메뉴 건너뛰기




Volumn 97, Issue 4, 1996, Pages 957-962

Induction of Fanconi anemia cellular phenotype in human 293 cells by overexpression of a mutant FAC allele

Author keywords

GST fusion; mitomycin C; multimeric complex; phenotype; transfection

Indexed keywords

CELL PROTEIN;

EID: 0030028557     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI118519     Document Type: Article
Times cited : (19)

References (26)
  • 1
    • 0028109326 scopus 로고
    • Fanconi anemia and novel strategies for therapy
    • Liu, J.M., M. Buchwald, C E. Walsh, and N.S. Young. 1994. Fanconi anemia and novel strategies for therapy. Blood. 84:3995-4007.
    • (1994) Blood , vol.84 , pp. 3995-4007
    • Liu, J.M.1    Buchwald, M.2    Walsh, C.E.3    Young, N.S.4
  • 2
    • 0017877785 scopus 로고
    • Repair deficient human disorders and cancer
    • Setlow, R.B. 1978. Repair deficient human disorders and cancer. Nature (Lond.). 271:713-717.
    • (1978) Nature (Lond.) , vol.271 , pp. 713-717
    • Setlow, R.B.1
  • 3
    • 0026878842 scopus 로고
    • Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9
    • Strathdee, C.A., A.M.V. Duncan, and M. Buchwald. 1992. Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9. Nature Genet. 1:196-198.
    • (1992) Nature Genet. , vol.1 , pp. 196-198
    • Strathdee, C.A.1    Duncan, A.M.V.2    Buchwald, M.3
  • 6
    • 0027999023 scopus 로고
    • Localization of Fanconi anemia C protein to the cytoplasm of mammalian cells
    • Youssoufian, H. 1994. Localization of Fanconi anemia C protein to the cytoplasm of mammalian cells. Proc Natl. Acad. Sci USA. 91:7975-7979.
    • (1994) Proc Natl. Acad. Sci USA , vol.91 , pp. 7975-7979
    • Youssoufian, H.1
  • 7
    • 0026521238 scopus 로고
    • Cloning of cDNAs for Fanconi's anaemia by functional complementation
    • Strathdee, C.A., H. Gavish, W.R. Shannon, and M. Buchwald. 1992. Cloning of cDNAs for Fanconi's anaemia by functional complementation. Nature (Lond.). 356:763-767.
    • (1992) Nature (Lond.) , vol.356 , pp. 763-767
    • Strathdee, C.A.1    Gavish, H.2    Shannon, W.R.3    Buchwald, M.4
  • 12
    • 0027339986 scopus 로고
    • A Leu554-to-Pro substitution completely abolishes the functional complementing activity of the Fanconi anemia (FACC) protein
    • Gavish, H., C.C. dos Santos, and M. Buchwald. 1993. A Leu554-to-Pro substitution completely abolishes the functional complementing activity of the Fanconi anemia (FACC) protein. Hum. Mol. Genet. 2:123-126.
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 123-126
    • Gavish, H.1    Dos Santos, C.C.2    Buchwald, M.3
  • 13
    • 0028968316 scopus 로고
    • Identification of cytosolic proteins that bind to the Fanconi anemia complementation group C polypeptide in vitro: Evidence for a multimeric complex
    • Youssoufian, H., A. D. Auerbach, P.C. Verlander, V. Steimle, and B. Mach. 1995. Identification of cytosolic proteins that bind to the Fanconi anemia complementation group C polypeptide in vitro: Evidence for a multimeric complex. J Biol. Chem. 270:9876-9882.
    • (1995) J Biol. Chem. , vol.270 , pp. 9876-9882
    • Youssoufian, H.1    Auerbach, A.D.2    Verlander, P.C.3    Steimle, V.4    Mach, B.5
  • 14
    • 0017710978 scopus 로고
    • Characteristics of a human cell line transformed by DNA from human adenovirus type 5
