Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Karima Habbout"'
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, Charifa Awada, Sébastien Bonnet, Roxane Paulin, Sandra Breuils-Bonnet, Karima Habbout, Steeve Provencher, Valérie Nadeau
Publikováno v:
Circulation. 142
Rationale: Pulmonary arterial hypertension (PAH) is a cardiopulmonary disorder characterized by elevation of pulmonary arterial (PA) pressure and premature death. PA smooth muscle cells (PASMCs) from PAH patients present a cancer-like hyperproliferat
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:
Yann Grobs, Olivier Boucherat, Sandra Breuils-Bonnet, Steeve Provencher, François Potus, Charlotte Romanet, Charifa Awada, Sandra Martineau, Wen-Hui Wu, Eve Tremblay, Karima Habbout, Sébastien Bonnet, Roxane Paulin
Publikováno v:
The European respiratory journal. 57(5)
Pulmonary hypertension (PH) is a life-threatening disease of multiple etiologies. Regardless of the underlying cause, PH is characterised by vasoconstriction and progressive thickening of the pulmonary vessel wall all of which is initiated by the los
Autor:
Olivier Boucherat, S. Provencher, Roxanne Paulin, Valérie Nadeau, Sandra Breuils Bonnet, Charifa Awada, Karima Habbout, S. Breuils Bonnet
Publikováno v:
D25. O BRAVE NEW WORLD! OMICS, SYSTEM BIOLOGY, AND NEW MOLECULAR MECHANISMS OF PULMONARY HYPERTENSION.
Autor:
François Potus, Sandra Martineau, Junichi Omura, Sandra Breuils-Bonnet, S. Provencher, Valérie Nadeau, Karima Habbout, Eve Tremblay, Hamza Zafar, Sandra Breuils Bonnet, Allan Lawrie, Jianhui Lin, Olivier Boucherat, Stephen L. Archer, Tsukasa Shimauchi, Roxane Paulin, David G. Kiely
Publikováno v:
C105. WITH ALL MY HEART: SEX, ESTROGEN, AND RIGHT VENTRICLE IN PULMONARY VASCULAR DISEASE AND BEYOND.
Autor:
Sandra Breuils Bonnet, Karima Habbout, François Potus, Roxane Paulin, Stephen L. Archer, Sandra Martineau, Sandra Breuils-Bonnet, Jianhui Lin, Olivier Boucherat, Eve Tremblay, Allan Lawrie, Valérie Nadeau, David G. Kiely, Junichi Omura, S. Provencher, Tsukasa Shimauchi, Hamza Zafar
Publikováno v:
A93. TRANSLATIONAL RESEARCH; EARLY CLINICAL FINDINGS AND OMICS ADVENTURE IN PULMONARY HYPERTENSION: FROM BIOMARKERS TO NEW THERAPEUTIC TARGETS.
Publikováno v:
The International Journal of Biochemistry & Cell Biology. 104:9-13
Pulmonary arterial hypertension (PAH) encompasses a group of clinical entities characterized by sustained vasoconstriction and progressive vascular remodeling that act in concert to elevate pulmonary vascular resistance. The current treatments for PA
Autor:
Saïd Bendahhou, Pascal Gosselin-Badaroudine, Serena Giuliano, Savine Vicart, Mohamed Chahine, Hugo Poulin, Sophie Nicole, Damien Sternberg, Karima Habbout, Bertrand Fontaine
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-13 (2018)
Scientific Reports
Scientific Reports, Nature Publishing Group, 2018, 8, pp.2041. ⟨10.1038/s41598-018-20468-0⟩
Scientific Reports, 2018, 8, pp.2041. ⟨10.1038/s41598-018-20468-0⟩
Scientific Reports
Scientific Reports, Nature Publishing Group, 2018, 8, pp.2041. ⟨10.1038/s41598-018-20468-0⟩
Scientific Reports, 2018, 8, pp.2041. ⟨10.1038/s41598-018-20468-0⟩
Mutations in NaV1.4, the skeletal muscle voltage-gated Na+ channel, underlie several skeletal muscle channelopathies. We report here the functional characterization of two substitutions targeting the R1451 residue and resulting in 3 distinct clinical
Autor:
Benoit Ranchoux, Sandra Breuils-Bonnet, Valérie Nadeau, Renée Paradis, Alice Bourgeois, Roxane Paulin, Olivier Boucherat, Karima Habbout, Sébastien Bonnet, Caroline Lambert, Stéphanie Paquet-Marceau, Steeve Provencher, Isabelle Trinh
Publikováno v:
Journal of Molecular Medicine. 96:223-235
Pulmonary arterial hypertension (PAH) is a progressive vascular remodeling disease characterized by a persistent elevation of pulmonary artery pressure, leading to right heart failure and premature death. Exaggerated proliferation and resistance to a