نتایج جستجو برای: tab2 composite

تعداد نتایج: 121748  

2004
David Owerbach Lazaro Piña Kenneth H. Gabbay

The IDDM5 gene, which is identified by whole-genome searches, is located on chromosome 6q25. TAB2 (MAP3K7IP2 [mitogen-activating protein kinase kinase kinase 7 interacting protein 2]) is a potential candidate gene for type 1 diabetes because it is located on chromosome 6q25 and is involved in nuclear factor (NF)B regulation. We have conducted familial association studies using 478 families and ...

2017
Mahmoud Gargouri Philip D. Bates Jeong-Jin Park Helmut Kirchhoff David R. Gang

BACKGROUND Nutrient deprivation causes significant stress to the unicellular microalga, Chlamydomonas reinhardtii, which responds by significantly altering its metabolic program. Following N deprivation, the accumulation of starch and triacylglycerols (TAGs) is significantly altered following massive reprogramming of cellular metabolism. One protein that was found to change dramatically and ear...

Journal: :Tropical Journal of Pharmaceutical Research 2023

Purpose: To investigate the effect of miR-493-5p in lipopolysaccharide (LPS) -induced ATDC5 chondrogenic cells.
 Methods: The MTT assay was used to determine viability LPS-induced cells. ENCORI (starbase.sysu.edu.cn/) predict target miR-493-5p. Quantitative reverse-transcription-polymerase chain reaction (qRT-PCR) expression controlled cells and treated with various combinations LPS, negat...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2003
Micah Luftig Efthimios Prinarakis Teruhito Yasui Theodore Tsichritzis Ellen Cahir-McFarland Jun-Ichiro Inoue Hiroyasu Nakano Tak Wah Mak Wen-Chen Yeh Xiaoxia Li Shizuo Akira Nobutaka Suzuki Shinobu Suzuki George Mosialos Elliott Kieff

Epstein-Barr virus latent membrane protein 1 (LMP1) activation of NF-kappaB is critical for Epstein-Barr virus-infected B lymphocyte survival. LMP1 activates the IkappaB kinase complex and NF-kappaB through two cytoplasmic signaling domains that engage tumor necrosis factor receptor-associated factor (TRAF)1/2/3/5 or TRADD and RIP. We now use cells lacking expression of TRAF2, TRAF5, TRAF6, IKK...

Journal: :EMBO reports 2006
Axel Thiefes Alexander Wolf Anneke Doerrie Guntram A Grassl Kunihiro Matsumoto Ingo Autenrieth Erwin Bohn Hiroaki Sakurai Rainer Niedenthal Klaus Resch Michael Kracht

The mechanism by which YopP simultaneously inhibits mitogen-activated protein kinase (MAPK) and nuclear factor-kappaB pathways has been elusive. Ectopic expression of YopP inhibits the activity and ubiquitination of a complex consisting of overexpressed TGF-beta-activated kinase 1 (TAK1) and its subunit TAK1-binding protein (TAB)1, but not of MEK kinase 1. YopP, but not the catalytically inacti...

Journal: :Molecular and cellular biology 2002
Zhengfan Jiang Jun Ninomiya-Tsuji Youcun Qian Kunihiro Matsumoto Xiaoxia Li

Interleukin-1 (IL-1) receptor-associated kinase (IRAK) plays an important role in the sequential formation and activation of IL-1-induced signaling complexes. Previous studies showed that IRAK is recruited to the IL-1-receptor complex, where it is hyperphosphorylated. We now find that the phosphorylated IRAK in turn recruits TRAF6 to the receptor complex (complex I), which differs from the prev...

Journal: :Cellular signalling 2006
Zi-Heng Zhuang Lei Sun Ling Kong Jun-Hao Hu Ming-Can Yu Peter Reinach Jing-Wu Zang Bao-Xue Ge

The TAK1 plays a pivotal role in the innate immune response of Drosophila by controlling the activation of JNK and NF-kappaB. Activation of TAK1 in mammals is mediated by two TAK1-binding proteins, TAB1 and TAB2, but the role of the TAB proteins in the immune response of Drosophila has not yet been established. Here, we report the identification of a TAB2-like protein in Drosophila called dTAB2...

Journal: :Bulletin of Materials Science 2016

Journal: :Cell 2006
Jan J. Brosens Eric W.-F. Lam Malcolm G. Parker

Homeostasis in reproductive tissues requires integration of hormonal and inflammatory signals. In this issue of Cell, Zhu et al. (2006) discover that proinflammatory signals switch repressed steroid hormone receptors into transcriptional activators by targeting TAB2, an adaptor protein that tethers corepressors. These findings have implications for the treatment of endocrine-resistant cancers.

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