نتایج جستجو برای: ipah

تعداد نتایج: 494  

Journal: :Pulmonary circulation 2015
Gerrina Ruiter Emmy Manders Chris M Happé Ingrid Schalij Herman Groepenhoff Luke S Howard Martin R Wilkins Harm J Bogaard Nico Westerhof Willem J van der Laarse Frances S de Man Anton Vonk-Noordegraaf

UNLABELLED In patients with idiopathic pulmonary arterial hypertension (iPAH), iron deficiency is common and has been associated with reduced exercise capacity and worse survival. Previous studies have shown beneficial effects of intravenous iron administration. In this study, we investigated the use of intravenous iron therapy in iron-deficient iPAH patients in terms of safety and effects on e...

2011
Bhola K Dahal Djuro Kosanovic Christina Kaulen Teodora Cornitescu Rajkumar Savai Julia Hoffmann Irwin Reiss Hossein A Ghofrani Norbert Weissmann Wolfgang M Kuebler Werner Seeger Friedrich Grimminger Ralph T Schermuly

BACKGROUND Mast cells (MCs) are implicated in inflammation and tissue remodeling. Accumulation of lung MCs is described in pulmonary hypertension (PH); however, whether MC degranulation and c-kit, a tyrosine kinase receptor critically involved in MC biology, contribute to the pathogenesis and progression of PH has not been fully explored. METHODS Pulmonary MCs of idiopathic pulmonary arterial...

Journal: :American journal of respiratory and critical care medicine 2008
Benjamin Terrier Mathieu C Tamby Luc Camoin Philippe Guilpain Cédric Broussard Guillaume Bussone Azzedine Yaïci Françoise Hotellier Gérald Simonneau Loïc Guillevin Marc Humbert Luc Mouthon

RATIONALE Pulmonary arterial hypertension (PAH) may be classified as idiopathic (IPAH) or familial (FPAH) or associated with various conditions and exposures such as dexfenfluramine intake (Dex-PAH) or systemic sclerosis (SSc-PAH). Because fibroblast dysfunction has been identified in SSc and IPAH and antifibroblast antibodies (AFAs) with a pathogenic role have been detected in the serum of SSc...

Journal: :American journal of physiology. Cell physiology 2007
Carmelle V Remillard Donna D Tigno Oleksandr Platoshyn Elyssa D Burg Elena E Brevnova Diane Conger Ann Nicholson Brinda K Rana Richard N Channick Lewis J Rubin Daniel T O'connor Jason X-J Yuan

The pore-forming alpha-subunit, Kv1.5, forms functional voltage-gated K(+) (Kv) channels in human pulmonary artery smooth muscle cells (PASMC) and plays an important role in regulating membrane potential, vascular tone, and PASMC proliferation and apoptosis. Inhibited Kv channel expression and function have been implicated in PASMC from patients with idiopathic pulmonary arterial hypertension (...

2017
Wenting Fan Huimin Qian Wenkang Shang Chen Ying Xuedi Zhang Song Cheng Bing Gu Ping Ma

Background The ability of Shigella to invade, colonize, and eventually kill host cells is influenced by many virulence factors. However, there is no analysis of related genes in Jiangsu Province of China so far. Shigella flexneri was collected from 13 cities of Jiangsu Province through the provincial Centers for Disease Control (CDC) for analysis of distribution of major virulence genes (ipaH, ...

2015
Shohreh Farshad Reza Ranjbar Marziyeh Hosseini

BACKGROUND Identification, understanding of antibiotic sensitivity patterns and molecular characterization of genetic elements of Shigella species are important because of both epidemiological and clinical indications in developing countries. OBJECTIVES The aim of this study was to analyze molecular epidemiology of Shigella isolates recovered from children with diarrhea in Shiraz (Southern Ir...

2015
Marius M. Hoeper Juergen Behr Matthias Held Ekkehard Grunig C. Dario Vizza Anton Vonk-Noordegraaf Tobias J. Lange Martin Claussen Christian Grohé Hans Klose Karen M. Olsson Thomas Zelniker Claus Neurohr Oliver Distler Hubert Wirtz Christian Opitz Doerte Huscher David Pittrow J. Simon R. Gibbs Masataka Kuwana

BACKGROUND Pulmonary hypertension (PH) is a common finding in patients with chronic fibrosing idiopathic interstitial pneumonias (IIP). Little is known about the response to pulmonary vasodilator therapy in this patient population. COMPERA is an international registry that prospectively captures data from patients with various forms of PH receiving pulmonary vasodilator therapies. METHODS We ...

2015
Thando Ndlovu Marcellous Le Roux Wesaal Khan Sehaam Khan

McNemar's test and the Pearson Chi-square were used to assess the co-detection and observed frequency, respectively, for potentially virulent E. coli genes in river water. Conventional multiplex Polymerase Chain Reaction (PCR) assays confirmed the presence of the aggR gene (69%), ipaH gene (23%) and the stx gene (15%) carried by Enteroaggregative E. coli (EAEC), Enteroinvasive E. coli (EIEC) an...

Journal: :Thorax 2005
M C Tamby Y Chanseaud M Humbert J Fermanian P Guilpain P Garcia-de-la-Peña-Lefebvre S Brunet A Servettaz B Weill G Simonneau L Guillevin M C Boissier L Mouthon

BACKGROUND It has previously been shown that IgG antibodies from patients with limited cutaneous systemic sclerosis (SSc) bind to specific microvascular endothelial cell antigens. Since patients with limited cutaneous SSc are prone to develop pulmonary arterial hypertension (PAH), and since endothelial cell activation is involved in the pathogenesis of idiopathic PAH (IPAH), a study was underta...

Journal: :American journal of physiology. Lung cellular and molecular physiology 2010
M Talati J West T R Blackwell J E Loyd B Meyrick

Macrophage derived-endothelin-1 (ET-1) has been suggested to contribute to a number of chronic lung diseases. Whether the ET-1 cascade from non-vascular sources (inflammatory cells) also contributes to pulmonary artery hypertension (PAH) and in particular to heritable PAH (HPAH) with known bone morphogenetic protein type 2 receptor (BMPR2) mutations is not known. We tested this notion using bon...

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