Nonsense mutations in the COX1 subunit impair the stability of respiratory chain complexes rather than their assembly.

PubWeight™: 1.10‹?› | Rank: Top 10%

🔗 View Article (PMC 3297988)

Published in EMBO J on January 17, 2012

Authors

Hue-Tran Hornig-Do1, Takashi Tatsuta, Angela Buckermann, Maria Bust, Gittan Kollberg, Agnes Rötig, Martin Hellmich, Leo Nijtmans, Rudolf J Wiesner

Author Affiliations

1: Institute for Vegetative Physiology, University of Cologne, Cologne, Germany. hue-tran.hornig@uni-koeln.de

Articles citing this

Spectinamides: a new class of semisynthetic antituberculosis agents that overcome native drug efflux. Nat Med (2014) 3.29

Mitochondrial Protein Synthesis Adapts to Influx of Nuclear-Encoded Protein. Cell (2016) 1.39

OXPHOS mutations and neurodegeneration. EMBO J (2012) 1.33

Sealing the mitochondrial respirasome. Mol Cell Biol (2012) 1.04

Comparison of mitochondrial mutation spectra in ageing human colonic epithelium and disease: absence of evidence for purifying selection in somatic mitochondrial DNA point mutations. PLoS Genet (2012) 1.01

Human mitochondrial leucyl tRNA synthetase can suppress non cognate pathogenic mt-tRNA mutations. EMBO Mol Med (2014) 0.98

AFG3L2 supports mitochondrial protein synthesis and Purkinje cell survival. J Clin Invest (2012) 0.95

A human mitochondrial poly(A) polymerase mutation reveals the complexities of post-transcriptional mitochondrial gene expression. Hum Mol Genet (2014) 0.94

Mitochondrial protein quality control: the mechanisms guarding mitochondrial health. Antioxid Redox Signal (2015) 0.88

Cytochrome c oxidase deficiency accelerates mitochondrial apoptosis by activating ceramide synthase 6. Cell Death Dis (2015) 0.83

Stress-triggered activation of the metalloprotease Oma1 involves its C-terminal region and is important for mitochondrial stress protection in yeast. J Biol Chem (2014) 0.82

MTO1 mediates tissue specificity of OXPHOS defects via tRNA modification and translation optimization, which can be bypassed by dietary intervention. Hum Mol Genet (2014) 0.82

Loss of the m-AAA protease subunit AFG₃L₂ causes mitochondrial transport defects and tau hyperphosphorylation. EMBO J (2014) 0.82

Methionine restriction slows down senescence in human diploid fibroblasts. Aging Cell (2014) 0.81

Metalloprotease OMA1 Fine-tunes Mitochondrial Bioenergetic Function and Respiratory Supercomplex Stability. Sci Rep (2015) 0.80

Novel MTND1 mutations cause isolated exercise intolerance, complex I deficiency and increased assembly factor expression. Clin Sci (Lond) (2015) 0.78

Cell Type-Specific Modulation of Respiratory Chain Supercomplex Organization. Int J Mol Sci (2016) 0.76

The Mitochondrial m-AAA Protease Prevents Demyelination and Hair Greying. PLoS Genet (2016) 0.75

High glucose uptake unexpectedly is accompanied by high levels of the mitochondrial ß-F1-ATPase subunit in head and neck squamous cell carcinoma. Oncotarget (2015) 0.75

NDUFAF4 variants are associated with Leigh syndrome and cause a specific mitochondrial complex I assembly defect. Eur J Hum Genet (2017) 0.75

Articles cited by this

The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 A. Science (1996) 9.32

Blue native PAGE. Nat Protoc (2006) 8.04

Biochemical and molecular investigations in respiratory chain deficiencies. Clin Chim Acta (1994) 4.93

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease. Cell (1998) 4.41

Neutral red uptake assay for the estimation of cell viability/cytotoxicity. Nat Protoc (2008) 3.76

The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria. Cell (2005) 3.72

Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms. Lancet Neurol (2008) 3.49

Quality control of mitochondria: protection against neurodegeneration and ageing. EMBO J (2008) 3.39

