Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q28511075)
Watch
English
Loss of wild-type carrier-mediated L-carnitine transport activity in hepatocytes of juvenile visceral steatosis mice
scientific journal article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
title
Loss of wild-type carrier-mediated L-carnitine transport activity in hepatocytes of juvenile visceral steatosis mice
(English)
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
main subject
Solute carrier family 22 (organic cation transporter), member 5
1 reference
stated in
GOA release 2020-03-11
steatosis
1 reference
based on heuristic
inferred from title
author name string
K. Yokogawa
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
M. Yonekawa
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
I. Tamai
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
R. Ohashi
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
Y. Tatsumi
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
Y. Higashi
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
M. Nomura
series ordinal
7
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
N. Hashimoto
series ordinal
8
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
H. Nikaido
series ordinal
9
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
J. Hayakawa
series ordinal
10
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
J. Nezu
series ordinal
11
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
A. Oku
series ordinal
12
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
M. Shimane
series ordinal
13
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
K. Miyamoto
series ordinal
14
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
A. Tsuji
series ordinal
15
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
language of work or name
English
0 references
publication date
1 October 1999
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
published in
Hepatology
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
volume
30
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
issue
4
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
page(s)
997–1001
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
cites work
EFFECTS OF CARNITINE ON ACETYL-COA OXIDATION BY HEART MUSCLE MITOCHONDRIA
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Carnitine deficiency syndromes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Carnitine deficiency presenting as familial cardiomyopathy: a treatable defect in carnitine transport
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sudden neonatal death in carnitine transporter deficiency.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular and functional identification of sodium ion-dependent, high affinity human carnitine transporter OCTN2
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary systemic carnitine deficiency is caused by mutations in a gene encoding sodium ion-dependent carnitine transporter
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Infantile disease with microvesicular fatty infiltration of viscera spontaneously occurring in the C3H-H-2° strain of mouse with similarities to Reye's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Urea cycle disorder in C3H-H-2 degree mice with juvenile steatosis of viscera
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac hypertrophy in juvenile visceral steatosis (jvs) mice with systemic carnitine deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation and use of liver cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A pharmacokinetic analysis program (multi) for microcomputer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary defect of juvenile visceral steatosis (jvs) mouse with systemic carnitine deficiency is probably in renal carnitine transport system
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Carnitine transport defect in fibroblasts of juvenile visceral steatosis (JVS) mouse
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gene-dose effect on carnitine transport activity in embryonic fibroblasts of JVS mice as a model of human carnitine transporter deficiency
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Carnitine uptake into human heart cells in culture
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
L-carnitine uptake in differentiating human cultured muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of the endogenous carnitine transport and expression of a rat renal Na(+)-dependent carnitine transport system in Xenopus laevis oocytes
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Carnitine biosynthesis: identification of the cDNA encoding human gamma-butyrobetaine hydroxylase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHEP.510300423
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/HEP.510300423
0 references
PubMed ID
10498652
1 reference
stated in
PubMed
PubMed ID
10498652
retrieved
25 January 2017
ResearchGate publication ID
12801022
0 references
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
