نتایج جستجو برای: eng protein

تعداد نتایج: 1241226  

Journal: :journal of dentistry, tehran university of medical sciences 0
maryam khalili nazanin mahdavi razieh beheshti fereshteh baghai naini

objectives : squamous cell carcinoma (scc) is the most common malignant neoplasm of the oral cavity and a public health threat. tumor progression is believed to be influenced by angiogenesis as well as tumor cell proliferation; however, the correlation of these two factors in tongue scc still remains unclear. this study aimed to assess the correlation of these two factors in tongue scc. materia...

Journal: :Molecular medicine reports 2015
Yanjun Lu Yaowu Zhu Lili Shi Hongtao Zhen Ziyong Sun Liming Cheng

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disorder characterized by aberrant vascular development. Mutations in two genes, endoglin (ENG) and activin receptor-like kinase 1 (ACVRL1) are associated with HHT. The present case study revealed the molecular diagnosis in a family exhibiting the clinical features of HHT disease. The coding exon and flanking intronic regions ...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2010
Mourad Toporsian Mirjana Jerkic Yu-Qing Zhou Mohammed G Kabir Lisa X Yu Brendan A S McIntyre Adrienne Davis Yu Jing Wang Duncan J Stewart Jaques Belik Mansoor Husain Mark Henkelman Michelle Letarte

OBJECTIVE Loss-of-function mutations in genes coding for transforming growth factor-beta/bone morphogenetic protein receptors and changes in nitric oxide(*) (NO(*)) bioavailability are associated with hereditary hemorrhagic telangiectasia and some forms of pulmonary arterial hypertension. How these abnormalities lead to seemingly disparate pulmonary pathologies remains unknown. Endoglin (Eng), ...

2011
Kristy Damjanovich Carmen Langa Francisco J Blanco Jamie McDonald Luisa M Botella Carmelo Bernabeu Whitney Wooderchak-Donahue David A Stevenson Pinar Bayrak-Toydemir

BACKGROUND Hereditary hemorrhagic telangiectasia (HHT) is a vascular disorder characterized by epistaxis, arteriovenous malformations, and telangiectases. The majority of the patients have a mutation in the coding region of the activin A receptor type II-like 1 (ACVRL1) or Endoglin (ENG) gene. However, in approximately 15% of cases, sequencing analysis and deletion/duplication testing fail to i...

2017
Takako Saito Marcel Bokhove Romina Croci Sara Zamora-Caballero Ling Han Michelle Letarte Daniele de Sanctis Luca Jovine

Endoglin (ENG)/CD105 is an essential endothelial cell co-receptor of the transforming growth factor β (TGF-β) superfamily, mutated in hereditary hemorrhagic telangiectasia type 1 (HHT1) and involved in tumor angiogenesis and preeclampsia. Here, we present crystal structures of the ectodomain of human ENG and its complex with the ligand bone morphogenetic protein 9 (BMP9). BMP9 interacts with a ...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2006
Neil G Docherty José M López-Novoa Miguel Arevalo Annette Düwel Ana Rodriguez-Peña Fernando Pérez-Barriocanal Carmelo Bernabeu Nélida Eleno

BACKGROUND Renal ischaemia-reperfusion (I-R) can cause acute tubular necrosis and chronic renal deterioration. Endoglin, an accessory receptor for Transforming Growth Factor-beta1 (TGF-beta1), is expressed on activated endothelium during macrophage maturation and implicated in the control of fibrosis, angiogenesis and inflammation. METHODS Endoglin expression was monitored over 14 days after ...

Journal: :Carcinogenesis 2015
Gaelle del Castillo Esther Sánchez-Blanco Ester Martín-Villar Ana C Valbuena-Diez Carmen Langa Eduardo Pérez-Gómez Jaime Renart Carmelo Bernabéu Miguel Quintanilla

Increased levels of soluble endoglin (Sol-Eng) correlate with poor outcome in human cancer. We have previously shown that shedding of membrane endoglin, and concomitant release of Sol-Eng is a late event in chemical mouse skin carcinogenesis associated with the development of undifferentiated spindle cell carcinomas (SpCCs). In this report, we show that mouse skin SpCCs exhibit a high expressio...

2014
Benoît Gore Mohamed Izikki Olaf Mercier Laurence Dewachter Elie Fadel Marc Humbert Philippe Dartevelle Gerald Simonneau Robert Naeije Franck Lebrin Saadia Eddahibi

Mutations affecting transforming growth factor-beta (TGF-β) superfamily receptors, activin receptor-like kinase (ALK)-1, and endoglin (ENG) occur in patients with pulmonary arterial hypertension (PAH). To determine whether the TGF-β/ALK1/ENG pathway was involved in PAH, we investigated pulmonary TGF-β, ALK1, ALK5, and ENG expressions in human lung tissue and cultured pulmonary-artery smooth-mus...

Ali AtashAbParvar, Azim Nejatizadeh, Fatemeh Mohseni, Kianoosh Malekzadeh, Minoo Rajaei, Pooneh Nikuei,

Background: The use of biomarkers for diagnosis of Preeclampsia (PE), a life-threatening pregnancy disorder, could reduce serious complications of this disease. In this study, we investigated dysregulation of endoglin (Eng) expression and diagnostic accuracy of soluble endoglin (sEng) in PE patients. Methods: For this case-control study, 26 mild and 15 severe preeclamptic women along with 20 no...

Journal: :Journal of animal science 2004
T A Baumann G P Lardy J S Caton V L Anderson

Two trials were conducted to determine the effect of energy source (ENG) and ruminally degradable protein (RDP) on lactating cow performance and intake and digestion in beef steers. In Trial 1, 78 cow-calf pairs were used in a 2 x 2 factorial design to determine the effect of ENG (corn or soyhulls; SH) and RDP (with our without sunflower meal) to a forage diet for lactating beef cows. The basal...

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