Mitochondrial biogenesis dysfunction and metabolic dysfunction from a novel mitochondrial tRNAMet 4467 C>A mutation in a Han Chinese family with maternally inherited hypertension-Reference-Cited by-同舟云学术

Mitochondrial biogenesis dysfunction and metabolic dysfunction from a novel mitochondrial tRNAMet 4467 C>A mutation in a Han Chinese family with maternally inherited hypertension

Published:2017-06-08 Issue:1 Volume:7 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Liu Yuqi,Li Yang,Zhu Chao,Tian Liuyang,Guan Minxin,Chen Yundai

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-017-03303-w.pdf

Reference41 articles.

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3. Brandao, A. P. et al. Familial aggregation of arterial blood pressure and possible genetic influence. Hypertension 19, II214–7, doi: 10.1161/01.HYP.19.2_Suppl.II214 (1992).

4. Chao, Z. et al. Mitochondrial tRNA mutation with high salt stimulation on cardiac damage: underlying mechanism associated with change of Bax and VDAC. Am J Physiol Heart Circ Physiol. 311, H1248–H1257, doi: 10.1152/ajpheart.00874.2015 (2016).

5. Chobanian, A. V. et al. Seventh report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure. Hypertension 42, 1206–52, doi: 10.1161/01.HYP.0000107251.49515.c2 (2003).

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