Publications by authors named "Xunwei Jiang"

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Effects of remimazolam on hemodynamics in children with congenital heart disease undergoing cardiac catheterization.
Hongyun Li, Zhaomeng Song, Xunwei Jiang, Wei Liu, Yan Jiang

Front Pharmacol· December 2025

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Gene and metabolite changes triggered by downregulation of JUNB and ZNF281 in idiopathic pulmonary arterial hypertension: potential mechanisms revealed by multi-omics study.
Yanfang Zong, Wei Liu, Jiahe Tian, Cuilan Hou, Tingting Xiao, Xunwei Jiang

Transl Pediatr· October 2025

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Delineation of single-cell Altas provides new insights for development of coronary artery lesions in Kawasaki disease: bad and good signaling molecules.
Qiuping Lin, Xin Lv, Qingzhu Qiu, Lianni Mei, Liqin Chen, Xunwei Jiang

Front Pediatr· June 2025

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The mechanism underlying B-cell developmental dysfunction in Kawasaki disease based on single-cell transcriptomic sequencing.
Qiuping Lin, Zhen Wang, Guohui Ding, Guang Li, Liqin Chen, Xunwei Jiang

Front Immunol· November 2024

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Torsades de Pointes electrical storm in children with KCNH2 mutations.
Li Zhang, Meng Xu, Zhen Yan, Yan Han, Xunwei Jiang

BMC Med Genomics· October 2024

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Case Report: Novel LIM domain-binding protein 3 (LDB3) mutations associated with hypertrophic cardiomyopathy family.
Junmin Zheng, Zhuangzhuang Huang, Shan Hou, Xunwei Jiang, Yongwei Zhang

Front Pediatr· November 2022

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Generation of an induced pluripotent stem cell line from a Chinese Han child with catecholaminergic polymorphic ventricular tachycardia.
Wei Liu, Ting Liu, Tingting Xiao, Lijian Xie, Cuilan Hou, Xunwei Jiang

Stem Cell Res· July 2022

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TECRL deficiency results in aberrant mitochondrial function in cardiomyocytes.
Cuilan Hou, Xunwei Jiang, Han Zhang, Junmin Zheng, Qingzhu Qiu

Commun Biol· May 2022

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A novel endoglin mutation in a family with hereditary hemorrhagic telangiectasia: a case report.
Yanfang Zong, Wei Liu, Cuilan Hou, Han Zhang, Xunwei Jiang

Transl Pediatr· August 2021

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A compound heterozygosity of Tecrl gene confirmed in a catecholaminergic polymorphic ventricular tachycardia family.
Lijian Xie, Cuilan Hou, Xunwei Jiang, Jian Zhao, Yun Li

Eur J Med Genet· July 2019

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A 10-year-old boy with dyspnea and hypoxia: abernathy malformation masquerading as pulmonary arteriovenous fistula.
Lijian Xie, Yun Li, Xunwei Jiang, Jian Zhao, Tingting Xiao

BMC Pediatr· February 2019

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