Treatment targets for right ventricular dysfunction in pulmonary arterial hypertension
Right ventricle (RV) dysfunction is the strongest predictor of mortality in pulmonary arterial
hypertension (PAH), but, at present, there are no therapies directly targeting the failing RV …
hypertension (PAH), but, at present, there are no therapies directly targeting the failing RV …
Estrogen-mediated mechanisms in hypertension and other cardiovascular diseases
B Visniauskas, I Kilanowski-Doroh, BO Ogola… - Journal of human …, 2023 - nature.com
Cardiovascular disease (CVD) is the leading cause of death globally for men and women.
Premenopausal women have a lower incidence of hypertension and other cardiovascular …
Premenopausal women have a lower incidence of hypertension and other cardiovascular …
Y-Chromosome Gene, Uty, Protects Against Pulmonary Hypertension by Reducing Proinflammatory Chemokines
CM Cunningham, M Li, G Ruffenach… - American journal of …, 2022 - atsjournals.org
Rationale: Idiopathic pulmonary arterial hypertension (PAH) is a terminal pulmonary
vascular disease characterized by increased pressure, right ventricular failure, and death …
vascular disease characterized by increased pressure, right ventricular failure, and death …
Biological heterogeneity in idiopathic pulmonary arterial hypertension identified through unsupervised transcriptomic profiling of whole blood
S Kariotis, E Jammeh, EM Swietlik, JA Pickworth… - Nature …, 2021 - nature.com
Idiopathic pulmonary arterial hypertension (IPAH) is a rare but fatal disease diagnosed by
right heart catheterisation and the exclusion of other forms of pulmonary arterial …
right heart catheterisation and the exclusion of other forms of pulmonary arterial …
Targeting Wnt-ß-catenin-FOSL signaling ameliorates right ventricular remodeling
SR Nayakanti, A Friedrich, P Sarode, L Jafari… - Circulation …, 2023 - Am Heart Assoc
Background: The ability of the right ventricle (RV) to adapt to an increased pressure
afterload determines survival in patients with pulmonary arterial hypertension. At present …
afterload determines survival in patients with pulmonary arterial hypertension. At present …
[HTML][HTML] Cannabidiol alleviates right ventricular fibrosis by inhibiting the transforming growth factor β pathway in monocrotaline-induced pulmonary hypertension in …
A Krzyżewska, M Baranowska-Kuczko… - … et Biophysica Acta (BBA …, 2023 - Elsevier
Cannabidiol (CBD) is a non-intoxicating compound of Cannabis with anti-fibrotic properties.
Pulmonary hypertension (PH) is a disease that can lead to right ventricular (RV) failure and …
Pulmonary hypertension (PH) is a disease that can lead to right ventricular (RV) failure and …
Pulmonary arterial hypertension: sex matters
JP Dignam, S Sharma, I Stasinopoulos… - British Journal of …, 2024 - Wiley Online Library
Pulmonary arterial hypertension (PAH) is a complex disease of multifactorial origin. While
registries have demonstrated that women are more susceptible to the disease, females with …
registries have demonstrated that women are more susceptible to the disease, females with …
mTOR signaling in pulmonary vascular disease: pathogenic role and therapeutic target
A Babicheva, A Makino, JXJ Yuan - International journal of molecular …, 2021 - mdpi.com
Pulmonary arterial hypertension (PAH) is a progressive and fatal disease without a cure.
The exact pathogenic mechanisms of PAH are complex and poorly understood, yet a …
The exact pathogenic mechanisms of PAH are complex and poorly understood, yet a …
[HTML][HTML] Characteristics of inflammation process in monocrotaline-induced pulmonary arterial hypertension in rats
C Tang, Y Luo, S Li, B Huang, S Xu, L Li - Biomedicine & Pharmacotherapy, 2021 - Elsevier
Objective A growing evidence demonstrates that inflammation is a major contributor to the
pathogenesis of pulmonary arterial hypertension (PAH). However, blocking inflammation …
pathogenesis of pulmonary arterial hypertension (PAH). However, blocking inflammation …
SOX17 deficiency mediates pulmonary hypertension: at the crossroads of sex, metabolism, and genetics
S Sangam, X Sun, TH Schwantes-An… - American journal of …, 2023 - atsjournals.org
Rationale: Genetic studies suggest that SOX17 (SRY-related HMG-box 17) deficiency
increases pulmonary arterial hypertension (PAH) risk. Objectives: On the basis of …
increases pulmonary arterial hypertension (PAH) risk. Objectives: On the basis of …