نتایج جستجو برای: doha development round ddr

تعداد نتایج: 1452695  

2009
Christina L. Davis

This paper examines how interest groups influence the decision to negotiate trade problems at the bilateral level, through adjudication, or in a comprehensive trade round. The institutional venues available for trade negotiations vary in terms of issues, rules, actors, and duration. Interest groups have preferences over the choice of institutional venue because differences in the scope and timi...

2011
Zeenia Kaul Anthony J Cesare Lily I Huschtscha Axel A Neumann Roger R Reddel

Replicative senescence is accompanied by a telomere-specific DNA damage response (DDR). We found that DDR+ telomeres occur spontaneously in early-passage normal human cells and increase in number with increasing cumulative cell divisions. DDR+ telomeres at replicative senescence retain TRF2 and RAP1 proteins, are not associated with end-to-end fusions and mostly result from strand-independent, ...

2017
Molly L Bristol Dipon Das Iain M Morgan

Human papillomaviruses (HPV) require the activation of the DNA damage response (DDR) in order to undergo a successful life cycle. This activation presents a challenge for the virus and the infected cell: how does viral and host replication proceed in the presence of a DDR that ordinarily arrests replication; and how do HPV16 infected cells retain the ability to proliferate in the presence of a ...

Journal: :Carcinogenesis 2015
Wen-Cheng Chou Ling-Yueh Hu Chia-Ni Hsiung Chen-Yang Shen

The DNA damage response (DDR) is activated by various genotoxic stresses. Base lesions, which are structurally simple and predominantly fixed by base excision repair (BER), can trigger the ataxia telangiectasia mutated (ATM)-checkpoint kinase 2 (Chk2) pathway, a DDR component. How these lesions trigger DDR remains unclear. Here we show that, for alkylation damage, methylpurine-DNA glycosylase (...

Journal: :Rechtsgeschichte - Legal History 2005

2016
Dong Wha Jun Mihwa Hwang Yun-Hee Kim Kyung-Tae Kim Sunshin Kim Chang-Hun Lee

The DNA damage response (DDR) is an emerging target for cancer therapy. By modulating the DDR, including DNA repair and cell cycle arrest, the efficacy of anticancer drugs can be enhanced and side effects reduced. We previously screened a chemical library and identified novel DDR inhibitors including DNA damage response inhibitor-9 (DDRI-9; 1H-Purine-2,6-dione,7-[(4-fluorophenyl)methyl]-3,7-dih...

2017
Jeff Rector Sasha Kapil Kelly J Treude Phyllis Kumm Jason G. Glanzer Brendan M. Byrne Shengqin Liu Lynette M Smith Dominick J DiMaio Peter Giannini Russell B Smith Greg G. Oakley

Oral cancers are easily accessible compared to many other cancers. Nevertheless, oral cancer is often diagnosed late, resulting in a poor prognosis. Most oral cancers are squamous cell carcinomas that predominantly develop from cell hyperplasias and dysplasias. DNA damage is induced in these tissues directly or indirectly in response to oncogene-induced deregulation of cellular proliferation. C...

2013
Federico Carafoli Erhard Hohenester

The discoidin domain receptors, DDR1 and DDR2, are two closely related receptor tyrosine kinases that are activated by triple-helical collagen in a slow and sustained manner. The DDRs have important roles in embryo development and their dysregulation is associated with human diseases, such as fibrosis, arthritis and cancer. The extracellular region of DDRs consists of a collagen-binding discoid...

Journal: :Genes & development 2017
Aleksandra Vancevska Kyle M Douglass Verena Pfeiffer Suliana Manley Joachim Lingner

Telomeres are specialized nucleoprotein structures that protect chromosome ends from DNA damage response (DDR) and DNA rearrangements. The telomeric shelterin protein TRF2 suppresses the DDR, and this function has been attributed to its abilities to trigger t-loop formation or prevent massive decompaction and loss of density of telomeric chromatin. Here, we applied stochastic optical reconstruc...

2013
Travis H. Stracker Ignasi Roig Philip A. Knobel Marko Marjanović

The DNA damage response (DDR) rapidly recognizes DNA lesions and initiates the appropriate cellular programs to maintain genome integrity. This includes the coordination of cell cycle checkpoints, transcription, translation, DNA repair, metabolism, and cell fate decisions, such as apoptosis or senescence (Jackson and Bartek, 2009). DNA double-strand breaks (DSBs) represent one of the most cytot...

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