Respiratory active mitochondrial supercomplexes. Mol Cell (2008) 3.35

In vivo labeling and analysis of human mitochondrial translation products. Methods Enzymol (1996) 2.84

The YTA10-12 complex, an AAA protease with chaperone-like activity in the inner membrane of mitochondria. Cell (1996) 2.80

Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. Nat Genet (2010) 2.66

Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1. J Cell Biol (2009) 2.65

Respiratory complex III is required to maintain complex I in mammalian mitochondria. Mol Cell (2004) 2.61

A molecular chaperone for mitochondrial complex I assembly is mutated in a progressive encephalopathy. J Clin Invest (2005) 2.21

The ratio of oxidative phosphorylation complexes I-V in bovine heart mitochondria and the composition of respiratory chain supercomplexes. J Biol Chem (2001) 2.15

Microtubule disassembly by ATP-dependent oligomerization of the AAA enzyme katanin. Science (1999) 2.15

Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia. Mol Cell Biol (2006) 2.00

A novel two-step mechanism for removal of a mitochondrial signal sequence involves the mAAA complex and the putative rhomboid protease Pcp1. J Mol Biol (2002) 1.80

Assembly of cytochrome-c oxidase in cultured human cells. Eur J Biochem (1998) 1.70

Significance of respirasomes for the assembly/stability of human respiratory chain complex I. J Biol Chem (2004) 1.68

Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defects. Biochim Biophys Acta (2008) 1.66

Cytochrome c oxidase is required for the assembly/stability of respiratory complex I in mouse fibroblasts. Mol Cell Biol (2006) 1.64

Electrophoresis techniques to investigate defects in oxidative phosphorylation. Methods (2008) 1.63

Architecture of active mammalian respiratory chain supercomplexes. J Biol Chem (2006) 1.58

Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase. Am J Hum Genet (2008) 1.54

A structural model of the cytochrome C reductase/oxidase supercomplex from yeast mitochondria. J Biol Chem (2007) 1.54

Shy1 couples Cox1 translational regulation to cytochrome c oxidase assembly. EMBO J (2007) 1.47

Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene. Biochem Biophys Res Commun (2000) 1.46

Cytochrome c oxidase subassemblies in fibroblast cultures from patients carrying mutations in COX10, SCO1, or SURF1. J Biol Chem (2003) 1.45

A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV. Am J Hum Genet (1999) 1.36

Assembly of respiratory complexes I, III, and IV into NADH oxidase supercomplex stabilizes complex I in Paracoccus denitrificans. J Biol Chem (2003) 1.29

Tissue-specific cytochrome c oxidase assembly defects due to mutations in SCO2 and SURF1. Biochem J (2005) 1.23

Identification of novel mutations in five patients with mitochondrial encephalomyopathy. Biochim Biophys Acta (2008) 1.22

Respiratory chain supercomplexes set the threshold for respiration defects in human mtDNA mutant cybrids. Hum Mol Genet (2006) 1.22

Isolation of functional pure mitochondria by superparamagnetic microbeads. Anal Biochem (2009) 1.21

Analysis of mouse models of cytochrome c oxidase deficiency owing to mutations in Sco2. Hum Mol Genet (2010) 1.21

Emerging roles of mitochondrial proteases in neurodegeneration. Biochim Biophys Acta (2009) 1.19

Afg3p, a mitochondrial ATP-dependent metalloprotease, is involved in degradation of mitochondrially-encoded Cox1, Cox3, Cob, Su6, Su8 and Su9 subunits of the inner membrane complexes III, IV and V. FEBS Lett (1996) 1.18

In vivo regulation of oxidative phosphorylation in cells harboring a stop-codon mutation in mitochondrial DNA-encoded cytochrome c oxidase subunit I. J Biol Chem (2001) 1.16

Pathological mutations of the human NDUFS4 gene of the 18-kDa (AQDQ) subunit of complex I affect the expression of the protein and the assembly and function of the complex. J Biol Chem (2003) 1.16

A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast. FEBS J (2005) 1.15

Dual functions of Mss51 couple synthesis of Cox1 to assembly of cytochrome c oxidase in Saccharomyces cerevisiae mitochondria. Mol Biol Cell (2009) 1.14

