Molecular base of biochemical complex I deficiency.
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[1] T. Wieland,et al. Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing , 2012, Journal of Medical Genetics.
[2] T. Rouault. Biogenesis of iron-sulfur clusters in mammalian cells: new insights and relevance to human disease , 2012, Disease Models & Mechanisms.
[3] T. Meitinger,et al. Mutation screening of 75 candidate genes in 152 complex I deficiency cases identifies pathogenic variants in 16 genes including NDUFB9 , 2011, Journal of Medical Genetics.
[4] I. D. de Coo,et al. Defective NDUFA9 as a novel cause of neonatally fatal complex I disease , 2011, Journal of Medical Genetics.
[5] J. Bridwell-Rabb,et al. Structure-function analysis of Friedreich's ataxia mutants reveals determinants of frataxin binding and activation of the Fe-S assembly complex. , 2011, Biochemistry.
[6] Morten Duno,et al. Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome , 2011, Journal of Medical Genetics.
[7] R. Rodenburg,et al. NDUFA10 mutations cause complex I deficiency in a patient with Leigh disease , 2011, European Journal of Human Genetics.
[8] H. Smeets,et al. Riboflavin-responsive oxidative phosphorylation complex I deficiency caused by defective ACAD9: new function for an old gene. , 2011, Brain : a journal of neurology.
[9] A. Pagnamenta,et al. FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy. , 2010, Human molecular genetics.
[10] Anamika Singh,et al. Characterization of the human HSC20, an unusual DnaJ type III protein, involved in iron-sulfur cluster biogenesis. , 2010, Human molecular genetics.
[11] Rutger O. Vogel,et al. Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex I. , 2010, Cell metabolism.
[12] M. Rivas,et al. Nature Genetics Advance Online Publication High-throughput, Pooled Sequencing Identifies Mutations in Nubpl and Foxred1 in Human Complex I Deficiency , 2022 .
[13] M. Ryan,et al. Assembly factors of human mitochondrial complex I and their defects in disease , 2010, IUBMB life.
[14] R. Rodenburg,et al. Novel mutations in the NDUFS1 gene cause low residual activities in human complex I deficiencies. , 2010, Molecular genetics and metabolism.
[15] Domenico de Rasmo,et al. cAMP-dependent protein kinase regulates post-translational processing and expression of complex I subunits in mammalian cells. , 2010, Biochimica et biophysica acta.
[16] Hans-Peter Braun,et al. Structure and function of mitochondrial supercomplexes. , 2010, Biochimica et biophysica acta.
[17] M. L. Genova,et al. Mitochondrial respiratory chain super-complex I-III in physiology and pathology. , 2010, Biochimica et biophysica acta.
[18] Cindy E J Dieteren,et al. Mammalian mitochondrial complex I: biogenesis, regulation, and reactive oxygen species generation. , 2010, Antioxidants & redox signaling.
[19] B. Merinero,et al. Mitochondrial bioenergetics and dynamics interplay in complex I-deficient fibroblasts. , 2010, Biochimica et biophysica acta.
[20] Rouslan G. Efremov,et al. The architecture of respiratory complex I , 2010, Nature.
[21] J. Enríquez,et al. Five Entry Points of the Mitochondrially Encoded Subunits in Mammalian Complex I Assembly , 2010, Molecular and Cellular Biology.
[22] Jun-Feng Wang,et al. Mitochondrial complex I activity and oxidative damage to mitochondrial proteins in the prefrontal cortex of patients with bipolar disorder. , 2010, Archives of general psychiatry.
[23] Allan Matte,et al. Structural Basis for Fe–S Cluster Assembly and tRNA Thiolation Mediated by IscS Protein–Protein Interactions , 2010, PLoS biology.
[24] K. Takahashi-Niki,et al. DJ-1 binds to mitochondrial complex I and maintains its activity. , 2009, Biochemical and biophysical research communications.
