Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Kulwant S. Aulak"'
Autor:
Kulwant S. Aulak, Jarrod W. Barnes, Liping Tian, Noel E. Mellor, Mohammad M. Haque, Belinda Willard, Ling Li, Suzy C. Comhair, Dennis J. Stuehr, Raed A. Dweik
Publikováno v:
Redox Biology, Vol 36, Iss , Pp 101625- (2020)
Idiopathic pulmonary arterial hypertension (IPAH) is a progressive and devastating disease characterized by vascular smooth muscle and endothelial cell proliferation leading to a narrowing of the vessels in the lung. The increased resistance in the l
Externí odkaz:
https://doaj.org/article/cb1104b7473e429ea36d8a6d877a814e
Autor:
Kulwant S Aulak, Lori Mavarakis, Liping Tian, Deborah Paul, Suzy A Comhair, Raed A Dweik, Adriano R Tonelli
Publikováno v:
PLoS ONE, Vol 19, Iss 10, p e0312535 (2024)
Pulmonary arterial hypertension (PAH) is a progressive disease characterized by elevated pulmonary arterial pressures that can lead to right heart failure and death. No cure exists for this disease, but therapeutic advancements have extended its medi
Externí odkaz:
https://doaj.org/article/7e4ed46e3a154cbeadfef80b9dac501d
Autor:
Adriano R Tonelli, Kulwant S Aulak, Mostafa K Ahmed, Alfred Hausladen, Batool Abuhalimeh, Charlie J Casa, Stephen C Rogers, David Timm, Allan Doctor, Benjamin Gaston, Raed A Dweik
Publikováno v:
PLoS ONE, Vol 14, Iss 8, p e0221777 (2019)
RationaleInhaled nitric oxide (NO) exerts a variety of effects through metabolites and these play an important role in regulation of hemodynamics in the body. A detailed investigation into the generation of these metabolites has been overlooked.Objec
Externí odkaz:
https://doaj.org/article/d68181fba0de4d389e5a1c3879811be1
Autor:
Kulwant S. Aulak, Raed A. Dweik, Tawfeq Naal, Kristin B. Highland, Celia A Melillo, Allaa Almoushref, Adriano R. Tonelli, Sami Al Abdi, Soumya Chatterjee, Mostafa Ahmed
Publikováno v:
Microcirculation. 29
Background It remains unknown whether the cutaneous microvascular responses are different between patients with scleroderma-associated pulmonary arterial hypertension (SSc-PAH) and SSc without pulmonary hypertension (PH). Methods We included 59 patie
Autor:
Jack S Crabb, Adriano R. Tonelli, Raed A. Dweik, Belinda Willard, Dennis J. Stuehr, John W. Crabb, Arnab Ghosh, Kulwant S. Aulak, Ling Li, Sami Al Abdi
Publikováno v:
Am J Physiol Lung Cell Mol Physiol
Idiopathic pulmonary arterial hypertension (IPAH) is a rapidly progressive disease with several treatment options. Long-term mortality remains high with great heterogeneity in treatment response. Even though most of the pathology of IPAH is observed
Autor:
Sami Al Ampnti, Allaa Almoushref, Tawfeq Naal, Celia Melillo, Kulwant S. Aulak, Mostafa K. Ahmed, Soumya Chatterjee, Kristin Highland, Raed A. Dweik, Adriano Tonelli
Background:It remains unknown whether the cutaneous microvascular responses are different between patients with scleroderma-associated pulmonary arterial hypertension (SSc-PAH) and SSc without pulmonary hypertension (PH).Methods:We included 59 patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6e880a9895be0f66080ee8e26b7eff5
https://doi.org/10.21203/rs.3.rs-144093/v1
https://doi.org/10.21203/rs.3.rs-144093/v1
Autor:
Dennis J. Stuehr, Suzy C. Comhair, Kulwant S. Aulak, Belinda Willard, Noël E. Mellor, Liping Tian, Jarrod W. Barnes, Raed A. Dweik, Ling Li, Mohammad Mahfuzul Haque
Publikováno v:
Redox Biology, Vol 36, Iss, Pp 101625-(2020)
Redox Biology
Redox Biology
Idiopathic pulmonary arterial hypertension (IPAH) is a progressive and devastating disease characterized by vascular smooth muscle and endothelial cell proliferation leading to a narrowing of the vessels in the lung. The increased resistance in the l
Autor:
Raed A. Dweik, Allaa Almoushref, James E Lane, Celia A Melillo, Kulwant S. Aulak, Adriano R. Tonelli
Publikováno v:
Annals of the American Thoracic Society
Autor:
Kulwant S. Aulak, Adriano R. Tonelli, Allaa Almoushref, Raed A. Dweik, Brittany E Brauer, Jennie Newman, Ruth E. McDowell, Celia A Melillo
Publikováno v:
Am J Physiol Lung Cell Mol Physiol
Group 1 pulmonary hypertension (PH), i.e., pulmonary arterial hypertension (PAH), is associated with a metabolic shift favoring glycolysis in cells comprising the lung vasculature as well as skeletal muscle and right heart. We sought to determine whe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d975d926c97f45974e1f9c1318d869df
https://europepmc.org/articles/PMC7099433/
https://europepmc.org/articles/PMC7099433/
Publikováno v:
B55. USE YOUR ILLUSION I: CLINICAL RESEARCH IN PAH.