Human NADH:ubiquinone oxidoreductase (Q28646241)

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English	Human NADH:ubiquinone oxidoreductase	scientific journal article

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instance of

scholarly article

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PubMed

PubMed publication ID

11695836

retrieved

3 February 2017

title

Human NADH:ubiquinone oxidoreductase (English)

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PubMed

PubMed publication ID

11695836

retrieved

3 February 2017

author name string

J. Smeitink

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1

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PubMed

PubMed publication ID

11695836

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3 February 2017

R. Sengers

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2

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PubMed

PubMed publication ID

11695836

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3 February 2017

F. Trijbels

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3

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PubMed

PubMed publication ID

11695836

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3 February 2017

L. van den Heuvel

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4

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PubMed

PubMed publication ID

11695836

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3 February 2017

publication date

1 June 2001

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PubMed

PubMed publication ID

11695836

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3 February 2017

published in

Journal of Bioenergetics and Biomembranes

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PubMed

PubMed publication ID

11695836

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3 February 2017

volume

33

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PubMed

PubMed publication ID

11695836

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3 February 2017

issue

3

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PubMed

PubMed publication ID

11695836

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3 February 2017

page(s)

259–266

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PubMed

PubMed publication ID

11695836

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3 February 2017

cites work

NADH:ubiquinone oxidoreductase from bovine heart mitochondria: sequence of a novel 17.2-kDa subunit.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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inferred from PubMed ID database lookup

Isolated complex I deficiency in children: clinical, biochemical and genetic aspects

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Human mitochondrial complex I in health and disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Lacticacidemia

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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The nuclear-encoded 18 kDa (IP) AQDQ subunit of bovine heart complex I is phosphorylated by the mitochondrial cAMP-dependent protein kinase

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Demonstration of a new pathogenic mutation in human complex I deficiency: a 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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The oxidative phosphorylation (OXPHOS) system: nuclear genes and human genetic diseases

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Mutation in the NDUFS4 gene of complex I abolishes cAMP-dependent activation of the complex in a child with fatal neurological syndrome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Genomic structure of the human NDUFS8 gene coding for the iron-sulfur TYKY subunit of the mitochondrial NADH:ubiquinone oxidoreductase

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Human NDUFB9 gene: genomic organization and a possible candidate gene associated with deafness disorder mapped to chromosome 8q13.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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A prognostic index as diagnostic strategy in children suspected of mitochondriocytopathy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Human complex I defects can be resolved by monoclonal antibody analysis into distinct subunit assembly patterns

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Characterization of the human complex I NDUFB7 and 17.2-kDa cDNAs and mutational analysis of 19 genes of the HP fraction in complex I-deficient-patients

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Isolation, mapping, and genomic structure of an X-linked gene for a subunit of human mitochondrial complex I.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Clinical features, investigation, and management of patients with defects of mitochondrial DNA.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Molecular Cloning and Characterization of the Human Mitochondrial NADH:Oxidoreductase 10-kDa Gene (NDUFV3)

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Practical problems in detecting abnormal mitochondrial function and genomes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Nuclear genes of human complex I of the mitochondrial electron transport chain: state of the art

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathies

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findings

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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inferred from PubMed ID database lookup

Structural organization and chromosomal localization of the human nuclear gene (NDUFV2) for the 24-kDa iron-sulfur subunit of complex I in mitochondrial respiratory chain

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Cloning of the human mitochondrial 51 kDa subunit (NDUFV1) reveals a 100% antisense homology of its 3'UTR with the 5'UTR of the gamma-interferon inducible protein (IP-30) precursor: is this a link between mitochondrial myopathy and inflammation?

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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inferred from PubMed ID database lookup

Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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cDNA of eight nuclear encoded subunits of NADH:ubiquinone oxidoreductase: human complex I cDNA characterization completed

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Human NDUFS3 gene coding for the 30-kDa subunit of mitochondrial complex I: genomic organization and expression

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical, genetic and immunoblot analyses of 17 patients with an isolated cytochrome c oxidase deficiency

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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inferred from PubMed ID database lookup

Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiency

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

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inferred from PubMed ID database lookup

Protein measurement with the Folin phenol reagent

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping of the NDUFA2, NDUFA6, NDUFA7, NDUFB8, and NDUFS8 electron transport chain genes by intron based radiation hybrid mapping

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intron based radiation hybrid mapping of 15 complex I genes of the human electron transport chain

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Membrane-bound ribosomes in HeLa cells. I. Their proportion to total cell ribosomes and their association with messenger RNA.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11695836

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1023/A:1010743321800

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4307644

Dimensions Publication ID

1013380789

0 references

OpenCitations bibliographic resource ID

4307644

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4307644

PubMed publication ID

11695836

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4307644

 

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