A novel frameshift mutation of the mtDNA COIII gene leads to impaired assembly of cytochrome c oxidase in a patient affected by Leigh-like syndrome. Hum Mol Genet (2000) 1.13

Role of nuclear-encoded subunit Vb in the assembly and stability of cytochrome c oxidase complex: implications in mitochondrial dysfunction and ROS production. Biochem J (2009) 1.13

Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA. Am J Hum Genet (1998) 1.11

Cytochrome c oxidase deficiency: patients and animal models. Biochim Biophys Acta (2009) 1.08

Complex I function is defective in complex IV-deficient Caenorhabditis elegans. J Biol Chem (2008) 1.08

An assembled complex IV maintains the stability and activity of complex I in mammalian mitochondria. J Biol Chem (2007) 1.07

Assembly of nuclear DNA-encoded subunits into mitochondrial complex IV, and their preferential integration into supercomplex forms in patient mitochondria. FEBS J (2009) 1.03

The carboxyl-terminal end of Cox1 is required for feedback assembly regulation of Cox1 synthesis in Saccharomyces cerevisiae mitochondria. J Biol Chem (2010) 0.96

MtDNA mutations associated with sideroblastic anaemia cause a defect of mitochondrial cytochrome c oxidase. Eur J Biochem (1998) 0.94

Forced extraction of targeted components from complex macromolecular assemblies. Proc Natl Acad Sci U S A (2008) 0.94

Cultivation in glucose-deprived medium stimulates mitochondrial biogenesis and oxidative metabolism in HepG2 hepatoma cells. Biol Chem (2002) 0.94

Novel SCO2 mutation (G1521A) presenting as a spinal muscular atrophy type I phenotype. Am J Med Genet A (2004) 0.93

de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency. J Pediatr (1988) 0.93

A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathy. Clin Neuropathol (2009) 0.92

Mitochondrial myopathy and rhabdomyolysis associated with a novel nonsense mutation in the gene encoding cytochrome c oxidase subunit I. J Neuropathol Exp Neurol (2005) 0.91

A novel mutation in the SCO2 gene in a neonate with early-onset cardioencephalomyopathy. Pediatr Neurol (2010) 0.89

Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy. Neuromuscul Disord (2005) 0.85

Phospholipid vesicles containing bovine heart mitochondrial cytochrome c oxidase and subunit III-deficient enzyme: analysis of respiratory control and proton translocating activities. Arch Biochem Biophys (1990) 0.84

Assembly factors and ATP-dependent proteases in cytochrome c oxidase biogenesis. Biochim Biophys Acta (2010) 0.84

Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA. Neurology (2000) 0.83

The subunit structure of cytochrome-c oxidase from tuna heart and liver. Eur J Biochem (1997) 0.79

Articles by these authors

Predicting drug susceptibility of non-small cell lung cancers based on genetic lesions. J Clin Invest (2009) 5.07

Mild therapeutic hypothermia in cardiogenic shock syndrome. Crit Care Med (2012) 4.61

Ischemic preconditioning for prevention of contrast medium-induced nephropathy: randomized pilot RenPro Trial (Renal Protection Trial). Circulation (2012) 3.42

MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion. Nat Genet (2006) 3.17

Random point mutations with major effects on protein-coding genes are the driving force behind premature aging in mtDNA mutator mice. Cell Metab (2009) 2.96

Prohibitins control cell proliferation and apoptosis by regulating OPA1-dependent cristae morphogenesis in mitochondria. Genes Dev (2008) 2.76

Use of a simple criteria set for guiding echocardiography in nosocomial Staphylococcus aureus bacteremia. Clin Infect Dis (2011) 2.62

Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex I. Cell Metab (2010) 2.21

An intersubunit signaling network coordinates ATP hydrolysis by m-AAA proteases. Mol Cell (2009) 2.12

Early prediction of nonprogression in advanced non-small-cell lung cancer treated with erlotinib by using [(18)F]fluorodeoxyglucose and [(18)F]fluorothymidine positron emission tomography. J Clin Oncol (2011) 2.10

Differential time to positivity is not predictive for central line-related Staphylococcus aureus bloodstream infection in routine clinical care. J Infect (2013) 2.00

