Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Jingsi Zhao"'
Autor:
Miranda K. Culley, Rashmi J. Rao, Monica Mehta, Jingsi Zhao, Wadih El Khoury, Lloyd D. Harvey, Dror Perk, Yi Yin Tai, Ying Tang, Sruti Shiva, Marlene Rabinovitch, Mingxia Gu, Thomas Bertero, Stephen Y. Chan
Publikováno v:
Vascular Pharmacology. 151:107181
Autor:
Miranda K. Culley, Monica Mehta, Jingsi Zhao, Dror Perk, Yi Yin Tai, Ying Tang, Sruti Shiva, Marlene Rabinovitch, Mingxia Gu, Thomas Bertero, Stephen Y. Chan
Deficiency of iron-sulfur (Fe-S) clusters promotes metabolic rewiring of the endothelium and the development of pulmonary hypertension (PH) in vivo. Joining a growing number of Fe-S biogenesis proteins critical to pulmonary endothelial function, rece
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9327249bba5c355366e259f4d12797e
https://doi.org/10.1101/2022.08.22.504849
https://doi.org/10.1101/2022.08.22.504849
Autor:
John Sembrat, Seyed Mehdi Nouraie, Bryan J. McVerry, Jeremy A. Mazurek, Neil J. Kelly, Sathish Badu Vasamsetti, Dennis M. McNamara, Yassmin Al Aaraj, Partha Dutta, Anjali Vaidya, Frank C. Sciurba, Yi-Yin Tai, Yuchi Han, Zeyu Xiong, Mauricio Rojas, Makenna E. Romanelli, Janet S. Lee, Annie M. Watson, Yingze Zhang, Marc A. Simon, Charles F. McTiernan, Adam Handen, Kerri Akaya Smith, Wei Sun, Jingsi Zhao, Stephen Y. Chan, Gil Speyer, Ying Tang, Seungchan Kim
Publikováno v:
JACC: Basic to Translational Science. 5:1073-1092
Utilizing publicly available ribonucleic acid sequencing data, we identified SCUBE1 as a BMPR2-related gene differentially expressed between induced pluripotent stem cell-endothelial cells derived from pulmonary arterial hypertension (PAH) patients c
Autor:
Jonathan Florentin, Jingsi Zhao, Yi-Yin Tai, Wei Sun, Lee Ohayon, Scott O'Neil, anagha arunkumar, xinyi zhang, Yassmin Al Aaraj, Annie Watson, John C Sembrat, mauricio rojas, Stephen Y Chan, Partha Dutta
Publikováno v:
Circulation. 144
Pulmonary hypertension (PH) is a vascular disease characterized by elevated pulmonary arterial pressure (PAP), leading to right ventricular failure and death. Pathogenic features of PH include endothelial apoptosis and vascular inflammation, which dr
Autor:
Maryam Sharifi-Sanjani, Andres Pulgarin, Ying Tang, Sébastien Bonnet, John Sembrat, Patricia Forsythe, Annie M. Watson, Imad Al Ghouleh, Miranda K. Culley, Bridget K. Wagner, Thomas Bertero, Vinny Negi, Seungchan Kim, Qiujun Yu, Jimin Yang, Xianglin Yin, Yassmin Al Aaraj, Anastasia Gorelova, Taijyu Satoh, Stéphanie Torrino, Arun Rajaratnam, Jingsi Zhao, Stephen Y. Chan, Stuart L. Schreiber, Gil Speyer, Mauricio Rojas, Sara O. Vargas, Mingji Dai, Steeve Provencher, Adam Handen, Yi Yin Tai
Publikováno v:
Science Advances
Description
A network dependency platform was generated to define a landscape of cancer drug mechanisms in pulmonary hypertension.
Cancer therapies are being considered for treating rare noncancerous diseases like pulmonary hypertension (PH
A network dependency platform was generated to define a landscape of cancer drug mechanisms in pulmonary hypertension.
Cancer therapies are being considered for treating rare noncancerous diseases like pulmonary hypertension (PH
Autor:
Jonathan Florentin, Jingsi Zhao, Yi-Yin Tai, Wei Sun, Lee L Ohayon, Scott P O’Neil, Anagha Arunkumar, Xinyi Zhang, Jianhui Zhu, Yassmin Al Aaraj, Annie Watson, John Sembrat, Mauricio Rojas, Stephen Y Chan, Partha Dutta
Publikováno v:
Life Science Alliance. 5:e202101264
Pulmonary hypertension (PH) is a vascular disease characterized by elevated pulmonary arterial pressure, leading to right ventricular failure and death. Pathogenic features of PH include endothelial apoptosis and vascular inflammation, which drive va
Autor:
Florentin, Jonathan, Jingsi Zhao, Yi-Yin Tai, Wei Sun, Ohayon, Lee L., O’Neil, Scott P., Arunkumar, Anagha, Xinyi Zhang, Jianhui Zhu, Aaraj, Yassmin Al, Watson, Annie, Sembrat, John, Rojas, Mauricio, Chan, Stephen Y., Dutta, Partha
Publikováno v:
Life Science Alliance; Nov2022, Vol. 5 Issue 11, p1-16, 16p
Autor:
John Sembrat, Marc A. Simon, Charles F. McTiernan, Partha Dutta, Wei Sun, Yuchi Han, Gil Speyer, Mehdi Nouraie, Mauricio Rojas, Adam Handen, Yingze Zhang, Frank C. Sciurba, Bryan J. McVerry, Ying Tang, Zeyu Xiong, Makenna E. Romanelli, Neil J. Kelly, Annie M. Watson, Yassmin Al Aaraj, Sathish Babu Vasamsetti, A. Smith, Seungchan Kim, Janet S. Lee, Dennis M. McNamara, Jeremy A. Mazurek, Yi-Yin Tai, Anjali Vaidya, Jingsi Zhao, Stephen Y. Chan
Publikováno v:
Circulation. 142
Introduction: Pulmonary arterial hypertension (PAH) is a morbid vascular disease where mutations of bone morphogenetic protein receptor 2 (BMPR2) control pulmonary endothelial pathophenotypes. Transcriptomic screening from endothelial cells (ECs) der
Autor:
Yi-Yin Tai, Thomas Bertero, Vinny Negi, Ying Tang, Jimin Yang, Jingsi Zhao, Partha Dutta, Stephen Y. Chan, Prithu Sundd, Stéphanie Torrino, Jonathan Florentin, Lee Ohayon, Michael G. Risbano, Tomasz Brzoska, Seyed Mehdi Nouraie, Chen-Shan Chen Woodcock
Publikováno v:
Circ Res
Circulation Research
Circulation Research, American Heart Association, 2020, 127 (5), pp.677-692. ⟨10.1161/CIRCRESAHA.119.316398⟩
Circulation Research
Circulation Research, American Heart Association, 2020, 127 (5), pp.677-692. ⟨10.1161/CIRCRESAHA.119.316398⟩
Rationale: Unproven theories abound regarding the long-range uptake and endocrine activity of extracellular blood-borne microRNAs into tissue. In pulmonary hypertension (PH), microRNA-210 (miR-210) in pulmonary endothelial cells promotes disease, but
Autor:
Jingsi Zhao, Stephen Y. Chan, Partha Dutta, Yi-Yin Tai, Annie M. Watson, Jonathan Florentin, John Sembrat, Mauricio Rojas
Publikováno v:
B57. INFLAMMATION AND PULMONARY HYPERTENSION! WHAT'S NEW.