Gu J N/A - Search Results

Year	Number of Results
1979	1
1980	1
1981	1
1987	1
1988	2
1993	1
2005	2
2007	2
2008	3
2009	3
2010	2
2011	2
2012	1
2013	5
2014	2
2015	2
2016	1
2017	1
2018	2
2019	2
2020	7
2021	6
2022	7
2023	5
2024	5
2025	6

1

VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy.

Shi HY, Xie MS, Guo YH, Yang CX, Gu JN, Qiao Q, Di RM, Qiu XB, Xu YJ, Yang YQ. Shi HY, et al. Among authors: gu jn. Eur J Med Genet. 2023 Mar;66(3):104705. doi: 10.1016/j.ejmg.2023.104705. Epub 2023 Jan 16. Eur J Med Genet. 2023. PMID: 36657711

2

Linezolid-Induced Pure Red Cell Aplasia: A Case Report.

Yang XY, Chen L, Gu JN, Zeng CJ, Pan DM. Yang XY, et al. Among authors: gu jn. Infect Drug Resist. 2022 Jul 20;15:3847-3856. doi: 10.2147/IDR.S362358. eCollection 2022. Infect Drug Resist. 2022. PMID: 35899083 Free PMC article.

3

Design, synthesis and antitumor evaluation of a novel nectin-4 targeting bicyclic toxin conjugate.

Gu JN, Liu F, Song YS, Ding HF, Feng XY, Ma XL, Huang YQ, Zhang Y. Gu JN, et al. Bioorg Med Chem Lett. 2025 Nov 1;127:130306. doi: 10.1016/j.bmcl.2025.130306. Epub 2025 Jun 10. Bioorg Med Chem Lett. 2025. PMID: 40505992

4

Somatic GATA4 mutation contributes to tetralogy of Fallot.

Abhinav P, Li YJ, Huang RT, Liu XY, Gu JN, Yang CX, Xu YJ, Wang J, Yang YQ. Abhinav P, et al. Among authors: gu jn. Exp Ther Med. 2024 Jan 8;27(2):91. doi: 10.3892/etm.2024.12379. eCollection 2024 Feb. Exp Ther Med. 2024. PMID: 38274337 Free PMC article.

5

Advances in endoscopic closure techniques for endoscopic full-thickness resection.

Zhang M, Liu J, Gu JN, Han K, Jia W, Li P, Sun Y, An N, Yang Z. Zhang M, et al. Among authors: gu jn. World J Gastrointest Endosc. 2025 Sep 16;17(9):107157. doi: 10.4253/wjge.v17.i9.107157. World J Gastrointest Endosc. 2025. PMID: 40979057 Free PMC article. Review.

6

SOX7 loss-of-function variation as a cause of familial congenital heart disease.

Huang RT, Guo YH, Yang CX, Gu JN, Qiu XB, Shi HY, Xu YJ, Xue S, Yang YQ. Huang RT, et al. Among authors: gu jn. Am J Transl Res. 2022 Mar 15;14(3):1672-1684. eCollection 2022. Am J Transl Res. 2022. PMID: 35422912 Free PMC article.

7

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

8

[Structural characterization of PCP-Ⅰ from Poria as vaccine adjuvant and its hydrolytic oligosaccharide].

Gu JN, Liu GX, Li S, Ma H, Shan JJ. Gu JN, et al. Zhongguo Zhong Yao Za Zhi. 2023 Aug;48(16):4429-4437. doi: 10.19540/j.cnki.cjcmm.20230124.201. Zhongguo Zhong Yao Za Zhi. 2023. PMID: 37802869 Chinese.

9

Benefits and risks of additional ablation of complex fractionated atrial electrograms for patients with atrial fibrillation: a systematic review and meta-analysis.

Wu SH, Jiang WF, Gu J, Zhao L, Wang YL, Liu YG, Zhou L, Gu JN, Xu K, Liu X. Wu SH, et al. Among authors: gu jn. Int J Cardiol. 2013 Oct 25;169(1):35-43. doi: 10.1016/j.ijcard.2013.08.083. Epub 2013 Sep 7. Int J Cardiol. 2013. PMID: 24083885

10

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.

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