메뉴 건너뛰기




Volumn 10, Issue 1, 1999, Pages 1-6

Isolation and characterization of novel CAG repeat containing genes expressed in human brain

Author keywords

[No Author keywords available]

Indexed keywords

CDNA LIBRARY; DEGENERATIVE DISEASE; GENE EXPRESSION; GLUTAMINE; OLIGONUCLEOTIDE PROBE;

EID: 0344223299     PISSN: 19401736     EISSN: 19401744     Source Type: Journal    
DOI: 10.3109/10425179909033929     Document Type: Article
Times cited : (5)

References (22)
  • 1
    • 0028986767 scopus 로고
    • Random amplification of cDNA ends allow for cloning of multiple novel human cDNA fragments containing CAG repeats
    • Carney, J. P., McKnight, C., Van Epps, S. and Kelley, M. R. (1994) Random amplification of cDNA ends allow for cloning of multiple novel human cDNA fragments containing CAG repeats. Gene, 155, 289-292.
    • (1994) Gene , vol.155 , pp. 289-292
    • Carney, J.P.1    McKnight, C.2    Epps, S.3    Kelley, M.R.4
  • 4
    • 0029792130 scopus 로고    scopus 로고
    • Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): Clinical description and genetic localization to chromosome 16q22.1
    • Flanigan, K., Gardner K., Alderson, K., Galster, B., Otterud, B., Leppert, M. F., Kaplan, C. and Ptácek, L. J. (1996) Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): Clinical description and genetic localization to chromosome 16q22.1. American Journal of Human Genetics, 59, 392-399. (Pubitemid 26266355)
    • (1996) American Journal of Human Genetics , vol.59 , Issue.2 , pp. 392-399
    • Flanigan, K.1    Gardner, K.2    Alderson, K.3    Galster, B.4    Otterud, B.5    Leppert, M.F.6    Kaplan, C.7    Ptacek, L.J.8
  • 6
    • 0028827297 scopus 로고
    • Characterization of four novel CAG repeat-containing cDNAs
    • Jiang, J. X., Deprez, R. H. L., Zwarthoff, E. C. and Riegman, P. H. J. (1995) Characterization of four novel CAG repeat-containing cDNAs. Genomics, 30, 91-93.
    • (1995) Genomics , vol.30 , pp. 91-93
    • Jiang, J.X.1    Deprez, R.H.L.2    Zwarthoff, E.C.3    Riegman, P.H.J.4
  • 9
    • 0025800526 scopus 로고
    • Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
    • La Spada, A. R., Wilson, E. M., Lubahn, D. B., Harding, A. E. and Fischbeck, K. H. (1991) Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature, 352, 77-79. (Pubitemid 21896702)
    • (1991) Nature , vol.352 , Issue.6330 , pp. 77-79
    • La Spada, A.R.1    Wilson, E.M.2    Lubahn, D.B.3    Harding, A.E.4    Fischbeck, K.H.5
  • 10
    • 0027297703 scopus 로고
    • Novel triplet repeat containing genes in human brain: Cloning, expression, and length polymorphisms
    • DOI 10.1006/geno.1993.1232
    • Li, S. H., Mclnnis, M., Margolis, R. L., Antonarakis, S. E. and Ross, C. (1993) Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms. Genomics, 16, 572-579. (Pubitemid 23183473)
    • (1993) Genomics , vol.16 , Issue.3 , pp. 572-579
    • Li, S.-H.1    McInnis, M.G.2    Margolis, R.L.3    Antonarakis, S.E.4    Ross, C.A.5
  • 11
    • 0028784037 scopus 로고
    • CAG repeat expansions and schizophrenia: Association with disease in females and with early age-at-onset
    • Morris, A. G., Gaitonde, E., McKenna, P. J., Mollon, J. D. and Hunt, D. M. (1995) CAG repeat expansions and schizophrenia: association with disease in females and with early age-at-onset. Human Molecular Genetics, 4, 1957-1961.
    • (1995) Human Molecular Genetics , vol.4 , pp. 1957-1961
    • Morris, A.G.1    Gaitonde, E.2    McKenna, P.J.3    Mollon, J.D.4    Hunt, D.M.5
  • 14
    • 0030807772 scopus 로고    scopus 로고
    • CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24
    • DOI 10.1093/hmg/6.11.1811
    • Nielsen, J. E., Koefoed, P., Abell, K., Hasholt, L., Eiberg, H., Fenger, K., Niebuhr, E. and Sorensen, S. A. (1997) CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24. Human Molecular Genetics, 6, 1811-1816. (Pubitemid 27460354)
    • (1997) Human Molecular Genetics , vol.6 , Issue.11 , pp. 1811-1816
    • Nielsen, J.E.1    Koefoed, P.2    Abell, K.3    Hasholt, L.4    Eiberg, H.5    Fenger, K.6    Niebuhr, E.7    Sorensen, S.A.8
  • 17
    • 0028020605 scopus 로고
    • Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11
    • DOI 10.1038/ng1194-280
    • Ranum, L. P. W., Schut, L. J., Lundgren, J. K., Orr, H. T. and Livingston, D. M. (1994) Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11. Nature Genetics, 8, 280-284. (Pubitemid 24338741)
    • (1994) Nature Genetics , vol.8 , Issue.3 , pp. 280-284
    • Ranum, L.P.W.1    Schut, L.J.2    Lundgren, J.K.3    Orr, H.T.4    Livingston, D.M.5
  • 20
    • 0027408526 scopus 로고
    • Finding new genes faster than ever
    • DOI 10.1038/ng0393-189
    • Sikela, J. M. and Auffray, C. (1993) Finding new genes faster than ever. Nature Genetics, 3, 189-191 (Pubitemid 23096549)
    • (1993) Nature Genetics , vol.3 , Issue.3 , pp. 189-191
    • Sikela, J.M.1    Auffray, C.2
  • 21
    • 0027480960 scopus 로고
    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
    • Huntington's Disease Collaborative Research Group
    • The Huntington's Disease Collaborative Research Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell, 72, 971-983.
    • (1993) Cell , vol.72 , pp. 971-983


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.