threonine and Electron Transport Chain Deficiencies, Mitochondrial

threonine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Alberti, JM; Baloh, RH; Biris, N; Dorn, GW; Franco, A; Gavathiotis, E; Janetka, JW; Kitsis, RN; Knight, WC; Krezel, AM; Mochly-Rosen, D; Rocha, AG; Rumsey, JM; Townsend, RR; Zacharioudakis, E	1
Abicht, A; Bindoff, LA; Chinnery, PF; Czermin, B; de Coo, IF; De Vries, M; Dimauro, S; Gorman, GG; Hirano, M; Holinski-Feder, E; Horvath, R; Hudson, G; Jardel, C; Keiling, BC; Klopstock, T; Lochmüller, H; Lombès, A; Neeve, VC; Saft, C; Samuels, DC; Smeets, H; Smeitink, J; Smits, BW; Taylor, RW; Turnbull, DM; van den Bosch, B; Van Goethem, G	1

Other Studies

2 other study(ies) available for threonine and Electron Transport Chain Deficiencies, Mitochondrial

Article	Year
MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A. Science (New York, N.Y.), 2018, 04-20, Volume: 360, Issue:6386 Topics: Amino Acid Substitution; Animals; Arginine; Axons; Charcot-Marie-Tooth Disease; Disease Models, Animal; Drug Design; Glutamine; GTP Phosphohydrolases; Humans; Methionine; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondrial Diseases; Mitochondrial Proteins; Oligopeptides; Phosphorylation; Protein Kinases; Sciatic Nerve; Small Molecule Libraries; Threonine	2018
What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr? Brain : a journal of neurology, 2012, Volume: 135, Issue:Pt 12 Topics: Adolescent; Adult; Age of Onset; Alanine; Child; Cohort Studies; Diffuse Cerebral Sclerosis of Schilder; DNA Mutational Analysis; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Europe; Family Health; Female; Genetic Predisposition to Disease; Homozygote; Humans; Male; Middle Aged; Mitochondrial Diseases; Muscle, Skeletal; Mutation; Ophthalmoplegia, Chronic Progressive External; Statistics as Topic; Statistics, Nonparametric; Threonine; Young Adult	2012

Article

Year

MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A.

Science (New York, N.Y.), 2018, 04-20, Volume: 360, Issue:6386

Topics: Amino Acid Substitution; Animals; Arginine; Axons; Charcot-Marie-Tooth Disease; Disease Models, Animal; Drug Design; Glutamine; GTP Phosphohydrolases; Humans; Methionine; Mice; Mice, Inbred C57BL; Mitochondria; Mitochondrial Diseases; Mitochondrial Proteins; Oligopeptides; Phosphorylation; Protein Kinases; Sciatic Nerve; Small Molecule Libraries; Threonine

2018

What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?

Brain : a journal of neurology, 2012, Volume: 135, Issue:Pt 12

Topics: Adolescent; Adult; Age of Onset; Alanine; Child; Cohort Studies; Diffuse Cerebral Sclerosis of Schilder; DNA Mutational Analysis; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Europe; Family Health; Female; Genetic Predisposition to Disease; Homozygote; Humans; Male; Middle Aged; Mitochondrial Diseases; Muscle, Skeletal; Mutation; Ophthalmoplegia, Chronic Progressive External; Statistics as Topic; Statistics, Nonparametric; Threonine; Young Adult

2012