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Literature DB >> 7626891

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

H Nikaido¹, M Horiuchi, N Hashimoto, T Saheki, J Hayakawa.

Abstract

Entities: Disease Gene Species

Mesh：

Substances：
DNA
Carnitine

Year: 1995 PMID： 7626891 DOI： 10.1007/bf00364804

Source DB: PubMed Journal: Mamm Genome ISSN： 0938-8990 Impact factor: 2.957

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15 in total

Review 1. Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathy.

Authors: I Tein; D C De Vivo; F Bierman; P Pulver; L J De Meirleir; L Cvitanovic-Sojat; R A Pagon; E Bertini; C Dionisi-Vici; S Servidei
Journal: Pediatr Res Date: 1990-09 Impact factor: 3.756

2. A genetic map of the mouse suitable for typing intraspecific crosses.

Authors: W Dietrich; H Katz; S E Lincoln; H S Shin; J Friedman; N C Dracopoli; E S Lander
Journal: Genetics Date: 1992-06 Impact factor: 4.562

Review 3. Primary carnitine deficiency.

Authors: H R Scholte; R Rodrigues Pereira; P C de Jonge; I E Luyt-Houwen; M Hedwig; M Verduin; J D Ross
Journal: J Clin Chem Clin Biochem Date: 1990-05

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

Authors: E Routman; J Cheverud
Journal: Mamm Genome Date: 1994-03 Impact factor: 2.957

5. 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.

Authors: T Koizumi; H Nikaido; J Hayakawa; A Nonomura; T Yoneda
Journal: Lab Anim Date: 1988-01 Impact factor: 2.471

6. Additional microsatellite markers for mouse genome mapping.

Authors: C M Hearne; M A McAleer; J M Love; T J Aitman; R J Cornall; S Ghosh; A M Knight; J B Prins; J A Todd
Journal: Mamm Genome Date: 1991 Impact factor: 2.957

Review 7. Carnitine metabolism and human carnitine deficiency.

Authors: V Tanphaichitr; P Leelahagul
Journal: Nutrition Date: 1993 May-Jun Impact factor: 4.008

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

Authors: M Horiuchi; K Kobayashi; S Yamaguchi; N Shimizu; T Koizumi; H Nikaido; J Hayakawa; M Kuwajima; T Saheki
Journal: Biochim Biophys Acta Date: 1994-04-12

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

Review 1. Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathy.

2. A genetic map of the mouse suitable for typing intraspecific crosses.

Review 3. Primary carnitine deficiency.

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

5. 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.

6. Additional microsatellite markers for mouse genome mapping.

Review 7. Carnitine metabolism and human carnitine deficiency.

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

Review 9. Carnitine function and requirements during the life cycle.

10. A child with valproic acid-associated carnitine deficiency and carnitine-responsive cardiac dysfunction.

Review 1. Carnitine transport: pathophysiology and metabolism of known molecular defects.

2. Evidence for linkage of human primary systemic carnitine deficiency with D5S436: a novel gene locus on chromosome 5q.