Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Tsukasa Shimauchi"'
Autor:
Sarah-Eve Lemay, Charifa Awada, Tsukasa Shimauchi, Wen-Hui Wu, Sébastien Bonnet, Steeve Provencher, Olivier Boucherat
Publikováno v:
Cells, Vol 10, Iss 6, p 1473 (2021)
Pulmonary arterial hypertension is a debilitating chronic disorder marked by the progressive obliteration of the pre-capillary arterioles. This imposes a pressure overload on the right ventricle (RV) pushing the latter to undergo structural and mecha
Externí odkaz:
https://doaj.org/article/a6ee1f26504042c7980de5283f7c61c0
Autor:
Sandra Breuils-Bonnet, Allan Lawrie, Stephen L. Archer, Eve Tremblay, Tsukasa Shimauchi, François Potus, David G. Kiely, Wen-Hui Wu, Jianhui Lin, Olivier Boucherat, Valérie Nadeau, Sébastien Bonnet, Kassandra Gagnon, Sandra Martineau, Karima Habbout, Hamza Zafar, Roxane Paulin, Steeve Provencher, Junichi Omura, Jean Perron, Florence Mazoyer
Publikováno v:
Circulation. 142:1464-1484
Background: Right ventricular (RV) function is the major determinant for both functional capacity and survival in patients with pulmonary arterial hypertension (PAH). Despite the recognized clinical importance of preserving RV function, the subcellul
Autor:
Olivier Boucherat, Steeve Provencher, Charifa Awada, Tsukasa Shimauchi, Sébastien Bonnet, Sarah-Eve Lemay, Wen-Hui Wu
Publikováno v:
Cells, Vol 10, Iss 1473, p 1473 (2021)
Cells
Cells
Pulmonary arterial hypertension is a debilitating chronic disorder marked by the progressive obliteration of the pre-capillary arterioles. This imposes a pressure overload on the right ventricle (RV) pushing the latter to undergo structural and mecha
Autor:
Sarah-Eve Lemay, Roxane Paulin, Alice Bourgeois, Eve Tremblay, Renée Paradis, Geraldine Vitry, Karima Habbout, Marie-Claude Lampron, Olivier Boucherat, Sandra Breuils-Bonnet, Florence Roux-Dalvai, Yann Grobs, Charifa Awada, Tsukasa Shimauchi, Mark Orcholski, Valérie Nadeau, Steeve Provencher, François Potus, Sébastien Bonnet
Publikováno v:
American Journal of Respiratory and Critical Care Medicine
Rationale: Pulmonary arterial hypertension (PAH) is a life-threatening condition characterized by abnormally elevated pulmonary pressures and right ventricular failure. Excessive proliferation and resistance to apoptosis of pulmonary artery smooth mu
Autor:
Wen-Hui Wu, Bonnet, Sébastien, Tsukasa Shimauchi, Toro, Victoria, Grobs, Yann, Romanet, Charlotte, Bourgeois, Alice, Vitry, Geraldine, Omura, Junichi, Tremblay, Eve, Nadeau, Valerie, Orcholski, Mark, Breuils-Bonnet, Sandra, Martineau, Sandra, Ferraro, Pasquale, Potus, Francois, Paulin, Roxane, Provencher, Steeve, Boucherat, Olivier, Wu, Wen-Hui
Publikováno v:
Thorax; Mar2022, Vol. 77 Issue 3, p247-258, 12p