cysteine and Complex IV Deficiency

cysteine has been researched along with Complex IV Deficiency in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Azan, G; Bonilla, E; DiMauro, S; Ferraris, S; Hirano, M; Krishna, S; Mancuso, M; Mauro, A; Nishigaki, Y; Romansky, SG; Sammarco, P; Tay, SK	1
Bonilla, E; Coster, RV; Davidson, MM; De Vivo, DC; DiMauro, S; Glerum, DM; Hirano, M; Kaplan, P; Krishna, S; Lebel, R; Lyon, G; Nishino, I; Papadopoulou, LC; Sadlock, JE; Scalais, E; Schon, EA; Selby, J; Shanske, S; Sue, CM; Tanji, K; Walker, W	1

Other Studies

2 other study(ies) available for cysteine and Complex IV Deficiency

Article	Year
Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation. Journal of the neurological sciences, 2005, Jan-15, Volume: 228, Issue:1 Topics: Cysteine; Cytochrome-c Oxidase Deficiency; Diabetes Complications; DNA Mutational Analysis; DNA, Mitochondrial; Electron Transport Complex I; Electron Transport Complex II; Electron Transport Complex III; Female; Humans; Infant; Male; Middle Aged; Mitochondrial Myopathies; Muscle, Skeletal; Point Mutation; RNA, Transfer; Threonine	2005
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene. Nature genetics, 1999, Volume: 23, Issue:3 Topics: Amino Acid Sequence; Base Sequence; Cardiomyopathies; Carrier Proteins; Cloning, Molecular; Conserved Sequence; Cysteine; Cytochrome-c Oxidase Deficiency; DNA Mutational Analysis; Electron Transport Complex IV; Fatal Outcome; Female; Humans; Infant; Infant, Newborn; Isoenzymes; Male; Mitochondrial Proteins; Molecular Chaperones; Molecular Sequence Data; Mutation; Myocardium; Neuromuscular Diseases; Polymorphism, Restriction Fragment Length; Proteins; RNA, Messenger; Saccharomyces cerevisiae Proteins	1999

Article

Year

Congenital or late-onset myopathy in patients with the T14709C mtDNA mutation.

Journal of the neurological sciences, 2005, Jan-15, Volume: 228, Issue:1

Topics: Cysteine; Cytochrome-c Oxidase Deficiency; Diabetes Complications; DNA Mutational Analysis; DNA, Mitochondrial; Electron Transport Complex I; Electron Transport Complex II; Electron Transport Complex III; Female; Humans; Infant; Male; Middle Aged; Mitochondrial Myopathies; Muscle, Skeletal; Point Mutation; RNA, Transfer; Threonine

2005

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.

Nature genetics, 1999, Volume: 23, Issue:3

Topics: Amino Acid Sequence; Base Sequence; Cardiomyopathies; Carrier Proteins; Cloning, Molecular; Conserved Sequence; Cysteine; Cytochrome-c Oxidase Deficiency; DNA Mutational Analysis; Electron Transport Complex IV; Fatal Outcome; Female; Humans; Infant; Infant, Newborn; Isoenzymes; Male; Mitochondrial Proteins; Molecular Chaperones; Molecular Sequence Data; Mutation; Myocardium; Neuromuscular Diseases; Polymorphism, Restriction Fragment Length; Proteins; RNA, Messenger; Saccharomyces cerevisiae Proteins

1999