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Volumn 55, Issue 10, 1998, Pages 1729-1732

Gene-dose effect on carnitine transport activity in embryonic fibroblasts of JVS mice as a model of human carnitine transporter deficiency

Author keywords

Embryonic fibroblast; JVS mouse; Membrane transporter; Systemic carnitine deficiency; Uptake kinetics

Indexed keywords

CARNITINE; CARRIER PROTEIN;

EID: 0032525016     PISSN: 00062952     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-2952(97)00670-9     Document Type: Article
Times cited : (40)

References (15)
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    • Horiuchi, M.1    Kobayashi, K.2    Tomomura, M.3    Kuwajima, M.4    Imamura, Y.5    Koizumi, T.6    Nikaido, H.7    Hayakawa, J.8    Saheki, T.9
  • 3
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    • Abnormal gene expression and regulation in the liver of jvs mice with systemic carnitine deficiency
    • Tomomura M, Imamura Y, Tomomura A, Horiuchi M, Saheki T. Abnormal gene expression and regulation in the liver of jvs mice with systemic carnitine deficiency. Biochim Biophys Acta. 1226:1994;307-314.
    • (1994) Biochim Biophys Acta , vol.1226 , pp. 307-314
    • Tomomura, M.1    Imamura, Y.2    Tomomura, A.3    Horiuchi, M.4    Saheki, T.5
  • 4
    • 0024246260 scopus 로고
    • Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts
    • Treem WR, Stanley CA, Finegold DN, Hale DN, Coates PM. Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts. N Engl J Med. 319:1988;1331-1336.
    • (1988) N Engl J Med , vol.319 , pp. 1331-1336
    • Treem, W.R.1    Stanley, C.A.2    Finegold, D.N.3    Hale, D.N.4    Coates, P.M.5
  • 9
    • 0029294041 scopus 로고
    • Mapping of jvs (juvenile visceral steatosis) gene, which causes systemic carnitine deficiency in mice, on Chromosome 11
    • Nikaido H, Horiuchi M, Hashimoto N, Saheki T, Hayakawa J. Mapping of jvs (juvenile visceral steatosis) gene, which causes systemic carnitine deficiency in mice, on Chromosome 11. Mamm Genome. 6:1995;369-370.
    • (1995) Mamm Genome , vol.6 , pp. 369-370
    • Nikaido, H.1    Horiuchi, M.2    Hashimoto, N.3    Saheki, T.4    Hayakawa, J.5
  • 12
    • 0023718446 scopus 로고
    • Hereditary defect in carnitine transport is expressed in fibroblasts
    • Eriksson BO, Lindstedt S, Nordin I. Hereditary defect in carnitine transport is expressed in fibroblasts. Eur J Pediatr. 147:1988;662-668.
    • (1988) Eur J Pediatr , vol.147 , pp. 662-668
    • Eriksson, B.O.1    Lindstedt, S.2    Nordin, I.3
  • 15
    • 0026014260 scopus 로고
    • Primary carnitine deficiency: Heterozygote and intrafamilial phenotypic variation
    • Garavaglia B, Uziel G, Dworzak F, Carrara F, DiDonato S. Primary carnitine deficiency Heterozygote and intrafamilial phenotypic variation . Neurology. 41:1991;1691-1693.
    • (1991) Neurology , vol.41 , pp. 1691-1693
    • Garavaglia, B.1    Uziel, G.2    Dworzak, F.3    Carrara, F.4    Didonato, S.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.