메뉴 건너뛰기




Volumn 75, Issue 4, 1996, Pages 222-223

Assignment of the gene for a ubiquitin-conjugating enzyme (UBE2I) to human chromosome band 16p13.3 by in situ hybridization

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; UBIQUITIN CONJUGATING ENZYME;

EID: 0030513198     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000134487     Document Type: Article
Times cited : (4)

References (12)
  • 1
    • 0028898059 scopus 로고
    • The Saccharomyces pombe hus5 gene encodes a ubiquitin conjugating enzyme required for normal mitosis
    • Al-Khodairy F, Enoch T, Hagan IM, Carr AM: The Saccharomyces pombe hus5 gene encodes a ubiquitin conjugating enzyme required for normal mitosis. J Cell Sci 108:475-486 (1995).
    • (1995) J Cell Sci , vol.108 , pp. 475-486
    • Al-Khodairy, F.1    Enoch, T.2    Hagan, I.M.3    Carr, A.M.4
  • 2
    • 0025331090 scopus 로고
    • In vivo degradation of a transcriptional regulator: The yeast α2 repressor
    • Hochstrasser M, Varshavsky A: In vivo degradation of a transcriptional regulator: the yeast α2 repressor. Cell 61:697-708 (1990).
    • (1990) Cell , vol.61 , pp. 697-708
    • Hochstrasser, M.1    Varshavsky, A.2
  • 3
    • 0028607143 scopus 로고
    • Regulated degradation of the transcription factor Gcn4
    • Kornitzer D, Raboy B, Kulka RG, Fink GR: Regulated degradation of the transcription factor Gcn4. EMBOJ 13:6021-6030 (1994).
    • (1994) EMBOJ , vol.13 , pp. 6021-6030
    • Kornitzer, D.1    Raboy, B.2    Kulka, R.G.3    Fink, G.R.4
  • 4
    • 0030012628 scopus 로고    scopus 로고
    • Analyses of loss-of-function mutations of the MITF gene suggests that haploinsufficiency is a cause of Waardenburg syndrome type 2A
    • Nobukuni Y, Watanabe A, Takeda K, Skarka H, Tachibana M: Analyses of loss-of-function mutations of the MITF gene suggests that haploinsufficiency is a cause of Waardenburg syndrome type 2A. Am J hum Genet 59:76-83 (1996).
    • (1996) Am J Hum Genet , vol.59 , pp. 76-83
    • Nobukuni, Y.1    Watanabe, A.2    Takeda, K.3    Skarka, H.4    Tachibana, M.5
  • 5
    • 0028967267 scopus 로고
    • Role of a ubiquitin-conjugating enzyme in degradation of S- and M-phase cyclins
    • Seufert W, Futcher B, Jentisch S: Role of a ubiquitin-conjugating enzyme in degradation of S- and M-phase cyclins. Nature 373:78-81 (1994).
    • (1994) Nature , vol.373 , pp. 78-81
    • Seufert, W.1    Futcher, B.2    Jentisch, S.3
  • 9
    • 0029741915 scopus 로고    scopus 로고
    • Ectopic expression of MITF a gene for Waardenburg syndrome type 2, converts fibroblasls to cells with melanocyte characteristics
    • Tachibana M, Takeda K, Nobukuni Y, Urabe K, Long JE, Meyers KA, Aaronson A, Miki T: Ectopic expression of MITF a gene for Waardenburg syndrome type 2, converts fibroblasls to cells with melanocyte characteristics. Nature Genet 14:50-54, 1996.
    • (1996) Nature Genet , vol.14 , pp. 50-54
    • Tachibana, M.1    Takeda, K.2    Nobukuni, Y.3    Urabe, K.4    Long, J.E.5    Meyers, K.A.6    Aaronson, A.7    Miki, T.8
  • 10
    • 0027943189 scopus 로고
    • Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene
    • Tassabehiji M, Newton VE, Read AP: Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene. Nature Genet 18:251-255 (1994).
    • (1994) Nature Genet , vol.18 , pp. 251-255
    • Tassabehiji, M.1    Newton, V.E.2    Read, A.P.3
  • 12
    • 0026802070 scopus 로고
    • Autosomal dominant congenital cataract and microphthalmia associated with familial t(2;16) translocation
    • Yokoyama Y, Narahara K, Tsuji K, Ninomiya S, Seino Y: Autosomal dominant congenital cataract and microphthalmia associated with familial t(2;16) translocation. Hum Genet 90:177-178 (1992).
    • (1992) Hum Genet , vol.90 , pp. 177-178
    • Yokoyama, Y.1    Narahara, K.2    Tsuji, K.3    Ninomiya, S.4    Seino, Y.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.