Related references
Note: Only part of the references are listed.Identification of CHCHD10 Mutation in Chinese Patients with Alzheimer Disease
Tingting Xiao et al.
MOLECULAR NEUROBIOLOGY (2017)
Genetic analysis of CHCHD2 and CHCHD10 in Italian patients with Parkinson's disease
Elisa Rubino et al.
NEUROBIOLOGY OF AGING (2017)
Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients
Federica Perrone et al.
NEUROBIOLOGY OF AGING (2017)
Loss of function CHCHD10 mutations in cytoplasmic TDP-43 accumulation and synaptic integrity
Jung-A A. Woo et al.
NATURE COMMUNICATIONS (2017)
Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies
Rene G. Feichtinger et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2017)
A CMC1-knockout reveals translation-independent control of human mitochondrial complex IV biogenesis
Myriam Bourens et al.
EMBO REPORTS (2017)
Intrafamilial clinical variability in individuals carrying the CHCHD10 mutation Gly66Val
P. Pasanen et al.
ACTA NEUROLOGICA SCANDINAVICA (2016)
High prevalence of CHCHD10 mutation in patients with frontotemporal dementia from China
Bin Jiao et al.
BRAIN (2016)
Mic60/Mitofilin determines MICOS assembly essential for mitochondrial dynamics and mtDNA nucleoid organization
H. Li et al.
CELL DEATH AND DIFFERENTIATION (2016)
CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis
Emmanuelle C. Genin et al.
EMBO MOLECULAR MEDICINE (2016)
Mitochondrial Protein Interaction Mapping Identifies Regulators of Respiratory Chain Function
Brendan J. Floyd et al.
MOLECULAR CELL (2016)
CHCHD2 gene mutations in familial and sporadic Parkinson's disease
Chang-he Shi et al.
NEUROBIOLOGY OF AGING (2016)
Analysis of the CHCHD10 gene in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Spain
Oriol Dols-Icardo et al.
BRAIN (2015)
CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis
Dario Ronchi et al.
BRAIN (2015)
Mutation analysis of CHCHD10 in different neurodegenerative diseases
Ming Zhang et al.
BRAIN (2015)
MNRR1 (formerly CHCHD2) is a bi-organellar regulator of mitochondrial metabolism
Siddhesh Aras et al.
MITOCHONDRION (2015)
Redox-regulated dynamic interplay between Cox19 and the copper-binding protein Cox11 in the intermembrane space of mitochondria facilitates biogenesis of cytochrome c oxidase
Manuela Bode et al.
MOLECULAR BIOLOGY OF THE CELL (2015)
CHCHD2 Is Coamplified with EGFR in NSCLC and Regulates Mitochondrial Function and Cell Migration
Yuhong Wei et al.
MOLECULAR CANCER RESEARCH (2015)
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders
Kotaro Ogaki et al.
NEUROLOGY (2015)
Human Mitochondrial DNA-Protein Complexes Attach to a Cholesterol-Rich Membrane Structure
Joachim M. Gerhold et al.
SCIENTIFIC REPORTS (2015)
Mitofilin and CHCHD6 physically interact with Sam50 to sustain cristae structure
Chengli Ding et al.
SCIENTIFIC REPORTS (2015)
Late Onset Spinal Motor Neuronopathy Is Caused by Mutation in CHCHD10
Sini Penttila et al.
ANNALS OF NEUROLOGY (2015)
Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy
Senda Ajroud-Driss et al.
NEUROGENETICS (2015)
CHCHD10 variant p.(Gly66Val) causes axonal Charcot-Marie-Tooth disease
Mari Auranen et al.
NEUROLOGY-GENETICS (2015)
Unbiased RNAi screen for hepcidin regulators links hepcidin suppression to proliferative Ras/RAF and nutrient-dependent mTOR signaling
Katarzyna Mleczko-Sanecka et al.
BLOOD (2014)
Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease
Kathrin Mueller et al.
BRAIN (2014)
Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis
Janel O. Johnson et al.
BRAIN (2014)
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement
Sylvie Bannwarth et al.
BRAIN (2014)
Human COX20 cooperates with SCO1 and SCO2 to mature COX2 and promote the assembly of cytochrome c oxidase
Myriam Bourens et al.
