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Qing Kenneth Wang

Showing results (41-50 of 51) with videos related to

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Investigative Ophthalmology & Visual Science|August 1, 2006
Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese familyMugen Liu, Tie Ke, Zhaoxiang Wang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 8, 2017
Identification of a new <i>adtrp1-tfpi</i> 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.
Cancer Letters|October 18, 2020
Angiogenic factor AGGF1 acts as a tumor suppressor by modulating p53 post-transcriptional modifications and stability via MDM2Wenxia Si, Bisheng Zhou, Wen Xie, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 13, 2010
Identification of NPPA variants associated with atrial fibrillation in a Chinese GeneID populationXiang Ren, Chengqi Xu, Chengxiong Zhan, et al.
Gene|May 24, 2020
ADTRP regulates TFPI expression via transcription factor POU1F1 involved in coronary artery diseaseChunyan Luo, Elisabeth Pook, Fan Wang, et al.
Human Genetics|August 27, 2009
Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han populationLisong Shi, Cong Li, Chuchu Wang, et al.
Human Molecular Genetics|June 2, 2019
De novo loss-of-function KCNMA1 variants are associated with a new multiple malformation syndrome and a broad spectrum of developmental and neurological phenotypesLina Liang, Xia Li, Sébastien Moutton, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Investigative Ophthalmology & Visual Science|August 1, 2006
Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese familyMugen Liu, Tie Ke, Zhaoxiang Wang, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|September 8, 2017
Identification of a new <i>adtrp1-tfpi</i> 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.
Cancer Letters|October 18, 2020
Angiogenic factor AGGF1 acts as a tumor suppressor by modulating p53 post-transcriptional modifications and stability via MDM2Wenxia Si, Bisheng Zhou, Wen Xie, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|January 13, 2010
Identification of NPPA variants associated with atrial fibrillation in a Chinese GeneID populationXiang Ren, Chengqi Xu, Chengxiong Zhan, et al.
Gene|May 24, 2020
ADTRP regulates TFPI expression via transcription factor POU1F1 involved in coronary artery diseaseChunyan Luo, Elisabeth Pook, Fan Wang, et al.
Human Genetics|August 27, 2009
Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han populationLisong Shi, Cong Li, Chuchu Wang, et al.
Human Molecular Genetics|June 2, 2019
De novo loss-of-function KCNMA1 variants are associated with a new multiple malformation syndrome and a broad spectrum of developmental and neurological phenotypesLina Liang, Xia Li, Sébastien Moutton, et al.
Pageof 6