Variation in germline mtDNA heteroplasmy is determined prenatally but modified during subsequent transmission. Nat Genet (2012) 1.94

Comparison of different video laryngoscopes for emergency intubation in a standardized airway manikin with immobilized cervical spine by experienced anaesthetists. A randomized, controlled crossover trial. Resuscitation (2011) 1.87

Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies. Hum Mol Genet (2004) 1.78

Success rates and endotracheal tube insertion times of experienced emergency physicians using five video laryngoscopes: a randomised trial in a simulated trapped car accident victim. Eur J Anaesthesiol (2011) 1.65

Electrophoresis techniques to investigate defects in oxidative phosphorylation. Methods (2008) 1.63

Prognostic impact of NT-proBNP and renal function in comparison to contemporary multi-marker risk scores in heart failure patients. Eur J Heart Fail (2008) 1.62

Acute infantile liver failure due to mutations in the TRMU gene. Am J Hum Genet (2009) 1.61

Renal impairment and transapical aortic valve implantation: impact of contrast medium dose on kidney function and survival. Eur J Cardiothorac Surg (2011) 1.58

Cytochrome oxidase in health and disease. Gene (2002) 1.57

Quality control of mitochondrial proteostasis. Cold Spring Harb Perspect Biol (2011) 1.55

Transient overexpression of mitochondrial transcription factor A (TFAM) is sufficient to stimulate mitochondrial DNA transcription, but not sufficient to increase mtDNA copy number in cultured cells. Nucleic Acids Res (2004) 1.53

A randomized controlled comparison of the Bonfils fiberscope and the GlideScope Cobalt AVL video laryngoscope for visualization of the larynx and intubation of the trachea in infants and small children with normal airways. Paediatr Anaesth (2013) 1.45

Fluid therapy and acute kidney injury in cardiogenic shock after cardiac arrest. Resuscitation (2012) 1.41

Targeted disruption of hepatic frataxin expression causes impaired mitochondrial function, decreased life span and tumor growth in mice. Hum Mol Genet (2005) 1.40

Dendritic cell based tumor vaccination in prostate and renal cell cancer: a systematic review and meta-analysis. PLoS One (2011) 1.38

Regulation of mitochondrial proliferation in the heart: power-plant failure contributes to cardiac failure in hypertrophy. Cardiovasc Res (2004) 1.38

Intramitochondrial transport of phosphatidic acid in yeast by a lipid transfer protein. Science (2012) 1.36

Simple flow cytometric method used to assess lipid accumulation in fat cells. J Lipid Res (2004) 1.33

Prohibitins interact genetically with Atp23, a novel processing peptidase and chaperone for the F1Fo-ATP synthase. Mol Biol Cell (2006) 1.26

CD4 T cell activation by myelin oligodendrocyte glycoprotein is suppressed by adult but not cord blood CD25+ T cells. Eur J Immunol (2003) 1.22

Isolation of functional pure mitochondria by superparamagnetic microbeads. Anal Biochem (2009) 1.21

Therapy of the neonatal abstinence syndrome with tincture of opium or morphine drops. Drug Alcohol Depend (2005) 1.21

TRIAP1/PRELI complexes prevent apoptosis by mediating intramitochondrial transport of phosphatidic acid. Cell Metab (2013) 1.16

Ultrasound guidance versus anatomical landmarks for internal jugular vein catheterization. Cochrane Database Syst Rev (2015) 1.16

Stress-induced OMA1 activation and autocatalytic turnover regulate OPA1-dependent mitochondrial dynamics. EMBO J (2014) 1.15

Import of mitochondrial transcription factor A (TFAM) into rat liver mitochondria stimulates transcription of mitochondrial DNA. Nucleic Acids Res (2003) 1.12

Activity of complex III of the mitochondrial electron transport chain is essential for early heart muscle cell differentiation. FASEB J (2004) 1.11

Mitochondrial complex III stabilizes complex I in the absence of NDUFS4 to provide partial activity. Hum Mol Genet (2011) 1.11

Binocular depth inversion as a paradigm of reduced visual information processing in prodromal state, antipsychotic-naïve and treated schizophrenia. Eur Arch Psychiatry Clin Neurosci (2009) 1.11

