278 related articles for article (PubMed ID: 30916346)
1. 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]
2. Ablation of Mto1 in zebrafish exhibited hypertrophic cardiomyopathy manifested by mitochondrion RNA maturation deficiency.
Zhang Q; He X; Yao S; Lin T; Zhang L; Chen D; Chen C; Yang Q; Li F; Zhu YM; Guan MX
Nucleic Acids Res; 2021 May; 49(8):4689-4704. PubMed ID: 33836087
[TBL] [Abstract][Full Text] [Related]
3. Deletion of Mtu1 (Trmu) in zebrafish revealed the essential role of tRNA modification in mitochondrial biogenesis and hearing function.
Zhang Q; Zhang L; Chen D; He X; Yao S; Zhang Z; Chen Y; Guan MX
Nucleic Acids Res; 2018 Nov; 46(20):10930-10945. PubMed ID: 30137487
[TBL] [Abstract][Full Text] [Related]
4. The defective expression of gtpbp3 related to tRNA modification alters the mitochondrial function and development of zebrafish.
Chen D; Li F; Yang Q; Tian M; Zhang Z; Zhang Q; Chen Y; Guan MX
Int J Biochem Cell Biol; 2016 Aug; 77(Pt A):1-9. PubMed ID: 27184967
[TBL] [Abstract][Full Text] [Related]
5. Defective Expression of the Mitochondrial-tRNA Modifying Enzyme GTPBP3 Triggers AMPK-Mediated Adaptive Responses Involving Complex I Assembly Factors, Uncoupling Protein 2, and the Mitochondrial Pyruvate Carrier.
Martínez-Zamora A; Meseguer S; Esteve JM; Villarroya M; Aguado C; Enríquez JA; Knecht E; Armengod ME
PLoS One; 2015; 10(12):e0144273. PubMed ID: 26642043
[TBL] [Abstract][Full Text] [Related]
6. Defects in the mitochondrial-tRNA modification enzymes MTO1 and GTPBP3 promote different metabolic reprogramming through a HIF-PPARγ-UCP2-AMPK axis.
Boutoual R; Meseguer S; Villarroya M; Martín-Hernández E; Errami M; Martín MA; Casado M; Armengod ME
Sci Rep; 2018 Jan; 8(1):1163. PubMed ID: 29348686
[TBL] [Abstract][Full Text] [Related]
7. Combination of the loss of cmnm5U34 with the lack of s2U34 modifications of tRNALys, tRNAGlu, and tRNAGln altered mitochondrial biogenesis and respiration.
Wang X; Yan Q; Guan MX
J Mol Biol; 2010 Feb; 395(5):1038-48. PubMed ID: 20004207
[TBL] [Abstract][Full Text] [Related]
8. Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy.
Kopajtich R; Nicholls TJ; Rorbach J; Metodiev MD; Freisinger P; Mandel H; Vanlander A; Ghezzi D; Carrozzo R; Taylor RW; Marquard K; Murayama K; Wieland T; Schwarzmayr T; Mayr JA; Pearce SF; Powell CA; Saada A; Ohtake A; Invernizzi F; Lamantea E; Sommerville EW; Pyle A; Chinnery PF; Crushell E; Okazaki Y; Kohda M; Kishita Y; Tokuzawa Y; Assouline Z; Rio M; Feillet F; Mousson de Camaret B; Chretien D; Munnich A; Menten B; Sante T; Smet J; Régal L; Lorber A; Khoury A; Zeviani M; Strom TM; Meitinger T; Bertini ES; Van Coster R; Klopstock T; Rötig A; Haack TB; Minczuk M; Prokisch H
Am J Hum Genet; 2014 Dec; 95(6):708-20. PubMed ID: 25434004
[TBL] [Abstract][Full Text] [Related]
9. A human mitochondrial GTP binding protein related to tRNA modification may modulate phenotypic expression of the deafness-associated mitochondrial 12S rRNA mutation.
