Early complex I assembly defects result in rapid turnover of the ND1 subunit
Published 2012 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Early complex I assembly defects result in rapid turnover of the ND1 subunit
Authors
Keywords
-
Journal
HUMAN MOLECULAR GENETICS
Volume 21, Issue 17, Pages 3815-3824
Publisher
Oxford University Press (OUP)
Online
2012-06-01
DOI
10.1093/hmg/dds209
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Mitochondrial AAA proteases — Towards a molecular understanding of membrane-bound proteolytic machines
- (2011) Florian Gerdes et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
- Presequence-dependent folding ensures MrpL32 processing by them-AAA protease in mitochondria
- (2011) Florian Bonn et al. EMBO JOURNAL
- Mutations in the Gene Encoding C8orf38 Block Complex I Assembly by Inhibiting Production of the Mitochondria-Encoded Subunit ND1
- (2011) Matthew McKenzie et al. JOURNAL OF MOLECULAR BIOLOGY
- Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect
- (2010) Hana Antonicka et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Acyl-CoA Dehydrogenase 9 Is Required for the Biogenesis of Oxidative Phosphorylation Complex I
- (2010) Jessica Nouws et al. Cell Metabolism
- FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy
- (2010) Elisa Fassone et al. HUMAN MOLECULAR GENETICS
- Five Entry Points of the Mitochondrially Encoded Subunits in Mammalian Complex I Assembly
- (2010) E. Perales-Clemente et al. MOLECULAR AND CELLULAR BIOLOGY
- LRPPRC and SLIRP Interact in a Ribonucleoprotein Complex That Regulates Posttranscriptional Gene Expression in Mitochondria
- (2010) Florin Sasarman et al. MOLECULAR BIOLOGY OF THE CELL
- High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency
- (2010) Sarah E Calvo et al. NATURE GENETICS
- Functional Modules and Structural Basis of Conformational Coupling in Mitochondrial Complex I
- (2010) C. Hunte et al. SCIENCE
- Mutations in NDUFAF3 (C3ORF60), Encoding an NDUFAF4 (C6ORF66)-Interacting Complex I Assembly Protein, Cause Fatal Neonatal Mitochondrial Disease
- (2009) Ann Saada et al. AMERICAN JOURNAL OF HUMAN GENETICS
- C6ORF66 Is an Assembly Factor of Mitochondrial Complex I
- (2008) Ann Saada et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease
- (2008) Canny Sugiana et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Subunits of Mitochondrial Complex I Exist as Part of Matrix- and Membrane-associated Subcomplexes in Living Cells
- (2008) Cindy E. J. Dieteren et al. JOURNAL OF BIOLOGICAL CHEMISTRY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreDiscover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversation