نتایج جستجو برای: fh

تعداد نتایج: 3804  

2015
Peter T Beernink Serena Giuntini Isabella Costa Alexander H Lucas Dan M Granoff

UNLABELLED Two licensed serogroup B meningococcal vaccines contain factor H binding protein (FHbp). The antigen specifically binds human FH, which downregulates complement. In wild-type mice whose mouse FH does not bind to FHbp vaccines, the serum anti-FHbp antibody response inhibited binding of human FH to FHbp. The inhibition was important for eliciting broad anti-FHbp serum bactericidal acti...

Journal: :The Journal of infectious diseases 2015
Dan M Granoff Isabella Costa Monica Konar Serena Giuntini Koen K A Van Rompay Peter T Beernink

BACKGROUND The meningococcal vaccine antigen, factor H (FH)-binding protein (FHbp), binds human complement FH. In human FH transgenic mice, binding decreased protective antibody responses. METHODS To investigate the effect of primate FH binding, we immunized rhesus macaques with a 4-component serogroup B vaccine (4CMenB). Serum FH in 6 animals bound strongly to FHbp (FHbp-FH(high)) and, in 6 ...

Journal: :Clinical and vaccine immunology : CVI 2014
Peter T Beernink Jutamas Shaughnessy Heather Stefek Sanjay Ram Dan M Granoff

Neisseria meningitidis causes disease only in humans. An important mechanism underlying this host specificity is the ability of the organism to resist complement by recruiting the complement downregulator factor H (FH) to the bacterial surface. In previous studies, binding of FH to one of the major meningococcal FH ligands, factor H binding protein (FHbp), was reported to be specific for human ...

Journal: :Atherosclerosis 2011
Hiroshi Mabuchi Atsushi Nohara Tohru Noguchi Junji Kobayashi Masa-Aki Kawashiri Hayato Tada Chiaki Nakanishi Mika Mori Masakazu Yamagishi Akihiro Inazu Junji Koizumi

AIM Familial hypercholesterolemia (FH) is caused by mutations of FH genes, i.e. LDL-receptor (LDLR), PCSK9 and apolipoprotein B (ApoB) gene. We evaluated the usefulness of DNA analysis for the diagnosis of homozygous FH (homo-FH), and studied the frequency of FH in the Hokuriku district of Japan. METHODS Twenty-five homo-FH patients were recruited. LDLR mutations were identified using the Inv...

2014
Isabella Costa Rolando Pajon Dan M. Granoff

UNLABELLED The meningococcal 4CMenB vaccine (Bexsero; Novartis) contains four antigens that can elicit serum bactericidal activity, one of which is factor H (FH)-binding protein (FHbp). FHbp specifically binds human complement FH. When humans are immunized, FHbp is expected to form a complex with FH, which could affect immunogenicity and safety. Wild-type mice (whose FH does not bind to FHbp) a...

2015
Jody L. Greaney Evan L. Matthews Megan M. Wenner

Greaney JL, Matthews EL, Wenner MM. Sympathetic reactivity in young women with a family history of hypertension. Am J Physiol Heart Circ Physiol 308: H816–H822, 2015. First published February 13, 2015; doi:10.1152/ajpheart.00867.2014.—Young adults with a family history of hypertension ( FH) have increased risk of developing hypertension. Furthermore, the blood pressure (BP) response to sympatho...

2005
Cheng-Yuan Chang Mao-Fu Lin Guu-Chang Yang Yu-Shing Liu Wing C. Kwong

In this paper, we propose a new fast-frequencyhopping code-division multiple-access (FH-CDMA) scheme for wireless communication systems, in which Reed-Solomon (RS) codes are modulated on top of FH-CDMA for supporting higher data rate than conventional M -ary frequency-shiftkeying FH-CDMA (MFSK/FH-CDMA) scheme and our recently proposed prime/FH-CDMA scheme. The performance of the RS/FH-CDMA sche...

Journal: :Circulation 2016
Angela Onorato Amy C Sturm

Familial hypercholesterolemia (FH) is a genetic condition that causes high low-density lipoprotein (LDL) cholesterol (sometimes referred to as bad cholesterol) from birth. FH means high cholesterol that runs in a family. FH is caused by specific DNA changes that are passed on from parents to their children. It is not caused by lifestyle factors such as a high-fat diet or lack of exercise. There...

Journal: :Journal of the American Society of Nephrology : JASN 2005
Marie-Agnès Dragon-Durey Chantal Loirat Sylvie Cloarec Marie-Alice Macher Jacques Blouin Hubert Nivet Laurence Weiss Wolf Herman Fridman Véronique Frémeaux-Bacchi

Several studies have demonstrated genetic predisposition in non-shigatoxin-associated hemolytic uremic syndrome (HUS), involving regulatory proteins of the complement alternative pathway: Factor H (FH) and membrane co-factor protein (CD46). Regarding the observations of thrombotic thrombocytopenic purpura patients, in whom a von Willebrand factor protease (ADAMST-13) deficiency may be inherited...

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