نتایج جستجو برای: fh

تعداد نتایج: 3804  

2018
Su-Fang Chen Feng-Mei Wang Zhi-Ying Li Feng Yu Min Chen Ming-Hui Zhao

Our previous study demonstrated that plasma levels of complement factor H (FH) were inversely associated with the disease activity of patients with anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (AAV). In addition to serving as an inhibitor of the alternative complement pathway, there is increasing evidence demonstrating direct regulatory roles of FH on several cell types...

Journal: :Blood 2008
Anne-lie Ståhl Fariba Vaziri-Sani Stefan Heinen Ann-Charlotte Kristoffersson Karl-Henrik Gydell Reem Raafat Alberto Gutierrez Ortraud Beringer Peter F Zipfel Diana Karpman

Atypical hemolytic uremic syndrome (aHUS) may be associated with mutations in the C-terminal of factor H (FH). FH binds to platelets via the C-terminal as previously shown using a construct consisting of short consensus repeats (SCRs) 15 to 20. A total of 4 FH mutations, in SCR15 (C870R) and SCR20 (V1168E, E1198K, and E1198Stop) in patients with aHUS, were studied regarding their ability to all...

2017
Eszter Trojnár Mihály Józsi Katalin Uray Dorottya Csuka Ágnes Szilágyi Danko Milosevic Vesna D. Stojanović Brankica Spasojević Krisztina Rusai Thomas Müller Klaus Arbeiter Kata Kelen Attila J. Szabó György S. Reusz Satu Hyvärinen T. Sakari Jokiranta Zoltán Prohászka

INTRODUCTION In autoimmune atypical hemolytic uremic syndrome (aHUS), the complement regulator factor H (FH) is blocked by FH autoantibodies, while 90% of the patients carry a homozygous deletion of its homolog complement FH-related protein 1 (CFHR1). The functional consequence of FH-blockade is widely established; however, the molecular basis of autoantibody binding and the role of CFHR1 defic...

2017
Heta P Desai Shatavia S Morrison Maureen H Diaz Alvaro J Benitez Bernard J Wolff Jonas M Winchell

Mycoplasma pneumoniae type 2 strain FH was previously sequenced with Illumina (FH-Illumina) and 454 (FH-454) technologies according to Xiao et al. (2015) and Krishnakumar et al. (2010). Comparative analyses revealed differences in genomic content between these sequences, including a 6-kb region absent from the FH-454 submission. Here, we present a complete genome sequence of FH sequenced with t...

Journal: :The Journal of infectious diseases 2002
Taru Meri T Sakari Jokiranta Jens Hellwage Alexandra Bialonski Peter F Zipfel Seppo Meri

The filarial parasite Onchocerca volvulus is the causative agent of river blindness. The adult worms produce microfilariae (mf), which are responsible for the disease pathogenesis; mf activate the complement system, but the activation stops before the formation of terminal complement complexes. Because of the arrest of complement activation, this study analyzed binding of the main alternative p...

2014
Suseok Oh Ci-Young Kim Jongrak Hong

OBJECTIVES The aim of this study was to verify the concordance of the measurement values when the same cephalometric analysis method was used for two-dimensional (2D) cephalometric radiography and three-dimensional computed tomography (3D CT), and to identify which 3D Frankfort horizontal (FH) plane was the most concordant with FH plane used for cephalometric radiography. MATERIALS AND METHOD...

2012
Anna Foltyn Zadura Peter F Zipfel Maria I Bokarewa Gunnar Sturfelt Andreas Jönsen Sara C Nilsson Andreas Hillarp Tore Saxne Leendert A Trouw Anna M Blom

INTRODUCTION Complement activation is involved in rheumatoid arthritis (RA), systemic lupus erythematosus (SLE) and atypical hemolytic uremic syndrome (aHUS). Autoantibodies to complement inhibitor factor H (FH), particularly in association with deletions of the gene coding for FH-related protein 1 (CFHR1), are associated with aHUS. METHODS Autoantibodies against FH, factor I (FI) and C4b-bin...

2017
Alexandra I Ershova Alexey N Meshkov Stepan S Bazhan Marina A Storozhok Alexey Y Efanov Irina V Medvedeva Elena V Indukaeva Yana V Danilchenko Olga K Kuzmina Olga L Barbarash Alexander D Deev Svetlana A Shalnova Sergey A Boytsov

BACKGROUND The prevalence of familial hypercholesterolemia (FH) in Russia has not previously been evaluated. The aim of our study was to investigate the prevalence of FH in the population of the West Siberian region of Russia, and then estimate the frequency of coronary artery disease (CAD) and treatment with cholesterol-lowering medication in FH patients. METHODS The sample of our study cons...

Journal: :The Medical journal of Australia 2016
Damon A Bell Gerald F Watts

Familial hypercholesterolaemia (FH) is the most common autosomal dominant condition, with a prevalence of between one in 200 and one in 350 people in the general population. Untreated FH is associated with premature atherosclerotic cardiovascular disease (CVD). The prevalence of homozygous or compound heterozygous FH is now considered to be about one in 300 000 people. Treating children with FH...

Journal: :Circulation 2003
Albert Wiegman Jessica Rodenburg Saskia de Jongh Joep C Defesche Henk D Bakker John J P Kastelein Eric J G Sijbrands

BACKGROUND Elevated LDL cholesterol (LDL-C) levels in childhood predict cardiovascular disease (CVD) later in life. Familial hypercholesterolemia (FH) represents the paradigm of this relation. METHODS AND RESULTS The objectives of this study were to (1) establish the LDL-C level that provides the most accurate diagnosis of FH in children from families with known FH and (2) assess whether lipo...

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