[25] Jay Shendure,et al. Next generation sequence analysis for mitochondrial disorders , 2009, Genome Medicine.
[26] J. Bennett,et al. The cybrid model of sporadic Parkinson's disease , 2009, Experimental Neurology.
[27] R. Rodenburg,et al. Baculovirus complementation restores a novel NDUFAF2 mutation causing complex I deficiency , 2009, Human mutation.
[28] Rutger O. Vogel,et al. Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease. , 2009, American journal of human genetics.
[29] R. Köster,et al. Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio). , 2009, Brain : a journal of neurology.
[30] J. Smeitink,et al. The antioxidant Trolox restores mitochondrial membrane potential and Ca2+-stimulated ATP production in human complex I deficiency , 2009, Journal of Molecular Medicine.
[31] M. Lazarou,et al. Assembly of mitochondrial complex I and defects in disease. , 2009, Biochimica et biophysica acta.
[32] S. Hosseinkhani,et al. A Novel Mitochondrial Heteroplasmic C13806A Point Mutation Associated with Iranian Friedreich’s Ataxia , 2009, Cellular and molecular neurobiology.
[33] A. Starkov. The Role of Mitochondria in Reactive Oxygen Species Metabolism and Signaling , 2008, Annals of the New York Academy of Sciences.
[34] J. Smeitink,et al. Electrophoresis techniques to investigate defects in oxidative phosphorylation. , 2008, Methods.
[35] J. Enríquez,et al. Respiratory active mitochondrial supercomplexes. , 2008, Molecular cell.
[36] V. Mootha,et al. Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease. , 2008, American journal of human genetics.
[37] J. Hirst,et al. The production of reactive oxygen species by complex I. , 2008, Biochemical Society transactions.
[38] S. Carr,et al. A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology , 2008, Cell.
[39] Domenico de Rasmo,et al. Mammalian complex I: a regulable and vulnerable pacemaker in mitochondrial respiratory function. , 2008, Biochimica et biophysica acta.
[40] M. Huynen,et al. The iron–sulphur protein Ind1 is required for effective complex I assembly , 2008, The EMBO journal.
[41] R. Rodenburg,et al. NDUFA2 complex I mutation leads to Leigh disease. , 2008, American journal of human genetics.
[42] Domenico de Rasmo,et al. cAMP-dependent protein kinase regulates the mitochondrial import of the nuclear encoded NDUFS4 subunit of complex I. , 2008, Cellular signalling.
[43] Ann Saada,et al. Mitochondrial complex I deficiency caused by a deleterious NDUFA11 mutation , 2008, Annals of neurology.
[44] J. Ganesh,et al. The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases. , 2008, Archives of neurology.
[45] Ann Saada,et al. C6ORF66 is an assembly factor of mitochondrial complex I. , 2008, American journal of human genetics.
[46] N. Yadava,et al. Investigations of the potential effects of phosphorylation of the MWFE and ESSS subunits on complex I activity and assembly. , 2008, The international journal of biochemistry & cell biology.
[47] Rutger O. Vogel,et al. Human mitochondrial complex I assembly: a dynamic and versatile process. , 2007, Biochimica et biophysica acta.
[48] J. Smeitink,et al. Mitochondrial and cytosolic thiol redox state are not detectably altered in isolated human NADH:ubiquinone oxidoreductase deficiency. , 2007, Biochimica et biophysica acta.
[49] J. Silke,et al. Human CIA30 is involved in the early assembly of mitochondrial complex I and mutations in its gene cause disease , 2007, The EMBO journal.
[50] Rutger O. Vogel,et al. Investigation of the complex I assembly chaperones B17.2L and NDUFAF1 in a cohort of CI deficient patients. , 2007, Molecular genetics and metabolism.
[51] M. Lazarou,et al. Analysis of the Assembly Profiles for Mitochondrial- and Nuclear-DNA-Encoded Subunits into Complex I , 2007, Molecular and Cellular Biology.
