نتایج جستجو برای: ژن pah

تعداد نتایج: 23292  

Journal: :European Heart Journal 2022

Abstract Background Pulmonary arterial hypertension (PAH) is characterized by the remodeling of pulmonary arteries, with an increased pressure and right ventricle (RV) overload. Until now, there still a lack effective treatment applied. Experimental research has reported beneficial effects mesenchymal stem cells (MSCs) therapy in PAH. However, are few studies on human umbilical cord (hUC-MSCs) ...

Journal: :Rapid communications in mass spectrometry : RCM 2012
Mohammad Eftekhari Ali I Ismail Richard N Zare

RATIONALE Polycyclic aromatic hydrocarbons (PAHs) are nonpolar and difficult to detect by desorption electrospray ionization. We present a new detection method based on cationization with silver ions, which has the added advantage of being able to differentiate PAHs with the same mass but different structure. METHODS 9,10-Diphenylanthracene and triptycene, in addition to four different groups...

2017
Kathleen Morrisroe Wendy Stevens Molla Huq David Prior Jo Sahhar Gene-Siew Ngian David Celermajer Jane Zochling Susanna Proudman Mandana Nikpour Catherine Hill Sue Lester Peter Nash Gian Ngian Mandana Nikpour Susanna Proudman Maureen Rischmueller Janet Roddy Joanne Sahhar Wendy Stevens Gemma Strickland Vivek Thakkar Jenny Walker Jane Zochling

BACKGROUND Pulmonary arterial hypertension (PAH) is a leading cause of mortality in systemic sclerosis (SSc). We sought to determine survival, predictors of mortality, and health-related quality of life (HRQoL) related to PAH in a large SSc cohort with PAH. METHODS We studied consecutive SSc patients with newly diagnosed (incident) World Health Organization (WHO) Group 1 PAH enrolled in a pro...

Journal: :Circulation research 2006
Evangelos D Michelakis

Although pulmonary arterial hypertension (PAH) was originally thought to be a disease of increased pulmonary arterial (PA) tone, we now know that vasoconstriction is important only in a minority of patients.1 PAH is characterized by increased proliferation of PA endothelial cells (PAECs) and PA smooth muscle cells (PASMCs), leading to narrowing or even obliteration of the PA lumen, increased pu...

Journal: :Respiration; international review of thoracic diseases 2010
Frank Reichenberger

tery pressure response to exercise and hypoxia, an early indicator of altered pulmonary vascular function [2] . The pathogenesis of PAH is complex and involves a variety of cellular and molecular mechanisms, including the serotoninand nitric oxide system. Therefore, genetic modifiers have been suggested to be involved in the development of PAH [3] . Are genetic changes relevant in our current c...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه دریانوردی و علوم دریایی چابهار - دانشکده علوم دریایی 1393

خلیج چابهار به دلیل موقعیت راهبردی، که نزدیک ترین راه دسترسی کشورهای محصور در خشکی آسیای میانه به آب های آزاد است از اهمیت فراوانی برخوردار است و سازندگی و سرمایه گذاری فراوانی در آن صورت می گیرد. از این رو ارزیابی مستمر منابع آلاینده، به خصوص هیدروکربن های نفتی در آن ضروری به نظر می رسد. هیدروکربن های آروماتیک حلقوی (pahs)، به علت پراکندگی سریع در محیط زیست و اثرات سرطان زایی و جهش زایی برای م...

2016
Masaki TERADA Yasuo TAKEHARA Haruo ISODA Tomohiro UTO Masaki MATSUNAGA Marcus ALLEY

PURPOSE Institutional Review Board (IRB)-approved prospective study was conducted to test whether objective and quantitative hemodynamic markers wall shear stress (WSS) and oscillatory shear index (OSI) measured by three-dimensional (3D) cine phase-contrast (PC) can reflect pulmonary arterial hypertension (PAH). PATIENTS AND METHODS Seventeen consecutive patients of suspected secondary PAH we...

Journal: :American journal of respiratory and critical care medicine 2016
Robert Szulcek Chris M Happé Nina Rol Ruud D Fontijn Chris Dickhoff Koen J Hartemink Katrien Grünberg Ly Tu Wim Timens George D Nossent Marinus A Paul Thomas A Leyen Anton J Horrevoets Frances S de Man Christophe Guignabert Paul B Yu Anton Vonk-Noordegraaf Geerten P van Nieuw Amerongen Harm J Bogaard

RATIONALE Altered pulmonary hemodynamics and fluid flow-induced high shear stress (HSS) are characteristic hallmarks in the pathogenesis of pulmonary arterial hypertension (PAH). However, the contribution of HSS to cellular and vascular alterations in PAH is unclear. OBJECTIVES We hypothesize that failing shear adaptation is an essential part of the endothelial dysfunction in all forms of PAH...

2012
Gene-Siew Ngian Wendy Stevens David Prior Eli Gabbay Janet Roddy Ai Tran Robert Minson Catherine Hill Ken Chow Joanne Sahhar Susanna Proudman Mandana Nikpour

INTRODUCTION Pulmonary arterial hypertension (PAH) is a major cause of mortality in connective tissue disease (CTD). We sought to quantify survival and determine factors predictive of mortality in a cohort of patients with CTD-associated PAH (CTD-PAH) in the current era of advanced PAH therapy. METHODS Patients with right heart catheter proven CTD-PAH were recruited from six specialised PAH t...

2014
Pavel Jansa Jiri Jarkovsky Hikmet Al-Hiti Jana Popelova David Ambroz Tomas Zatocil Regina Votavova Pavel Polacek Jana Maresova Michael Aschermann Petr Brabec Ladislav Dusek Ales Linhart

BACKGROUND Pulmonary arterial hypertension (PAH) is a severe and progressive disease characterized by increased pulmonary vascular resistance, ultimately leading to right heart failure and death. Epidemiological data from national registries are growing worldwide, but are still unavailable in Eastern Europe. METHODS A PAH registry was initiated in January 2007 using a nationwide network of ec...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید