382 related articles for article (PubMed ID: 28740091)
21. Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency.
Hathazi D; Griffin H; Jennings MJ; Giunta M; Powell C; Pearce SF; Munro B; Wei W; Boczonadi V; Poulton J; Pyle A; Calabrese C; Gomez-Duran A; Schara U; Pitceathly RDS; Hanna MG; Joost K; Cotta A; Paim JF; Navarro MM; Duff J; Mattman A; Chapman K; Servidei S; Della Marina A; Uusimaa J; Roos A; Mootha V; Hirano M; Tulinius M; Giri M; Hoffmann EP; Lochmüller H; DiMauro S; Minczuk M; Chinnery PF; Müller JS; Horvath R
EMBO J; 2020 Dec; 39(23):e105364. PubMed ID: 33128823
[TBL] [Abstract][Full Text] [Related]
22. Significance of Mitochondria DNA Mutations in Diseases.
Zhu Z; Wang X
Adv Exp Med Biol; 2017; 1038():219-230. PubMed ID: 29178079
[TBL] [Abstract][Full Text] [Related]
23. Defective oxidative phosphorylation in thyroid oncocytic carcinoma is associated with pathogenic mitochondrial DNA mutations affecting complexes I and III.
Bonora E; Porcelli AM; Gasparre G; Biondi A; Ghelli A; Carelli V; Baracca A; Tallini G; Martinuzzi A; Lenaz G; Rugolo M; Romeo G
Cancer Res; 2006 Jun; 66(12):6087-96. PubMed ID: 16778181
[TBL] [Abstract][Full Text] [Related]
24. Molecular characterization of putative modulatory factors in two Spanish families with A1555G deafness.
Otaegui D; Irizar H; Goicoechea M; Pérez-Tur J; Belar M; López de Munain A
Audiol Neurootol; 2008; 13(5):320-7. PubMed ID: 18391568
[TBL] [Abstract][Full Text] [Related]
25. Analyzing the suppression of respiratory defects in the yeast model of human mitochondrial tRNA diseases.
Montanari A; Zhou YF; D'Orsi MF; Bolotin-Fukuhara M; Frontali L; Francisci S
Gene; 2013 Sep; 527(1):1-9. PubMed ID: 23727608
[TBL] [Abstract][Full Text] [Related]
26. Deletion of Gtpbp3 in zebrafish revealed the hypertrophic cardiomyopathy manifested by aberrant mitochondrial tRNA metabolism.
Chen D; Zhang Z; Chen C; Yao S; Yang Q; Li F; He X; Ai C; Wang M; Guan MX
Nucleic Acids Res; 2019 Jun; 47(10):5341-5355. PubMed ID: 30916346
[TBL] [Abstract][Full Text] [Related]
27. Bromodomain Inhibitors Correct Bioenergetic Deficiency Caused by Mitochondrial Disease Complex I Mutations.
Barrow JJ; Balsa E; Verdeguer F; Tavares CD; Soustek MS; Hollingsworth LR; Jedrychowski M; Vogel R; Paulo JA; Smeitink J; Gygi SP; Doench J; Root DE; Puigserver P
Mol Cell; 2016 Oct; 64(1):163-175. PubMed ID: 27666594
[TBL] [Abstract][Full Text] [Related]
28. Mutations of the mitochondrial-tRNA modifier MTO1 cause hypertrophic cardiomyopathy and lactic acidosis.
Ghezzi D; Baruffini E; Haack TB; Invernizzi F; Melchionda L; Dallabona C; Strom TM; Parini R; Burlina AB; Meitinger T; Prokisch H; Ferrero I; Zeviani M
Am J Hum Genet; 2012 Jun; 90(6):1079-87. PubMed ID: 22608499
[TBL] [Abstract][Full Text] [Related]
