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Volumn 431, Issue , 1998, Pages 147-150

Delayed hypersensitivity to 5-fluorouracil associated with reduced dihydropyrimidine dehydrogenase (DPD) activity

Author keywords

[No Author keywords available]

Indexed keywords

DIHYDROPYRIMIDINE DEHYDROGENASE; FLUOROURACIL;

EID: 0031861795     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-4615-5381-6_28     Document Type: Conference Paper
Times cited : (2)

References (13)
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  • 3
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    • Elevated urine, blood and cerebrospinal fluid levels of uracil and thymine in a child with dihydrothymine dehydrogenase deficiency
    • Bakkeren JAJM, De Abreu RA, Sengers RCA, Gabreels FJM, Maas JM, Renier WO (1984). Elevated urine, blood and cerebrospinal fluid levels of uracil and thymine in a child with dihydrothymine dehydrogenase deficiency. Clin. Chim. Acta 140: 247-56.
    • (1984) Clin. Chim. Acta , vol.140 , pp. 247-256
    • Bakkeren, J.A.J.M.1    De Abreu, R.A.2    Sengers, R.C.A.3    Gabreels, F.J.M.4    Maas, J.M.5    Renier, W.O.6
  • 7
    • 0027426408 scopus 로고
    • Dihydropyrimidine dehydrogenase activity in human peripheral blood mononuclear cells and liver
    • Lu Z, Zhang R, Diasio RB (1993). Dihydropyrimidine dehydrogenase activity in human peripheral blood mononuclear cells and liver. Cancer Res. 53:5433-8.
    • (1993) Cancer Res. , vol.53 , pp. 5433-5438
    • Lu, Z.1    Zhang, R.2    Diasio, R.B.3
  • 8
    • 0025990479 scopus 로고
    • Severe 5-fluorouracil toxicity secondary to dihydropyrimidine dehydrogenase deficiency. A potentially more common pharmacogenetic syndrome
    • Harris BE, Carpenter JT, Diasio RB (1991). Severe 5-fluorouracil toxicity secondary to dihydropyrimidine dehydrogenase deficiency. A potentially more common pharmacogenetic syndrome. Cancer 68: 499-501.
    • (1991) Cancer , vol.68 , pp. 499-501
    • Harris, B.E.1    Carpenter, J.T.2    Diasio, R.B.3
  • 9
    • 0029133354 scopus 로고
    • Diagnostic analysis, clinical importance and molecular basis of dihydropyrimidine dehydrogenase deficiency
    • Gonzalez FJ, Fernandez-Salguero P (1995). Diagnostic analysis, clinical importance and molecular basis of dihydropyrimidine dehydrogenase deficiency. TiPS 16:325-7.
    • (1995) TiPS , vol.16 , pp. 325-327
    • Gonzalez, F.J.1    Fernandez-Salguero, P.2
  • 11
    • 0002695311 scopus 로고
    • Hereditary orotic aciduria and other disorders of pyrimidine metabolism
    • ed. CR Scriver, AL Beaudet, WS Sly, D Valle, chapter 55, McGraw-Hill, NY
    • Webster DR, Becroft DM, Suttle DP (1995). Hereditary orotic aciduria and other disorders of pyrimidine metabolism. In: The Metabolic and Molecular Bases of Inherited Disease, ed. CR Scriver, AL Beaudet, WS Sly, D Valle, chapter 55, McGraw-Hill, NY, pp 1799-1837.
    • (1995) The Metabolic and Molecular Bases of Inherited Disease , pp. 1799-1837
    • Webster, D.R.1    Becroft, D.M.2    Suttle, D.P.3
  • 12
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    • Potential importance of dihydropyrimidine dehydrogenase in cancer chemotherapy
    • Milano G, Etienne M-C (1994) Potential importance of dihydropyrimidine dehydrogenase in cancer chemotherapy. Pharmacogen. 4:301-6.
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    • cDNA cloning and chromosome mapping of human dihydropyrimidine dehydrogenase, an enzyme associated with 5-fluorouracil toxicity and congenital thymine uraciluria
    • Yokota H, Fernandez-Salguero P, Furuya H, Lin K, McBride OW, Podschun B, Schnackerz KD, Gonzalez FJ (1994). cDNA cloning and chromosome mapping of human dihydropyrimidine dehydrogenase, an enzyme associated with 5-fluorouracil toxicity and congenital thymine uraciluria. J. Biol. Chem. 269:23192-6.
    • (1994) J. Biol. Chem. , vol.269 , pp. 23192-23196
    • Yokota, H.1    Fernandez-Salguero, P.2    Furuya, H.3    Lin, K.4    McBride, O.W.5    Podschun, B.6    Schnackerz, K.D.7    Gonzalez, F.J.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.