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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 30, 2019
Mutation in NPPA causes atrial fibrillation by activating inflammation and cardiac fibrosis in a knock-in rat modelChen Cheng, Huixia Liu, Chengcheng Tan, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 8, 2017
Identification of a new adtrp1-tfpi regulatory axis for the specification of primitive myelopoiesis and definitive hematopoiesisLi Wang, Xiaojing Wang, Longfei Wang, et al.
Journal of Lipid Research|January 16, 2010
A genome-wide linkage scan identifies multiple quantitative trait loci for HDL-cholesterol levels in families with premature CAD and MIRong Yang, Lin Li, Sara Bretschger Seidelmann, et al.
Cell|December 17, 2008
Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac deathXianqin Zhang, Shenghan Chen, Shin Yoo, et al.
The Journal of Biological Chemistry|January 11, 2008
Identification of a new co-factor, MOG1, required for the full function of cardiac sodium channel Nav 1.5Ling Wu, Sandro L Yong, Chun Fan, et al.
Nature|February 13, 2004
Identification of an angiogenic factor that when mutated causes susceptibility to Klippel-Trenaunay syndromeXiao-Li Tian, Rajkumar Kadaba, Sun-Ah You, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|March 5, 2018
Significant Association between OPG/TNFRSF11B Variant and Common Complex Ischemic StrokeXin Xiong, Duraid Hamied Naji, Binbin Wang, et al.
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