These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
138 related articles for article (PubMed ID: 33553162)
1. Mitochondrial tRNA Mutation and Regulation of the Adiponectin Pathway in Maternally Inherited Hypertension in Chinese Han. Bai J; Ma Q; Lan Y; Chen Y; Ma S; Li J; Liu C; Fu Z; Lu X; Huang Y; Li Y Front Cell Dev Biol; 2020; 8():623450. PubMed ID: 33553162 [TBL] [Abstract][Full Text] [Related]
2. Maternally Inherited Essential Hypertension May Be Associated with the Mutations in Mitochondrial tRNA Wang C; Deng X; Li L; Li M Pharmgenomics Pers Med; 2024; 17():13-26. PubMed ID: 38222291 [TBL] [Abstract][Full Text] [Related]
3. Novel mitochondrial tRNA Fu Y; Jing P; Yao L; Wang H; Zhou C Ir J Med Sci; 2023 Apr; 192(2):615-623. PubMed ID: 35657541 [TBL] [Abstract][Full Text] [Related]
4. Molecular characterization of two Chinese pedigrees with maternally inherited hypertension. Ding Y; Yu J; Guo Q; Gao B; Huang J J Gene Med; 2021 Apr; 23(4):e3328. PubMed ID: 33625761 [TBL] [Abstract][Full Text] [Related]
5. Mitochondrial tRNA Yang P; Wu P; Liu X; Feng J; Zheng S; Wang Y; Fan Z Ir J Med Sci; 2020 May; 189(2):489-496. PubMed ID: 31776834 [TBL] [Abstract][Full Text] [Related]
6. Mitochondrial tRNA mutations are associated with maternally inherited hypertension in two Han Chinese pedigrees. Qiu Q; Li R; Jiang P; Xue L; Lu Y; Song Y; Han J; Lu Z; Zhi S; Mo JQ; Guan MX Hum Mutat; 2012 Aug; 33(8):1285-93. PubMed ID: 22549939 [TBL] [Abstract][Full Text] [Related]
7. Systematic analysis of the clinical and biochemical characteristics of maternally inherited hypertension in Chinese Han families associated with mitochondrial. Liu Y; Zhu Q; Zhu C; Wang X; Yang J; Yin T; Gao J; Li Z; Ma Q; Guan M; Li Y; Chen Y BMC Med Genomics; 2014 Dec; 7():73. PubMed ID: 25539907 [TBL] [Abstract][Full Text] [Related]
8. Mitochondrial biogenesis dysfunction and metabolic dysfunction from a novel mitochondrial tRNA Liu Y; Li Y; Zhu C; Tian L; Guan M; Chen Y Sci Rep; 2017 Jun; 7(1):3034. PubMed ID: 28596595 [TBL] [Abstract][Full Text] [Related]
9. Associations of mitochondrial DNA 3777-4679 region mutations with maternally inherited essential hypertensive subjects in China. Zhu Y; You J; Xu C; Gu X BMC Med Genet; 2020 May; 21(1):105. PubMed ID: 32414374 [TBL] [Abstract][Full Text] [Related]
10. Maternally inherited coronary heart disease is associated with a novel mitochondrial tRNA mutation. Zhang Z; Liu M; He J; Zhang X; Chen Y; Li H BMC Cardiovasc Disord; 2019 Dec; 19(1):293. PubMed ID: 31842766 [TBL] [Abstract][Full Text] [Related]
11. Mitochondrial DNA mutation m.5512A > G in the acceptor-stem of mitochondrial tRNA Guo L; Yuan Y; Bi R Biochem Biophys Res Commun; 2016 Oct; 479(4):800-807. PubMed ID: 27687549 [TBL] [Abstract][Full Text] [Related]
12. Mitochondrial tRNA Li H; Geng J; Yu H; Tang X; Yang X; Xue L Biochem Biophys Res Commun; 2018 Jan; 495(1):574-581. PubMed ID: 29129694 [TBL] [Abstract][Full Text] [Related]
13. Contribution of the tRNA Meng F; He Z; Tang X; Zheng J; Jin X; Zhu Y; Ren X; Zhou M; Wang M; Gong S; Mo JQ; Shu Q; Guan MX J Biol Chem; 2018 Mar; 293(9):3321-3334. PubMed ID: 29348176 [TBL] [Abstract][Full Text] [Related]
14. Mitochondrial tRNA Mutations Associated With Essential Hypertension: From Molecular Genetics to Function. Liu Y; Chen Y Front Cell Dev Biol; 2020; 8():634137. PubMed ID: 33585472 [TBL] [Abstract][Full Text] [Related]
15. A Deafness- and Diabetes-associated tRNA Mutation Causes Deficient Pseudouridinylation at Position 55 in tRNAGlu and Mitochondrial Dysfunction. Wang M; Liu H; Zheng J; Chen B; Zhou M; Fan W; Wang H; Liang X; Zhou X; Eriani G; Jiang P; Guan MX J Biol Chem; 2016 Sep; 291(40):21029-21041. PubMed ID: 27519417 [TBL] [Abstract][Full Text] [Related]
16. Mitochondrial tRNA Zheng P; Li S; Liu C; Zha Z; Wei X; Yuan Y Clin Exp Hypertens; 2018; 40(6):595-600. PubMed ID: 29211511 [TBL] [Abstract][Full Text] [Related]
17. Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene. Yan X; Wang X; Wang Z; Sun S; Chen G; He Y; Mo JQ; Li R; Jiang P; Lin Q; Sun M; Li W; Bai Y; Zhang J; Zhu Y; Lu J; Yan Q; Li H; Guan MX J Med Genet; 2011 Oct; 48(10):682-90. PubMed ID: 21931169 [TBL] [Abstract][Full Text] [Related]
18. The mitochondrial calcium uniporter is involved in mitochondrial calcium cycle dysfunction: Underlying mechanism of hypertension associated with mitochondrial tRNA(Ile) A4263G mutation. Chen X; Zhang Y; Xu B; Cai Z; Wang L; Tian J; Liu Y; Li Y Int J Biochem Cell Biol; 2016 Sep; 78():307-314. PubMed ID: 27471128 [TBL] [Abstract][Full Text] [Related]
19. Maternally inherited hypertension is associated with the mitochondrial tRNA(Ile) A4295G mutation in a Chinese family. Li Z; Liu Y; Yang L; Wang S; Guan MX Biochem Biophys Res Commun; 2008 Mar; 367(4):906-11. PubMed ID: 18177739 [TBL] [Abstract][Full Text] [Related]
20. Identification of a Novel Mitochondrial tRNA Mutation in Chinese Family with Type 2 Diabetes Mellitus. Li X; Shang J; Li S; Wang Y Pharmgenomics Pers Med; 2024; 17():149-161. PubMed ID: 38645701 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]