Yan Q - Search Results

1

1-Deoxynojirimycin promotes cardiac function and rescues mitochondrial cristae in mitochondrial hypertrophic cardiomyopathy.

Zhuang Q, Guo F, Fu L, Dong Y, Xie S, Ding X, Hu S, Zhou XD, Jiang Y, Zhou H, Qiu Y, Lei Z, Li M, Cai H, Fan M, Sang L, Fu Y, Zhang D, Lin A, Li X, Kunath T, Zhou R, Liang P, Liu Z, Yan Q. Zhuang Q, et al. Among authors: yan q. J Clin Invest. 2023 Jul 17;133(14):e164660. doi: 10.1172/JCI164660. J Clin Invest. 2023. PMID: 37200096 Free PMC article.

2

[Advances in the molecular pathogenesis of hypertrophic cardiomyopathy].

Song YR, Liu Z, Gu SL, Qian LJ, Yan QF. Song YR, et al. Yi Chuan. 2011 Jun;33(6):549-57. doi: 10.3724/sp.j.1005.2011.00549. Yi Chuan. 2011. PMID: 21684859 Review. Chinese.

3

Mitochondrial ND5 12338T>C variant is associated with maternally inherited hypertrophic cardiomyopathy in a Chinese pedigree.

Liu Z, Song Y, Gu S, He X, Zhu X, Shen Y, Wu B, Wang W, Li S, Jiang P, Lu J, Huang W, Yan Q. Liu Z, et al. Among authors: yan q. Gene. 2012 Sep 15;506(2):339-43. doi: 10.1016/j.gene.2012.06.071. Epub 2012 Jul 1. Gene. 2012. PMID: 22759514

4

The novel mitochondrial 16S rRNA 2336T>C mutation is associated with hypertrophic cardiomyopathy.

Liu Z, Song Y, Li D, He X, Li S, Wu B, Wang W, Gu S, Zhu X, Wang X, Zhou Q, Dai Y, Yan Q. Liu Z, et al. Among authors: yan q. J Med Genet. 2014 Mar;51(3):176-84. doi: 10.1136/jmedgenet-2013-101818. Epub 2013 Dec 23. J Med Genet. 2014. PMID: 24367055 Free PMC article.

5

Mechanistic study on the nuclear modifier gene MSS1 mutation suppressing neomycin sensitivity of the mitochondrial 15S rRNA C1477G mutation in Saccharomyces cerevisiae.

Zhou Q, Wang W, He X, Zhu X, Shen Y, Yu Z, Wang X, Qi X, Zhang X, Fan M, Dai Y, Yang S, Yan Q. Zhou Q, et al. Among authors: yan q. PLoS One. 2014 Mar 3;9(3):e90336. doi: 10.1371/journal.pone.0090336. eCollection 2014. PLoS One. 2014. PMID: 24595024 Free PMC article.

6

Bile acid signaling and liver regeneration.

Fan M, Wang X, Xu G, Yan Q, Huang W. Fan M, et al. Among authors: yan q. Biochim Biophys Acta. 2015 Feb;1849(2):196-200. doi: 10.1016/j.bbagrm.2014.05.021. Epub 2014 May 27. Biochim Biophys Acta. 2015. PMID: 24878541 Free PMC article. Review.

7

A deafness-associated tRNAHis mutation alters the mitochondrial function, ROS production and membrane potential.

Gong S, Peng Y, Jiang P, Wang M, Fan M, Wang X, Zhou H, Li H, Yan Q, Huang T, Guan MX. Gong S, et al. Among authors: yan q. Nucleic Acids Res. 2014 Jul;42(12):8039-48. doi: 10.1093/nar/gku466. Epub 2014 Jun 11. Nucleic Acids Res. 2014. PMID: 24920829 Free PMC article.

8

Mitochondrial Dysfunctions Contribute to Hypertrophic Cardiomyopathy in Patient iPSC-Derived Cardiomyocytes with MT-RNR2 Mutation.

Li S, Pan H, Tan C, Sun Y, Song Y, Zhang X, Yang W, Wang X, Li D, Dai Y, Ma Q, Xu C, Zhu X, Kang L, Fu Y, Xu X, Shu J, Zhou N, Han F, Qin D, Huang W, Liu Z, Yan Q. Li S, et al. Among authors: yan q. Stem Cell Reports. 2018 Mar 13;10(3):808-821. doi: 10.1016/j.stemcr.2018.01.013. Epub 2018 Feb 15. Stem Cell Reports. 2018. PMID: 29456182 Free PMC article.

9

Mitochondrial dysfunction caused by m.2336T>C mutation with hypertrophic cardiomyopathy in cybrid cell lines.

Li D, Sun Y, Zhuang Q, Song Y, Wu B, Jia Z, Pan H, Zhou H, Hu S, Zhang B, Qiu Y, Dai Y, Chen S, Xu X, Zhu X, Lin A, Huang W, Liu Z, Yan Q. Li D, et al. Among authors: yan q. Mitochondrion. 2019 May;46:313-320. doi: 10.1016/j.mito.2018.08.005. Epub 2018 Sep 6. Mitochondrion. 2019. PMID: 30196098

10

Cell models and drug discovery for mitochondrial diseases.

Hu SY, Zhuang QQ, Qiu Y, Zhu XF, Yan QF. Hu SY, et al. J Zhejiang Univ Sci B. 2019 May;20(5):449-456. doi: 10.1631/jzus.B1900196. J Zhejiang Univ Sci B. 2019. PMID: 31090270 Free PMC article. Review.

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