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Volumn 32, Issue 2, 1996, Pages 297-298

Assignment of human KH-box-containing genes by in situ hybridization: HNRNPK maps to 9q21.32-q21.33, PCBP1 to 2p12-p13, and PCBP2 to 12q13.12-q13.13, distal to FRA12A

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 12Q; CHROMOSOME 2P; CHROMOSOME 9Q; DNA DETERMINATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCATION; GENE MAPPING; HUMAN; MOLECULAR CLONING; PRIORITY JOURNAL;

EID: 0029866905     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1996.0121     Document Type: Article
Times cited : (21)

References (10)
  • 1
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    • Dejgaard, K., Leffers, H., Rasmussen, H. H., Madsen, P., Kruse, T. A., Gesser, B., Nielsen, H., and Celis, J. (1994). Identification, molecular cloning, expression and chromosome mapping of a family of transformation upregulated hnRNP-K proteins derived by alternative splicing. J. Mol. Biol. 236: 33-48.
    • (1994) J. Mol. Biol. , vol.236 , pp. 33-48
    • Dejgaard, K.1    Leffers, H.2    Rasmussen, H.H.3    Madsen, P.4    Kruse, T.A.5    Gesser, B.6    Nielsen, H.7    Celis, J.8
  • 2
    • 0027947017 scopus 로고
    • Digitized and differentially shaded human chromosome ideograms for genomic applications
    • Francke, U. (1994). Digitized and differentially shaded human chromosome ideograms for genomic applications. Cytogenet. Cell Genet. 65: 206-219.
    • (1994) Cytogenet. Cell Genet. , vol.65 , pp. 206-219
    • Francke, U.1
  • 3
    • 0027258576 scopus 로고
    • The KH domain occurs in a diverse set of RNA-binding proteins that include the antitumour NusA and is probably involved in binding to nucleic acids
    • Gibson, T. J., Thompson, J. D., and Heringa, J. (1993). The KH domain occurs in a diverse set of RNA-binding proteins that include the antitumour NusA and is probably involved in binding to nucleic acids. FEBS Lett. 324: 361-366.
    • (1993) FEBS Lett. , vol.324 , pp. 361-366
    • Gibson, T.J.1    Thompson, J.D.2    Heringa, J.3
  • 4
    • 0028557941 scopus 로고
    • Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3
    • Jones, C., Slijepcevic, P., Marsh, S., Baker, E., Langdon, W. Y., Richards, R. I., and Tunnacliffe, A. (1994). Physical linkage of the fragile site FRA11B and a Jacobsen syndrome chromosome deletion breakpoint in 11q23.3. Hum. Mol. Genet. 3: 2123-2130.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 2123-2130
    • Jones, C.1    Slijepcevic, P.2    Marsh, S.3    Baker, E.4    Langdon, W.Y.5    Richards, R.I.6    Tunnacliffe, A.7
  • 6
    • 0029076374 scopus 로고
    • Characterization of two major cellular poly(rC)-binding human proteins, each containing three K-homologous (KH) domains
    • Leffers, H., Dejgaard, K., and Celis, J. (1995). Characterization of two major cellular poly(rC)-binding human proteins, each containing three K-homologous (KH) domains. Eur. J. Biochem. 230: 447-453.
    • (1995) Eur. J. Biochem. , vol.230 , pp. 447-453
    • Leffers, H.1    Dejgaard, K.2    Celis, J.3
  • 8
    • 0028567730 scopus 로고
    • The cloning of FRAXF: Trinucleotide repeat expansion and methylation at a third fragile site in distal xqter
    • Ritchie, R. J., Knight, S. J. L., Hirst, M. C., Grewal, P. K., Bobrow, M., Cross, G. S., and Davies, K. E. (1994). The cloning of FRAXF: Trinucleotide repeat expansion and methylation at a third fragile site in distal Xqter. Hum. Mol. Genet. 3: 2115-2121.
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 2115-2121
    • Ritchie, R.J.1    Knight, S.J.L.2    Hirst, M.C.3    Grewal, P.K.4    Bobrow, M.5    Cross, G.S.6    Davies, K.E.7
  • 9
    • 0027327486 scopus 로고
    • The protein product of the fragile X gene, FMR1, has characteristics of an RNA binding protein
    • Siomi, H., Siomi, M. C., Nussbaum, R. L., and Dreyfuss, G. (1993). The protein product of the fragile X gene, FMR1, has characteristics of an RNA binding protein. Cell 74: 291-298.
    • (1993) Cell , vol.74 , pp. 291-298
    • Siomi, H.1    Siomi, M.C.2    Nussbaum, R.L.3    Dreyfuss, G.4
  • 10
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    • Essential role for KH domains in RNA binding: Impaired RNA binding by a mutation in the KH domain of FMR1 causes fragile X syndrome
    • Siomi, H., Choi, M., Siomi, M. C., Nussbaum, R. L., and Dreyfuss, G. (1994). Essential role for KH domains in RNA binding: Impaired RNA binding by a mutation in the KH domain of FMR1 causes fragile X syndrome. Cell 77: 33-39.
    • (1994) Cell , vol.77 , pp. 33-39
    • Siomi, H.1    Choi, M.2    Siomi, M.C.3    Nussbaum, R.L.4    Dreyfuss, G.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.