[52] Rutger O. Vogel,et al. Identification of Mitochondrial Complex I Assembly Intermediates by Tracing Tagged NDUFS3 Demonstrates the Entry Point of Mitochondrial Subunits* , 2007, Journal of Biological Chemistry.
[53] Gary W Miller,et al. Mechanism of toxicity of pesticides acting at complex I: relevance to environmental etiologies of Parkinson’s disease , 2007, Journal of neurochemistry.
[54] J. Smeitink,et al. Superoxide production is inversely related to complex I activity in inherited complex I deficiency. , 2007, Biochimica et biophysica acta.
[55] Rutger O. Vogel,et al. Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly. , 2007, Genes & development.
[56] L. Sazanov,et al. Respiratory complex I: mechanistic and structural insights provided by the crystal structure of the hydrophilic domain. , 2007, Biochemistry.
[57] R. Rodenburg,et al. X‐linked NDUFA1 gene mutations associated with mitochondrial encephalomyopathy , 2007, Annals of neurology.
[58] D. Leibfritz,et al. Free radicals and antioxidants in normal physiological functions and human disease. , 2007, The international journal of biochemistry & cell biology.
[59] John E. Walker,et al. Bovine Complex I Is a Complex of 45 Different Subunits* , 2006, Journal of Biological Chemistry.
[60] M. Lazarou,et al. Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients. , 2006, Journal of molecular biology.
[61] J. Smeitink,et al. Mitochondrial complex I: Structure, function and pathology , 2006, Journal of Inherited Metabolic Disease.
[62] H. Fukui,et al. Cytochrome c Oxidase Is Required for the Assembly/Stability of Respiratory Complex I in Mouse Fibroblasts , 2006, Molecular and Cellular Biology.
[63] Ulrich Brandt,et al. Energy converting NADH:quinone oxidoreductase (complex I). , 2006, Annual review of biochemistry.
[64] J. Xie,et al. Parkinson's Disease Brain Mitochondrial Complex I Has Oxidatively Damaged Subunits and Is Functionally Impaired and Misassembled , 2006, The Journal of Neuroscience.
[65] C. Geula,et al. Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons , 2006, Nature Genetics.
[66] Jun-Feng Wang,et al. Downregulation in components of the mitochondrial electron transport chain in the postmortem frontal cortex of subjects with bipolar disorder. , 2006, Journal of psychiatry & neuroscience : JPN.
[67] Robert W. Taylor,et al. High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease , 2006, Nature Genetics.
[68] Philip Hinchliffe,et al. Structure of the Hydrophilic Domain of Respiratory Complex I from Thermus thermophilus , 2006, Science.
[69] N. Pfanner,et al. Essential role of Isd11 in mitochondrial iron–sulfur cluster synthesis on Isu scaffold proteins , 2006, The EMBO journal.
[70] E. Shoubridge,et al. A molecular chaperone for mitochondrial complex I assembly is mutated in a progressive encephalopathy. , 2005, The Journal of clinical investigation.
[71] Rutger O. Vogel,et al. Human mitochondrial complex I assembly is mediated by NDUFAF1 , 2005, The FEBS journal.
[72] Tomoko Ohnishi,et al. Conformation‐driven and semiquinone‐gated proton‐pump mechanism in the NADH‐ubiquinone oxidoreductase (complex I) , 2005, FEBS letters.
[73] L. Sazanov,et al. Organization of Iron-Sulfur Clusters in Respiratory Complex I , 2005, Science.
[74] Robert W. Taylor,et al. A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast , 2005, The FEBS journal.
[75] D. Dean,et al. Structure, function, and formation of biological iron-sulfur clusters. , 2005, Annual review of biochemistry.
[76] M. Huynen,et al. Tracing the evolution of a large protein complex in the eukaryotes, NADH:ubiquinone oxidoreductase (Complex I). , 2005, Journal of molecular biology.
