Accessory subunits are integral for assembly and function of human mitochondrial complex I
Published 2016 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Accessory subunits are integral for assembly and function of human mitochondrial complex I
Authors
Keywords
-
Journal
NATURE
Volume 538, Issue 7623, Pages 123-126
Publisher
Springer Nature
Online
2016-09-13
DOI
10.1038/nature19754
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Mitochondrial complex I-linked disease
- (2016) Richard J. Rodenburg BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- Unraveling the complexity of mitochondrial complex I assembly: A dynamic process
- (2016) Laura Sánchez-Caballero et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- Mitochondrial unfolded protein response controls matrix pre-RNA processing and translation
- (2016) Christian Münch et al. NATURE
- Structure of mammalian respiratory complex I
- (2016) Jiapeng Zhu et al. NATURE
- Exome sequencing of patients with histiocytoid cardiomyopathy reveals a de novoNDUFB11mutation that plays a role in the pathogenesis of histiocytoid cardiomyopathy
- (2015) Bahig M. Shehata et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- The BioPlex Network: A Systematic Exploration of the Human Interactome
- (2015) Edward L. Huttlin et al. CELL
- Mutation in NDUFA13/GRIM19 leads to early onset hypotonia, dyskinesia and sensorial deficiencies, and mitochondrial complex I instability
- (2015) Claire Angebault et al. HUMAN MOLECULAR GENETICS
- COA6 is a mitochondrial complex IV assembly factor critical for biogenesis of mtDNA-encoded COX2
- (2015) David A. Stroud et al. HUMAN MOLECULAR GENETICS
- Characterization of mitochondrial FOXRED1 in the assembly of respiratory chain complex I
- (2015) Luke E. Formosa et al. HUMAN MOLECULAR GENETICS
- Mistargeted mitochondrial proteins activate a proteostatic response in the cytosol
- (2015) Lidia Wrobel et al. NATURE
- New roles for mitochondrial proteases in health, ageing and disease
- (2015) Pedro M. Quirós et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- A giant molecular proton pump: structure and mechanism of respiratory complex I
- (2015) Leonid A. Sazanov NATURE REVIEWS MOLECULAR CELL BIOLOGY
- MitoCarta2.0: an updated inventory of mammalian mitochondrial proteins
- (2015) Sarah E. Calvo et al. NUCLEIC ACIDS RESEARCH
- PAT-seq: a method to study the integration of 3'-UTR dynamics with gene expression in the eukaryotic transcriptome
- (2015) P. F. Harrison et al. RNA
- Mechanistic insight from the crystal structure of mitochondrial complex I
- (2015) V. Zickermann et al. SCIENCE
- Structural and functional analysis of MiD51, a dynamin receptor required for mitochondrial fission
- (2014) Viviane Richter et al. JOURNAL OF CELL BIOLOGY
- Architecture of mammalian respiratory complex I
- (2014) Kutti R. Vinothkumar et al. NATURE
- Minimal, encapsulated proteomic-sample processing applied to copy-number estimation in eukaryotic cells
- (2014) Nils A Kulak et al. NATURE METHODS
- CHOPCHOP: a CRISPR/Cas9 and TALEN web tool for genome editing
- (2014) Tessa G. Montague et al. NUCLEIC ACIDS RESEARCH
- PINK1 Loss-of-Function Mutations Affect Mitochondrial Complex I Activity via NdufA10 Ubiquinone Uncoupling
- (2014) V. A. Morais et al. SCIENCE
- Low abundance of the matrix arm of complex I in mitochondria predicts longevity in mice
- (2014) Satomi Miwa et al. Nature Communications
- Mitochondrial Complex I
- (2013) Judy Hirst Annual Review of Biochemistry
- Partial complex I deficiency due to the CNS conditional ablation of Ndufa5 results in a mild chronic encephalopathy but no increase in oxidative damage
- (2013) Susana Peralta et al. HUMAN MOLECULAR GENETICS
- Crystal structure of the entire respiratory complex I
- (2013) Rozbeh Baradaran et al. NATURE
- Genome engineering using the CRISPR-Cas9 system
- (2013) F Ann Ran et al. Nature Protocols
- Assembly factors for the membrane arm of human complex I
- (2013) B. Andrews et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Supercomplex Assembly Determines Electron Flux in the Mitochondrial Electron Transport Chain
- (2013) E. Lapuente-Brun et al. SCIENCE
- A constant and similar assembly defect of mitochondrial respiratory chain complex I allows rapid identification of NDUFS4 mutations in patients with Leigh syndrome
- (2012) Z. Assouline et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
- Complexome Profiling Identifies TMEM126B as a Component of the Mitochondrial Complex I Assembly Complex
- (2012) Heinrich Heide et al. Cell Metabolism
- Gene Knockout Using Transcription Activator-like Effector Nucleases (TALENs) Reveals That Human NDUFA9 Protein Is Essential for Stabilizing the Junction between Membrane and Matrix Arms of Complex I
- (2012) David A. Stroud et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing
- (2012) Tobias B Haack et al. JOURNAL OF MEDICAL GENETICS
- Mitochondrial disorders as windows into an ancient organelle
- (2012) Scott B. Vafai et al. NATURE
- FLASH assembly of TALENs for high-throughput genome editing
- (2012) Deepak Reyon et al. NATURE BIOTECHNOLOGY
- NIH Image to ImageJ: 25 years of image analysis
- (2012) Caroline A Schneider et al. NATURE METHODS
- ePAT: A simple method to tag adenylated RNA to measure poly(A)-tail length and other 3' RACE applications
- (2012) A. Janicke et al. RNA
- Understanding mitochondrial complex I assembly in health and disease
- (2011) Masakazu Mimaki et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- Using control genes to correct for unwanted variation in microarray data
- (2011) J. A. Gagnon-Bartsch et al. BIOSTATISTICS
- Defective NDUFA9 as a novel cause of neonatally fatal complex I disease
- (2011) B J C van den Bosch et al. JOURNAL OF MEDICAL GENETICS
- Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes includingNDUFB9
- (2011) Tobias B Haack et al. JOURNAL OF MEDICAL GENETICS
- Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome
- (2011) E. Ostergaard et al. JOURNAL OF MEDICAL GENETICS
- Composition and Topology of the Endoplasmic Reticulum–Mitochondria Encounter Structure
- (2011) David A. Stroud et al. JOURNAL OF MOLECULAR BIOLOGY
- Andromeda: A Peptide Search Engine Integrated into the MaxQuant Environment
- (2011) Jürgen Cox et al. JOURNAL OF PROTEOME RESEARCH
- Dual Function of Sdh3 in the Respiratory Chain and TIM22 Protein Translocase of the Mitochondrial Inner Membrane
- (2011) Natalia Gebert et al. MOLECULAR CELL
- NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease
- (2010) Saskia J G Hoefs et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Quantitative proteomics combined with BAC TransgeneOmics reveals in vivo protein interactions
- (2010) Nina C. Hubner et al. JOURNAL OF CELL BIOLOGY
- ZiFiT (Zinc Finger Targeter): an updated zinc finger engineering tool
- (2010) J. D. Sander et al. NUCLEIC ACIDS RESEARCH
- Enrichment Map: A Network-Based Method for Gene-Set Enrichment Visualization and Interpretation
- (2010) Daniele Merico et al. PLoS One
- A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology
- (2008) David J. Pagliarini et al. CELL
- Respiratory Active Mitochondrial Supercomplexes
- (2008) Rebeca Acín-Pérez et al. MOLECULAR CELL
- MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification
- (2008) Jürgen Cox et al. NATURE BIOTECHNOLOGY
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started