نتایج جستجو برای: ncf2

تعداد نتایج: 100  

2001
Bryan Kautz Renu Kakar Ebenezer David Elizabeth A. Eklund

The CYBB and NCF2 genes encode the phagocyte respiratory burst oxidase proteins, gp91 and p67. Previously, we identified homologous CYBB and NCF2 cis elements that are necessary for lineage-specific transcription during late myeloid differentiation. We determined that these homologous cis elements are activated by PU.1, IRF1, interferon consensus sequence-binding protein (ICSBP), and the CREB-b...

Journal: :Journal of immunology 2005
Stephan Lindsey Chunliu Zhu Yu Feng Lu Elizabeth A Eklund

p67(phox) and gp91(phox) are components of the phagocyte-specific respiratory burst oxidase that are encoded by the NCF2 and CYBB genes, respectively. These genes are transcribed exclusively in myeloid cells that have differentiated beyond the promyelocyte stage. In mature phagocytes, NCF2 and CYBB transcription continues until cell death and further increases in response to IFN-gamma and other...

2004
Katherine A. Gauss Peggy L. Bunger Trina C. Larson Catherine J. Young Laura K. Nelson-Overton Daniel W. Siemsen Mark T. Quinn

The phagocyte reduced nicotinamide adenine dinucleotide phosphate oxidase is a multiprotein enzyme that catalyzes the production of microbicidal oxidants. Although oxidase assembly involves association of several membrane and cytosolic oxidase proteins, one of the cytosolic cofactors, p67, appears to play a more prominent role in final activation of the enzyme complex. Based on the importance o...

Journal: :Human molecular genetics 2014
Xana Kim-Howard Celi Sun Julio E Molineros Amit K Maiti Hema Chandru Adam Adler Graham B Wiley Kenneth M Kaufman Leah Kottyan Joel M Guthridge Astrid Rasmussen Jennifer Kelly Elena Sánchez Prithvi Raj Quan-Zhen Li So-Young Bang Hye-Soon Lee Tae-Hwan Kim Young Mo Kang Chang-Hee Suh Won Tae Chung Yong-Beom Park Jung-Yoon Choe Seung Cheol Shim Shin-Seok Lee Bok-Ghee Han Nancy J Olsen David R Karp Kathy Moser Bernardo A Pons-Estel Edward K Wakeland Judith A James John B Harley Sang-Cheol Bae Patrick M Gaffney Marta Alarcón-Riquelme Loren L Looger Swapan K Nath

Recent reports have associated NCF2, encoding a core component of the multi-protein NADPH oxidase (NADPHO), with systemic lupus erythematosus (SLE) susceptibility in individuals of European ancestry. To identify ethnicity-specific and -robust variants within NCF2, we assessed 145 SNPs in and around the NCF2 gene in 5325 cases and 21 866 controls of European-American (EA), African-American (AA),...

Journal: :Journal of immunology 2006
Vanessa Sancho-Shimizu Danielle Malo

A recessive Salmonella Typhimurium susceptibility locus (immunity to Typhimurium (Ity3) was reported previously on distal mouse chromosome 1 using a cross between C57BL/6J and wild-derived MOLF/Ei mice. This quantitative trait locus is located in a genomic region spanning 84 Mb, rich in candidate genes for which a role in host resistance to Salmonella infection is either known or can be envisio...

2008
Ioannis Emiris Michael Hemmer Menelaos Karavelas Sebastian Limbach Bernard Mourrain Elias P. Tsigaridas Zafeirakis Zafeirakopoulos I. Emiris E. P. Tsigaridas Luis Peñaranda

We summarize the results of the cross-benchmarks for two univariate algebraic kernels (AK) developed in ACS. The kernels, developed at INRIA and MPI, were tested on 6 types of univariate polynomials of various degrees and bitsizes. The methods included were: Sturm, Sleeve, CF, NCF, NCF2 for the INRIA kernel, and Descartes and Bitstream-Descartes for the MPI kernel. NCF, NCF2, Descartes and Bits...

Journal: :Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia 2011
Jiri Vrba Katerina Trtkova Jitka Ulrichova

UNLABELLED AIM. This study was designed to examine whether the class I and class IIa histone deacetylase (HDAC) inhibitors, sodium butyrate and sodium valproate alter the expression of human NCOR1 and/or NCOR2 genes coding for N-CoR (nuclear receptor corepressor) and SMRT (silencing mediator for retinoid and thyroid hormone receptors), respectively. METHODS Human leukemia HL-60 cells were tre...

Journal: :Iranian journal of allergy, asthma, and immunology 2012
Mohsen Badalzadeh Fatemeh Fattahi Mohammad Reza Fazlollahi Shaghayegh Tajik Mohammad Hassan Bemanian Fatemeh Behmanesh Massoud Movahedi Massoud Houshmand Zahra Pourpak

Chronic granulomatous disease (CGD), a rare inherited primary immunodeficiency disorder, is caused by mutation in any one of the genes encoding components of nicotinamide adenine dinucleotide phosphate (NADPH)-oxidase enzyme. NCF2 gene (encoding P67-phox component) is one of them and its mutation is less common to cause CGD (around 5-6%). Here, we assessed mutation analysis of NCF2 in 4 CGD pat...

2013
Patricia A.J. Muller

in the popular tale " Ozma of Oz, " Lyman Frank Baum describes the princess Langwidere, who is capable of interchanging her currently worn head with another one, using a collection of heads stored in a cabinet. Remarkably, she changes her character as well when putting a new head on her neck. in the December 15, 2012 issue of Cell Cycle, Kurt Engeland and colleagues report a similar phenomenon ...

Journal: :iranian journal of allergy, asthma and immunology 0
mohsen badalzadeh immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran fatemeh fattahi immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran mohammad reza fazlollahi immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran shaghayegh tajik immunology, asthma and allergy research institute, tehran university of medical sciences, tehran, iran mohammad hassan bemanian department of pediatrics, division of allergy and immunology, shahid sadoughi hospital, school of medicine, shahid sadoughi university of medical sciences, yazd, iran fatemeh behmanesh allergy research center, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran

chronic granulomatous disease (cgd), a rare inherited primary immunodeficiency disorder,  is  caused  by  mutation  in  any  one  of  the  genes  encoding  components   of nicotinamide adenine dinucleotide phosphate (nadph)-oxidase enzyme. ncf2 gene (encoding p67-phox component) is one of them and its mutation is less common to cause cgd (around 5-6%). here, we assessed mutation analysis of ncf...

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