[77] R. Laframboise,et al. NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findings , 1996, Journal of Inherited Metabolic Disease.
[78] N. Yadava,et al. Molecular genetics of complex I-deficient Chinese hamster cell lines. , 2004, Biochimica et biophysica acta.
[79] S. Nanko,et al. Mitochondrial DNA 3644T-->C mutation associated with bipolar disorder. , 2004, Genomics.
[80] B. Barbiroli,et al. The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy , 2004 .
[81] Rutger O. Vogel,et al. Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies. , 2004, Human molecular genetics.
[82] Q. Zeng,et al. GRIM-19, a Cell Death Regulatory Protein, Is Essential for Assembly and Function of Mitochondrial Complex I , 2004, Molecular and Cellular Biology.
[83] D. Turnbull,et al. Mutations of the mitochondrial ND1 gene as a cause of MELAS , 2004, Journal of Medical Genetics.
[84] Robert W. Taylor,et al. NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency. , 2004, The Journal of clinical investigation.
[85] M. Beal,et al. Mitochondrial α-Ketoglutarate Dehydrogenase Complex Generates Reactive Oxygen Species , 2004, The Journal of Neuroscience.
[86] M. Bauer,et al. Significance of Respirasomes for the Assembly/Stability of Human Respiratory Chain Complex I* , 2004, Journal of Biological Chemistry.
[87] I. Fearnley,et al. The Phosphorylation of Subunits of Complex I from Bovine Heart Mitochondria* , 2004, Journal of Biological Chemistry.
[88] E. Klein,et al. Mitochondrial complex i subunits expression is altered in schizophrenia: a postmortem study , 2004, Biological Psychiatry.
[89] N. Yadava,et al. Development and Characterization of a Conditional Mitochondrial Complex I Assembly System* , 2004, Journal of Biological Chemistry.
[90] M. Finel,et al. Assembly of Respiratory Complexes I, III, and IV into NADH Oxidase Supercomplex Stabilizes Complex I in Paracoccus denitrificans* , 2004, Journal of Biological Chemistry.
[91] B. Böttcher,et al. The gross structure of the respiratory complex I: a Lego System. , 2004, Biochimica et biophysica acta.
[92] P. Bénit,et al. Mutant NDUFS3 subunit of mitochondrial complex I causes Leigh syndrome , 2004, Journal of Medical Genetics.
[93] A. Schapira. Primary and secondary defects of the mitochondrial respiratory chain , 2002, Journal of Inherited Metabolic Disease.
[94] A. Ballabio,et al. Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia , 2003, The Journal of cell biology.
[95] V. Petruzzella,et al. 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* , 2003, Journal of Biological Chemistry.
[96] K. Majamaa,et al. Impaired complex I assembly in a Leigh syndrome patient with a novel missense mutation in the ND6 gene , 2003, Annals of neurology.
[97] J. Hirst,et al. The nuclear encoded subunits of complex I from bovine heart mitochondria. , 2003, Biochimica et biophysica acta.
[98] S. Nanko,et al. Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder , 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.
[99] U. Brandt,et al. Proton pumping by NADH:ubiquinone oxidoreductase. A redox driven conformational change mechanism? , 2003, FEBS letters.
[100] P. Bénit,et al. Mutant NDUFV2 subunit of mitochondrial complex I causes early onset hypertrophic cardiomyopathy and encephalopathy , 2003, Human mutation.
[101] D. Turnbull,et al. The epidemiology of Leber hereditary optic neuropathy in the North East of England. , 2003, American journal of human genetics.
[102] J. Hirst,et al. Analysis of the Subunit Composition of Complex I from Bovine Heart Mitochondria*S , 2003, Molecular & Cellular Proteomics.
[103] Todd B. Sherer,et al. Subcutaneous Rotenone Exposure Causes Highly Selective Dopaminergic Degeneration and α-Synuclein Aggregation , 2003, Experimental Neurology.
