نتایج جستجو برای: but mps

تعداد نتایج: 2058103  

2004
David G. Simons Jan Dommerholt

During the past few months, several new studies, reviews and case studies on myofascial pain syndrome [MPS] and myofascial trigger points [TrPs] have been published. Myofascial pain syndrome and TrPs are increasingly being recognized not only in the United States, but also in Europe. Testa and colleagues [Milan, Italy] published an excellent review article detailing the clinical signs that lead...

Journal: :IEEE Access 2021

Spectroscopic technology is widely used in identifying the categories of microplastics (MPs) for its non-destructive, rapid, and without pretreatment characters. Recognition spectral category often conducted by matching with reference library, this works well a known material but fails to blindly identify unknown source environmental MPs. In work, robust classifier was proposed differentiate ch...

Journal: :American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons 2004
Klemens Budde John Curtis Gregory Knoll Lawrence Chan Hans-Hellmut Neumayer Yodit Seifu Michael Hall

With the objective of enhancing upper gastrointestinal (GI) tolerability, enteric-coated mycophenolate sodium (EC-MPS, myfortic, Novartis Pharma AG, Basel, Switzerland) has been developed. This double-blinded, 12-month study investigated whether renal transplant patients taking mycophenolate mofetil (MMF) can be safely converted to EC-MPS. Stable kidney transplant patients were randomized to re...

2014
Chin-Chou Wang Chia-Cheng Tseng Chang-Chun Hsiao Huang-Chih Chang Li-Teh Chang Wen-Feng Fang Steve Leu Yi-Hsi Wang Tzu-Hsien Tsai Cheng-Ta Yang Chih-Hung Chen Hon-Kan Yip Chi-Kung Ho Meng-Chih Lin

BACKGROUND This study tested the hypothesis that circulating microparticles (MPs) are useful biomarkers for predicting one-year mortality in patients with end-stage non-small cell lung cancer (ES-NSCLC). METHODS AND RESULTS One hundred seven patients were prospectively enrolled into the study between April 2011 and February 2012, and each patient received regular follow-up after enrollment. L...

Journal: :American journal of physiology. Endocrinology and metabolism 2011
Timothy Etheridge Philip J Atherton Daniel Wilkinson Anna Selby Debbie Rankin Nick Webborn Kenneth Smith Peter W Watt

Chronic reductions in tissue O(2) tension (hypoxia) are associated with muscle atrophy and blunted hypertrophic responses to resistance exercise (RE) training. However, the effect of hypoxia on muscle protein synthesis (MPS) at rest and after RE is unknown. In a crossover study, seven healthy men (21.4 ± 0.7 yr) performed unilateral leg RE (6 × 8 repetitions at 70% 1-repetition maximum) under n...

Journal: :Journal of experimental & clinical cancer research : CR 2016
Liangliang Zhao Yayan Bi Junjie Kou Jialan Shi Daxun Piao

BACKGROUND Colon cancer is invariably accompanied by altered coagulation activity; however, the precise role of phosphatidylserine (PS) in the hypercoagulable state of colon cancer patients remains unclear. We explored the exposure of PS on platelets and microparticles (MPs), and evaluate its role in procoagulant activity in colon cancer patients. METHODS PS-positive platelets and MPs, mainly...

Journal: :Advanced drug delivery reviews 2000
A K Agrawal C M Gupta

The use of liposomes as drug carriers in treatment of various diseases has been explored extensively for more than 20 years. 'Conventional' liposomes, when administered in vivo by a variety of routes, rapidly accumulate in the mononuclear phagocyte system (MPS). The inherent tendency of the liposomes to concentrate in MPS can be exploited in enhancing the non-specific host defence against infec...

Journal: :Frontiers in bioscience 2016
Joanna Jakobkiewicz-Banecka Magdalena Gabig-Ciminska Anna Kloska Marcelina Malinowska Ewa Piotrowska Zyta Banecka-Majkutewicz Bogdan Banecki Alicja Wegrzyn Grzegorz Wegrzyn

Mucopolysaccharidosis type III (MPS III), or Sanfilippo syndrome, is a lysosomal storage disease in which heparan sulfate is accumulated in lysosomes, as well as outside of cells, as the primary storage material. This disease is a complex of four conditions caused by dysfunctions of one of genes coding for lysosomal enzymes involved in degradation of heparan sulfate: SGSH (coding for heparan N-...

2015
Thomas G. Watkinson Antonio N. Calabrese Fabrice Giusti Manuela Zoonens Sheena E. Radford Alison E. Ashcroft

Membrane proteins (MPs) are essential for numerous important biological processes. Recently, mass spectrometry (MS), coupled with an array of related techniques, has been used to probe the structural properties of MPs and their complexes. Typically, detergent micelles have been employed for delivering MPs into the gas-phase, but these complexes have intrinsic properties that can limit the utili...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Christian Hinderer Peter Bell Brittney L Gurda Qiang Wang Jean-Pierre Louboutin Yanqing Zhu Jessica Bagel Patricia O'Donnell Tracey Sikora Therese Ruane Ping Wang Mark E Haskins James M Wilson

Patients with mucopolysaccharidosis type I (MPS I), a genetic deficiency of the lysosomal enzyme α-l-iduronidase (IDUA), exhibit accumulation of glycosaminoglycans in tissues, with resulting diverse clinical manifestations including neurological, ocular, skeletal, and cardiac disease. MPS I is currently treated with hematopoietic stem cell transplantation or weekly enzyme infusions, but these t...

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