نتایج جستجو برای: روش mps

تعداد نتایج: 374469  

Journal: :Annals of gastroenterology 2016
Evangelos Voudoukis Eleni-Kyriaki Vetsika Konstantina Giannakopoulou Konstantinos Karmiris Angeliki Theodoropoulou Aekaterini Sfiridaki Vassilis Georgoulias Gregorios A Paspatis Ioannis E Koutroubakis

BACKGROUND There is evidence that circulating microparticles (MPs) and annexin (+) platelet-derived MPs (PDMPs) are increased in inflammatory bowel disease (IBD). The aim of our study was to characterize the abundance, origin, and annexin V binding of MPs in patients with IBD and correlate them with the disease characteristics. METHODS Case-control study of 46 IBD patients (23 Crohn's disease...

2014
Hoon Young Choi Sung Jin Moon Brian B. Ratliff Sun Hee Ahn Ara Jung Mirae Lee Seol Lee Beom Jin Lim Beom Seok Kim Matthew D. Plotkin Sung Kyu Ha Hyeong Cheon Park

We recently demonstrated the use of in vitro expanded kidney-derived mesenchymal stem cells (KMSC) protected peritubular capillary endothelial cells in acute renal ischemia-reperfusion injury. Herein, we isolated and characterized microparticles (MPs) from KMSC. We investigated their in vitro biologic effects on human endothelial cells and in vivo renoprotective effects in acute ischemia-reperf...

2015
Pamela Arn Iain A. Bruce James E. Wraith Helen Travers Shari Fallet

OBJECTIVE Mucopolysaccharidosis I (MPS I) is a progressive, debilitating, and life-threatening genetic disease, which, owing to the nonspecific nature of the early symptoms, is often unrecognized and associated with significant diagnostic delays. To improve early recognition leading to early diagnosis and initiation of treatment, we characterized the extent of airway-related symptoms and surger...

Journal: :American journal of physiology. Heart and circulatory physiology 2011
Nathan J Palpant Fikru B Bedada Brandon Peacock Bruce R Blazar Joseph M Metzger Jakub Tolar

Cardiac dysfunction is a common cause of death among pediatric patients with mutations in the lysosomal hydrolase α-l-iduronidase (IDUA) gene, which causes mucopolysaccharidosis type I (MPS-I). The purpose of this study was to analyze adrenergic regulation of cardiac hemodynamic function in MPS-I. An analysis of murine heart function was performed using conductance micromanometry to assess in v...

Journal: :Genetic Vaccines and Therapy 2007
Donald S Anson Chantelle McIntyre Belinda Thomas Rachel Koldej Enzo Ranieri Ainslie Roberts Peter R Clements Kylie Dunning Sharon Byers

BACKGROUND Mucopolysaccharidosis type IIIA (MPS IIIA) is the most common of the mucopolysaccharidoses. The disease is caused by a deficiency of the lysosomal enzyme sulphamidase and results in the storage of the glycosaminoglycan (GAG), heparan sulphate. MPS IIIA is characterised by widespread storage and urinary excretion of heparan sulphate, and a progressive and eventually profound neurologi...

Journal: :Circulation research 2011
A Phillip Owens Nigel Mackman

Blood contains microparticles (MPs) derived from a variety of cell types, including platelets, monocytes, and endothelial cells. In addition, tumors release MPs into the circulation. MPs are formed from membrane blebs that are released from the cell surface by proteolytic cleavage of the cytoskeleton. All MPs are procoagulant because they provide a membrane surface for the assembly of component...

2010
Chiara Porro Silvia Lepore Teresa Trotta Stefano Castellani Luigi Ratclif Anna Battaglino Sante Di Gioia Maria C Martínez Massimo Conese Angela B Maffione

BACKGROUND Microparticles (MPs) are membrane vesicles released during cell activation and apoptosis. MPs have different biological effects depending on the cell from they originate. Cystic fibrosis (CF) lung disease is characterized by massive neutrophil granulocyte influx in the airways, their activation and eventually apoptosis. We investigated on the presence and phenotype of MPs in the sput...

2016
Fariborz Mobarrez Anna Vikerfors Johanna T. Gustafsson Iva Gunnarsson Agneta Zickert Anders Larsson David S. Pisetsky Håkan Wallén Elisabet Svenungsson

Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease characterized by circulating autoantibodies and the formation of immune complexes. In these responses, the selecting self-antigens likely derive from the remains of dead and dying cells, as well as from disturbances in clearance. During cell death/activation, microparticles (MPs) can be released to the circulation. Previous M...

Journal: :Blood 2013
Julia E Geddings Nigel Mackman

Patients with cancer have an increased risk for venous thrombosis. Interestingly, different cancer types have different rates of thrombosis, with pancreatic cancer having one of the highest rates. However, the mechanisms responsible for the increase in venous thrombosis in patients with cancer are not understood. Tissue factor (TF) is a transmembrane receptor and primary initiator of blood coag...

Journal: :Blood 1995
M S Sands L C Erway C Vogler W S Sly E H Birkenmeier

MPS VII mice are deficient in beta-glucuronidase and share many clinical, biochemical, and pathologic characteristics with human mucopolysaccharidosis type VII (MPS VII). We have shown that syngeneic bone marrow transplantation (BMT) prolongs survival and reduces lysosomal storage in many organs of the MPS VII mouse. In this report, we quantify the hearing loss and determine the impact of synge...

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