نتایج جستجو برای: cd95

تعداد نتایج: 2385  

Journal: :Journal of leukocyte biology 2001
P Gorak-Stolinska J P Truman D M Kemeny A Noble

Human primary effector T cells were analyzed for their susceptibility to anti-CD3-induced activation-induced cell death (AICD). Th1 and Tc1 cells were more susceptible to AICD than their type 2 counterparts. Type 1 and type 2 subsets were also found to be differentially susceptible to CD95-mediated apoptosis, although cell-surface expression of CD95 and CD95L was at similar levels on all subset...

2017
William Putzbach Quan Q Gao Monal Patel Stijn van Dongen Ashley Haluck-Kangas Aishe A Sarshad Elizabeth T Bartom Kwang-Youn A Kim Denise M Scholtens Markus Hafner Jonathan C Zhao Andrea E Murmann Marcus E Peter

Over 80% of multiple-tested siRNAs and shRNAs targeting CD95 or CD95 ligand (CD95L) induce a form of cell death characterized by simultaneous activation of multiple cell death pathways preferentially killing transformed and cancer stem cells. We now show these si/shRNAs kill cancer cells through canonical RNAi by targeting the 3'UTR of critical survival genes in a unique form of off-target effe...

Journal: :Communicative & Integrative Biology 2012

Journal: :The Journal of Experimental Medicine 1999
Jan Paul Medema Joan de Jong Thorbald van Hall Cornelis J.M. Melief Rienk Offringa

The antiapoptotic protein cellular FLICE (Fas-associated death domain-like IL-1beta-converting enzyme) inhibitory protein (cFLIP) protects cells from CD95(APO-1/Fas)-induced apoptosis in vitro and was found to be overexpressed in human melanomas. However, cytotoxic T cell-induced apoptosis, which is critically involved in tumor control in vivo, is not inhibited by cFLIP in vitro, as only CD95- ...

2011
Mohamed A. Al-Ahmady Takwa E. Meawed Hoda Gouda Bakr Ihab M Salem

Diabetes mellitus (DM) and its complications are complex syndromes representing universal health problems. Egypt ranks ninth among countries with diabetes where the problem is magnified. Researchers have discussed the effect of hyper glycaemia on apoptosis. However, the aims of this study were to assess CD95 positive cells in controlled and uncontrolled type II diabetic patients and to elucidat...

2016
Amanda Poissonnier Doriane Sanséau Matthieu Le Gallo Marine Malleter Nicolas Levoin Roselyne Viel Lucie Morere Aubin Penna Patrick Blanco Alain Dupuy Florence Poizeau Alain Fautrel Julien Seneschal Florence Jouan Jerome Ritz Edouard Forcade Nathalie Rioux Cécile Contin-Bordes Thomas Ducret Anne-Marie Vacher Paul A. Barrow Robin J. Flynn Pierre Vacher Patrick Legembre

CD95 ligand (CD95L) is expressed by immune cells and triggers apoptotic death. Metalloprotease-cleaved CD95L (cl-CD95L) is released into the bloodstream but does not trigger apoptotic signaling. Hence, the pathophysiological role of cl-CD95L remains unclear. We observed that skin-derived endothelial cells from systemic lupus erythematosus (SLE) patients expressed CD95L and that after cleavage, ...

2013
A. Sallam Kareem Y. Shaheen

INTRODUCTION The tumor necrosis factor receptor (TNFR) family consists of a number of type I transmembrane glycoproteins characterized by homologous cysteine-rich domains in their extracellular region. The intracellular parts of these proteins vary in size and structure, corresponding to the wide array of functions of TNFR proteins, ranging from regulation of cell activation and differentiation...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2008
Guo Zhang Margaret A Park Clint Mitchell Hossein Hamed Mohamed Rahmani Aditi Pandya Martin David T Curiel Adly Yacoub Martin Graf Ray Lee John D Roberts Paul B Fisher Steven Grant Paul Dent

PURPOSE AND DESIGN Mechanism(s) by which the multikinase inhibitor sorafenib and the histone deacetylase inhibitor vorinostat interact to kill hepatic, renal, and pancreatic adenocarcinoma cells has been defined. RESULTS Low doses of sorafenib and vorinostat interacted in vitro in a synergistic fashion to kill hepatic, renal, and pancreatic adenocarcinoma cells in multiple short-term viabilit...

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