نتایج جستجو برای: binding protein c mutation

تعداد نتایج: 2414558  

Journal: :The Journal of biological chemistry 1998
C Cazaux J S Blanchet D Dupuis G Villani M Defais N P Johnson

The L2 loop is a DNA-binding site of RecA protein, a recombinase from Eschericha coli. Two DNA-binding sites have been functionally defined in this protein. To determine whether the L2 loop of RecA protein is part of the primary or secondary binding site, we have constructed proteins with site-specific mutations in the loop and investigated their biological, biochemical, and DNA binding propert...

Journal: :iranian journal of public health 0
m niyyati s rezaie f rahimi m mohebali ah maghsood sh farnia

background: acanthamoeba castellanii is the important cause of amoebic keratitis in iran. the key molecule in pathogene­sis of acanthamoeba keratitis is mannose binding protein (mbp) led to adhesion of amoeba to corneal epithelium. subse­quent to adhesion other cytopathic effects occur. the goal of this study was to identify the molecular characterization of a gene encoding mbp in an iranian is...

F. Tohidinejad M.R. Mohammadabadi,

The aim of the present study was todeterminecharacteristics of Rheb gene and protein in Raini Cashmere goat. Comparative analyses of the nucleotide sequences were performed. Open reading frames (ORFs), theoretical molecular weights of deduced polypeptides, the protein isoelectric point, protein characteristics and three-dimensional structures was predicted using online standard softwares. The f...

Abbas Shirdel, Abdol Rahim Rezaee Akram Beyk yazdi Hassan Rahimi Houshang Rafatpanah Ian V Hutchinson Mahmoud Reza Azarpajooh

Introduction Genetic background has known to be associated with the outcome of human T cell lymphotropic virus (HTLV) type I infection. In The present study we investigate the association between GM-CSF gene polymorphisms with the outcome of HTLV-I infection. Materials and Methods We analyzed 3 single-nucleotide polymorphisms in the promter region of granulocyte macrophage colony stimulating...

Journal: :iranian red crescent medical journal 0
habib onsori cell and molecular biology department, marand branch, islamic azad university, marand, ir iran; cell and molecular biology department, marand branch, islamic azad university, marand university sq., p.o. box: 54165-161, marand, ir iran, tel.: +98-4912263444, fax.: +98-4912260566 mohammad ali hosseinpour feizi biology department, tabriz university, tabriz, ir iran abbas ali hosseinpour feizi hematology and oncology research center, tabriz university of medical sciences, tabriz, ir iran

introduction: haemophilia a is the most common inherited x-linked recessive bleeding disorder. the severity of the resultant bleeding diathesis depends on the fviii levels associated with the mutation. analysis of carrier state can be made indirectly by dna linkage analysis or directly by identifying the mutation that leads to the disease. the aim of this study was to identification of the caus...

فریدونی, محمدامین, بصیری, زهرا , شمس, مقدسه ,

Introduction: Wegener’s Granolomatosis (WG) is a systemic, necrotizing, small-vessel vasculitis. Vascular inflammation and occlusion leading to tissue ischemia is a hallmark of WG. WG has a clinical predilection for the upper airways, lungs, and kidneys. Thromboembolic events do not usually occur and arterial thrombosis is extremely rare. Case Report: Here we reported 2 rare cases of arteria...

Journal: :iranian journal of basic medical sciences 0
abbas shirdel internal medicine department, ghaem hospital, mashhad university of medical sciences, mashhad, iran houshang rafatpanah immunology research centre, buali reserch institute, mashhad university of medical sciences, mashhad, iran centre for integrated genomic medical research (cigmr), the university of manchester, manchester, uk hassan rahimi internal medicine department, ghaem hospital, mashhad university of medical sciences, mashhad, iran abdol rahim rezaee immunology research centre, buali reserch institute, mashhad university of medical sciences, mashhad, iran mahmoud reza azarpajooh neurology department, ghaem hospital, mashhad university of medical sciences, mashhad, iran

introduction genetic background has known to be associated with the outcome of human t cell lymphotropic virus (htlv) type i infection. in the present study we investigate the association between gm-csf gene polymorphisms with the outcome of htlv-i infection. materials and methods we analyzed 3 single-nucleotide polymorphisms in the promter region of granulocyte macrophage colony stimulating fa...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2011
Brie E Paddock Zhao Wang Laurie M Biela Kaiyun Chen Michael D Getzy Amelia Striegel Janet E Richmond Edwin R Chapman David E Featherstone Noreen E Reist

The vesicle protein synaptotagmin I is the Ca(2+) sensor that triggers fast, synchronous release of neurotransmitter. Specifically, Ca(2+) binding by the C(2)B domain of synaptotagmin is required at intact synapses, yet the mechanism whereby Ca(2+) binding results in vesicle fusion remains controversial. Ca(2+)-dependent interactions between synaptotagmin and SNARE (soluble N-ethylmaleimide-sen...

Journal: :The American journal of physiology 1999
Zvjezdana Sever-Chroneos Cindy J Bachurski Cong Yan Jeffrey A Whitsett

The regulatory role of activator protein-1 (AP-1) family members in mouse surfactant protein (SP) B (mSP-B) promoter function was assessed in the mouse lung epithelial cell line MLE-15. Expression of recombinant Jun B and c-Jun inhibited mSP-B promoter activity by 50-75%. Although c-Fos expression did not alter mSP-B transcription, Jun D enhanced mSP-B promoter activity and reversed inhibition ...

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