Gu JN - Search Results

1

Identification of BMP10 as a Novel Gene Contributing to Dilated Cardiomyopathy.

Gu JN, Yang CX, Ding YY, Qiao Q, Di RM, Sun YM, Wang J, Yang L, Xu YJ, Yang YQ. Gu JN, et al. Diagnostics (Basel). 2023 Jan 9;13(2):242. doi: 10.3390/diagnostics13020242. Diagnostics (Basel). 2023. PMID: 36673052 Free PMC article.

2

Early identification and treatment of PV re-connections: role of observation time and impact on clinical results of atrial fibrillation ablation.

Wang XH, Liu X, Sun YM, Gu JN, Shi HF, Zhou L, Hu W. Wang XH, et al. Among authors: gu jn. Europace. 2007 Jul;9(7):481-6. doi: 10.1093/europace/eum101. Epub 2007 May 23. Europace. 2007. PMID: 17522081 Clinical Trial.

3

Circumferential pulmonary vein isolation: the role of key target sites.

Wang XH, Shi HF, Sun YM, Gu JN, Zhou L, Liu X. Wang XH, et al. Among authors: gu jn. Europace. 2008 Feb;10(2):197-204. doi: 10.1093/europace/eum298. Europace. 2008. PMID: 18256124

4

Pulmonary vein isolation combined with superior vena cava isolation for atrial fibrillation ablation: a prospective randomized study.

Wang XH, Liu X, Sun YM, Shi HF, Zhou L, Gu JN. Wang XH, et al. Among authors: gu jn. Europace. 2008 May;10(5):600-5. doi: 10.1093/europace/eun077. Europace. 2008. PMID: 18442966 Clinical Trial.

5

Identification of long non-coding RNAs as novel biomarker and potential therapeutic target for atrial fibrillation in old adults.

Xu Y, Huang R, Gu J, Jiang W. Xu Y, et al. Oncotarget. 2016 Mar 8;7(10):10803-11. doi: 10.18632/oncotarget.7514. Oncotarget. 2016. PMID: 26908457 Free PMC article.

6

Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy.

Xu YJ, Wang ZS, Yang CX, Di RM, Qiao Q, Li XM, Gu JN, Guo XJ, Yang YQ. Xu YJ, et al. Among authors: gu jn. J Cardiovasc Transl Res. 2019 Jun;12(3):257-267. doi: 10.1007/s12265-018-9851-8. Epub 2018 Dec 10. J Cardiovasc Transl Res. 2019. PMID: 30536204

7

Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy.

Di RM, Yang CX, Zhao CM, Yuan F, Qiao Q, Gu JN, Li XM, Xu YJ, Yang YQ. Di RM, et al. Among authors: gu jn. Eur J Med Genet. 2020 Apr;63(4):103827. doi: 10.1016/j.ejmg.2019.103827. Epub 2019 Dec 16. Eur J Med Genet. 2020. PMID: 31857253

8

A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block.

Zhang Y, Sun YM, Xu YJ, Zhao CM, Yuan F, Guo XJ, Guo YH, Yang CX, Gu JN, Qiao Q, Wang J, Yang YQ. Zhang Y, et al. Among authors: gu jn. Int Heart J. 2020 Jul 30;61(4):761-768. doi: 10.1536/ihj.19-650. Epub 2020 Jul 8. Int Heart J. 2020. PMID: 32641638 Free article.

9

ISL1 loss-of-function variation causes familial atrial fibrillation.

Wu SH, Wang XH, Xu YJ, Gu JN, Yang CX, Qiao Q, Guo XJ, Guo YH, Qiu XB, Jiang WF, Yang YQ. Wu SH, et al. Among authors: gu jn. Eur J Med Genet. 2020 Nov;63(11):104029. doi: 10.1016/j.ejmg.2020.104029. Epub 2020 Aug 6. Eur J Med Genet. 2020. PMID: 32771629

10

Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy.

Qiao Q, Zhao CM, Yang CX, Gu JN, Guo YH, Zhang M, Li RG, Qiu XB, Xu YJ, Yang YQ. Qiao Q, et al. Among authors: gu jn. Clin Chem Lab Med. 2020 Dec 3;59(5):955-963. doi: 10.1515/cclm-2020-1318. Print 2021 Apr 27. Clin Chem Lab Med. 2020. PMID: 33554560

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