Related references
Note: Only part of the references are listed.Assembly factors as a new class of disease genes for mitochondrial complex I deficiency: cause, pathology and treatment options
Jessica Nouws et al.
BRAIN (2012)
Complexome Profiling Identifies TMEM126B as a Component of the Mitochondrial Complex I Assembly Complex
Heinrich Heide et al.
CELL METABOLISM (2012)
Early complex I assembly defects result in rapid turnover of the ND1 subunit
Olga Zurita Rendon et al.
HUMAN MOLECULAR GENETICS (2012)
Combined OXPHOS complex I and IV defect, due to mutated complex I assembly factor C20ORF7
Ann Saada et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2012)
A proteolytic cleavage assay to monitor autophagy in Dictyostelium discoideum
Javier Calvo-Garrido et al.
AUTOPHAGY (2011)
The induction of autophagy by mechanical stress
Jason S. King et al.
AUTOPHAGY (2011)
Why does mitochondrial complex I have so many subunits?
Judy Hirst
BIOCHEMICAL JOURNAL (2011)
Biochemical diagnosis of mitochondrial disorders
Richard J. T. Rodenburg
JOURNAL OF INHERITED METABOLIC DISEASE (2011)
Mutations in the Gene Encoding C8orf38 Block Complex I Assembly by Inhibiting Production of the Mitochondria-Encoded Subunit ND1
Matthew McKenzie et al.
JOURNAL OF MOLECULAR BIOLOGY (2011)
The AMPK signalling pathway coordinates cell growth, autophagy and metabolism
Maria M. Mihaylova et al.
NATURE CELL BIOLOGY (2011)
CDD: a Conserved Domain Database for the functional annotation of proteins
Aron Marchler-Bauer et al.
NUCLEIC ACIDS RESEARCH (2011)
Dictyostelium as a model for human disease
Ricardo Escalante
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2011)
The Dictyostelium model for mitochondrial disease
Lisa M. Francione et al.
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2011)
Two modes of mitochondrial dysfunction lead independently to lifespan extension in Caenorhabditis elegans
Wen Yang et al.
AGING CELL (2010)
Mammalian Mitochondrial Complex I: Biogenesis, Regulation, and Reactive Oxygen Species Generation
Werner J. H. Koopman et al.
ANTIOXIDANTS & REDOX SIGNALING (2010)
Autophagy in Dictyostelium Genes and pathways, cell death and infection
Javier Calvo-Garrido et al.
AUTOPHAGY (2010)
Mitochondrial fatty acid synthesis and respiration
J. Kalervo Hiltunen et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2010)
Acyl-CoA Dehydrogenase 9 Is Required for the Biogenesis of Oxidative Phosphorylation Complex I
Jessica Nouws et al.
CELL METABOLISM (2010)
FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy
Elisa Fassone et al.
HUMAN MOLECULAR GENETICS (2010)
Assembly Factors of Human Mitochondrial Complex I and Their Defects in Disease
Matthew Mckenzie et al.
IUBMB LIFE (2010)
MidA is a putative methyltransferase that is required for mitochondrial complex I function
Sergio Carilla-Latorre et al.
JOURNAL OF CELL SCIENCE (2010)
Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome
M. Gerards et al.
JOURNAL OF MEDICAL GENETICS (2010)
The Subunit Composition of Mitochondrial NADH:Ubiquinone Oxidoreductase (Complex I) From Pichia pastoris
Hannah R. Bridges et al.
MOLECULAR & CELLULAR PROTEOMICS (2010)
The architecture of respiratory complex I
Rouslan G. Efremov et al.
NATURE (2010)
Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency
Tobias B. Haack et al.
NATURE GENETICS (2010)
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency
Sarah E. Calvo et al.
NATURE GENETICS (2010)
Regulation of Mammalian Autophagy in Physiology and Pathophysiology
Brinda Ravikumar et al.
PHYSIOLOGICAL REVIEWS (2010)
Genome-wide analysis reveals mechanisms modulating autophagy in normal brain aging and in Alzheimer's disease
Marta M. Lipinski et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Mutations in NDUFAF3 (C3ORF60), Encoding an NDUFAF4 (C6ORF66)-interacting Complex I Assembly Protein, Cause Fatal Neonatal Mitochondrial Disease
Ann Saada et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Assembly of mitochondrial complex I and defects in disease
Michael Lazarou et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2009)
Jalview Version 2-a multiple sequence alignment editor and analysis workbench
Andrew M. Waterhouse et al.
BIOINFORMATICS (2009)
Databases of homologous gene families for comparative genomics
Simon Penel et al.
BMC BIOINFORMATICS (2009)
Mitochondrial Respiratory Complex I: Structure, Function and Implication in Human Diseases
Lokendra K. Sharma et al.
CURRENT MEDICINAL CHEMISTRY (2009)
Baculovirus Complementation Restores a Novel NDUFAF2 Mutation Causing Complex I Deficiency
Saskia J. G. Hoefs et al.
HUMAN MUTATION (2009)
Mitochondrial Fatty Acid Synthesis Type II: More than Just Fatty Acids
J. Kalervo Hiltunen et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Dictyostelium discoideum-a model for many reasons
Sarah J. Annesley et al.
MOLECULAR AND CELLULAR BIOCHEMISTRY (2009)
Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease
Canny Sugiana et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
A mitochondrial protein compendium elucidates complex I disease biology
David J. Pagliarini et al.
CELL (2008)
Clustal W and clustal X version 2.0
M. A. Larkin et al.
BIOINFORMATICS (2007)
From endosymbiont to host-controlled organelle:: The hijacking of mitochondrial protein synthesis and metabolism
Toni Gabaldon et al.
PLOS COMPUTATIONAL BIOLOGY (2007)
Diverse cytopathologies in mitochondrial disease are caused by AMP-activated protein kinase signaling
Paul B. Bokko et al.
MOLECULAR BIOLOGY OF THE CELL (2007)
Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly
Rutger O. Vogel et al.
GENES & DEVELOPMENT (2007)
Mitochondrial complex I: Structure, function and pathology
Rolf J. R. J. Janssen et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2006)
Functional genomics in Dictyostelium:: MidA, a new conserved protein, is required for mitochondrial function and development
P Torija et al.
JOURNAL OF CELL SCIENCE (2006)
Human mitochondrial complex I assembly is mediated by NDUFAF1
RO Vogel et al.
FEBS JOURNAL (2005)
A molecular chaperone for mitochondrial complex I assembly is mutated in a progressive encephalopathy
I Ogilvie et al.
JOURNAL OF CLINICAL INVESTIGATION (2005)
The post-translational modifications of the nuclear encoded subunits of complex I from bovine heart mitochondria
J Carroll et al.
MOLECULAR & CELLULAR PROTEOMICS (2005)
Two Dictyostelium orthologs of the prokaryotic cell division protein FtsZ localize to mitochondria and are required for the maintenance of normal mitochondrial morphology
PR Gilson et al.
EUKARYOTIC CELL (2003)
A method for the comprehensive proteomic analysis of membrane proteins
CC Wu et al.
NATURE BIOTECHNOLOGY (2003)
Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60
JJ Hansen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Tortoise, a novel mitochondrial protein, is required for directional responses of Dictyostelium in chemotactic gradients
S van Es et al.
JOURNAL OF CELL BIOLOGY (2001)
Share Paper