    • Graham, F.L., J. Smiley, W.C. Russell, and R. Nairn. 1977. Characteristics of a human cell line transformed by DNA from human adenovirus type 5. J. Gen. Virol. 36:59-72.
    • (1977) J. Gen. Virol. , vol.36 , pp. 59-72
    • Graham, F.L.1    Smiley, J.2    Russell, W.C.3    Nairn, R.4
  • 15
    • 0026533752 scopus 로고
    • The sequence context of the inttiation codon in the encephalomyocarditis virus leader modulates efficiency of internal translation initiation
    • Davies, M.V., and R.J. Kaufman. 1992. The sequence context of the inttiation codon in the encephalomyocarditis virus leader modulates efficiency of internal translation initiation. J. Virol. 66:1924-1932.
    • (1992) J. Virol. , vol.66 , pp. 1924-1932
    • Davies, M.V.1    Kaufman, R.J.2
  • 16
    • 0003694904 scopus 로고
    • Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York
    • Harlow, E., and D. Lane. 1988. Antibodies. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York.
    • (1988) Antibodies
    • Harlow, E.1    Lane, D.2
  • 17
    • 0027212498 scopus 로고
    • Solubilization and purification of enzymatically active glutathione S-transferase (pGEX) fusion proteins
    • Frangioni J.V., and B.G. Neel. 1993. Solubilization and purification of enzymatically active glutathione S-transferase (pGEX) fusion proteins. Anal. Biochem. 210:179-187.
    • (1993) Anal. Biochem. , vol.210 , pp. 179-187
    • Frangioni, J.V.1    Neel, B.G.2
  • 19
    • 0018065032 scopus 로고
    • Human disorders showing increased sensitivity to the induction of genetic damage
    • Arlett, C.F., and Lehmann, A.R. 1978. Human disorders showing increased sensitivity to the induction of genetic damage. Annu. Rev. Genet. 12:95-115.
    • (1978) Annu. Rev. Genet. , vol.12 , pp. 95-115
    • Arlett, C.F.1    Lehmann, A.R.2
  • 20
    • 0026075929 scopus 로고
    • Induction of a mutant phenotype in human repair proficient cells after overexpression of a mutated human DNA repair gene
    • Belt, P.B.G.M., M.F. van Oosterwijk, H Odijk, J.H.J. Hoeijmakers, and C. Backendorf. 1991. Induction of a mutant phenotype in human repair proficient cells after overexpression of a mutated human DNA repair gene. Nucleic Acids Res. 19:5633-5637.
    • (1991) Nucleic Acids Res. , vol.19 , pp. 5633-5637
    • Belt, P.B.G.M.1    Van Oosterwijk, M.F.2    Odijk, H.3    Hoeijmakers, J.H.J.4    Backendorf, C.5
  • 23
    • 0028934368 scopus 로고
    • Mutations in XPA that prevent association with ERCC1 are defective in nucleotide excision repair
    • Li, L., C.A. Peterson, X. Lu, and R.J. Legerski. 1995. Mutations in XPA that prevent association with ERCC1 are defective in nucleotide excision repair. Mol. Cell. Blol. 15:1993-1998.
    • (1995) Mol. Cell. Blol. , vol.15 , pp. 1993-1998
    • Li, L.1    Peterson, C.A.2    Lu, X.3    Legerski, R.J.4
  • 26
    • 0026234831 scopus 로고
    • Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa
    • Gal, A., A. Artlich, M. Ludwig, G. Niemeyer, K. Olek, E. Schwinger, and A. Schinzel. 1991. Pro-347-Arg mutation of the rhodopsin gene in autosomal dominant retinitis pigmentosa. Genomics. 11:468-470.
    • (1991) Genomics , vol.11 , pp. 468-470
    • Gal, A.1    Artlich, A.2    Ludwig, M.3    Niemeyer, G.4    Olek, K.5    Schwinger, E.6    Schinzel, A.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.