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

about

Mitochondrial Chaperones in the Brain: Safeguarding Brain Health and Metabolism?Assembly of mammalian oxidative phosphorylation complexes I-V and supercomplexes Mitochondrial complex I assembly model OXPHOS system Human diseases associated with defects in assembly of OXPHOS complexes

P2860

Q55283805-BE29198E-2DEC-4FB4-BB2D-BCE55150F078 Q56760543-6C88D8AB-BEE5-455E-A26C-CDE7E630361B Q56854959-D42D267F-C261-4B77-A501-0ED34B92958C Q57175222-EE30C46F-69B3-4D9D-930A-1799F1069DA6

P2860

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

Item

http://www.wikidata.org/entity/Q38769102

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

A Mutation in the Flavin Adeni ...... horylation Complexes I and II.

@en

type

Item

label

A Mutation in the Flavin Adeni ...... horylation Complexes I and II.

@en

prefLabel

A Mutation in the Flavin Adeni ...... horylation Complexes I and II.

@en

P1476

A Mutation in the Flavin Adeni ...... horylation Complexes I and II.

@en

P2093

Eric A Shoubridge

http://www.w3.org/2001/XMLSchema#string

Hana Antonicka

http://www.w3.org/2001/XMLSchema#string

Olga Zurita Rendón

http://www.w3.org/2001/XMLSchema#string

P2860

Molecular characterization of mitochondrial apoptosis-inducing factor

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

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

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

C6ORF66 is an assembly factor of mitochondrial complex I

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

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

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

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

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

P304

2132-2140

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1128/MCB.00066-16

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Rita Horvath

P577

2016-05-23T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

27215383

http://www.w3.org/2001/XMLSchema#string

P921

phosphorylation

P932

4968213

http://www.w3.org/2001/XMLSchema#string

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

about

P2860

P2860

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

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932