Jiang X - Search Results

1

A compound heterozygosity of Tecrl gene confirmed in a catecholaminergic polymorphic ventricular tachycardia family.

Xie L, Hou C, Jiang X, Zhao J, Li Y, Xiao T. Xie L, et al. Among authors: jiang x. Eur J Med Genet. 2019 Jul;62(7):103631. doi: 10.1016/j.ejmg.2019.01.018. Epub 2019 Feb 18. Eur J Med Genet. 2019. PMID: 30790670

2

A 10-year-old boy with dyspnea and hypoxia: abernathy malformation masquerading as pulmonary arteriovenous fistula.

Xie L, Li Y, Jiang X, Zhao J, Xiao T. Xie L, et al. Among authors: jiang x. BMC Pediatr. 2019 Feb 11;19(1):55. doi: 10.1186/s12887-019-1422-x. BMC Pediatr. 2019. PMID: 30744582 Free PMC article.

3

A novel endoglin mutation in a family with hereditary hemorrhagic telangiectasia: a case report.

Zong Y, Liu W, Hou C, Zhang H, Jiang X, Sun X, Xie L, Xiao T, Zhang Y, Li Y. Zong Y, et al. Among authors: jiang x. Transl Pediatr. 2021 Aug;10(8):2123-2130. doi: 10.21037/tp-20-156. Transl Pediatr. 2021. PMID: 34584883 Free PMC article.

4

TECRL deficiency results in aberrant mitochondrial function in cardiomyocytes.

Hou C, Jiang X, Zhang H, Zheng J, Qiu Q, Zhang Y, Sun X, Xu M, Chang ACY, Xie L, Xiao T. Hou C, et al. Among authors: jiang x. Commun Biol. 2022 May 16;5(1):470. doi: 10.1038/s42003-022-03414-9. Commun Biol. 2022. PMID: 35577932 Free PMC article.

5

Generation of an induced pluripotent stem cell line from a Chinese Han child with catecholaminergic polymorphic ventricular tachycardia.

Liu W, Liu T, Xiao T, Xie L, Hou C, Jiang X. Liu W, et al. Among authors: jiang x. Stem Cell Res. 2022 Jul;62:102811. doi: 10.1016/j.scr.2022.102811. Epub 2022 May 11. Stem Cell Res. 2022. PMID: 35679758 Free article.

6

Case Report: Novel LIM domain-binding protein 3 (LDB3) mutations associated with hypertrophic cardiomyopathy family.

Zheng J, Huang Z, Hou S, Jiang X, Zhang Y, Liu W, Jia J, Li Y, Sun X, Xie L, Zhao X, Hou C, Xiao T. Zheng J, et al. Among authors: jiang x. Front Pediatr. 2022 Nov 14;10:947963. doi: 10.3389/fped.2022.947963. eCollection 2022. Front Pediatr. 2022. PMID: 36452351 Free PMC article.

7

Torsades de Pointes electrical storm in children with KCNH2 mutations.

Zhang L, Xu M, Yan Z, Han Y, Jiang X, Xiao T, Hou C, Li Y. Zhang L, et al. Among authors: jiang x. BMC Med Genomics. 2024 Oct 11;17(1):250. doi: 10.1186/s12920-024-02025-z. BMC Med Genomics. 2024. PMID: 39394151 Free PMC article.

8

The mechanism underlying B-cell developmental dysfunction in Kawasaki disease based on single-cell transcriptomic sequencing.

Lin Q, Wang Z, Ding G, Li G, Chen L, Qiu Q, Song S, Liu W, Jiang X, Huang M, Shen L, Xiao T, Xie L. Lin Q, et al. Among authors: jiang x. Front Immunol. 2024 Oct 23;15:1438640. doi: 10.3389/fimmu.2024.1438640. eCollection 2024. Front Immunol. 2024. PMID: 39507528 Free PMC article.

9

Influence of starch on freeze-thaw stability of Hypophthalmichthys molitrix surimi gel observed via ice crystal distribution and gel properties.

Jiang X, Liang Q, Shi W. Jiang X, et al. Food Chem X. 2024 Nov 12;24:101995. doi: 10.1016/j.fochx.2024.101995. eCollection 2024 Dec 30. Food Chem X. 2024. PMID: 39850935 Free PMC article.

10

DET induces apoptosis and suppresses tumor invasion in glioma cells via PI3K/AKT pathway.

Zhao R, Wang M, Wu Z, Zhao P, Dong H, Su Y, Zhao C, Qi M, Ling S, Jiang X. Zhao R, et al. Among authors: jiang x. Front Oncol. 2025 Jan 9;14:1528454. doi: 10.3389/fonc.2024.1528454. eCollection 2024. Front Oncol. 2025. PMID: 39850823 Free PMC article.

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