نتایج جستجو برای: il 23r

تعداد نتایج: 139911  

Journal: :Annual review of genomics and human genetics 2009
Johan Van Limbergen David C Wilson Jack Satsangi

From epidemiological data, based on concordance data in family studies, via linkage analysis to genome-wide association studies, we and others have accumulated robust evidence implicating more than 30 distinct genomic loci involved in the genetic susceptibility to Crohn's disease (CD). These loci encode genes involved in a number of homeostatic mechanisms: innate pattern recognition receptors (...

Journal: :Frontiers in immunology 2016
Sakshi Malik Muzamil Yaqub Want Amit Awasthi

γδ (gamma-delta) T cells, a small population of unconventional T cells, have been found in central nervous system lesions of multiple sclerosis (MS) patients, but their function in disease activity is not clearly understood. Previous studies in experimental autoimmune encephalomyelitis (EAE) were inconsistent in identifying their specific roles in suppressing or promoting disease pathogenesis. ...

Journal: :The Journal of Experimental Medicine 2003
Craig A. Murphy Claire L. Langrish Yi Chen Wendy Blumenschein Terrill McClanahan Robert A. Kastelein Jonathon D. Sedgwick Daniel J. Cua

Interleukin (IL) 23 is a heterodimeric cytokine composed of a p19 subunit and the p40 subunit of IL-12. IL-23 affects memory T cell and inflammatory macrophage function through engagement of a novel receptor (IL-23R) on these cells. Recent analysis of the contribution of IL-12 and IL-23 to central nervous system autoimmune inflammation demonstrated that IL-23 rather than IL-12 was the essential...

2011
Sanne P. Smeekens Theo S. Plantinga Frank L. van de Veerdonk Bas Heinhuis Alexander Hoischen Leo A. B. Joosten Peter D. Arkwright Andrew Gennery Bart Jan Kullberg Joris A. Veltman Desa Lilic Jos W. M. van der Meer Mihai G. Netea

We recently reported the genetic cause of autosomal dominant chronic mucocutaneous candidiasis (AD-CMC) as a mutation in the STAT1 gene. In the present study we show that STAT1 Arg274Trp mutations in the coiled-coil (CC) domain is the genetic cause of AD-CMC in three families of patients. Cloning and transfection experiments demonstrate that mutated STAT1 inhibits IL12R/IL-23R signaling, with h...

2013
Wu Chuan Nir Yosef Theresa Thalhamer Chen Zhu Sheng Xiao Yasuhiro Kishi Aviv Regev Vijay K. Kuchroo Chuan Wu Vijay Kuchroo

Induction of pathogenic TH17 cells by inducible salt-sensing kinase SGK1. Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. The MIT Faculty has made this article openly available. Please share how this access benefits you. Your story matters. Th17 response and induces pathogenic effe...

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