메뉴 건너뛰기




Volumn 36, Issue 2, 1996, Pages 219-226

DRPLA gene (Atrophin-1) sequence and mRNA expression in human brain

Author keywords

Dentatorubral pallidoluysian atrophy; Huntington's disease; Microsatellite; Trinucleotide repeat

Indexed keywords

COMPLEMENTARY DNA; GLUTAMINE; MESSENGER RNA; SERINE;

EID: 0029912378     PISSN: 0169328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0169-328X(95)00241-J     Document Type: Article
Times cited : (36)

References (39)
  • 2
    • 0026772992 scopus 로고
    • Spatial and temporal expression of α and β thyroid hormone receptor mRNAs, including the β2 subtype, in the developing mammalian nervous system
    • Bradley, D.J., Towle, H.C. and Young, W.S.III, Spatial and temporal expression of α and β thyroid hormone receptor mRNAs, including the β2 subtype, in the developing mammalian nervous system, J. Neurosci., 12 (1992) 2288-2302.
    • (1992) J. Neurosci. , vol.12 , pp. 2288-2302
    • Bradley, D.J.1    Towle, H.C.2    Young W.S. III3
  • 6
    • 0027507667 scopus 로고
    • Human genetic diseases due to condon reiteration: Relationship to an evolutionary mechanism
    • Green, H., Human genetic diseases due to condon reiteration: Relationship to an evolutionary mechanism, Cell, 74 (1993) 955-956.
    • (1993) Cell , vol.74 , pp. 955-956
    • Green, H.1
  • 7
    • 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, A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes, Cell, 72 (1993) 971-983.
    • (1993) Cell , vol.72 , pp. 971-983
  • 8
    • 85047678013 scopus 로고
    • Denatao-rubro-pallidoluysian atrophy: A clinico-pathological study
    • Iizuka, R., Hirayama, K., and Maehara, K. Denatao-rubro-pallidoluysian atrophy: a clinico-pathological study, J. Neurol. Neurosurg. Psychiatry, 47 (1984) 1288-1298.
    • (1984) J. Neurol. Neurosurg. Psychiatry , vol.47 , pp. 1288-1298
    • Iizuka, R.1    Hirayama, K.2    Maehara, K.3
  • 11
    • 0028080406 scopus 로고
    • Trinucleotide repeat expansion in neurological disease
    • La Spada, A.R., Paulson, H.L. and Fischbeck, K.H., Trinucleotide repeat expansion in neurological disease, Ann. Neurol., 36 (1994) 814-822.
    • (1994) Ann. Neurol. , vol.36 , pp. 814-822
    • La Spada, A.R.1    Paulson, H.L.2    Fischbeck, K.H.3
  • 12
    • 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., Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy, Nature, 352 (1991) 77-79.
    • (1991) Nature , vol.352 , pp. 77-79
    • La Spada, A.R.1    Wilson, E.M.2    Lubahn, D.B.3    Harding, A.E.4    Fischbeck, K.H.5
  • 13
    • 0343927697 scopus 로고
    • Expression of mRNA for DRPLA gene (atrophin-1) and HD gene (IT15) in developmental and adult brain
    • Li, S-H., Margolis, R.L., Li, X-J. and Ross, C.A., Expression of mRNA for DRPLA gene (atrophin-1) and HD gene (IT15) in developmental and adult brain, Neurosci. Abstr., 24 (1994) 1648.
    • (1994) Neurosci. Abstr. , vol.24 , pp. 1648
    • Li, S.-H.1    Margolis, R.L.2    Li, X.-J.3    Ross, C.A.4
  • 14
    • 0027297703 scopus 로고
    • Novel triplet repeat containing genes in human brain: Cloning, expression, and length polymorphisms
    • Li, S-H., Mclnnis, M.G., Margolis, R.L., Antonarakis, S.E. and Ross, C.A., Novel triplet repeat containing genes in human brain: Cloning, expression, and length polymorphisms, Genomics, 16 (1993) 572-579.
    • (1993) Genomics , vol.16 , pp. 572-579
    • Li, S.-H.1    McLnnis, M.G.2    Margolis, R.L.3    Antonarakis, S.E.4    Ross, C.A.5