[104] L. V. D. Heuvel,et al. Some practical aspects of providing a diagnostic service for respiratory chain defects , 2003, Annals of clinical biochemistry.
[105] H. Schägger. Respiratory chain supercomplexes of mitochondria and bacteria. , 2002, Biochimica et biophysica acta.
[106] Erin N. Smith,et al. Species-specific and Mutant MWFE Proteins , 2002, The Journal of Biological Chemistry.
[107] E. Starikovskaya,et al. The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J , 2002, Human Genetics.
[108] M. Runswick,et al. GRIM-19, a Cell Death Regulatory Gene Product, Is a Subunit of Bovine Mitochondrial NADH:Ubiquinone Oxidoreductase (Complex I)* , 2001, The Journal of Biological Chemistry.
[109] E. Shoubridge. Nuclear genetic defects of oxidative phosphorylation. , 2001, Human molecular genetics.
[110] Robert W. Taylor,et al. Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene , 2001, Annals of neurology.
[111] P. Bénit,et al. Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiency. , 2001, American journal of human genetics.
[112] T. Friedrich. Complex I: A Chimaera of a Redox and Conformation-Driven Proton Pump? , 2001, Journal of bioenergetics and biomembranes.
[113] J. Smeitink,et al. Human NADH:Ubiquinone Oxidoreductase , 2001, Journal of bioenergetics and biomembranes.
[114] N. Cairns,et al. The reduction of NADH ubiquinone oxidoreductase 24- and 75-kDa subunits in brains of patients with Down syndrome and Alzheimer's disease. , 2001, Life sciences.
[115] S. Dimauro,et al. The genetics and pathology of oxidative phosphorylation , 2001, Nature Reviews Genetics.
[116] J. Smeitink,et al. Respiratory chain complex I deficiency. , 2001, American journal of medical genetics.
[117] H. Mandel,et al. Mutations in the complex I NDUFS2 gene of patients with cardiomyopathy and encephalomyopathy , 2001, Annals of neurology.
[118] D. Turnbull,et al. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy. , 2001, Brain : a journal of neurology.
[119] Todd B. Sherer,et al. Chronic systemic pesticide exposure reproduces features of Parkinson's disease , 2000, Nature Neuroscience.
[120] P. Shapiro,et al. Identification of GRIM-19, a Novel Cell Death-regulatory Gene Induced by the Interferon-β and Retinoic Acid Combination, Using a Genetic Approach* , 2000, The Journal of Biological Chemistry.
[121] L. V. D. Heuvel,et al. Combined enzymatic complex I and III deficiency associated with mutations in the nuclear encoded NDUFS4 gene. , 2000, Biochemical and biophysical research communications.
[122] L. V. D. Heuvel,et al. Clinical differences in patients with mitochondriocytopathies due to nuclear versus mitochondrial DNA mutations , 2000, Human mutation.
[123] J. Walker,et al. Resolution of the membrane domain of bovine complex I into subcomplexes: implications for the structural organization of the enzyme. , 2000, Biochemistry.
[124] K. Pfeiffer,et al. Supercomplexes in the respiratory chains of yeast and mammalian mitochondria , 2000, The EMBO journal.
[125] L. P. Van den Heuvel,et al. Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects , 2000, Human mutation.
[126] J. Cooper,et al. Clinical, biochemical and molecular genetic correlations in Friedreich's ataxia. , 2000, Human molecular genetics.
[127] S. Dimauro,et al. Does the Patient Have a Mitochondrial Encephalomyopathy? , 1999, Journal of child neurology.
[128] S. Dimauro,et al. Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene , 1999, Annals of neurology.
[129] P. Barth,et al. Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I , 1999, Annals of neurology.
[130] A. Matsuno-Yagi,et al. The NDUFA1 gene product (MWFE protein) is essential for activity of complex I in mammalian mitochondria. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[131] D. Thorburn,et al. Respiratory chain complex I deficiency , 1999, Neurology.
