نتایج جستجو برای: eng 2008

تعداد نتایج: 153747  

Journal: :The European respiratory journal 2008
S Barry M Lipman R Breen G Janossy

REFERENCES 1 Birring SS, Fleming T, Matos S, Raj AA, Evans DH, Pavord ID. The Leicester Cough Monitor: preliminary validation of an automated cough detection system in patients with chronic cough. Eur Respir J 2008; 31: 1013–1018. 2 Birring SS, Matos S, Patel RB, Prudon B, Evans DH, Pavord ID. Cough frequency, cough sensitivity and health status in patients with chronic cough. Respir Med 2006; ...

2012
Petra Gromova Brian P Rubin An Thys Pierre Cullus Christophe Erneux Jean-Marie Vanderwinden

ENDOGLIN/CD105 (ENG) is a transmembrane glycoprotein and an auxiliary unit of the transforming growth factor-β (TGF-β); receptor, expressed predominantly in vascular endothelium. Noteworthy, Eng mRNA expression has been reported also in Kit(+) interstitial cells of Cajal (ICC) in the mouse intestine. Gastrointestinal stromal tumours (GIST) are thought to derive from ICC. Here we have investiga...

2014
Zhen Liu Franck Lebrin Janita A. Maring Sander van den Driesche Stieneke van der Brink Maarten van Dinther Midory Thorikay Sabrina Martin Kazuki Kobayashi Lukas J. A. C. Hawinkels Laurens A. van Meeteren Evangelia Pardali Jeroen Korving Michelle Letarte Helen M. Arthur Charles Theuer Marie-José Goumans Christine Mummery Peter ten Dijke

ENDOGLIN (ENG) is a co-receptor for transforming growth factor-β (TGF-β) family members that is highly expressed in endothelial cells and has a critical function in the development of the vascular system. Mutations in Eng are associated with the vascular disease known as hereditary hemorrhagic telangiectasia type l. Using mouse embryonic stem cells we observed that angiogenic factors, including...

Journal: :Stroke 2003
Junichiro Satomi Richard J Mount Mourad Toporsian Andrew D Paterson M Christopher Wallace Robert V Harrison Michelle Letarte

BACKGROUND AND PURPOSE Hereditary hemorrhagic telangiectasia type 1 (HHT1) is an autosomal dominant vascular dysplasia caused by mutations in the endoglin gene and characterized by dilated vessels and arteriovenous malformations (AVMs). To understand the etiology of this disorder, we evaluated the cerebral vasculature of endoglin heterozygous (Eng+/-) mice, which represent the only animal model...

2015
Rabab Nasrallah Kathy Knezevic Thuan Thai Shane R. Thomas Berthold Göttgens Georges Lacaud Valerie Kouskoff John E. Pimanda

During embryonic development, hematopoietic cells develop by a process of endothelial-to hematopoietic transition of a specialized population of endothelial cells. These hemogenic endothelium (HE) cells in turn develop from a primitive population of FLK1(+) mesodermal cells. Endoglin (ENG) is an accessory TGF-β receptor that is enriched on the surface of endothelial and hematopoietic stem cells...

2015
José M. Abril

The reliability of the narrative of the Biblical Exodus has been subject of heated debate for decades. Recent archaeological studies seem to provide new insight of the exodus path, and although with a still controversial chronology, the effects of the Minoan Santorini eruption have been proposed as a likely explanation of the biblical plagues. Particularly, it has been suggested that flooding b...

2017
Calinda K E Dingenouts Wineke Bakker Kirsten Lodder Karien C Wiesmeijer Asja T Moerkamp Janita A Maring Helen M Arthur Anke M Smits Marie-José Goumans

AIMS Hereditary Hemorrhagic Telangiectasia type-1 (HHT1) is a genetic vascular disorder caused by haploinsufficiency of the TGFβ co-receptor endoglin. Dysfunctional homing of HHT1 mononuclear cells (MNCs) towards the infarcted myocardium hampers cardiac recovery. HHT1-MNCs have elevated expression of dipeptidyl peptidase-4 (DPP4/CD26), which inhibits recruitment of CXCR4-expressing MNCs by inac...

2015
Rabab Nasrallah Kathy Knezevic Thuan Thai Shane R. Thomas Berthold Göttgens John E. Pimanda

During embryonic development, hematopoietic cells develop by a process of endothelial-to hematopoietic transition of a specialized population of endothelial cells. These hemogenic endothelium (HE) cells in turn develop from a primitive population of FLK1 mesodermal cells. Endoglin (ENG) is an accessory TGF-β receptor that is enriched on the surface of endothelial and hematopoietic stem cells an...

2016
June Baik Alessandro Magli Naoyuki Tahara Scott A. Swanson Naoko Koyano-Nakagawa Luciene Borges Ron Stewart Daniel J. Garry Yasuhiko Kawakami James A. Thomson Rita C. R. Perlingeiro

Mechanisms of haematopoietic and cardiac patterning remain poorly understood. Here we show that the BMP and Wnt signalling pathways are integrated in an endoglin (Eng)-dependent manner in cardiac and haematopoietic lineage specification. Eng is expressed in early mesoderm and marks both haematopoietic and cardiac progenitors. In the absence of Eng, yolk sacs inappropriately express the cardiac ...

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