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy. Brain (2009) 1.10

Epigenetic silencing of the candidate tumor suppressor gene PROX1 in sporadic breast cancer. Int J Cancer (2007) 1.09

Anandamide levels in cerebrospinal fluid of first-episode schizophrenic patients: impact of cannabis use. Schizophr Res (2007) 1.09

Role of the novel metallopeptidase Mop112 and saccharolysin for the complete degradation of proteins residing in different subcompartments of mitochondria. J Biol Chem (2005) 1.08

Molecular analysis of ANT1, TWINKLE and POLG in patients with multiple deletions or depletion of mitochondrial DNA by a dHPLC-based assay. Eur J Hum Genet (2006) 1.08

Conclusions need to be based on sound data: keep an eye on both bias and imprecision. Eur J Anaesthesiol (2013) 1.08

Tracheal intubation with the Bonfils fiberscope in the difficult pediatric airway: a comparison with fiberoptic intubation. Paediatr Anaesth (2014) 1.08

Anandamide elevation in cerebrospinal fluid in initial prodromal states of psychosis. Br J Psychiatry (2009) 1.06

Deoxyribonucleotide metabolism in cycling and resting human fibroblasts with a missense mutation in p53R2, a subunit of ribonucleotide reductase. J Biol Chem (2011) 1.06

Complex I assembly: a puzzling problem. Curr Opin Neurol (2004) 1.06

Association of anti-RNA polymerase III autoantibodies and cancer in scleroderma. Arthritis Res Ther (2014) 1.04

The mitochondrial electron transport chain is dispensable for proliferation and differentiation of epidermal progenitor cells. Stem Cells (2011) 1.03

Mitochondrial AAA proteases--towards a molecular understanding of membrane-bound proteolytic machines. Biochim Biophys Acta (2011) 1.02

Effect of a capsular tension ring on refractive outcomes in eyes with high myopia. J Cataract Refract Surg (2010) 1.01

Mitochondrial (mt)DNA changes in tissue may not be reflected by depletion of mtDNA in peripheral blood mononuclear cells in HIV-infected patients. Antivir Ther (2006) 1.01

Functional consequences of mitochondrial tRNA Trp and tRNA Arg mutations causing combined OXPHOS defects. Eur J Hum Genet (2009) 1.01

Ultrasound guidance versus anatomical landmarks for subclavian or femoral vein catheterization. Cochrane Database Syst Rev (2015) 1.00

Genotype-phenotype spectrum of PYCR1-related autosomal recessive cutis laxa. Mol Genet Metab (2013) 1.00

NOA1 is an essential GTPase required for mitochondrial protein synthesis. Mol Biol Cell (2010) 1.00

Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9. J Med Genet (2011) 0.99

Reactive oxygen species derived from the mitochondrial respiratory chain are not responsible for the basal levels of oxidative base modifications observed in nuclear DNA of Mammalian cells. Free Radic Biol Med (2004) 0.99

Clinically defined chemotherapy-associated bowel syndrome predicts severe complications and death in cancer patients. Haematologica (2011) 0.98

Development and validation of a risk-score model for subjects with impaired glucose tolerance for the assessment of the risk of type 2 diabetes mellitus-The STOP-NIDDM risk-score. Diabetes Res Clin Pract (2009) 0.98

Impaired mitochondrial Ca2+ homeostasis in respiratory chain-deficient cells but efficient compensation of energetic disadvantage by enhanced anaerobic glycolysis due to low ATP steady state levels. Exp Cell Res (2007) 0.98

A dominant-negative isoform of hypoxia-inducible factor-1 alpha specifically expressed in human testis. Biol Reprod (2004) 0.96

Screening for ovarian cancer by transvaginal ultrasound and serum CA125 measurement in women with a familial predisposition: a prospective cohort study. Gynecol Oncol (2006) 0.96

Neoadjuvant radiochemotherapy and surgery for advanced rectal cancer : prognostic significance of tumor regression. Strahlenther Onkol (2011) 0.95

Preoperative aspirin use in cardiac surgery. Ann Surg (2013) 0.95

Vardenafil for the treatment of raynaud phenomenon: a randomized, double-blind, placebo-controlled crossover study. Arch Intern Med (2012) 0.95

