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JOURNAL OF RADIATION RESEARCH, ISSN 0449-3060, 2012, Volume 53, Issue 2, pp. 257 - 263
The purpose of this study is to investigate the influence of mitochondrial respiratory chain complex I inhibition on the radiosensitivity of HepG2 cells. The... 
Journal Article
Nan fang yi ke da xue xue bao = Journal of Southern Medical University, ISSN 1673-4254, 09/2013, Volume 33, Issue 9, p. 1357
To investigate the relationship between heroin spongiform leucoencephalopathy and respiratory chain complex I deficiency. The activity of respiratory chain... 
Electron Transport | Humans | Middle Aged | Mitochondrial Diseases - metabolism | Male | Canavan Disease - etiology | Case-Control Studies | Heroin Dependence - complications | Young Adult | Canavan Disease - metabolism | Adult | Female | Canavan Disease - pathology | Heroin Dependence - metabolism | Heroin Dependence - pathology
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 08/2012, Volume 14, Issue 8, p. 561
This study reviews a case of mitochondrial respiratory chain complex I deficiency due to the 10191T>C mutation in mitochondrial ND3 gene. The previously... 
Mitochondrial Diseases - genetics | Magnetic Resonance Imaging | Electron Transport Complex I - genetics | Electron Transport Complex I - deficiency | Humans | Adolescent | Brain - pathology | Male | Mutation | Leigh Disease - genetics
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 04/2012, Volume 14, Issue 4, p. 241
Mitochondrial respiratory chain deficiency is a common cause of mitochondrial disease in children. This study aimed to review the clinical, enzymatic and... 
Mitochondrial Diseases - complications | Diagnosis, Differential | Cholestasis, Intrahepatic - diagnosis | Electron Transport Complex I - deficiency | Humans | Cholestasis, Intrahepatic - etiology | Infant | Male
Journal Article
Cocuk Sagligi ve Hastaliklari Dergisi, ISSN 0010-0161, 2015, Volume 58, Issue 2, pp. 68 - 71
Journal Article
Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, ISSN 1008-8830, 05/2009, Volume 11, Issue 5, p. 333
Leigh syndrome is a genetically heterogeneous disease caused by defects in enzymes involved in aerobic energy metabolism and the Krebs', cycle. Mitonchondrial... 
DNA, Mitochondrial - genetics | Electron Transport Complex I - deficiency | Humans | Adolescent | Male | Mutation | Leigh Disease - genetics
Journal Article
Journal Article
KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, ISSN 0023-2165, 03/2014, Volume 231, Issue 3, pp. 216 - 221
Zusammenfassung Die Lebersche hereditare Optikusneuropathie ist eine seltene erbliche Erkrankung der retinalen Ganglienzellen und fuhrt innerhalb von Wochen... 
CENTRAL SCOTOMA | Lebersche hereditare Optikus-Neuropathie | CLINICAL EXPRESSION | MITOCHONDRIAL-DNA MUTATION | VISUAL RECOVERY | mitochondrial disease | Genetik | mitochondriale Erkrankung | LARGE BRAZILIAN PEDIGREE | COMPLEX-I | LHON | TOO OLD | OPHTHALMOLOGY | Genetics | LATE-ONSET | DYSFUNCTION | Lebers hereditary optic neuropathy | MTDNA MUTATIONS
Journal Article
Journal of Pesticide Science, ISSN 1348-589X, 2004, Volume 29, Issue 2, pp. 127 - 161
Natural acetogenins are the most potent inhibitors of mitochondrial complex I. By synthesizing a ubiquinone-acetogenin hybrid inhibitor (named Q-acetogenin),... 
Journal Article
by Huang, J and Xu, XY and Wang, LX
CHINESE JOURNAL OF ORGANIC CHEMISTRY, ISSN 0253-2786, 08/2010, Volume 30, Issue 8, pp. 1233 - 1236
3-Aryloxypropanals are important intermediates for the preparations of medicines, plasticizers and surfactants. An improved preparation of 3-aryloxypropanal is... 
3-aryloxypropanal | synthesis | OXIDATION | MITOCHONDRIAL COMPLEX-I | CHEMISTRY, ORGANIC | phenol | DELTA-LAC-ACETOGENINS | HYDROFORMYLATION
Journal Article
Zhonghua er ke za zhi = Chinese journal of pediatrics, ISSN 0578-1310, 11/2011, Volume 49, Issue 11, p. 848
Journal Article
Yi chuan = Hereditas, ISSN 0253-9772, 11/2012, Volume 34, Issue 11, p. 1434
The complete sequence of mitochondrial genome of Larus brunnicephalus was determined using long PCR and conserved primers walking approaches. The results... 
Animals | Codon | Electron Transport Complex I - genetics | Base Sequence | Charadriiformes - classification | RNA, Ribosomal - chemistry | Molecular Sequence Data | Charadriiformes - genetics | Genome, Mitochondrial | Phylogeny
Journal Article
YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, ISSN 0031-6903, 2008, Volume 128, pp. 170 - 171
Since the discovery of the 1-methyl 4-phenyl 1,2,3,6-tetrahydropyridine (MPTP)-induced Parkinsonism, mitochondrial dysfunction has been thought as a major... 
MITOCHONDRIAL COMPLEX-I | mitochondria | DISEASE | Parkinson disease | complex I | PHARMACOLOGY & PHARMACY | MPTP
Journal Article
BBA - Bioenergetics, ISSN 0005-2728, 07/2016, Volume 1857, Issue 7, pp. 938 - 945
Complex I deficiency is the most frequently encountered single mitochondrial single enzyme deficiency in patients with a mitochondrial disorder. Although... 
Complex I | Enzyme measurement | mtDNA | Whole exome sequencing | Mitochondrial disease | RESPIRATORY-CHAIN | EXOME | SUPEROXIDE-PRODUCTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CLINICAL-FEATURES | DEFICIENCY | ATP PRODUCTION | BIOPHYSICS | LEIGH-SYNDROME | CALCIUM UNIPORTER | MUTATION | HEREDITARY OPTIC NEUROPATHY | Enzymes | Genes | Genomics | Genetic screening
Journal Article
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