Search Results - "Pu, William t."

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  1. 1

    Endocardial and Epicardial Epithelial to Mesenchymal Transitions in Heart Development and Disease by von Gise, Alexander, Pu, William T

    Published in Circulation research (08-06-2012)
    “…Epithelial to mesenchymal transition (EMT) converts epithelial cells to mobile and developmentally plastic mesenchymal cells. All cells in the heart arise from…”
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  2. 2

    Cellular Origin and Developmental Program of Coronary Angiogenesis by Tian, Xueying, Pu, William T, Zhou, Bin

    Published in Circulation research (30-01-2015)
    “…Coronary artery disease causes acute myocardial infarction and heart failure. Identifying coronary vascular progenitors and their developmental program could…”
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  3. 3

    Strategies for cardiac regeneration and repair by Lin, Zhiqiang, Pu, William T

    Published in Science translational medicine (04-06-2014)
    “…Heart failure is a growing epidemic caused by cardiomyocyte depletion. Current therapies prolong survival by protecting remaining cardiomyocytes but are unable…”
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  4. 4

    Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association by Pierpont, Mary Ella, Brueckner, Martina, Chung, Wendy K., Garg, Vidu, Lacro, Ronald V., McGuire, Amy L., Mital, Seema, Priest, James R., Pu, William T., Roberts, Amy, Ware, Stephanie M., Gelb, Bruce D., Russell, Mark W.

    Published in Circulation (New York, N.Y.) (20-11-2018)
    “…This review provides an updated summary of the state of our knowledge of the genetic contributions to the pathogenesis of congenital heart disease. Since 2007,…”
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  5. 5

    Co-occupancy by multiple cardiac transcription factors identifies transcriptional enhancers active in heart by He, Aibin, Kong, Sek Won, Ma, Qing, Pu, William T

    “…Identification of genomic regions that control tissue-specific gene expression is currently problematic. ChIP and high-throughput sequencing (ChIP-seq) of…”
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  6. 6

    Molecular mechanisms of arrhythmogenic cardiomyopathy by Austin, Karyn M., Trembley, Michael A., Chandler, Stephanie F., Sanders, Stephen P., Saffitz, Jeffrey E., Abrams, Dominic J., Pu, William T.

    Published in Nature reviews cardiology (01-09-2019)
    “…Arrhythmogenic cardiomyopathy is a genetic disorder characterized by the risk of life-threatening arrhythmias, myocardial dysfunction and fibrofatty…”
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  7. 7

    Therapeutic role of miR-19a/19b in cardiac regeneration and protection from myocardial infarction by Gao, Feng, Kataoka, Masaharu, Liu, Ning, Liang, Tian, Huang, Zhan-Peng, Gu, Fei, Ding, Jian, Liu, Jianming, Zhang, Feng, Ma, Qing, Wang, Yingchao, Zhang, Mingming, Hu, Xiaoyun, Kyselovic, Jan, Hu, Xinyang, Pu, William T., Wang, Jian’an, Chen, Jinghai, Wang, Da-Zhi

    Published in Nature communications (17-04-2019)
    “…The primary cause of heart failure is the loss of cardiomyocytes in the diseased adult heart. Previously, we reported that the miR-17-92 cluster plays a key…”
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  8. 8

    Optimization of genome engineering approaches with the CRISPR/Cas9 system by Li, Kai, Wang, Gang, Andersen, Troels, Zhou, Pingzhu, Pu, William T

    Published in PloS one (28-08-2014)
    “…Designer nucleases such as TALENS and Cas9 have opened new opportunities to scarlessly edit the mammalian genome. Here we explored several parameters that…”
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  9. 9

    Enhancing the precision of genetic lineage tracing using dual recombinases by He, Lingjuan, Li, Yan, Li, Yi, Pu, Wenjuan, Huang, Xiuzhen, Tian, Xueying, Wang, Yue, Zhang, Hui, Liu, Qiaozhen, Zhang, Libo, Zhao, Huan, Tang, Juan, Ji, Hongbin, Cai, Dongqing, Han, Zhibo, Han, Zhongchao, Nie, Yu, Hu, Shengshou, Wang, Qing-Dong, Sun, Ruilin, Fei, Jian, Wang, Fengchao, Chen, Ting, Yan, Yan, Huang, Hefeng, Pu, William T, Zhou, Bin

    Published in Nature medicine (01-12-2017)
    “…Genetic cell-lineage tracing studies in mice are crucial for delineating the contribution of stem and progenitor cells to different cell types, both in disease…”
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  10. 10

    Gene therapy for inherited arrhythmias by Bezzerides, Vassilios J, Prondzynski, Maksymilian, Carrier, Lucie, Pu, William T

    Published in Cardiovascular research (15-07-2020)
    “…Abstract Inherited arrhythmias are disorders caused by one or more genetic mutations that increase the risk of arrhythmia, which result in life-long risk of…”
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  11. 11

    Acetylation of VGLL4 Regulates Hippo-YAP Signaling and Postnatal Cardiac Growth by Lin, Zhiqiang, Guo, Haidong, Cao, Yuan, Zohrabian, Sylvia, Zhou, Pingzhu, Ma, Qing, VanDusen, Nathan, Guo, Yuxuan, Zhang, Jin, Stevens, Sean M., Liang, Feng, Quan, Qimin, van Gorp, Pim R., Li, Amy, dos Remedios, Cristobal, He, Aibin, Bezzerides, Vassilios J., Pu, William T.

