(Q38769102)

English

A Mutation in the Flavin Adenine Dinucleotide-Dependent Oxidoreductase FOXRED1 Results in Cell-Type-Specific Assembly Defects in Oxidative Phosphorylation Complexes I and II.

scientific article published on 23 May 2016

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

6 September 2017

A Mutation in the Flavin Adenine Dinucleotide-Dependent Oxidoreductase FOXRED1 Results in Cell-Type-Specific Assembly Defects in Oxidative Phosphorylation Complexes I and II. (English)

1 reference

Europe PubMed Central

PMC publication ID

6 September 2017

phosphorylation

1 reference

based on heuristic

inferred from title

object named as

Rita Horvath

3

0 references

author name string

Olga Zurita Rendón

1

1 reference

Europe PubMed Central

PMC publication ID

6 September 2017

Hana Antonicka

2

1 reference

Europe PubMed Central

PMC publication ID

6 September 2017

Eric A Shoubridge

4

1 reference

Europe PubMed Central

PMC publication ID

6 September 2017

language of work or name

0 references

publication date

23 May 2016

1 reference

Europe PubMed Central

PMC publication ID

6 September 2017

Molecular and Cellular Biology

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Europe PubMed Central

PMC publication ID

6 September 2017

36

1 reference

Europe PubMed Central

PMC publication ID

6 September 2017

16

1 reference

Europe PubMed Central

PMC publication ID

6 September 2017

2132-2140

1 reference

Europe PubMed Central

PMC publication ID

6 September 2017

Characterization of mitochondrial FOXRED1 in the assembly of respiratory chain complex I

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

The arginine methyltransferase NDUFAF7 is essential for complex I assembly and early vertebrate embryogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Assembly factors for the membrane arm of human complex I.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

NDUFAF7 methylates arginine 85 in the NDUFS2 subunit of human complex I

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Crystal structure of the entire respiratory complex I

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Understanding mitochondrial complex I assembly in health and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex I

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Assembly factors of human mitochondrial complex I and their defects in disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma

1 reference

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6 September 2017

Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome

1 reference

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6 September 2017

Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Mitochondrial complex I deficiency: from organelle dysfunction to clinical disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

A mitochondrial protein compendium elucidates complex I disease biology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Assembly of mitochondrial complex I and defects in disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

The iron-sulphur protein Ind1 is required for effective complex I assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

C6ORF66 is an assembly factor of mitochondrial complex I

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

The mitochondrial transcription factor TFAM coordinates the assembly of multiple DNA molecules into nucleoid-like structures

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Identification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Dissociating the dual roles of apoptosis-inducing factor in maintaining mitochondrial structure and apoptosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Mitochondrial complex I: structure, function and pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Human mitochondrial complex I assembly is mediated by NDUFAF1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

A molecular chaperone for mitochondrial complex I assembly is mutated in a progressive encephalopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

AIF deficiency compromises oxidative phosphorylation

1 reference

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6 September 2017

Mitochondrial disorders: prevalence, myths and advances.

1 reference

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6 September 2017

Riboflavin uptake and FAD synthesis in Saccharomyces cerevisiae mitochondria: involvement of the Flx1p carrier in FAD export

1 reference

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6 September 2017

Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Molecular characterization of mitochondrial apoptosis-inducing factor

1 reference

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6 September 2017

Blue native electrophoresis for isolation of membrane protein complexes in enzymatically active form

1 reference

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6 September 2017

Mutations in SDHD lead to autosomal recessive encephalomyopathy and isolated mitochondrial complex II deficiency

1 reference

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6 September 2017

Early complex I assembly defects result in rapid turnover of the ND1 subunit

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

6 September 2017

Five entry points of the mitochondrially encoded subunits in mammalian complex I assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

14 September 2017

Riboflavin-responsive defects of beta-oxidation

1 reference

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14 September 2017

A structural model for FOXRED1, an FAD-dependent oxidoreductase necessary for NADH: Ubiquinone oxidoreductase (complex I) assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

25 September 2017

Mass estimation of native proteins by blue native electrophoresis: principles and practical hints

1 reference

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23 June 2018

Expression of the E6 and E7 genes of human papillomavirus (HPV16) extends the life span of human myoblasts

1 reference

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23 June 2018

Evolution of FOXRED1, an FAD-dependent oxidoreductase necessary for NADH:ubiquinone oxidoreductase (Complex I) assembly.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

31 August 2018

Complexome profiling identifies TMEM126B as a component of the mitochondrial complex I assembly complex.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

31 August 2018

Analysis of oxidative phosphorylation complexes in cultured human fibroblasts and amniocytes by blue-native-electrophoresis using mitoplasts isolated with the help of digitonin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

31 August 2018

Radioactive labeling of mitochondrial translation products in cultured cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4968213

4 November 2018

Identifiers

10.1128/MCB.00066-16

1 reference

Europe PubMed Central

PMC publication ID

6 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

6 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

6 September 2017

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