Respiratory chain defects in the mitochondria of cultured skin fibroblasts from three patients with lacticacidemia (Q34577359)

From Wikidata

Jump to navigation Jump to search

scientific article

edit

Language	Label	Description	Also known as
English	Respiratory chain defects in the mitochondria of cultured skin fibroblasts from three patients with lacticacidemia	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

title

Respiratory chain defects in the mitochondria of cultured skin fibroblasts from three patients with lacticacidemia (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

main subject

mitochondrion

1 reference

based on heuristic

inferred from title

author name string

Robinson BH

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

Ward J

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

Goodyer P

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

Baudet A

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

language of work or name

English

0 references

publication date

1 May 1986

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

published in

Journal of Clinical Investigation

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

volume

77

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

issue

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

page(s)

1422-1427

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

cites work

Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis

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=424541

retrieved

7 July 2018

Deficiency in ubiquinone cytochrome c reductase in a patient with mitochondrial myopathy and lactic acidosis

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=424541

retrieved

7 July 2018

Progressive poliodystrophy (Alpers' disease) with a defect in cytochrome aa3 in muscle: a report of two unrelated 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=424541

retrieved

7 July 2018

Transport of reduced nicotinamide-adenine dinucleotide into mitochondria of rat white adipose tissue

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=424541

retrieved

7 July 2018

Pyridine nucleotides and rate control

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=424541

retrieved

7 July 2018

Defective intramitochondrial NADH oxidation in skin fibroblasts from an infant with fatal neonatal lacticacidemia

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=424541

retrieved

7 July 2018

Investigation of mitochondrial metabolism in small human skeletal muscle biopsy specimens. Improvement of preparation procedure.

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=424541

retrieved

7 July 2018

Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH 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=424541

retrieved

7 July 2018

Fatal infantile cytochrome c oxidase deficiency: decrease of immunologically detectable enzyme in muscle

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=424541

retrieved

7 July 2018

A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.

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=424541

retrieved

7 July 2018

An analysis of the polypeptide composition of bovine heart mitochondrial NADH-ubiquinone oxidoreductase by two-dimensional polyacrylamide-gel electrophoresis

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=424541

retrieved

7 July 2018

Leigh's encephalomyelopathy in a patient with cytochrome c oxidase deficiency in muscle tissue

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=424541

retrieved

7 July 2018

Letter: A metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness

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=424541

retrieved

28 July 2018

Mitochondrial encephalomyopathies: biochemical studies in two cases revealing defects in the respiratory chain

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=424541

retrieved

27 October 2018

Lactic acidosis, neurological deterioration and compromised cellular pyruvate oxidation due to a defect in the reoxidation of cytoplasmically generated NADH.

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=424541

retrieved

27 October 2018

Two siblings with cytochromec oxidase 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=424541

retrieved

27 October 2018

A mitochondrial myopathy with a defective respiratory chain and carnitine 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=424541

retrieved

27 October 2018

Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Revised assays for the investigation of congenital lactic acidosis using 14C keto acids, eliminating problems associated with spontaneous decarboxylation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of cytochromes b and aa3 in muscle from a floppy infant with cytochrome oxidase deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cytochrome-related inherited disorder of the nervous system and muscle

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oxidative phosphorylation in mitochondria isolated from human fibroblasts

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal infhntile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactic acidosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitochondrial myopathy. Biochemical studies revealing a deficiency of NADH--cytochrome b reductase activity

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Childhood mitochondrial myopathy with ophthalmoplegia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Progressive infantile poliodystrophy. Association with disturbed pyruvate oxidation in muscle and liver

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytochrome-c-oxidase deficiency in a floppy infant

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3009544

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1172/JCI112453

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

PMC publication ID

424541

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

PubMed publication ID

3009544

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3009544

retrieved

3 August 2017

 

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

Retrieved from "https://www.wikidata.org/w/index.php?title=Q34577359&oldid=1975899555"