نتایج جستجو برای: عضله fhl

تعداد نتایج: 3176  

Journal: :Infection and immunity 2005
Kate von Lackum Jennifer C Miller Tomasz Bykowski Sean P Riley Michael E Woodman Volker Brade Peter Kraiczy Brian Stevenson Reinhard Wallich

During the natural mammal-tick infection cycle, the Lyme disease spirochete Borrelia burgdorferi comes into contact with components of the alternative complement pathway. B. burgdorferi, like many other human pathogens, has evolved the immune evasion strategy of binding two host-derived fluid-phase regulators of complement, factor H and factor H-like protein 1 (FHL-1). The borrelial complement ...

2001
Antun Milas

We consider a class of weak modules for vertex operator algebras that we call logarithmic modules. We also construct nontrivial examples of intertwining operators between certain logarithmic modules for the Virasoro vertex operator algebra. At the end we speculate about some possible logarithmic intertwiners at the level c = 0. Introduction This work is an attempt to explain an algebraic reform...

Journal: :Blood 2005
Eiichi Ishii Ikuyo Ueda Ryutaro Shirakawa Ken Yamamoto Hisanori Horiuchi Shouichi Ohga Kenji Furuno Akira Morimoto Miyoko Imayoshi Yoshiyasu Ogata Masafumi Zaitsu Masahiro Sako Kenichi Koike Akifumi Sakata Hidetoshi Takada Toshiro Hara Shinsaku Imashuku Takehiko Sasazuki Masaki Yasukawa

Mutations of the perforin (PRF1) and MUNC13-4 genes distinguish 2 forms of familial hemophagocytic lymphohistiocytosis (FHL2 and FHL3, respectively), but the clinical and biologic correlates of these genotypes remain in question. We studied the presenting features and cytotoxic T lymphocyte/natural killer (CTL/NK) cell functions of 35 patients for their relationship to distinct FHL subtypes. FH...

2018
Robin C Willenbring Yasuhiro Ikeda Larry R Pease Aaron J Johnson

BACKGROUND Deleterious mutations in PRF1 result in lethal, childhood disease, familial hemophagocytic lymphohistiocytosis type 2 (FHL 2). However, not all mutations in PRF1 are deleterious and result in FHL 2. Currently, these nondeleterious mutations are being investigated in the onset of numerous disorders, such as lymphomas and diabetes. Yet, there is still an overwhelmingly large amount of ...

Journal: :Journal of biochemistry 2008
Muneaki Takahata Takashi Tamura Katsumasa Abe Hisaaki Mihara Suguru Kurokawa Yoshihiro Yamamoto Ryuhei Nakano Nobuyoshi Esaki Kenji Inagaki

Escherichia coli growing under anaerobic conditions produce H(2) and CO(2) by the enzymatic cleavage of formate that is produced from pyruvate at the end of glycolysis. Selenium is an integral part of formate dehydrogenase H (FDH H), which catalyses the first step in the formate hydrogen lyase (FHL) system. The genes of FHL system are transcribed only under anaerobic conditions, in the presence...

2008
Toshinari Maeda Viviana Sanchez‐Torres Thomas K. Wood

Hydrogen fuel is renewable, efficient and clean, and fermentative bacteria hold great promise for its generation. Here we use the isogenic Escherichia coli K-12 KEIO library to rapidly construct multiple, precise deletions in the E. coli genome to direct the metabolic flux towards hydrogen production. Escherichia coli has three active hydrogenases, and the genes involved in the regulation of th...

2015
Marlene Carmo Kimberly A Risma Paritha Arumugam Swati Tiwari Adrianne E Hontz Claudia A Montiel-Equihua Maria E Alonso-Ferrero Michael P Blundell Axel Schambach Christopher Baum Punam Malik Adrian J Thrasher Michael B Jordan H Bobby Gaspar

Defects in perforin lead to the failure of T and NK cell cytotoxicity, hypercytokinemia, and the immune dysregulatory condition known as familial hemophagocytic lymphohistiocytosis (FHL). The only curative treatment is allogeneic hematopoietic stem cell transplantation which carries substantial risks. We used lentiviral vectors (LV) expressing the human perforin gene, under the transcriptional ...

2013
Maurizio Aricò Elena Boggio Valentina Cetica Matteo Melensi Elisabetta Orilieri Nausicaa Clemente Giuseppe Cappellano Sara Buttini Maria Felicia Soluri Cristoforo Comi Carlo Dufour Daniela Pende Irma Dianzani Steven R. Ellis Sara Pagliano Stefania Marcenaro Ugo Ramenghi Annalisa Chiocchetti Umberto Dianzani

Autoimmune lymphoproliferative syndrome (ALPS) is caused by genetic defects decreasing Fas function and is characterized by lymphadenopathy/splenomegaly and expansion of CD4/CD8 double-negative T cells. This latter expansion is absent in the ALPS variant named Dianzani Autoimmune/lymphoproliferative Disease (DALD). In addition to the causative mutations, the genetic background influences ALPS a...

2011
Serenella Cerrito Marta Cialdea Mayer

In this paper we provide the first (as far as we know) direct calculus deciding satisfiability of formulae in negation normal form in the fragment of FHL (full hybrid logic with the binder, including the global and converse modalities), where no occurrence of a universal operator is in the scope of a binder. By means of a satisfiability preserving translation of formulae, the calculus can be tu...

2017
Simon J. Clark Selina McHarg Viranga Tilakaratna Nicole Brace Paul N. Bishop

Age-related macular degeneration (AMD) is the leading cause of blindness in the western world and affects nearly 200 million people globally. Local inflammation driven by complement system dysregulation is currently a therapeutic target. Bruch's membrane (BrM) is a sheet of extracellular matrix that separates the retina from the underlying choroid, a highly vascularized layer that supplies oxyg...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید