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(Q28505245)
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English
Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death
scientific journal article
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Statements
instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
title
Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden death
(English)
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
main subject
hypoglycemia
1 reference
based on heuristic
inferred from title
Hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta
1 reference
stated in
GOA release 2020-03-11
Hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha
1 reference
stated in
GOA release 2020-03-11
mitochondrion
1 reference
based on heuristic
inferred from title
author name string
J. A. Ibdah
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
H. Paul
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
Y. Zhao
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
S. Binford
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
K. Salleng
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
M. Cline
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
D. Matern
series ordinal
7
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
M. J. Bennett
series ordinal
8
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
P. Rinaldo
series ordinal
9
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
A. W. Strauss
series ordinal
10
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
language of work or name
English
0 references
publication date
1 June 2001
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
published in
Journal of Clinical Investigation
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
volume
107
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
page(s)
1403–1409
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
issue
11
1 reference
stated in
PubMed
PubMed ID
11390422
retrieved
24 January 2017
cites work
Liver disease in pregnancy and fetal fatty acid oxidation defects
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
19 March 2017
Disorders of mitochondrial fatty acyl-CoA beta-oxidation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
19 March 2017
Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
19 March 2017
Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
19 March 2017
Q28287645
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
19 March 2017
Structural analysis of cDNAs for subunits of human mitochondrial fatty acid beta-oxidation trifunctional protein
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
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19 March 2017
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
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19 March 2017
Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction
2 references
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
19 March 2017
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
29 September 2017
Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. II. Purification and properties of enoyl-coenzyme A (CoA) hydratase/3-hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase trifunctional protein
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
19 March 2017
Combined enzyme defect of mitochondrial fatty acid oxidation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
19 March 2017
Recognition and management of fatty acid oxidation defects: a series of 107 patients.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
29 September 2017
A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
29 September 2017
Mitochondrial trifunctional protein deficiency. Catalytic heterogeneity of the mutant enzyme in two patients
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
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29 September 2017
The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
29 September 2017
Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
29 September 2017
Molecular characterization of mitochondrial trifunctional protein deficiency: formation of the enzyme complex is important for stabilization of both alpha- and beta-subunits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
2 June 2018
Arrhythmias and conduction defects as presenting symptoms of fatty acid oxidation disorders in children
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
27 November 2018
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: variable expressivity of maternal illness during pregnancy and unusual presentation with infantile cholestasis and hypocalcaemia.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
27 November 2018
Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liver.
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
27 November 2018
Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=209324
retrieved
27 November 2018
Pregnancy and fetal long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11390422
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Clinical and biochemical presentation of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11390422
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11390422
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/11390422
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1172/JCI12590
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
962173
OpenCitations bibliographic resource ID
962173
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
962173
PMCID
209324
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
962173
PubMed ID
11390422
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
962173
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