Li X; Guan MX
Mol Cell Biol; 2002 Nov; 22(21):7701-11. PubMed ID: 12370316
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Characterization of human GTPBP3, a GTP-binding protein involved in mitochondrial tRNA modification.
Villarroya M; Prado S; Esteve JM; Soriano MA; Aguado C; Pérez-Martínez D; Martínez-Ferrandis JI; Yim L; Victor VM; Cebolla E; Montaner A; Knecht E; Armengod ME
Mol Cell Biol; 2008 Dec; 28(24):7514-31. PubMed ID: 18852288
[TBL] [Abstract][Full Text] [Related]
12. An animal model for mitochondrial tyrosyl-tRNA synthetase deficiency reveals links between oxidative phosphorylation and retinal function.
Jin X; Zhang Z; Nie Z; Wang C; Meng F; Yi Q; Chen M; Sun J; Zou J; Jiang P; Guan MX
J Biol Chem; 2021; 296():100437. PubMed ID: 33610547
[TBL] [Abstract][Full Text] [Related]
13. FARS2 Deficiency Causes Cardiomyopathy by Disrupting Mitochondrial Homeostasis and the Mitochondrial Quality Control System.
Li B; Liu F; Chen X; Chen T; Zhang J; Liu Y; Yao Y; Hu W; Zhang M; Wang B; Liu L; Chen K; Wu Y
Circulation; 2024 Apr; 149(16):1268-1284. PubMed ID: 38362779
[TBL] [Abstract][Full Text] [Related]
14. Identification and characterization of mouse GTPBP3 gene encoding a mitochondrial GTP-binding protein involved in tRNA modification.
Li X; Guan MX
Biochem Biophys Res Commun; 2003 Dec; 312(3):747-54. PubMed ID: 14680828
[TBL] [Abstract][Full Text] [Related]
15. Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation.
Meng F; Cang X; Peng Y; Li R; Zhang Z; Li F; Fan Q; Guan AS; Fischel-Ghosian N; Zhao X; Guan MX
J Biol Chem; 2017 Feb; 292(7):2881-2892. PubMed ID: 28049726
[TBL] [Abstract][Full Text] [Related]
16. The human tRNA taurine modification enzyme GTPBP3 is an active GTPase linked to mitochondrial diseases.
Peng GX; Zhang Y; Wang QQ; Li QR; Xu H; Wang ED; Zhou XL
Nucleic Acids Res; 2021 Mar; 49(5):2816-2834. PubMed ID: 33619562
[TBL] [Abstract][Full Text] [Related]
17. The ROS-sensitive microRNA-9/9* controls the expression of mitochondrial tRNA-modifying enzymes and is involved in the molecular mechanism of MELAS syndrome.
Meseguer S; Martínez-Zamora A; García-Arumí E; Andreu AL; Armengod ME
Hum Mol Genet; 2015 Jan; 24(1):167-84. PubMed ID: 25149473
[TBL] [Abstract][Full Text] [Related]
18. Mutations in the Caenorhabditis elegans orthologs of human genes required for mitochondrial tRNA modification cause similar electron transport chain defects but different nuclear responses.
Navarro-González C; Moukadiri I; Villarroya M; López-Pascual E; Tuck S; Armengod ME
PLoS Genet; 2017 Jul; 13(7):e1006921. PubMed ID: 28732077
[TBL] [Abstract][Full Text] [Related]
19. Mutation in MTO1 involved in tRNA modification impairs mitochondrial RNA metabolism in the yeast Saccharomyces cerevisiae.
Wang X; Yan Q; Guan MX
Mitochondrion; 2009 Jun; 9(3):180-5. PubMed ID: 19460296
[TBL] [Abstract][Full Text] [Related]
20. Human cardiomyopathy mutations induce myocyte hyperplasia and activate hypertrophic pathways during cardiogenesis in zebrafish.
Becker JR; Deo RC; Werdich AA; Panàkovà D; Coy S; MacRae CA
Dis Model Mech; 2011 May; 4(3):400-10. PubMed ID: 21245263
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
