(Q38299817)

1 September 2017

title

Mitochondrial respiratory chain deficiency in Caenorhabditis elegans results in developmental arrest and increased life span (English)

1 reference

ATP synthase subunit beta, mitochondrial CELE_C34E10.6

1 September 2017

main subject

Caenorhabditis elegans

0 references

1 reference

NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial CELE_C09H10.3

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

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Tsang WY

1

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1 September 2017

Sayles LC

2

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1 September 2017

Grad LI

3

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1 September 2017

Pilgrim DB

4

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1 September 2017

Lemire BD

5

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1 September 2017

language of work or name

English

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publication date

15 June 2001

1 reference

Journal of Biological Chemistry

1 September 2017

number of pages

7

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based on heuristic

inferred from page(s)

published in

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1 September 2017

volume

276

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1 September 2017

issue

34

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1 September 2017

page(s)

32240-32246

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

1 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Iron-sulfur clusters/semiquinones in complex I.

21 January 2018

1 reference

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Deficiency of respiratory chain complex I is a common cause of Leigh disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Human complex I deficiency: clinical spectrum and involvement of oxygen free radicals in the pathogenicity of the defect

21 January 2018

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Human mitochondrial complex I in health and disease

21 January 2018

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Mutant NDUFV1 subunit of mitochondrial complex I causes leukodystrophy and myoclonic epilepsy

21 January 2018

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The ATP synthase--a splendid molecular machine

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Structure at 2.8 A resolution of F1-ATPase from bovine heart mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M103999200

Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice

21 January 2018

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Mitochondrial diseases in man and mouse

21 January 2018

1 reference

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Role of the mitochondrial genome during early development in mice. Effects of ethidium bromide and chloramphenicol

21 January 2018

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Genome sequence of the nematode C. elegans: a platform for investigating biology

21 January 2018

1 reference

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Reverse genetics by chemical mutagenesis in Caenorhabditis elegans

21 January 2018

1 reference

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The Saccharomyces cerevisiae TCM62 gene encodes a chaperone necessary for the assembly of the mitochondrial succinate dehydrogenase (complex II).

21 January 2018

1 reference

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RNA interference: genetic wand and genetic watchdog

21 January 2018

1 reference

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Disruption of the gene encoding the NADH-binding subunit of NADH: ubiquinone oxidoreductase in Neurospora crassa. Formation of a partially assembled enzyme without FMN and the iron-sulphur cluster N-3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Computational method to predict mitochondrially imported proteins and their targeting sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Specific interference by ingested dsRNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

A common muscarinic pathway for diapause recovery in the distantly related nematode species Caenorhabditis elegans and Ancylostoma caninum

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

A mutation in succinate dehydrogenase cytochrome b causes oxidative stress and ageing in nematodes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

GAS-1: a mitochondrial protein controls sensitivity to volatile anesthetics in the nematode Caenorhabditis elegans

21 January 2018

1 reference

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Mitochondrial expression and function of GAS-1 in Caenorhabditis elegans

21 January 2018

1 reference

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Genomic analysis of gene expression in C. elegans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Cytochrome c deficiency causes embryonic lethality and attenuates stress-induced apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Functional genomic analysis of C. elegans chromosome I by systematic RNA interference

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Functional genomic analysis of cell division in C. elegans using RNAi of genes on chromosome III

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Requirement of NAD and SIR2 for life-span extension by calorie restriction in Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

The genetics of caloric restriction in Caenorhabditis elegans

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Aging, energy, and oxidative stress in neurodegenerative diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Medical significance of Caenorhabditis elegans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

A role for Caenorhabditis elegans in understanding the function and interactions of human disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

A novel deficiency of mitochondrial ATPase of nuclear origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Mutations in mtDNA: are we scraping the bottom of the barrel?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Clinical differences in patients with mitochondriocytopathies due to nuclear versus mitochondrial DNA mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Mitochondrial respiratory chain diseases and mutations in nuclear DNA: a promising start?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

21 January 2018

Mitochondrial disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Assembly of mitochondrial ATP synthase in cultured human cells: implications for mitochondrial diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

Reverse genetics: from gene sequence to mutant worm.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

RNAi in C. elegans: soaking in the genome sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

21 January 2018

Mitochondrial medicine

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103999200

21 January 2018

Identifiers

DOI

10.1074/JBC.M103999200

1 reference

1 September 2017

1 reference