    Published in Developmental cell (21-11-2016)
    “…Binding of the transcriptional co-activator YAP with the transcription factor TEAD stimulates growth of the heart and other organs. YAP overexpression potently…”
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  12. 12
  13. 13

    Cardiac-Specific YAP Activation Improves Cardiac Function and Survival in an Experimental Murine MI Model by Lin, Zhiqiang, von Gise, Alexander, Zhou, Pingzhu, Gu, Fei, Ma, Qing, Jiang, Jianming, Yau, Allan L, Buck, Jessica N, Gouin, Katryna A, van Gorp, Pim R.R, Zhou, Bin, Chen, Jinghai, Seidman, Jonathan G, Wang, Da-Zhi, Pu, William T

    Published in Circulation research (18-07-2014)
    “…RATIONALE:Yes-associated protein (YAP), the terminal effector of the Hippo signaling pathway, is crucial for regulating embryonic cardiomyocyte proliferation…”
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  14. 14

    Genetic Cre-loxP Assessment of Epicardial Cell Fate Using Wt1-Driven Cre Alleles by Zhou, Bin, Pu, William T

    Published in Circulation research (09-11-2012)
    “…RATIONALE:Wt1-Cre-based tools are important reagents for studying epicardial cell fate and gene function. OBJECTIVE:To better describe the properties of…”
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  15. 15

    De novo formation of a distinct coronary vascular population in neonatal heart by Tian, Xueying, Hu, Tianyuan, Zhang, Hui, He, Lingjuan, Huang, Xiuzhen, Liu, Qiaozhen, Yu, Wei, He, Liang, Yang, Zhen, Yan, Yan, Yang, Xiao, Zhong, Tao P., Pu, William T., Zhou, Bin

    “…The postnatal coronary vessels have been viewed as developing through expansion of vessels formed during the fetal period. Using genetic lineage tracing, we…”
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  16. 16

    Gene Therapy for Catecholaminergic Polymorphic Ventricular Tachycardia by Inhibition of Ca2+/Calmodulin-Dependent Kinase II by Bezzerides, Vassilios J, Caballero, Ana, Wang, Suya, Ai, Yulan, Hylind, Robyn J, Lu, Fujian, Heims-Waldron, Danielle A, Chambers, Kristina D, Zhang, Donghui, Abrams, Dominic J, Pu, William T

    Published in Circulation (New York, N.Y.) (30-07-2019)
    “…BACKGROUND:Catecholaminergic polymorphic ventricular tachycardia (CPVT), an inherited cardiac arrhythmia characterized by adrenergically triggered arrhythmias,…”
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  17. 17

    Reassessment of Isl1 and Nkx2-5 cardiac fate maps using a Gata4-based reporter of Cre activity by Ma, Qing, Zhou, Bin, Pu, William T.

    Published in Developmental biology (01-11-2008)
    “…Isl1 and Nkx2-5-expressing cardiovascular progenitors play pivotal roles in cardiogenesis. Previously reported Cre-based fate-mapping studies showed that Isl1…”
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    Mitochondrial Cardiomyopathy Caused by Elevated Reactive Oxygen Species and Impaired Cardiomyocyte Proliferation by Zhang, Donghui, Li, Yifei, Heims-Waldron, Danielle, Bezzerides, Vassilios, Guatimosim, Silvia, Guo, Yuxuan, Gu, Fei, Zhou, Pingzhu, Lin, Zhiqiang, Ma, Qing, Liu, Jianming, Wang, Da-Zhi, Pu, William T

    Published in Circulation research (05-01-2018)
    “…RATIONALE:Although mitochondrial diseases often cause abnormal myocardial development, the mechanisms by which mitochondria influence heart growth and function…”
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  20. 20

    De novo cardiomyocytes from within the activated adult heart after injury by Smart, Nicola, Bollini, Sveva, Dubé, Karina N., Vieira, Joaquim M., Zhou, Bin, Davidson, Sean, Yellon, Derek, Riegler, Johannes, Price, Anthony N., Lythgoe, Mark F., Pu, William T., Riley, Paul R.

    Published in Nature (London) (30-06-2011)
    “…Repairs of the heart The prospect of cell-based therapy in cardiovascular regenerative medicine comes a step closer with the demonstration that a peptide can…”
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