139 related articles for article (PubMed ID: 18194667)
1. 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]
2. Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.
Zhou X; Zhang H; Zhao F; Ji Y; Tong Y; Zhang J; Zhang Y; Yang L; Qian Y; Lu F; Qu J; Guan MX
Mol Genet Metab; 2010 Aug; 100(4):379-84. PubMed ID: 20627642
[TBL] [Abstract][Full Text] [Related]
3. Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafness.
Li X; Fischel-Ghodsian N; Schwartz F; Yan Q; Friedman RA; Guan MX
Nucleic Acids Res; 2004; 32(3):867-77. PubMed ID: 14960712
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation.
Tong Y; Sun YH; Zhou X; Zhao F; Mao Y; Wei QP; Yang L; Qu J; Guan MX
Mol Genet Metab; 2010 Apr; 99(4):417-24. PubMed ID: 20053576
[TBL] [Abstract][Full Text] [Related]
7. Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated ND1 G3460A mutation in Chinese families.
Ji Y; Liang M; Zhang J; Zhang M; Zhu J; Meng X; Zhang S; Gao M; Zhao F; Wei QP; Jiang P; Tong Y; Liu X; Qin Mo J; Guan MX
J Hum Genet; 2014 Mar; 59(3):134-40. PubMed ID: 24430572
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Clinical and molecular features of two diabetes families carrying mitochondrial ND1 T3394C mutation.
You X; Huang X; Bi L; Li R; Zheng L; Xin C
Ir J Med Sci; 2022 Apr; 191(2):749-758. PubMed ID: 33840063
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. The mitochondrial tRNA(Glu) A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathy.
Tong Y; Mao Y; Zhou X; Yang L; Zhang J; Cai W; Zhao F; Wang X; Lu F; Qu J; Guan MX
Biochem Biophys Res Commun; 2007 Jun; 357(2):524-30. PubMed ID: 17434142
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation.
Zhang M; Zhou X; Li C; Zhao F; Zhang J; Yuan M; Sun YH; Wang J; Tong Y; Liang M; Yang L; Cai W; Wang L; Qu J; Guan MX
Mol Genet Metab; 2010; 101(2-3):192-9. PubMed ID: 20728388
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees.
Chen B; Sun D; Yang L; Zhang C; Yang A; Zhu Y; Zhao J; Chen Y; Guan M; Wang X; Li R; Tang X; Wang J; Tao Z; Lu J; Guan MX
Am J Med Genet A; 2008 May; 146A(10):1248-58. PubMed ID: 18386806
[TBL] [Abstract][Full Text] [Related]
15. [Identification of mitochondrial DNA ND1 T3866C mutation in three ethnic Han Chinese families affected with Leber's hereditary optic neuropathy].
Zhang S; Gao M; Zhang Z; Liu X; Guan M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):198-203. PubMed ID: 25863085
[TBL] [Abstract][Full Text] [Related]
16. [Leber's hereditary optic neuropathy and limbs abnormity claudication may be associated with the mitochondrial ND1 T3866C mutation].
Liu Y; Zhuang SL; Tong Y; Qu J; Zhou XT; Zhao FX; Zhang JJ; Zhang YM; Zhang Y; Guan MX
Yi Chuan; 2010 Feb; 32(2):141-7. PubMed ID: 20176558
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation.
Qu J; Zhou X; Zhao F; Liu X; Zhang M; Sun YH; Liang M; Yuan M; Liu Q; Tong Y; Wei QP; Yang L; Guan MX
Biochim Biophys Acta; 2010 Mar; 1800(3):305-12. PubMed ID: 19733221
[TBL] [Abstract][Full Text] [Related]
19. Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese Families.
Zhou X; Qian Y; Zhang J; Tong Y; Jiang P; Liang M; Dai X; Zhou H; Zhao F; Ji Y; Mo JQ; Qu J; Guan MX
Invest Ophthalmol Vis Sci; 2012 Jul; 53(8):4586-94. PubMed ID: 22577081
[TBL] [Abstract][Full Text] [Related]
20. Mitochondrial tRNAAla 5601C>T variant may affect the clinical expression of the LHON‑related ND4 11778G>A mutation in a family.
Ding Y; Ye YF; Li MY; Xia BH; Leng JH
Mol Med Rep; 2020 Jan; 21(1):201-208. PubMed ID: 31939618
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]