Pu J - Search Results

1

Genome-Wide Association Study for Idiopathic Ventricular Tachyarrhythmias Identifies Key Role of CCR7 and PKN2 in Calcium Homeostasis and Cardiac Rhythm Maintenance.

Fang C, Wang P, Yu D, Zhang X, Gou D, Liang L, Bai X, Xie W, Li H, Pu J, Yao Y, Wang B, Ren X, Ke T, Tu X, Xu C, Wang QK. Fang C, et al. Among authors: pu j. Circ Genom Precis Med. 2022 Oct;15(5):e003603. doi: 10.1161/CIRCGEN.121.003603. Epub 2022 Jul 27. Circ Genom Precis Med. 2022. PMID: 35895078

2

De Novo FGF12 (Fibroblast Growth Factor 12) Functional Variation Is Potentially Associated With Idiopathic Ventricular Tachycardia.

Li Q, Zhao Y, Wu G, Chen S, Zhou Y, Li S, Zhou M, Fan Q, Pu J, Hong K, Cheng X, Kenneth Wang Q, Tu X. Li Q, et al. Among authors: pu j. J Am Heart Assoc. 2017 Aug 3;6(8):e006130. doi: 10.1161/JAHA.117.006130. J Am Heart Assoc. 2017. PMID: 28775062 Free PMC article.

3

Identification of rare variants in cardiac sodium channel β4-subunit gene SCN4B associated with ventricular tachycardia.

Yang Q, Xiong H, Xu C, Huang Y, Tu X, Wu G, Fu F, Wang Z, Wang L, Zhao Y, Li S, Huang Y, Wang C, Wang D, Yao Y, Wang F, Wang Y, Xue Y, Wang P, Chen Q, Pu J, Wang QK. Yang Q, et al. Among authors: pu j. Mol Genet Genomics. 2019 Aug;294(4):1059-1071. doi: 10.1007/s00438-019-01567-7. Epub 2019 Apr 17. Mol Genet Genomics. 2019. PMID: 31020414 Free PMC article.

4

The role of variability in night-time mean heart rate on the prediction of ventricular arrhythmias and all-cause mortality in implantable cardioverter defibrillator patients.

Zhao S, Chen K, Su Y, Hua W, Pu J, Li H, Dai Y, Tang M, Fan X, Zhao Y, Zheng X, Cai C, Li Z, Zhang S. Zhao S, et al. Among authors: pu j. Europace. 2015 Oct;17 Suppl 2:ii76-82. doi: 10.1093/europace/euv209. Europace. 2015. PMID: 26842120

5

Clinical implications of sarcomere and nonsarcomere gene variants in patients with left ventricular noncompaction cardiomyopathy.

Li S, Zhang C, Liu N, Bai H, Hou C, Pu J. Li S, et al. Among authors: pu j. Mol Genet Genomic Med. 2019 Sep;7(9):e874. doi: 10.1002/mgg3.874. Epub 2019 Aug 9. Mol Genet Genomic Med. 2019. PMID: 31397097 Free PMC article.

6

LRP6 Polymorphisms Is Associated With Sudden Cardiac Death in Patients With Chronic Heart Failure in the Chinese Han Population.

Guo Q, Lai Y, Chu J, Chen X, Gao M, Sang C, Dong J, Pu J, Ma C. Guo Q, et al. Among authors: pu j. Front Cardiovasc Med. 2022 Feb 4;8:815595. doi: 10.3389/fcvm.2021.815595. eCollection 2021. Front Cardiovasc Med. 2022. PMID: 35187114 Free PMC article.

7

Novel SCN5A frame‑shift mutation underlying in patient with idiopathic ventricular fibrillation manifested with J wave in inferior lead and prolonged S‑wave in precordial lead.

Zhou X, Ren L, Huang J, Zhang Y, Cai Y, Pu J. Zhou X, et al. Among authors: pu j. Exp Ther Med. 2023 May 2;25(6):287. doi: 10.3892/etm.2023.11986. eCollection 2023 Jun. Exp Ther Med. 2023. PMID: 37206574 Free PMC article.

8

Common RyR2 variants associate with ventricular arrhythmias and sudden cardiac death in chronic heart failure.

Ran Y, Chen J, Li N, Zhang W, Feng L, Wang R, Hui R, Zhang S, Pu J. Ran Y, et al. Among authors: pu j. Clin Sci (Lond). 2010 Jun 4;119(5):215-23. doi: 10.1042/CS20090656. Clin Sci (Lond). 2010. PMID: 20408814

9

Genotype-Positive Status Is Associated With Poor Prognoses in Patients With Left Ventricular Noncompaction Cardiomyopathy.

Li S, Zhang C, Liu N, Bai H, Hou C, Wang J, Song L, Pu J. Li S, et al. Among authors: pu j. J Am Heart Assoc. 2018 Oct 16;7(20):e009910. doi: 10.1161/JAHA.118.009910. J Am Heart Assoc. 2018. PMID: 30371277 Free PMC article.

10

Titin-truncating variants are associated with heart failure events in patients with left ventricular non-compaction cardiomyopathy.

Li S, Zhang C, Liu N, Bai H, Hou C, Song L, Pu J. Li S, et al. Among authors: pu j. Clin Cardiol. 2019 May;42(5):530-535. doi: 10.1002/clc.23172. Epub 2019 Apr 16. Clin Cardiol. 2019. PMID: 30851055 Free PMC article.

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