Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Yi Yin Tai"'
Publikováno v:
Journal of Translational Medicine, Vol 20, Iss 1, Pp 1-3 (2022)
Externí odkaz:
https://doaj.org/article/6637d2c19b824db3b5f57c666a03d324
Autor:
Neha Hafeez, Anna Kirillova, Yunshan Yue, Rashmi J. Rao, Neil J. Kelly, Wadih El Khoury, Yassmin Al Aaraj, Yi‐Yin Tai, Adam Handen, Ying Tang, Danli Jiang, Ting Wu, Yingze Zhang, Dennis McNamara, Tatiana V. Kudryashova, Elena A. Goncharova, Dmitry Goncharov, Thomas Bertero, Mehdi Nouraie, Gang Li, Wei Sun, Stephen Y. Chan
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 7 (2023)
Background Pulmonary arterial hypertension (PAH) is a complex, fatal disease where disease severity has been associated with the single nucleotide polymorphism (SNP) rs2856830, located near the human leukocyte antigen DPA1 (HLA‐DPA1) gene. We aimed
Externí odkaz:
https://doaj.org/article/9664f574fd8840f292c4a425b64c4fd2
Autor:
Abhinav P. Acharya, Ying Tang, Thomas Bertero, Yi‐Yin Tai, Lloyd D. Harvey, Chen‐Shan C. Woodcock, Wei Sun, Ricardo Pineda, Nilay Mitash, Melanie Königshoff, Steven R. Little, Stephen Y. Chan
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 12 (2021)
Background Pulmonary hypertension (PH) is a deadly disease characterized by vascular stiffness and altered cellular metabolism. Current treatments focus on vasodilation and not other root causes of pathogenesis. Previously, it was demonstrated that g
Externí odkaz:
https://doaj.org/article/1d0dd61ad805414d920fcbfe662dfad0
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:
Hafeez, Neha, Kirillova, Anna, Yunshan Yue, Rao, Rashmi J., Kelly, Neil J., El Khoury, Wadih, Al Aaraj, Yassmin, Yi-Yin Tai, Handen, Adam, Ying Tang, Danli Jiang, Ting Wu, Yingze Zhang, McNamara, Dennis, Kudryashova, Tatiana V., Goncharova, Elena A., Goncharov, Dmitry, Bertero, Thomas, Nouraie, Mehdi, Gang Li
Publikováno v:
Journal of the American Heart Association; 4/4/2023, Vol. 12 Issue 7, p1-18, 37p
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:
Thomas Bertero, Abhinav P. Acharya, Wei Sun, Nilay Mitash, Ricardo Pineda, Stephen Y. Chan, Lloyd D. Harvey, Melanie Königshoff, Chen Shan C. Woodcock, Ying Tang, Steven R. Little, Yi Yin Tai
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Journal of the American Heart Association
Journal of the American Heart Association, Wiley-Blackwell, 2021, 10, ⟨10.1161/jaha.120.019091⟩
Journal of the American Heart Association
Journal of the American Heart Association, Wiley-Blackwell, 2021, 10, ⟨10.1161/jaha.120.019091⟩
Background Pulmonary hypertension (PH) is a deadly disease characterized by vascular stiffness and altered cellular metabolism. Current treatments focus on vasodilation and not other root causes of pathogenesis. Previously, it was demonstrated that g