نتایج جستجو برای: mfs

تعداد نتایج: 1749  

2014
Bela F. Asztalos Michael S. Horan Katalin V. Horvath Ann Y. McDermott Naga P. Chalasani Ernst J. Schaefer Ranji Cui

OBJECTIVE To describe novel C-reactive protein (CRP) molecular forms (mf) in human plasma. DESIGN AND METHODS Five novel CRP-mfs, disctinct from the previously described native (nCRP) and modified (mCRP) C-reactive proteins, were separated from human plasma by polyacrylamide gel electrophoresis and immunodetected by western blot in subjects with or without increased BMI, cardiovascular diseas...

2015
Garima Gupta Antonio Liu

Miller Fisher syndrome is a variant of Guillain-Barre syndrome characterized by the classic triad of ophthalmoplegia, ataxia, and areflexia. Pupillary involvement is common in MFS and has been reported in 35-42% of MFS patients. Although case reports have discussed isolated ophthalmoplegia as a presentation of MFS, anisocoria and rapid fluctuation of pupillary diameter have not been reported in...

Journal: :Blood 1993
F Fauvel-Lafève V Tabaka J P Caen Y J Legrand

Bernard-Soulier syndrome (BSS) platelets, which lack the membrane glycoprotein complex Ib-IX, do not adhere to subendothelium. The adhesion of platelets from two patients with BSS to subendothelial microfibrils (MFs) and type I collagen was compared in an in vitro assay adapted to patients with low platelet count. With both patients, platelet adhesion to MFs was strongly defective, whereas the ...

1998
Stephen D. Bay

Combining multiple classi ers is an e ective technique for improving accuracy. There are many general combining algorithms, such as Bagging or Error Correcting Output Coding, that signi cantly improve classi ers like decision trees, rule learners, or neural networks. Unfortunately, many combining methods do not improve the nearest neighbor classi er. In this paper, we present MFS, a combining a...

Journal: :Journal of medical genetics 2006
P N Robinson E Arteaga-Solis C Baldock G Collod-Béroud P Booms A De Paepe H C Dietz G Guo P A Handford D P Judge C M Kielty B Loeys D M Milewicz A Ney F Ramirez D P Reinhardt K Tiedemann P Whiteman M Godfrey

Marfan syndrome (MFS), a relatively common autosomal dominant hereditary disorder of connective tissue with prominent manifestations in the skeletal, ocular, and cardiovascular systems, is caused by mutations in the gene for fibrillin-1 (FBN1). The leading cause of premature death in untreated individuals with MFS is acute aortic dissection, which often follows a period of progressive dilatatio...

2015
Sudha Bhingardive Dhirendra Singh Rudramurthy V Hanumant Harichandra Redkar Pushpak Bhattacharyya

An acid test for any new Word Sense Disambiguation (WSD) algorithm is its performance against the Most Frequent Sense (MFS). The field of WSD has found the MFS baseline very hard to beat. Clearly, if WSD researchers had access to MFS values, their striving to better this heuristic will push the WSD frontier. However, getting MFS values requires sense annotated corpus in enormous amounts, which ...

Journal: :Science 2006
Jennifer P Habashi Daniel P Judge Tammy M Holm Ronald D Cohn Bart L Loeys Timothy K Cooper Loretha Myers Erin C Klein Guosheng Liu Carla Calvi Megan Podowski Enid R Neptune Marc K Halushka Djahida Bedja Kathleen Gabrielson Daniel B Rifkin Luca Carta Francesco Ramirez David L Huso Harry C Dietz

Aortic aneurysm and dissection are manifestations of Marfan syndrome (MFS), a disorder caused by mutations in the gene that encodes fibrillin-1. Selected manifestations of MFS reflect excessive signaling by the transforming growth factor-beta (TGF-beta) family of cytokines. We show that aortic aneurysm in a mouse model of MFS is associated with increased TGF-beta signaling and can be prevented ...

Journal: :Langmuir : the ACS journal of surfaces and colloids 2010
P R Sajanlal T Pradeep

A strategy for the preparation of bimetallic mesoflowers (MFs) has been demonstrated by a simple overgrowth reaction. We make hybrid MFs containing Au core and shells of different metals, such as Ag and Pt, by tuning the experimental conditions so as to study region-specific overgrowth. This selective growth is attributed to the specific binding affinity of cetyltrimethylammonium bromide (CTAB)...

Journal: :Investigative ophthalmology & visual science 2002
Gilles Sultan Christophe Baudouin Olivier Auzerie Magdalena De Saint Jean Marie Goldschild Pierre-Jean Pisella

PURPOSE To investigate corneal thickness, curvature, and morphology with the Orbscan Topography System I (Bausch & Lomb, Inc., Salt Lake City, UT) in patients with Marfan syndrome (MFS) and to study MFS with in vivo confocal microscopy. METHODS This prospective, clinical, comparative case series included 60 eyes of 31 patients with MFS and 32 eyes of 17 control subjects. First, biomicroscopic...

2017
Jung Woo Park Li Yan Chris Stoddard Xiaofang Wang Zhichao Yue Leann Crandall Tiwanna Robinson Yuxiao Chang Kyle Denton Enqin Li Bin Jiang Zhenwu Zhang Kristen Martins-Taylor Siu-Pok Yee Hong Nie Feng Gu Wei Si Ting Xie Lixia Yue Ren-He Xu

Marfan syndrome (MFS) is a connective tissue disorder caused by mutations in FBN1 gene, which encodes a key extracellular matrix protein FIBRILLIN-1. The haplosufficiency of FBN1 has been implicated in pathogenesis of MFS with manifestations primarily in cardiovascular, muscular, and ocular tissues. Due to limitations in animal models to study the late-onset diseases, human pluripotent stem cel...

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