Human epidermal keratinocytes accumulate superoxide due to low activity of Mn-SOD, leading to mitochondrial functional impairment. J Invest Dermatol (2006) 0.94

Glucocorticoid hormone stimulates mitochondrial biogenesis specifically in skeletal muscle. Endocrinology (2002) 0.94

Elevated MMP-7 levels in patients with systemic sclerosis: correlation with pulmonary involvement. Exp Dermatol (2011) 0.94

Presequence-dependent folding ensures MrpL32 processing by the m-AAA protease in mitochondria. EMBO J (2011) 0.94

CREB-1alpha is recruited to and mediates upregulation of the cytochrome c promoter during enhanced mitochondrial biogenesis accompanying skeletal muscle differentiation. Mol Cell Biol (2008) 0.94

Conditional targeting of tumor necrosis factor receptor-associated factor 6 reveals opposing functions of Toll-like receptor signaling in endothelial and myeloid cells in a mouse model of atherosclerosis. Circulation (2012) 0.94

NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvement. Mol Genet Metab (2009) 0.94

Cultivation in glucose-deprived medium stimulates mitochondrial biogenesis and oxidative metabolism in HepG2 hepatoma cells. Biol Chem (2002) 0.94

Electron cryomicroscopy structure of a membrane-anchored mitochondrial AAA protease. J Biol Chem (2010) 0.93

Nasal irrigation as an adjunctive treatment in allergic rhinitis: a systematic review and meta-analysis. Am J Rhinol Allergy (2012) 0.93

Recommending early integration of palliative care - does it work? Support Care Cancer (2011) 0.93

A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria. Eur J Pediatr (2009) 0.93

Nijmegen paediatric CDG rating scale: a novel tool to assess disease progression. J Inherit Metab Dis (2011) 0.92

N-acetylcysteine prevents reactive oxygen species-mediated myocardial stress in patients undergoing cardiac surgery: results of a randomized, double-blind, placebo-controlled clinical trial. J Thorac Cardiovasc Surg (2003) 0.91

Human polyomaviruses 6, 7, 9, 10 and Trichodysplasia spinulosa-associated polyomavirus in HIV-infected men. J Gen Virol (2014) 0.91

Negative regulation of mitochondrial transcription by mitochondrial topoisomerase I. Nucleic Acids Res (2013) 0.90

Clinical and biochemical characteristics in patients with a high mutant load of the mitochondrial T8993G/C mutations. Am J Med Genet A (2006) 0.90

Pearson syndrome in the neonatal period: two case reports and review of the literature. J Pediatr Hematol Oncol (2009) 0.90

Respiratory chain deficiencies. Handb Clin Neurol (2013) 0.89

Experimental radiofrequency ablation near the portal and the hepatic veins in pigs: differences in efficacy of a monopolar ablation system. J Surg Res (2006) 0.88

A stepwise psychotherapy intervention for reducing risk in coronary artery disease (SPIRR-CAD) - rationale and design of a multicenter, randomized trial in depressed patients with CAD. J Psychosom Res (2011) 0.88

Alpha-actinin 4 and BAT1 interaction with the cytochrome c promoter upon skeletal muscle differentiation. Curr Genet (2005) 0.88

Human mitochondrial ATP-binding cassette transporter ABCB10 is required for efficient red blood cell development. Br J Haematol (2011) 0.87

Molecular dysfunction associated with the human mitochondrial 3302A>G mutation in the MTTL1 (mt-tRNALeu(UUR)) gene. Nucleic Acids Res (2006) 0.87

Effects of deep brain stimulation in dyskinetic cerebral palsy: a meta-analysis. Mov Disord (2013) 0.87

Respiratory chain deficiency slows down cell-cycle progression via reduced ROS generation and is associated with a reduction of p21CIP1/WAF1. J Cell Physiol (2006) 0.86

Neurobehavioural deficits after severe traumatic brain injury (TBI). Brain Inj (2006) 0.86

Thyrotropin powers human mitochondria. FASEB J (2010) 0.85

BOLA1 is an aerobic protein that prevents mitochondrial morphology changes induced by glutathione depletion. Antioxid Redox Signal (2012) 0.85