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Volumn 56, Issue 3, 1999, Pages 350-352

Mapping of the KHSRP gene to a region of conserved synteny on human chromosome 19p13.3 and mouse chromosome 17

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PROTEIN KHSRP; REGULATOR PROTEIN; UNCLASSIFIED DRUG;

EID: 0033559057     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1998.5725     Document Type: Article
Times cited : (10)

References (12)
  • 1
    • 0029956656 scopus 로고    scopus 로고
    • The far upstream element-binding proteins comprise an ancient family of single-strand DNA-binding transactivators
    • Davis-Smyth T., Duncan R. C., Zheng T., Michelotti G., Levens D. The far upstream element-binding proteins comprise an ancient family of single-strand DNA-binding transactivators. J. Biol. Chem. 271:1996;31679-31687.
    • (1996) J. Biol. Chem. , vol.271 , pp. 31679-31687
    • Davis-Smyth, T.1    Duncan, R.C.2    Zheng, T.3    Michelotti, G.4    Levens, D.5
  • 2
    • 0028206551 scopus 로고
    • A sequence-specific, single-strand binding protein activates the far upstream element of c-myc and defines a new DNA-binding motif
    • Duncan R., Bazar L., Michelotti G., Tomonaga T., Krutzsch H., Avigan M., Levens D. A sequence-specific, single-strand binding protein activates the far upstream element of c-myc and defines a new DNA-binding motif. Genes Dev. 8:1994;465-480.
    • (1994) Genes Dev. , vol.8 , pp. 465-480
    • Duncan, R.1    Bazar, L.2    Michelotti, G.3    Tomonaga, T.4    Krutzsch, H.5    Avigan, M.6    Levens, D.7
  • 6
    • 0001334170 scopus 로고
    • Recessive congenital cerebellar disorder in a genetic isolate: CPD type VII
    • Johnson W. G., Murphy M., Murphy W. I., Bloom A. D. Recessive congenital cerebellar disorder in a genetic isolate: CPD type VII. Neurology. 28:1978;352-353.
    • (1978) Neurology , vol.28 , pp. 352-353
    • Johnson, W.G.1    Murphy, M.2    Murphy, W.I.3    Bloom, A.D.4
  • 7
    • 0015305199 scopus 로고
    • Thin fur, a recessive mutant on chromosome 17 of the mouse
    • Key M., Hollander W. F. Thin fur, a recessive mutant on chromosome 17 of the mouse. J. Hered. 63:1972;97-98.
    • (1972) J. Hered. , vol.63 , pp. 97-98
    • Key, M.1    Hollander, W.F.2
  • 8
    • 0030969572 scopus 로고    scopus 로고
    • A new regulatory protein, KSRP, mediates exon inclusion through an intronic splicing enhancer
    • Min H., Turck C. W., Nikolic J. M., Black D. L. A new regulatory protein, KSRP, mediates exon inclusion through an intronic splicing enhancer. Genes Dev. 11:1997;1023-1036.
    • (1997) Genes Dev. , vol.11 , pp. 1023-1036
    • Min, H.1    Turck, C.W.2    Nikolic, J.M.3    Black, D.L.4
  • 9
    • 0029925102 scopus 로고    scopus 로고
    • A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman Islands
    • Nystuen A., Benke P. J., Merren J., Stone E. M., Sheffield V. C. A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman Islands. Hum. Mol. Genet. 5:1996;525-531.
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 525-531
    • Nystuen, A.1    Benke, P.J.2    Merren, J.3    Stone, E.M.4    Sheffield, V.C.5
  • 11
    • 0028914042 scopus 로고
    • Soma-specific expression and cloning of PSI, a negative regulator of P element pre-mRNA splicing
    • Siebel C. W., Admon A., Rio D. C. Soma-specific expression and cloning of PSI, a negative regulator of P element pre-mRNA splicing. Genes Dev. 9:1995;269-283.
    • (1995) Genes Dev. , vol.9 , pp. 269-283
    • Siebel, C.W.1    Admon, A.2    Rio, D.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.