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Results: 1 to 20 of 113

1.

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. doi: 10.1038/ejhg.2011.111. Epub 2011 Jun 22.

PMID:
21694735
[PubMed - indexed for MEDLINE]
Free PMC Article
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. doi: 10.1161/HYPERTENSIONAHA.109.128702. Epub 2009 Apr 27.

PMID:
19398658
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

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.

PMID:
16431939
[PubMed - indexed for MEDLINE]
Free Article
4.

The 12S rRNA A1555G mutation in the mitochondrial haplogroup D5a is responsible for maternally inherited hypertension and hearing loss in two Chinese pedigrees.

Chen H, Zheng J, Xue L, Meng Y, Wang Y, Zheng B, Fang F, Shi S, Qiu Q, Jiang P, Lu Z, Mo JQ, Lu J, Guan MX.

Eur J Hum Genet. 2012 Jun;20(6):607-12. doi: 10.1038/ejhg.2011.259. Epub 2012 Feb 8.

PMID:
22317974
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

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. doi: 10.1161/HYPERTENSIONAHA.109.129270. Epub 2009 Jun 22.

PMID:
19546379
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

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 21;367(4):906-11. doi: 10.1016/j.bbrc.2007.12.150. Epub 2008 Jan 3.

PMID:
18177739
[PubMed - indexed for MEDLINE]
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. Chinese.

PMID:
24846941
[PubMed - indexed for MEDLINE]
8.

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. doi: 10.1016/j.ophtha.2010.09.003. Epub 2010 Dec 4.

PMID:
21131053
[PubMed - indexed for MEDLINE]
9.

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. doi: 10.1002/humu.22109. Epub 2012 May 30.

PMID:
22549939
[PubMed - indexed for MEDLINE]
10.

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. doi: 10.1016/j.ymgme.2010.01.008. Epub 2010 Jan 25.

PMID:
20153673
[PubMed - indexed for MEDLINE]
11.

[The analysis of Leber's hereditary optic neuropathy associated with mitochondrial tRNAAla C5601T mutation in seven Han Chinese families].

Zhou HH, Dai XN, Lin B, Mi H, Liu XL, Zhao FX, Zhang JJ, Zhou XT, Sun YH, Wei QP, Qu J, Guan MX.

Yi Chuan. 2012 Aug;34(8):1031-42. Chinese.

PMID:
22917908
[PubMed - indexed for MEDLINE]
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. doi: 10.3109/19401736.2012.710205. Epub 2012 Aug 24.

PMID:
22917175
[PubMed - indexed for MEDLINE]
13.

Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese families.

Wang X, Lu J, Zhu Y, Yang A, Yang L, Li R, Chen B, Qian Y, Tang X, Wang J, Zhang X, Guan MX.

Pharmacogenet Genomics. 2008 Dec;18(12):1059-70. doi: 10.1097/FPC.0b013e3283131661.

PMID:
18820594
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy.

Qian Y, Zhou X, Hu Y, Tong Y, Li R, Lu F, Yang H, Mo JQ, Qu J, Guan MX.

Biochem Biophys Res Commun. 2005 Jul 1;332(2):614-21.

PMID:
15896721
[PubMed - indexed for MEDLINE]
15.

Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation.

Qu J, Zhou X, Zhang J, Zhao F, Sun YH, Tong Y, Wei QP, Cai W, Yang L, West CE, Guan MX.

Ophthalmology. 2009 Mar;116(3):558-564.e3. doi: 10.1016/j.ophtha.2008.10.022. Epub 2009 Jan 22.

PMID:
19167085
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.

Chen J, Yang L, Yang A, Zhu Y, Zhao J, Sun D, Tao Z, Tang X, Wang J, Wang X, Tsushima A, Lan J, Li W, Wu F, Yuan Q, Ji J, Feng J, Wu C, Liao Z, Li Z, Greinwald JH, Lu J, Guan MX.

Gene. 2007 Oct 15;401(1-2):4-11. Epub 2007 Jun 20.

PMID:
17698299
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

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 28;368(1):18-22. doi: 10.1016/j.bbrc.2007.12.193. Epub 2008 Jan 14.

PMID:
18194667
[PubMed - indexed for MEDLINE]
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. doi: 10.1016/j.bbagen.2009.08.010. Epub 2009 Sep 3.

PMID:
19733221
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families.

Qu J, Wang Y, Tong Y, Zhou X, Zhao F, Yang L, Zhang S, Zhang J, West CE, Guan MX.

Invest Ophthalmol Vis Sci. 2010 Oct;51(10):4906-12. doi: 10.1167/iovs.09-5027. Epub 2010 Apr 30.

PMID:
20435583
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

[Hearing loss may be associated with the novel mitochondrial tRNA(Asp) A7551G mutation in a Chinese family].

Wu Y, Liang LZ, Xiao HL, Yang YL, Yu X, Zheng J, Fang F, Zheng BJ, Tang XW, Jin LJ, Guan MX.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2013 Dec;48(12):978-84. Chinese.

PMID:
24506995
[PubMed - indexed for MEDLINE]

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