Mapping of jvs (juvenile visceral steatosis) gene, which causes systemic carnitine deficiency in mice, on chromosome 11.

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作者信息

Nikaido H, Horiuchi M, Hashimoto N, Saheki T, Hayakawa J

机构信息

Institute for Experimental Animals, School of Medicine, Kanazawa University, Japan.

出版信息

Mamm Genome. 1995 May;6(5):369-70. doi: 10.1007/BF00364804.

DOI:10.1007/BF00364804

PMID:7626891

Abstract

摘要

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本文引用的文献

Carnitine metabolism and human carnitine deficiency.

Nutrition. 1993 May-Jun;9(3):246-54.

Serum carnitine concentrations in coeliac disease.

Gut. 1993 Jul;34(7):933-5. doi: 10.1136/gut.34.7.933.

Cardiac hypertrophy in juvenile visceral steatosis (jvs) mice with systemic carnitine deficiency.

FEBS Lett. 1993 Jul 12;326(1-3):267-71. doi: 10.1016/0014-5793(93)81805-a.

Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 11.

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A rapid method of scoring simple sequence repeat polymorphisms with agarose gel electrophoresis.

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Primary defect of juvenile visceral steatosis (jvs) mouse with systemic carnitine deficiency is probably in renal carnitine transport system.

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Infantile disease with microvesicular fatty infiltration of viscera spontaneously occurring in the C3H-H-2(0) strain of mouse with similarities to Reye's syndrome.

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Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathy.

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Primary carnitine deficiency.

J Clin Chem Clin Biochem. 1990 May;28(5):351-7.

Animal model of systemic carnitine deficiency: analysis in C3H-H-2 degrees strain of mouse associated with juvenile visceral steatosis.

Biochem Biophys Res Commun. 1991 Feb 14;174(3):1090-4. doi: 10.1016/0006-291x(91)91532-h.

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