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Results: 1 to 20 of 102

Similar articles for PubMed (Select 23627313)

1.

The mitochondrial tRNA(Met) 4454T > C variant may not be associated with essential hypertension in Han Chinese population.

Wang Y, Dong P, Li L, Li X, Wang H, Yang X, Wang S, Li Z, Shang X.

Mitochondrial DNA. 2014 Apr;25(2):124-5. doi: 10.3109/19401736.2013.786705. Epub 2013 Apr 29. No abstract available.

PMID:
23627313
2.

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.

3.

Genetic variants in mitochondrial tRNA genes are associated with essential hypertension in a Chinese Han population.

Zhu HY, Wang SW, Liu L, Chen R, Wang L, Gong XL, Zhang ML.

Clin Chim Acta. 2009 Dec;410(1-2):64-9. doi: 10.1016/j.cca.2009.09.023. Epub 2009 Sep 22.

PMID:
19778529
4.

[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
5.

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. doi: 10.1038/ejhg.2008.151. Epub 2008 Aug 13.

6.

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.

7.

[Mitochondrial tRNAMet mutation in Chinese Han essential hypertensive individuals].

Li ZB, Liu YQ, Li YH, Chen R, Wang L, Zhu QL, Li Y, Wang SW.

Yi Chuan. 2011 Jun;33(6):601-6. Chinese.

PMID:
21684865
8.
9.

A potato mitochondrial isoleucine tRNA is coded for by a mitochondrial gene possessing a methionine anticodon.

Weber F, Dietrich A, Weil JH, Maréchal-Drouard L.

Nucleic Acids Res. 1990 Sep 11;18(17):5027-30.

10.

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.

11.

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
12.

Endothelial nitric oxide synthase genetic variation and essential hypertension risk in Han Chinese: the Fangshan study.

Niu WQ, Qi Y, Zhang LT, Qi YX, Wang B, Hou SQ, Zhai XY, Qiu CC.

J Hum Hypertens. 2009 Feb;23(2):136-9. doi: 10.1038/jhh.2008.111. Epub 2008 Sep 4. No abstract available.

PMID:
18769442
13.

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
15.

Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family.

Ding Y, Li Y, You J, Yang L, Chen B, Lu J, Guan MX.

J Genet Genomics. 2009 Apr;36(4):241-50. doi: 10.1016/S1673-8527(08)60111-3.

PMID:
19376484
17.
18.

Sequence analysis of Saccharomyces exiguus mitochondrial DNA reveals an RNase P RNA gene flanked by two tRNA genes.

Wise C, Martin NC.

Nucleic Acids Res. 1991 Sep 11;19(17):4773. No abstract available.

19.

Nucleotide sequences of animal mitochondrial tRNAs(Met) possibly recognizing both AUG and AUA codons.

Takemoto C, Ueda T, Miura K, Watanabe K.

Nucleic Acids Symp Ser. 1999;(42):77-8.

20.

The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss.

Han D, Dai P, Zhu Q, Liu X, Huang D, Yuan Y, Yuan H, Wang X, Qian Y, Young WY, Guan MX.

Biochem Biophys Res Commun. 2007 Jun 1;357(2):554-60. Epub 2007 Apr 9.

PMID:
17434445
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