234 related articles for article (PubMed ID: 19546379)
1. Failures in mitochondrial tRNAMet and tRNAGln metabolism caused by the novel 4401A>G mutation are involved in essential hypertension in a Han Chinese Family.
Li R; Liu Y; Li Z; Yang L; Wang S; Guan MX
Hypertension; 2009 Aug; 54(2):329-37. PubMed ID: 19546379
[TBL] [Abstract][Full Text] [Related]
2. Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree.
Liu Y; Li R; Li Z; Wang XJ; Yang L; Wang S; Guan MX
Hypertension; 2009 Jun; 53(6):1083-90. PubMed ID: 19398658
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Hypertension-associated mitochondrial DNA 4401A>G mutation caused the aberrant processing of tRNAMet, all 8 tRNAs and ND6 mRNA in the light-strand transcript.
Zhao X; Cui L; Xiao Y; Mao Q; Aishanjiang M; Kong W; Liu Y; Chen H; Hong F; Jia Z; Wang M; Jiang P; Guan MX
Nucleic Acids Res; 2019 Nov; 47(19):10340-10356. PubMed ID: 31504769
[TBL] [Abstract][Full Text] [Related]
5. Molecular characterization of a pedigree carrying the hypertension‑associated mitochondrial tRNAGln T4363C mutation.
Wang L; Dong Z; Lin W; Gao R; Chen C; Xu J
Mol Med Rep; 2017 Nov; 16(5):6029-6033. PubMed ID: 28849157
[TBL] [Abstract][Full Text] [Related]
6. Molecular characterization of a Chinese family carrying a novel C4329A mutation in mitochondrial tRNAIle and tRNAGln genes.
Liu Y; Li Y; Gao J; Zhu C; Lan Y; Yang J; Li Z; Guan M; Chen Y
BMC Med Genet; 2014 Jul; 15():84. PubMed ID: 25056089
[TBL] [Abstract][Full Text] [Related]
7. [The mitochondrial tRNAMet/tRNAGlnA4401G and tRNACysG5821A mutations may be associated with hypertension in two Han Chinese families].
Xu M; He Y; Geng J; Meng Y; Yu H; Lin Z; Shi S; Xue L; Lu Z; Guan M
Yi Chuan; 2014 Feb; 36(2):127-34. PubMed ID: 24846941
[TBL] [Abstract][Full Text] [Related]
8. Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese family.
Tang X; Li R; Zheng J; Cai Q; Zhang T; Gong S; Zheng W; He X; Zhu Y; Xue L; Yang A; Yang L; Lu J; Guan MX
Mol Genet Metab; 2010 May; 100(1):57-64. PubMed ID: 20153673
[TBL] [Abstract][Full Text] [Related]
9. The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree.
Lu Z; Chen H; Meng Y; Wang Y; Xue L; Zhi S; Qiu Q; Yang L; Mo JQ; Guan MX
Eur J Hum Genet; 2011 Nov; 19(11):1181-6. PubMed ID: 21694735
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation.
Qu J; Li R; Zhou X; Tong Y; Lu F; Qian Y; Hu Y; Mo JQ; West CE; Guan MX
Invest Ophthalmol Vis Sci; 2006 Feb; 47(2):475-83. PubMed ID: 16431939
[TBL] [Abstract][Full Text] [Related]
12. Coronary heart disease is associated with a mutation in mitochondrial tRNA.
Jia Z; Wang X; Qin Y; Xue L; Jiang P; Meng Y; Shi S; Wang Y; Qin Mo J; Guan MX
Hum Mol Genet; 2013 Oct; 22(20):4064-73. PubMed ID: 23736300
[TBL] [Abstract][Full Text] [Related]
13. A mitochondrial mutation A4401G is involved in the pathogenesis of left ventricular hypertrophy in Chinese hypertensives.
Zhu HY; Wang SW; Liu L; Li YH; Chen R; Wang L; Holliman CJ
Eur J Hum Genet; 2009 Feb; 17(2):172-8. PubMed ID: 18701880
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Clinical and molecular characterization of a Han Chinese family with high penetrance of essential hypertension.
Teng L; Zheng J; Leng J; Ding Y
Mitochondrial DNA; 2012 Dec; 23(6):461-5. PubMed ID: 22917175
[TBL] [Abstract][Full Text] [Related]
16. Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families.
Liu XL; Zhou X; Zhou J; Zhao F; Zhang J; Li C; Ji Y; Zhang Y; Wei QP; Sun YH; Yang L; Lin B; Yuan Y; Li Y; Qu J; Guan MX
Ophthalmology; 2011 May; 118(5):978-85. PubMed ID: 21131053
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Mitochondrial tRNA
Ding Y; Xia BH; Zhang CJ; Zhuo GC
Gene; 2018 Feb; 642():299-306. PubMed ID: 29155328
[TBL] [Abstract][Full Text] [Related]
19. The mitochondrial ND1 T3308C mutation in a Chinese family with the secondary hypertension.
Liu Y; Li Z; Yang L; Wang S; Guan MX
Biochem Biophys Res Commun; 2008 Mar; 368(1):18-22. PubMed ID: 18194667
[TBL] [Abstract][Full Text] [Related]
20. Molecular characterization of a Han Chinese family with essential hypertension.
Zhu JF; Zhang X; Ling L
Genet Mol Res; 2016 May; 15(2):. PubMed ID: 27323027
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