[132] K. Nagashima,et al. Adult Leigh syndrome with mitochondrial DNA mutation at 8993 , 1999, Acta Neuropathologica.
[133] E. Mariman,et al. Mutant NDUFV1 subunit of mitochondrial complex I causes leukodystrophy and myoclonic epilepsy , 1999, Nature Genetics.
[134] C. Elkan,et al. A common ancestor for a subunit in the mitochondrial proton-translocating NADH:ubiquinone oxidoreductase (complex I) and short-chain dehydrogenases/reductases , 1999, Cellular and Molecular Life Sciences (CMLS).
[135] S. Dimauro,et al. A double mutation (A8296G and G8363A) in the mitochondrial DNA tRNALys gene associated with myoclonus epilepsy with ragged-red fibers , 1999, Neurology.
[136] B. Hamel,et al. The first nuclear-encoded complex I mutation in a patient with Leigh syndrome. , 1998, American journal of human genetics.
[137] R. Küffner,et al. Involvement of two novel chaperones in the assembly of mitochondrial NADH:Ubiquinone oxidoreductase (complex I). , 1998, Journal of molecular biology.
[138] J. Arenas,et al. Complex I Defect in muscle from patients with Huntington's disease , 1998, Annals of neurology.
[139] E. Mariman,et al. Demonstration of a new pathogenic mutation in human complex I deficiency: a 5-bp duplication in the nuclear gene encoding the 18-kD (AQDQ) subunit. , 1998, American journal of human genetics.
[140] S. Dimauro,et al. Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS. , 1997, Biochemical and biophysical research communications.
[141] U. Brandt,et al. Proton-translocation by membrane-bound NADH:ubiquinone-oxidoreductase (complex I) through redox-gated ligand conduction. , 1997, Biochimica et biophysica acta.
[142] R. Swerdlow,et al. Origin and functional consequences of the complex I defect in Parkinson's disease , 1996, Annals of neurology.
[143] D. Turnbull,et al. Deficiency of respiratory chain complex I is a common cause of leigh disease , 1996, Annals of neurology.
[144] J. Christodoulou,et al. Leigh syndrome: Clinical features and biochemical and DNA abnormalities , 1996, Annals of neurology.
[145] D. Wallace,et al. Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia , 1996, Molecular and cellular biology.
[146] J. Walker,et al. Conservation of sequences of subunits of mitochondrial complex I and their relationships with other proteins. , 1992, Biochimica et biophysica acta.
[147] J. Walker,et al. The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains , 1992, Quarterly Reviews of Biophysics.
[148] A. Torroni,et al. Mitochondrial DNA Complex I and I11 Mutations Associated With Leber’s Hereditary Optic Neuropathy , 2002 .
[149] K. Leonard,et al. Electron microscopic analysis of the peripheral and membrane parts of mitochondrial NADH dehydrogenase (complex I). , 1991, Journal of molecular biology.
[150] C. Marsden,et al. Mitochondrial Complex I Deficiency in Parkinson's Disease , 1990, Lancet.
[151] Y. Kagawa,et al. Deficiencies in complex I subunits of the respiratory chain in Parkinson's disease. , 1989, Biochemical and biophysical research communications.
[152] A. H. V. Schapira,et al. MITOCHONDRIAL COMPLEX I DEFICIENCY IN PARKINSON'S DISEASE , 1989, The Lancet.
[153] J. Veerkamp,et al. Investigation of mitochondrial metabolism in small human skeletal muscle biopsy specimens. Improvement of preparation procedure. , 1985, Clinica chimica acta; international journal of clinical chemistry.
[154] M. Wikström. Two protons are pumped from the mitochondrial matrix per electron transferred between NADH and ubiquinone , 1984, FEBS letters.
[155] J. Langston,et al. Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis. , 1983, Science.
[156] C. Scoppetta,et al. CENTRAL CERVICAL CORD SYNDROME AFTER HEADING A FOOTBALL , 1978, The Lancet.