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Volumn 533, Issue , 2003, Pages 13-18

On the role of IMPDH1 in retinal degeneration

Author keywords

[No Author keywords available]

Indexed keywords

INOSINATE DEHYDROGENASE; NUCLEOTIDE;

EID: 0346271789     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4615-0067-4_2     Document Type: Conference Paper
Times cited : (12)

References (11)
  • 2
    • 0027717956 scopus 로고
    • Characterization of human type I and type II IMP dehydrogenases
    • Carr, S.F., Papp, E., Wu, J.C., and Natsumeda, Y., 1993, Characterization of human type I and type II IMP dehydrogenases. J Biol Chem. 268: 27286.
    • (1993) J Biol Chem , vol.268 , pp. 27286
    • Carr, S.F.1    Papp, E.2    Wu, J.C.3    Natsumeda, Y.4
  • 3
    • 0001213543 scopus 로고    scopus 로고
    • Regulation of the human inosine monophosphate dehydrogenase type 1 gene. Utilization of alternative promoters
    • Gu, J.J., Spychala, J., and Mitchell, B.S., 1997, Regulation of the human inosine monophosphate dehydrogenase type 1 gene. Utilization of alternative promoters. J Biol Chem. 272: 4458.
    • (1997) J Biol Chem , vol.272 , pp. 4458
    • Gu, J.J.1    Spychala, J.2    Mitchell, B.S.3
  • 5
    • 0036501462 scopus 로고    scopus 로고
    • Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice
    • Kennan, A., Aherne, A., Palfi, A., Humphries, M., McKee, A., Stitt, A., Simpson, D.A., Demtroder, K., Orntoft, T., Ayuso, C., Kenna, P.F., Farrar, G.J., and Humphries, P., 2002, Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice. Hum Mol Genet. 11:547.
    • (2002) Hum Mol Genet , vol.11 , pp. 547
    • Kennan, A.1    Aherne, A.2    Palfi, A.3    Humphries, M.4    McKee, A.5    Stitt, A.6    Simpson, D.A.7    Demtroder, K.8    Orntoft, T.9    Ayuso, C.10    Kenna, P.F.11    Farrar, G.J.12    Humphries, P.13
  • 7
    • 0028831395 scopus 로고
    • Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: Linkage mapping in a second, unrelated family
    • McGuire, R.E., Gannon, A.M., Sullivan, L.S., Rodriguez, J.A., and Daiger, S.P., 1995, Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family. Hum Genet. 95:71.
    • (1995) Hum Genet , vol.95 , pp. 71
    • McGuire, R.E.1    Gannon, A.M.2    Sullivan, L.S.3    Rodriguez, J.A.4    Daiger, S.P.5
  • 10
    • 0028343293 scopus 로고
    • Tissue-differential expression of two distinct genes for human IMP dehydrogenase (E.C.1.1.1.205)
    • Senda, M., and Natsumeda, Y., 1994, Tissue-differential expression of two distinct genes for human IMP dehydrogenase (E.C.1.1.1.205). Life Sci. 54: 1917.
    • (1994) Life Sci , vol.54 , pp. 1917
    • Senda, M.1    Natsumeda, Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.