(Q33894446)

English

Carnitine-acylcarnitine translocase deficiency with severe hypoglycemia and auriculo ventricular block. Translocase assay in permeabilized fibroblasts

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Carnitine-acylcarnitine translocase deficiency with severe hypoglycemia and auriculo ventricular block. Translocase assay in permeabilized fibroblasts (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

carnitine-acylcarnitine translocase deficiency

0 references

1 reference

based on heuristic

inferred from title

author name string

Pande SV

1

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Brivet M

2

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Slama A

3

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Demaugre F

4

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Aufrant C

5

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Saudubray JM

6

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

language of work or name

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publication date

1 March 1993

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Journal of Clinical Investigation

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Europe PubMed Central

PubMed publication ID

29 July 2017

91

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

1247-1252

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Protein measurement with the Folin phenol reagent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Oxidation of fatty acids in cultured fibroblasts: a model system for the detection and study of defects in oxidation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Regulation of hepatic fatty acid oxidation and ketone body production

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Muscle Carnitine Palmityltransferase Deficiency and Myoglobinuria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Myocardial metabolism of free fatty acids. Studies with 14C-labeled substrates in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Complementation analysis of fatty acid oxidation disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

A carnitine/acylcarnitine translocase assay applicable to biopsied muscle specimens without requiring mitochondrial isolation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Prophylaxis of early ventricular fibrillation by inhibition of acylcarnitine accumulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

2,4-Dienoyl-coenzyme A reductase deficiency: a possible new disorder of fatty acid oxidation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. Physiopathological approach to carnitine palmitoyltransferase II deficiencies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Brief report: a deficiency of carnitine-acylcarnitine translocase in the inner mitochondrial membrane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

Approach to the patient with a fatty acid oxidation disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

A mitochondrial carnitine acylcarnitine translocase system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

5 July 2018

The L-3-hydroxyacyl-CoA dehydrogenase deficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

29 October 2018

Identification and purification of the carnitine carrier from rat liver mitochondria

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=288085

29 October 2018

Fuel Homeostasis in Exercise

1 reference

https://pubmed.ncbi.nlm.nih.gov/8450053

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Decreased ketogenesis due to deficiency of hepatic carnitine acyl transferase

1 reference

https://pubmed.ncbi.nlm.nih.gov/8450053

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carnitine-acylcarnitine translocase catalyzes an equilibrating unidirectional transport as well

1 reference

https://pubmed.ncbi.nlm.nih.gov/8450053

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inhibition of mitochondrial carnitine-acylcarnitine translocase by sulfobetaines

1 reference

https://pubmed.ncbi.nlm.nih.gov/8450053

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8450053

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Protein microinjection by protease permeabilization of fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/8450053

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI116288

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

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