apparent 'founder' HD haplotype. Hum. Mol. Genet. 4, 203 206.
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 203-206
    • Rubinsztein, D.C.1    Leggo, J.2    Goodburn, S.3    Barton, D.E.4    Ferguson-Smith, M.A.5
  • 14
    • 0035504960 scopus 로고    scopus 로고
    • Centrosome disorganization in fibroblast cultures derived from R6/2 Huntington's disease (HD) transgenic mice and HD patients
    • Sathasivam K., Woodman B., Mahal A., Bertaux F., Wanker E. E., Shima D. T. Bates G. P. (2001) Centrosome disorganization in fibroblast cultures derived from R6/2 Huntington's disease (HD) transgenic mice and HD patients. Hum. Mol. Genet. 10, 2425 2435.
    • (2001) Hum. Mol. Genet. , vol.10 , pp. 2425-2435
    • Sathasivam, K.1    Woodman, B.2    Mahal, A.3    Bertaux, F.4    Wanker, E.E.5    Shima, D.T.6    Bates, G.P.7
  • 16
    • 19744380273 scopus 로고    scopus 로고
    • Loss of wild-type huntingtin influences motor dysfunction and survival in the YAC128 mouse model of Huntington disease
    • Van Raamsdonk J. M., Pearson J., Rogers D. A., Bissada N., Vogl A. W., Hayden M. R. Leavitt B. R. (2005) Loss of wild-type huntingtin influences motor dysfunction and survival in the YAC128 mouse model of Huntington disease. Hum. Mol. Genet. 14, 1379 1392.
    • (2005) Hum. Mol. Genet. , vol.14 , pp. 1379-1392
    • Van Raamsdonk, J.M.1    Pearson, J.2    Rogers, D.A.3    Bissada, N.4    Vogl, A.W.5    Hayden, M.R.6    Leavitt, B.R.7
  • 17
    • 0031747231 scopus 로고    scopus 로고
    • Genetic polymorphisms adjacent to the CAG repeat influence clinical features at onset in Huntington's disease
    • Vuillaume I., Vermersch P., Destee A., Petit H. Sablonniere B. (1998) Genetic polymorphisms adjacent to the CAG repeat influence clinical features at onset in Huntington's disease. J. Neurol. Neurosurg. Psychiatry 64, 758 762.
    • (1998) J. Neurol. Neurosurg. Psychiatry , vol.64 , pp. 758-762
    • Vuillaume, I.1    Vermersch, P.2    Destee, A.3    Petit, H.4    Sablonniere, B.5
  • 18
    • 0034737299 scopus 로고    scopus 로고
    • Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease
    • Yamamoto A., Lucas J. J. Hen R. (2000) Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease. Cell 101, 57 66.
    • (2000) Cell , vol.101 , pp. 57-66
    • Yamamoto, A.1    Lucas, J.J.2    Hen, R.3
  • 20
    • 0035919701 scopus 로고    scopus 로고
    • Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease
    • Zuccato C., Ciammola A., Rigamonti D. et al. (2001) Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease. Science 293, 493 498.
    • (2001) Science , vol.293 , pp. 493-498
    • Zuccato, C.1    Ciammola, A.2    Rigamonti, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.