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Article

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

Mammalian genome : official journal of the International Mammalian Genome Society - 1 May 1995

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

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Share to Carnitine
Share to Chromosome Mapping
Share to Chromosomes
Share to Crosses, Genetic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Recessive

Share to Mice, Inbred C57BL

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PMID: 7626891
DOI: 10.1007/BF00364804

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Related research

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Research trail→

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Mapping of jvs (juvenile visceral steatosis) gene, which causes systemic carnitine deficiency in mice, on chromosome 11.PMID 7626891Read ↗

A missense mutation of mouse OCTN2, a sodium-dependent carnitine cotransporter, in the juvenile visceral steatosis mouse.Semantic proximity Read ↗

Spontaneous development of intestinal and colonic atrophy and inflammation in the carnitine-deficient jvs (OCTN2(-/-)) mice.Semantic proximity Read ↗

Pressure overload-induced cardiomyopathy in heterozygous carrier mice of carnitine transporter gene mutation.Semantic proximity Read ↗

Effect of carnitine deprivation on carnitine homeostasis and energy metabolism in mice with systemic carnitine deficiency.Semantic proximity Read ↗

A heterozygote phenotype is present in the jvs +/- mutant mouse livers.Semantic proximity Read ↗

Decreased tissue distribution of L-carnitine in juvenile visceral steatosis mice.Semantic proximity Read ↗

Age-associated cardiomyopathy in heterozygous carrier mice of a pathological mutation of carnitine transporter gene, OCTN2.Semantic proximity Read ↗

The human obesity gene map: the 2004 update.Semantic proximity Read ↗

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