HUMAN MOLECULAR GENETICS (2014)
Metabolic consequences of NDUFS4 gene deletion in immortalized mouse embryonic fibroblasts
Federica Valsecchi et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2012)
The mitochondrial calcium regulator cyclophilin D is an essential component of oestrogen-mediated neuroprotection in amyotrophic lateral sclerosis
Hyun Jeong Kim et al.
BRAIN (2012)
Role of Twin Cys-Xaa9-Cys Motif Cysteines in Mitochondrial Import of the Cytochrome c Oxidase Biogenesis Factor Cmc1
Myriam Bourens et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
Template-based protein structure modeling using the RaptorX web server
Morten Kaellberg et al.
NATURE PROTOCOLS (2012)
In Vivo Pathogenic Role of Mutant SOD1 Localized in the Mitochondrial Intermembrane Space
Anissa Igoudjil et al.
JOURNAL OF NEUROSCIENCE (2011)
The molecular identity of the mitochondrial Ca2+sequestration system
Anatoly A. Starkov
FEBS JOURNAL (2010)
Mitochondrial Iron Metabolism and Its Role in Neurodegeneration
Maxx P. Horowitz et al.
JOURNAL OF ALZHEIMERS DISEASE (2010)
The Conserved Mitochondrial Twin Cx9C Protein Cmc2 Is a Cmc1 Homologue Essential for Cytochrome c Oxidase Biogenesis
Darryl Horn et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Genome-wide analysis of eukaryotic twin CX9C proteins
Gabriele Cavallaro
MOLECULAR BIOSYSTEMS (2010)
Systems survey of endocytosis by multiparametric image analysis
Claudio Collinet et al.
NATURE (2010)
Redox regulation of protein folding in the mitochondrial intermembrane space
Carla M. Koehler et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2009)
Systematic Analysis of the Twin Cx9C Protein Family
Sebastian Longen et al.
JOURNAL OF MOLECULAR BIOLOGY (2009)
The Erv1-Mia40 disulfide relay system in the intermembrane space of mitochondria
Kai Hell
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2008)
Excessive reactive oxygen species induces apoptosis in fibroblasts: Role of mitochondrially accumulated hyaluronic acid binding protein 1 (HABP1/p32/gC1qR)
Anindya Roy Chowdhury et al.
EXPERIMENTAL CELL RESEARCH (2008)
Cmc1p is a conserved mitochondrial twin CX9C protein involved in cytochrome c oxidase biogenesis
Darryl Horn et al.
MOLECULAR AND CELLULAR BIOLOGY (2008)
A structural-dynamical characterization of human Cox17
Lucia Banci et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Characterization of the cytochrome c oxidase assembly factor Cox19 of Saccharomyces cerevisiae
Kevin Rigby et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Neural mitochondrial Ca2+ capacity impairment precedes the onset of motor symptoms in G93A Cu/Zn-superoxide dismutase mutant mice
M Damiano et al.
JOURNAL OF NEUROCHEMISTRY (2006)
Simultaneous quantitative measurement and automated analysis of mitochondrial morphology, mass, potential, and motility in livig human skin fibroblasts
WJH Koopman et al.
CYTOMETRY PART A (2006)
Mitochondrial network complexity and pathological decrease in complex I activity are tightly correlated in isolated human complex I deficiency
WJH Koopman et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2005)
A disulfide relay system in the intermembrane space of mitochondria that mediates protein import
N Mesecke et al.
CELL (2005)
Folding studies of Cox17 reveal an important interplay of cysteine oxidation and copper binding
F Arnesano et al.
STRUCTURE (2005)
Tim50 is a subunit of the TIM23 complex that links protein translocation across the outer and inner mitochondrial membranes
H Yamamoto et al.
CELL (2002)
The mitochondrial presequence translocase: An essential role of Tim50 in directing preproteins to the import channel
A Geissler et al.
CELL (2002)
The role of the Tim8p-Tim13p complex in a conserved import pathway for mitochondrial polytopic inner membrane proteins
SP Curran et al.
JOURNAL OF CELL BIOLOGY (2002)
Share Paper