  • 16
    • 0024306555 scopus 로고
    • Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity
    • Lubahn, D.B., Brown, T.R., Simental, J.A., Higgs, H.N., Migeon, C.J., Wilson, E.M. and French, F.S., Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity, Proc. Natl. Acad. Sci. USA, 86 (1989) 9534-9538.
    • (1989) Proc. Natl. Acad. Sci. USA , vol.86 , pp. 9534-9538
    • Lubahn, D.B.1    Brown, T.R.2    Simental, J.A.3    Higgs, H.N.4    Migeon, C.J.5    Wilson, E.M.6    French, F.S.7
  • 17
    • 0028843242 scopus 로고
    • Abnormal androgen receptor binding affinity in subjects with Kennedy's disease (spinal and bulbar muscular atropy)
    • MacLean, H.E., Choi, W-T., Rekaris, G., Warne, G.L. and Zajac, J.D., Abnormal androgen receptor binding affinity in subjects with Kennedy's disease (spinal and bulbar muscular atropy), J. Clin. Endocrinol. Metab., 80 (1995) 508-516.
    • (1995) J. Clin. Endocrinol. Metab. , vol.80 , pp. 508-516
    • MacLean, H.E.1    Choi, W.-T.2    Rekaris, G.3    Warne, G.L.4    Zajac, J.D.5
  • 18
    • 0026550512 scopus 로고
    • Molecular characterization of a novel rat protein structurally related to poly(A) binding protein and the 70K protein of the U1 small nuclear ribonucleoprotein particle (snRNP)
    • Mueller, D, Rehbein, M., Baumeister, H., Richter, D., Molecular characterization of a novel rat protein structurally related to poly(A) binding protein and the 70K protein of the U1 small nuclear ribonucleoprotein particle (snRNP), Nucleic Acid Res., 20 (1992) 1471-1475.
    • (1992) Nucleic Acid Res. , vol.20 , pp. 1471-1475
    • Mueller, D.1    Rehbein, M.2    Baumeister, H.3    Richter, D.4
  • 20
    • 0028060244 scopus 로고
    • Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA)
    • Nagafuchi, S., Yanagisawa, H., Ohsaki, E., Shirayama, T., Tadokoro, K., Inoue, T. and Yamada, M., Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA), Nature Genet., 8 (1994) 177-182.
    • (1994) Nature Genet. , vol.8 , pp. 177-182
    • Nagafuchi, S.1    Yanagisawa, H.2    Ohsaki, E.3    Shirayama, T.4    Tadokoro, K.5    Inoue, T.6    Yamada, M.7
  • 22
    • 0020064620 scopus 로고
    • Familial myoclonus epilepsy and choreoathetosis: Hereditary dentatorubral-pallidoluysian atrophy
    • Naito, H. and Oyanagi, S., Familial myoclonus epilepsy and choreoathetosis: Hereditary dentatorubral-pallidoluysian atrophy, Neurology, 32 (1982) 798-807.
    • (1982) Neurology , vol.32 , pp. 798-807
    • Naito, H.1    Oyanagi, S.2
  • 25
    • 0022322597 scopus 로고
    • Design and characterization of peptides with amphiphilic B-strand structures
    • Osterman, D.G., and Kaiser, E.T., Design and characterization of peptides with amphiphilic B-strand structures, J Cell. Biochem., 29 (1985) 57-72.
    • (1985) J Cell. Biochem. , vol.29 , pp. 57-72
    • Osterman, D.G.1    Kaiser, E.T.2
  • 26
    • 0027988041 scopus 로고
    • Polar zippers: Their role in human disease
    • Perutz, M., Polar zippers: Their role in human disease, Protein Sci., 3 (1995) 1629-1637.
    • (1995) Protein Sci. , vol.3 , pp. 1629-1637
    • Perutz, M.1
  • 27
    • 0027300219 scopus 로고
    • Genes with triplet repeats: Candidate mediators of neuropsychiatric disorders
    • Ross, C.A., Mclnnis, M.G., Margolis, R.L. and Li, S-H., Genes with triplet repeats: Candidate mediators of neuropsychiatric disorders, Trends Neurosci., 16 (1993) 254-260.
