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Your search keyword '"Qiongqiong Zhou"' showing total 5 results
Start Over Author "Qiongqiong Zhou" Journal journal of the american college of cardiology
5 results on '"Qiongqiong Zhou"'

1. GW29-e0267 FAT10 attenuates hypoxia-induced cardiomyocyte apoptosis by stabilizing caveolin-3

Author

Qiongqiong Zhou and Kui Hong

Subjects
Caveolin 3, business.industry, cardiovascular system, Medicine, Hypoxia (medical), medicine.symptom, Cardiology and Cardiovascular Medicine, business, Cardiomyocyte apoptosis, Cell biology
Abstract

This study explored whether FAT10 inhibits hypoxia-induced cardiomyocyte apoptosis by regulating Cav-3 expression, and whether the expression of Cav-3 is stabilized by inhibiting ubiquitin-mediated cardiomyocyte degradation. Together, these findings revealed the novel role of FAT10 in protection

Published
2018

2. GW26-e2300 Gender differences in clinical characteristics and inpatient outcomes amongst 2442 hospitalized Chinese patients with nonvalvular atrial fibrillation: The Nanchang Atrial Fibrillation Registry

Author

Alena Shantsila, Qinmei Xiong, Kui Hong, Deirdre A. Lane, Qiongqiong Zhou, Yang Shen, Gregory Y.H. Lip, Xiaoshu Cheng, and Ying Liu

Subjects
medicine.medical_specialty, business.industry, Medicine, Atrial fibrillation, Cardiology and Cardiovascular Medicine, business, medicine.disease, Intensive care medicine
Published
2015

4. GW26-e4458 A long-term misdiagnosis of catecholaminergic polymorphic ventricular tachycardia as epilepsy caused by RyR2 mutation

Author

Xin Liu, Qiongqiong Zhou, Kui Hong, Wenfeng He, Jiejing Jin, Yang Shen, Jinzhu Hu, Juxiang Li, and Wengen Zhu

Subjects
medicine.medical_specialty, biology, business.industry, Syncope (genus), Catecholaminergic polymorphic ventricular tachycardia, medicine.disease, biology.organism_classification, Ryanodine receptor 2, Epilepsy, Internal medicine, Mutation (genetic algorithm), cardiovascular system, medicine, Cardiology, cardiovascular diseases, Cardiology and Cardiovascular Medicine, business
Abstract

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare lethal disorder among inherited arrhythmogenic channelopathies, and would be misdiagnosed by neurologists for the analogous symptom of syncope. We aim to describe a long-term misdiagnosis case of CPVT as epilepsy caused by

Published
2015

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