نتایج جستجو برای: h2ax gene

تعداد نتایج: 1142668  

2013
Matthew Hoare Arun Shankar Meera Shah Simon Rushbrook William Gelson Susan Davies Arne Akbar Graeme J.M. Alexander

BACKGROUND & AIMS Age is the dominant prognostic factor influencing the natural history of hepatitis C virus (HCV) infection and treatment response. Accelerated lymphocyte telomere shortening in HCV infection correlates with adverse clinical outcomes. Critical telomere shortening generates double-stranded DNA breaks (DSB) inducing the DNA damage response, leading to replicative senescence. The ...

Journal: :Cell cycle 2006
Toshiki Tanaka H Dorota Halicka Frank Traganos Zbigniew Darzynkiewicz

Oxidative burst is a defense mechanism used by specialized phagocytes such as granulocytes or monocytes to kill the invading microorganisms through generation of superoxide anions. Oxidative burst also results in DNA damage of the phagocytes. Phagocytes are terminally differentiated cells, some of very short life-span cells. We could find no reports whether oxidative burst-mediated DNA damage t...

2014
Gernot Neumayer Minh Dang Nguyen

During interphase, the spindle assembly factor TPX2 is compartmentalized in the nucleus where its roles remain largely uncharacterized. Recently, we found that TPX2 regulates the levels of serine 139-phosphoryated H2AX (γ-H2AX) at chromosomal breaks induced by ionizing radiation. Here, we report that TPX2 readily associates with the chromatin in the absence of ionizing radiation. Overexpression...

2014
Juliane Heydenreich Christoph Otto Frank Mayer Anja Carlsohn

Background. Analysis of γ-H2AX foci is a promising approach to evaluate exercise-induced DNA damage. However, baseline levels and day-to-day variability of γ-H2AX foci have not been investigated in healthy subjects at rest. Methods. Blood was taken from eight moderately trained healthy males (29 ± 3 yrs, 1.84 ± 0.03 m, and 85 ± 6 kg) at two separate days (M1/M2) after 24-hour exercise cessation...

Journal: :Frontiers in bioscience 2017
Masayuki Mishima

Current anticancer therapy may be one of the most important exogenous sources of exposure to genotoxic agents in US, Japan, and Europe, where approximately 40-55 percent of the population is diagnosed with cancer at a certain point in their life. This review focuses on recent efforts to integrate a novel biomarker, gamma-H2AX, into anticancer drug screening to classify the mode of action (MoA) ...

Journal: :The EMBO journal 2010
Cédric Artus Hanan Boujrad Aïda Bouharrour Marie-Noëlle Brunelle Sylviane Hoos Victor J Yuste Pascal Lenormand Jean-Claude Rousselle Abdelkader Namane Patrick England Hans K Lorenzo Santos A Susin

Programmed necrosis induced by DNA alkylating agents, such as MNNG, is a caspase-independent mode of cell death mediated by apoptosis-inducing factor (AIF). After poly(ADP-ribose) polymerase 1, calpain, and Bax activation, AIF moves from the mitochondria to the nucleus where it induces chromatinolysis and cell death. The mechanisms underlying the nuclear action of AIF are, however, largely unkn...

2016
Joris Pauty Marie-France Côté Amélie Rodrigue Denis Velic Jean-Yves Masson Sébastien Fortin

2-Ethylphenyl 4-(3-ethylureido)benzenesulfonate (SFOM-0046) is a novel anticancer agent that arrests cell cycle in S-phase and causes DNA replication stress leading to the phosphorylation of H2AX into γ-H2AX. First, using the M21, HT29, HT-1080 and HeLa cell lines, we confirmed that S-phase cell cycle arrest and γ-H2AX foci induction by SFOM-0046 is a general mechanism occurring in diverse canc...

2011
Darryl Hudson Igor Kovalchuk Igor Koturbash Bryan Kolb Olga A. Martin Olga Kovalchuk

Younger individuals are more prone to develop cancer upon ionizing radiation (IR) exposure. Radiation-induced tumors are associated with inefficient repair of IR-induced DNA damage and genome instability. Phosphorylation of histone H2AX (γ-H2AX) is the initial event in repair of IR-induced DNA damage on the chromatin flanking the DNA strand breaks. This step is crucially important for the repai...

Journal: :Human molecular genetics 2013
Lauren A Solomon Bailey A Russell L Ashley Watson Frank Beier Nathalie G Bérubé

ATR-X syndrome is a rare genetic disorder caused by mutations in the ATRX gene. Affected individuals are cognitively impaired and display a variety of developmental abnormalities, including skeletal deformities. To investigate the function of ATRX during skeletal development, we selectively deleted the gene in the developing forelimb mesenchyme of mice. The absence of ATRX in the limb mesenchym...

Journal: :Journal of Cell Biology 2003

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