Loss of COX4I1 Leads to Combined Respiratory Chain Deficiency and Impaired Mitochondrial Protein Synthesis
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Title
Loss of COX4I1 Leads to Combined Respiratory Chain Deficiency and Impaired Mitochondrial Protein Synthesis
Authors
Keywords
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Journal
Cells
Volume 10, Issue 2, Pages 369
Publisher
MDPI AG
Online
2021-02-12
DOI
10.3390/cells10020369
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Note: Only part of the references are listed.- Respiratory supercomplexes act as a platform for complex III ‐mediated maturation of human mitochondrial complexes I and IV
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- (2020) David Pajuelo Reguera et al. Cells
- HIGD2A is required for assembly of the COX3 module of human mitochondrial complex IV
- (2020) Daniella H Hock et al. MOLECULAR & CELLULAR PROTEOMICS
- Distinct Roles of Mitochondrial HIGD1A and HIGD2A in Respiratory Complex and Supercomplex Biogenesis
- (2020) Alba Timón-Gómez et al. Cell Reports
- Multiple pathways coordinate assembly of human mitochondrial complex IV and stabilization of respiratory supercomplexes
- (2020) Teresa Lobo‐Jarne et al. EMBO JOURNAL
- MITRAC15/COA1 promotes mitochondrial translation in a ND2 ribosome–nascent chain complex
- (2019) Cong Wang et al. EMBO REPORTS
- COA6 Is Structurally Tuned to Function as a Thiol-Disulfide Oxidoreductase in Copper Delivery to Mitochondrial Cytochrome c Oxidase
- (2019) Shivatheja Soma et al. Cell Reports
- Structure of the intact 14-subunit human cytochrome c oxidase
- (2018) Shuai Zong et al. CELL RESEARCH
- Assembly of mammalian oxidative phosphorylation complexes I–V and supercomplexes
- (2018) Alba Signes et al. Essays in Biochemistry
- Spatial orchestration of mitochondrial translation and OXPHOS complex assembly
- (2018) Stefan Stoldt et al. NATURE CELL BIOLOGY
- Mitochondrial cytochrome c oxidase biogenesis: Recent developments
- (2018) Alba Timón-Gómez et al. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
- COX16 promotes COX2 metallation and assembly during respiratory complex IV biogenesis
- (2018) Abhishek Aich et al. eLife
- Multi-omics analysis identifies ATF4 as a key regulator of the mitochondrial stress response in mammals
- (2017) Pedro M. Quirós et al. JOURNAL OF CELL BIOLOGY
- Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies
- (2017) René G. Feichtinger et al. Oxidative Medicine and Cellular Longevity
- MR-1S Interacts with PET100 and PET117 in Module-Based Assembly of Human Cytochrome c Oxidase
- (2017) Sara Vidoni et al. Cell Reports
- Unraveling the complexity of mitochondrial complex I assembly: A dynamic process
- (2016) Laura Sánchez-Caballero et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- Mitochondrial Protein Synthesis Adapts to Influx of Nuclear-Encoded Protein
- (2016) Ricarda Richter-Dennerlein et al. CELL
- A Genome-wide CRISPR Death Screen Identifies Genes Essential for Oxidative Phosphorylation
- (2016) Jason D. Arroyo et al. Cell Metabolism
- Ground control to major TOM: mitochondria-nucleus communication
- (2016) Michal Eisenberg-Bord et al. FEBS Journal
- Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6
- (2016) Hana Hartmannová et al. HUMAN MOLECULAR GENETICS
- The architecture of respiratory supercomplexes
- (2016) James A. Letts et al. NATURE
- The architecture of the mammalian respirasome
- (2016) Jinke Gu et al. NATURE
- Accessory subunits are integral for assembly and function of human mitochondrial complex I
- (2016) David A. Stroud et al. NATURE
- Human mitochondrial COX1 assembly into cytochrome c oxidase at a glance
- (2015) S. Dennerlein et al. JOURNAL OF CELL SCIENCE
- Making Proteins in the Powerhouse
- (2014) B. Martin Hällberg et al. Cell Metabolism
- A Novel in-Frame 18-bp Microdeletion inMT-CYBCauses a Multisystem Disorder with Prominent Exercise Intolerance
- (2014) Valeria Carossa et al. HUMAN MUTATION
- Double Nicking by RNA-Guided CRISPR Cas9 for Enhanced Genome Editing Specificity
- (2013) F. Ann Ran et al. CELL
- Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression
- (2013) Elena J. Tucker et al. PLoS Genetics
- MITRAC Links Mitochondrial Protein Translocation to Respiratory-Chain Assembly and Translational Regulation
- (2012) David U. Mick et al. CELL
- NDUFA4 Is a Subunit of Complex IV of the Mammalian Electron Transport Chain
- (2012) Eduardo Balsa et al. Cell Metabolism
- Mitochondrial Complex I Plays an Essential Role in Human Respirasome Assembly
- (2012) David Moreno-Lastres et al. Cell Metabolism
- Complexome Profiling Identifies TMEM126B as a Component of the Mitochondrial Complex I Assembly Complex
- (2012) Heinrich Heide et al. Cell Metabolism
- Nonsense mutations in the COX1 subunit impair the stability of respiratory chain complexes rather than their assembly
- (2012) Hue-Tran Hornig-Do et al. EMBO JOURNAL
- Biogenesis and assembly of eukaryotic cytochrome c oxidase catalytic core
- (2011) Ileana C. Soto et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- Mice deleted for heart-type cytochrome c oxidase subunit 7a1 develop dilated cardiomyopathy
- (2011) Maik Hüttemann et al. MITOCHONDRION
- Novel insights into the assembly and function of human nuclear-encoded cytochromecoxidase subunits 4, 5a, 6a, 7a and 7b
- (2010) Daniela Fornuskova et al. BIOCHEMICAL JOURNAL
- Proton-Coupled Electron Transfer in Cytochrome Oxidase
- (2010) Ville R. I. Kaila et al. CHEMICAL REVIEWS
- Isolation of mitochondria for biogenetical studies: An update
- (2009) Erika Fernández-Vizarra et al. MITOCHONDRION
- Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ
- (2008) Ortal Barel et al. AMERICAN JOURNAL OF HUMAN GENETICS
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