    • (1993) Trends Neurosci. , vol.16 , pp. 254-260
    • Ross, C.A.1    McLnnis, M.G.2    Margolis, R.L.3    Li, S.-H.4
  • 28
    • 33744887360 scopus 로고    scopus 로고
    • When more is less: Pathogenesis of glutamine repeat neurodegenerative diseases
    • in press
    • Ross, C.A., When more is less: Pathogenesis of glutamine repeat neurodegenerative diseases, Neuron, in press.
    • Neuron
    • Ross, C.A.1
  • 30
    • 0029014180 scopus 로고
    • Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals
    • Servadio, A., Koshy, B., Armstrong, D., Antalffy, B., Orr, H.T. and Zoghbi, H.Y., Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals, Nature Genet., 10 (1995) 94-98.
    • (1995) Nature Genet. , vol.10 , pp. 94-98
    • Servadio, A.1    Koshy, B.2    Armstrong, D.3    Antalffy, B.4    Orr, H.T.5    Zoghbi, H.Y.6
  • 32
    • 0001294843 scopus 로고
    • Unusual form of cerebellar ataxia: Combined dentato-rubral and pallido-Luysian degeneration
    • Smith, J.K., Gonda, V.E. and Malamud, N., Unusual form of cerebellar ataxia: Combined dentato-rubral and pallido-Luysian degeneration, Neurology, 8 (1958) 205-209.
    • (1958) Neurology , vol.8 , pp. 205-209
    • Smith, J.K.1    Gonda, V.E.2    Malamud, N.3
  • 33
    • 0024825955 scopus 로고
    • Structure of the human RD gene: A highly conserved gene in the class III region of the major histocompatability complex
    • Speiser, P.W., White, P.C., Structure of the human RD gene: A highly conserved gene in the class III region of the major histocompatability complex, DNA, 8 (1989) 745-751.
    • (1989) DNA , vol.8 , pp. 745-751
    • Speiser, P.W.1    White, P.C.2
  • 34
    • 0028997643 scopus 로고
    • Simple tandem DNA repeats and human genetic disease
    • Sutherland, G.R. and Richards, R.I., Simple tandem DNA repeats and human genetic disease, Proc. Natl. Acad. Sci. USA, 92 (1995) 3636-3641.
    • (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 3636-3641
    • Sutherland, G.R.1    Richards, R.I.2
  • 35
    • 0023680089 scopus 로고
    • Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family
    • Takahashi, H., Ohama, E., Naito, H., Takeda, S., Nakashima, S., Makifuchi, T., and Ikuta, F., Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family, Neurology, 38 (1988) 1065-1070
    • (1988) Neurology , vol.38 , pp. 1065-1070
    • Takahashi, H.1    Ohama, E.2    Naito, H.3    Takeda, S.4    Nakashima, S.5    Makifuchi, T.6    Ikuta, F.7
  • 37
    • 0022780331 scopus 로고
    • The nucleotide sequence of the fission yeast DNA toposiomerase II gene: Sturctural and functional relationships to other DNA topoisomerases
    • Uemura, T., Morikawa, K., and Yanagida, M., The nucleotide sequence of the fission yeast DNA toposiomerase II gene: sturctural and functional relationships to other DNA topoisomerases, EMBO J., 5 (1986) 2355-2361.
    • (1986) EMBO J. , vol.5 , pp. 2355-2361
    • Uemura, T.1    Morikawa, K.2    Yanagida, M.3
  • 39
    • 0029015557 scopus 로고
    • Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain
    • Yazawa, I., Nukina, N., Hashida, H., Goto, J., Yamada, M. and Kanazawa, I., Abnormal gene product identified in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) brain, Nature Genet., 10 (1995) 99-103.
    • (1995) Nature Genet. , vol.10 , pp. 99-103
    • Yazawa, I.1    Nukina, N.2    Hashida, H.3    Goto, J.4    Yamada, M.5    Kanazawa, I.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.