Literature DB >> 3352223

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.

T Koizumi1, H Nikaido, J Hayakawa, A Nonomura, T Yoneda.   

Abstract

The clinical, biochemical and histopathological findings of an infantile disease occurring in the C3H-H-2 degree strain of mice, which has similarities with Reye's syndrome in children, is described.

Entities:  

Mesh：

Year:  1988        PMID： 3352223     DOI： 10.1258/002367788780746511

Source DB:  PubMed          Journal:  Lab Anim        ISSN： 0023-6772            Impact factor:   2.471


  14 in total

Review 1.  Uptake carriers and oncology drug safety.

Authors:  Jason A Sprowl; Alex Sparreboom
Journal:  Drug Metab Dispos       Date:  2013-12-30       Impact factor: 3.922

2.  Slc22a5 haploinsufficiency does not aggravate the phenotype of the long-chain acyl-CoA dehydrogenase KO mouse.

Authors:  Pablo Ranea-Robles; Chunli Yu; Naomi van Vlies; Frédéric M Vaz; Sander M Houten
Journal:  J Inherit Metab Dis       Date:  2019-12-23       Impact factor: 4.982

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

Authors:  H Nikaido; M Horiuchi; N Hashimoto; T Saheki; J Hayakawa
Journal:  Mamm Genome       Date:  1995-05       Impact factor: 2.957

4.  Cisplatin-induced downregulation of OCTN2 affects carnitine wasting.

Authors:  Cynthia S Lancaster; Chaoxin Hu; Ryan M Franke; Kelly K Filipski; Shelley J Orwick; Zhaoyuan Chen; Zhili Zuo; Walter J Loos; Alex Sparreboom
Journal:  Clin Cancer Res       Date:  2010-09-21       Impact factor: 12.531

5.  Hyperammonemia in carnitine-deficient adult JVS mice used by starvation.

Authors:  Xiang Xian Li; Keiko Kobayashi; Masahisa Horiuchi; Abdul Jalil; Goichiro Yoshida; Takeyori Saheki
Journal:  Metab Brain Dis       Date:  2002-12       Impact factor: 3.584

Review 6.  A general introduction to the biochemistry of mitochondrial fatty acid β-oxidation.

Authors:  Sander Michel Houten; Ronald J A Wanders
Journal:  J Inherit Metab Dis       Date:  2010-03-02       Impact factor: 4.982

Review 7.  Carnitine transport: pathophysiology and metabolism of known molecular defects.

Authors:  I Tein
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

8.  Identification of human CDV-1R and mouse Cdv-1R, two novel proteins with putative signal peptides, especially highly expressed in testis and increased with the male sex maturation.

Authors:  Jisong Peng; Long Yu; Masahisa Horiuchi; Pingzhao Zhang; Xinghua Huang; Yazhou Zhang; Dan Li; Md Abdul Jalil; Shouyyan Zhao
Journal:  Mol Biol Rep       Date:  2002-12       Impact factor: 2.316

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

Authors:  Y Shoji; A Koizumi; T Kayo; T Ohata; T Takahashi; K Harada; G Takada
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025

10.  Mitochondrial abnormalities of muscle tissue in mice with juvenile visceral steatosis associated with systemic carnitine deficiency.

Authors:  J Miyagawa; M Kuwajima; T Hanafusa; K Ozaki; H Fujimura; A Ono; R Uenaka; I Narama; T Oue; K Yamamoto
Journal:  Virchows Arch       Date:  1995       Impact factor: 4.064
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