29. Cysteine Supplementation May be Beneficial in a Subgroup of Mitochondrial Translation Deficiencies.
Bartsakoulia M; Mϋller JS; Gomez-Duran A; Yu-Wai-Man P; Boczonadi V; Horvath R
J Neuromuscul Dis; 2016 Aug; 3(3):363-379. PubMed ID: 27854233
[TBL] [Abstract][Full Text] [Related]
30. The 2-thiouridylase function of the human MTU1 (TRMU) enzyme is dispensable for mitochondrial translation.
Sasarman F; Antonicka H; Horvath R; Shoubridge EA
Hum Mol Genet; 2011 Dec; 20(23):4634-43. PubMed ID: 21890497
[TBL] [Abstract][Full Text] [Related]
31. Nuclear factors: roles related to mitochondrial deafness.
Luo LF; Hou CC; Yang WX
Gene; 2013 May; 520(2):79-89. PubMed ID: 23510774
[TBL] [Abstract][Full Text] [Related]
32. [Mitochondrial liver disease caused by TRMU gene mutation].
Zhang ZH; Ma XP; Guo HM
Zhonghua Er Ke Za Zhi; 2020 Jul; 58(7):602-604. PubMed ID: 32605348
[TBL] [Abstract][Full Text] [Related]
33. Identification and characterization of mouse TRMU gene encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase.
Yan Q; Guan MX
Biochim Biophys Acta; 2004 Jan; 1676(2):119-26. PubMed ID: 14746906
[TBL] [Abstract][Full Text] [Related]
34. Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment.
Iommarini L; Kurelac I; Capristo M; Calvaruso MA; Giorgio V; Bergamini C; Ghelli A; Nanni P; De Giovanni C; Carelli V; Fato R; Lollini PL; Rugolo M; Gasparre G; Porcelli AM
Hum Mol Genet; 2014 Mar; 23(6):1453-66. PubMed ID: 24163135
[TBL] [Abstract][Full Text] [Related]
35. MitoTALEN: A General Approach to Reduce Mutant mtDNA Loads and Restore Oxidative Phosphorylation Function in Mitochondrial Diseases.
Hashimoto M; Bacman SR; Peralta S; Falk MJ; Chomyn A; Chan DC; Williams SL; Moraes CT
Mol Ther; 2015 Oct; 23(10):1592-9. PubMed ID: 26159306
[TBL] [Abstract][Full Text] [Related]
36. Metabolic and chemical regulation of tRNA modification associated with taurine deficiency and human disease.
Asano K; Suzuki T; Saito A; Wei FY; Ikeuchi Y; Numata T; Tanaka R; Yamane Y; Yamamoto T; Goto T; Kishita Y; Murayama K; Ohtake A; Okazaki Y; Tomizawa K; Sakaguchi Y; Suzuki T
Nucleic Acids Res; 2018 Feb; 46(4):1565-1583. PubMed ID: 29390138
[TBL] [Abstract][Full Text] [Related]
37. The mitochondrial genome in human adaptive radiation and disease: on the road to therapeutics and performance enhancement.
Wallace DC
Gene; 2005 Jul; 354():169-80. PubMed ID: 16024186
[TBL] [Abstract][Full Text] [Related]
38. Mitochondrial DNA mutations in disease and aging.
Wallace DC
Environ Mol Mutagen; 2010 Jun; 51(5):440-50. PubMed ID: 20544884
[TBL] [Abstract][Full Text] [Related]
39. Generation and Characterization of Induced Pluripotent Stem Cells from Patients with mtDNA Mutations.
Hämäläinen RH; Suomalainen A
Methods Mol Biol; 2016; 1353():65-75. PubMed ID: 26187202
[TBL] [Abstract][Full Text] [Related]
40. SIRT3 gene expression: a link between inherited mitochondrial DNA variants and oxidative stress.
D'Aquila P; Rose G; Panno ML; Passarino G; Bellizzi D
Gene; 2012 Apr; 497(2):323-9. PubMed ID: 22326535
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]