نتایج جستجو برای: fluctuation hypothesis fh

تعداد نتایج: 247227  

Journal: :Hormones and behavior 2006
Wendy Saltzman Shahen Ahmed Atefeh Fahimi Daniel J Wittwer Frederick H Wegner

In several cooperatively breeding species, reproductively suppressed, nonbreeding females are attracted to infants and routinely provide alloparental care, while breeding females may attack or kill other females' infants. The mechanisms underlying the transition from alloparental to infanticidal behavior are unknown. In this study, we tested the hypothesis that this transition is associated wit...

2006
I. V. L. Costa M. H. Vainstein L. C. Lapas A. A. Batista F. A. Oliveira

Investigations on diffusion in systems with memory [1] have established a hierarchical connection between mixing, ergodicity, and the fluctuation-dissipation theorem (FDT). This hierarchy means that ergodicity is a necessary condition for the validity of the FDT, and mixing is a necessary condition for ergodicity. In this work, we compare those results with recent investigations using the Lee r...

Journal: :Infection and immunity 2006
Kelley M Hovis Janice P Jones Tania Sadlon Gauri Raval David L Gordon Richard T Marconi

Borrelia hermsii, the primary etiological agent of tick-borne relapsing fever in North America, binds the complement regulatory protein factor H (FH) as a means of evading opsonophagocytosis and the alternative complement pathway. The ability of FH-binding protein A (FhbA) to bind FH-like protein 1 (FHL-1) has not been assessed previously. In this study, using a whole-cell absorption assay, we ...

Journal: :Journal of immunology 2008
Livija Deban Hanna Jarva Markus J Lehtinen Barbara Bottazzi Antonio Bastone Andrea Doni T Sakari Jokiranta Alberto Mantovani Seppo Meri

The long pentraxin PTX3 is a multifunctional soluble molecule involved in inflammation and innate immunity. As an acute phase protein, PTX3 binds to the classical pathway complement protein C1q, limits tissue damage in inflammatory conditions by regulating apoptotic cell clearance, and plays a role in the phagocytosis of selected pathogens. This study was designed to investigate the interaction...

Journal: :Journal of atherosclerosis and thrombosis 2012
Mariko Harada-Shiba Hidenori Arai Tomonori Okamura Koutaro Yokote Shinichi Oikawa Atsushi Nohara Tomoo Okada Takao Ohta Hideaki Bujo Makoto Watanabe Akihiko Wakatsuki Shizuya Yamashita

AIM Heterozygous patients of familial hypercholesterolemia (FH) are known to have a high risk of coronary artery disease (CAD). Early diagnosis and prompt treatment are necessary to prevent their CAD. In this study we tried to amend the Japanese diagnostic criteria of FH for general practitioners by examining each component of the current criteria. METHODS A multicenter study was performed, w...

Journal: :Biological psychiatry 1998
D Malaspina J H Friedman C Kaufmann G Bruder X Amador D Strauss S Clark S Yale E Lukens H Thorning R Goetz J Gorman

BACKGROUND Although schizophrenia is presumed to be heterogeneous, there has been limited success distinguishing familial from sporadic cases. We used psychobiological measures to examine heterogeneity, as they may be closer to neurobiology than symptoms. Smooth pursuit eye movement quality (SPEM) and dichotic listening (DL) tests to tones and words were used to assess hemispheric laterality as...

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...

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