Primary defect of juvenile visceral steatosis (jvs) mouse with systemic carnitine deficiency is probably in renal carnitine transport system-Reference-Cited by-同舟云学术

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

Published:1994-04 Issue:1 Volume:1226 Page:25-30
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Horiuchi Masahisa,Kobayashi Keiko,Yamaguchi Seiji,Shimizu Nobuo,Koizumi Tsutomu,Nikaido Hiroko,Hayakawa Jun-ichiro,Kuwajima Masamichi,Saheki Takeyori

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference47 articles.

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

2. Urea cycle disorder in C3H-H-2° mice with juvenile steatosis of viscera

3. Abnormal expression of urea cycle enzyme genes in juvenile visceral steatosis (jvs) mice

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

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