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A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation.
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  • 相关项目：病理生理学
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病理生理学
期刊论文 15
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Mapping a Novel Locus for Familial Atrial Fibrillation on Chromosome 10p11-q21.
Spatial heterogeneity of muscarinic type 2 receptors in the atrium.
Kir2.3 knock-down decreases IK1 current in neonatal rat cardiomyocytes.
Refractoriness of the Sheep Superior Vena Cava Myocardial Sleeve.
Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.
High sensitivity of the sheep pulmonary vein antrum to acetylcholine stimulation.
Cardiac Electrophysiology in China.
GATA4基因突变与散发型先天性心脏病
NKX2—5基因与先天性心脏病的关系
心肌特异性表达人KCNE4转基因小鼠模型的建立
hKCNE5基因克隆及其重组腺病毒表达载体的构建
氯吡格雷和质子泵抑制剂联用的安全性