Gene-dose effect on carnitine transport activity in embryonic fibroblasts of JVS mice as a model of human carnitine transporter deficiency (Q28512898)

25 January 2017

title

Gene-dose effect on carnitine transport activity in embryonic fibroblasts of JVS mice as a model of human carnitine transporter deficiency (English)

1 reference

Solute carrier family 22 (organic cation transporter), member 5

25 January 2017

main subject

1 reference

GOA release 2020-03-11

author name string

N. Hashimoto

1

1 reference

25 January 2017

F. Suzuki

2

1 reference

25 January 2017

I. Tamai

3

1 reference

25 January 2017

H. Nikaido

4

1 reference

25 January 2017

M. Kuwajima

5

1 reference

25 January 2017

J. Hayakawa

6

1 reference

25 January 2017

A. Tsuji

7

1 reference

25 January 2017

language of work or name

English

0 references

publication date

15 May 1998

1 reference

25 January 2017

published in

Biochemical Pharmacology

1 reference

25 January 2017

volume

55

1 reference

25 January 2017

issue

10

1 reference

25 January 2017

page(s)

1729–1732

1 reference

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

25 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

Abnormal gene expression and regulation in the liver of jvs mice with systemic carnitine deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

Carnitine transport defect in fibroblasts of juvenile visceral steatosis (JVS) mouse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

Hereditary defect in carnitine membrane transport is expressed in skin fibroblasts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

First prenatal diagnosis of the carnitine transporter defect

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

Primary carnitine deficiency: Heterozygote and intrafamilial phenotypic variation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-2952%2897%2900670-9

10.1016/S0006-2952(97)00670-9

7 January 2021

Identifiers

DOI

0 references

1 reference