نتایج جستجو برای: chromatid breaks

تعداد نتایج: 33390  

Journal: :Industrial health 1981
K Morimoto A Koizumi

MATERIALS AND METHODS Chromium is known to be an essential element1. Epidemiological and experimental studies have, however, demonstrated that some chromium compouds (mainly hexavalent salts) are mutagenic carcinogens2-5) (see ref. 1 for review). Recent studies have also shown that the hexavalent compounds induce dose-related increases in chromosomal aberrations and sister chromatid exchanges i...

Journal: :Current Biology 2005
Juraj Gregan Peter K. Rabitsch Benjamin Sakem Ortansa Csutak Vitaly Latypov Elisabeth Lehmann Juerg Kohli Kim Nasmyth

Two rounds of chromosome segregation after only a single round of DNA replication enable the production of haploid gametes from diploid precursors during meiosis. To identify genes involved in meiotic chromosome segregation, we developed an efficient strategy to knock out genes in the fission yeast on a large scale. We used this technique to delete 180 functionally uncharacterized genes whose e...

Journal: :EMBO reports 2013
Vincent Dion Véronique Kalck Andrew Seeber Thomas Schleker Susan M Gasser

The regulation of chromatin mobility in response to DNA damage is important for homologous recombination in yeast. Anchorage reduces rates of recombination, whereas increased chromatin mobility correlates with more efficient homology search. Here we tracked the mobility and localization of spontaneous S-phase lesions bound by Rad52, and find that these foci have reduced movement, unlike enzymat...

Journal: :Cancer genetics and cytogenetics 1983
A B Mitra V V Murty U K Luthra

Double-minute chromosomes (DMs) were observed in repeated samples in the leukocytes of a patient with a previous history of cervical carcinoma. The most interesting cytogenetic finding was the coexistence of DMs and a dicentric chromosome along with chromosome- and chromatid-type breaks and gaps. This observation suggests that DMs might originate through the breakage of existing chromosomes. Th...

2017
Guochao Liu Hui Wang Fengmei Zhang Youjia Tian Zhujun Tian Zuchao Cai David Lim Zhihui Feng

This study explored whether valproic acid (VPA, a histone deacetylase inhibitor) could radiosensitize osteosarcoma and primary-culture tumor cells, and determined the mechanism of VPA-induced radiosensitization. The working system included osteosarcoma cells (U2OS) and primary-culture cells from chemical carcinogen (DMBA)-induced breast cancer in rats; and clonogenic survival, immunofluorescenc...

2012
Sabine S. Lange John P. Wittschieben Richard D. Wood

Unique among translesion synthesis (TLS) DNA polymerases, pol ζ is essential during embryogenesis. To determine whether pol ζ is necessary for proliferation of normal cells, primary mouse fibroblasts were established in which Rev3L could be conditionally inactivated by Cre recombinase. Cells were grown in 2% O(2) to prevent oxidative stress-induced senescence. Cells rapidly became senescent or ...

2011
Huimei Lu Yi-Yuan Huang Sonam Mehrotra Roberto Droz-Rosario Jingmei Liu Mantu Bhaumik Eileen White Zhiyuan Shen

BCCIP is a BRCA2- and CDKN1A(p21)-interacting protein that has been implicated in the maintenance of genomic integrity. To understand the in vivo functions of BCCIP, we generated a conditional BCCIP knockdown transgenic mouse model using Cre-LoxP mediated RNA interference. The BCCIP knockdown embryos displayed impaired cellular proliferation and apoptosis at day E7.5. Consistent with these resu...

2015
Ying Yuan Sébastien Britton Christine Delteil Julia Coates Stephen P. Jackson Nadia Barboule Philippe Frit Patrick Calsou

In humans, DNA double-strand breaks (DSBs) are repaired by two mutually-exclusive mechanisms, homologous recombination or end-joining. Among end-joining mechanisms, the main process is classical non-homologous end-joining (C-NHEJ) which relies on Ku binding to DNA ends and DNA Ligase IV (Lig4)-mediated ligation. Mostly under Ku- or Lig4-defective conditions, an alternative end-joining process (...

M SAADAT, MR NOORI-DALOII, P MEHDIPOUR,

Cytogenetic studies were performed on 150 cases of Down's syndrome (DS) in Iran. The standard trisomy 21 was found in 132 (88 % ) and translocation-trisomy 21 (+21) in 18 (12%) patients, i.e., t(21,21) in 1(0.63%) and mosaicism in 17(11.33%) cases. The comparison of the frequencies for mosaicism between different populations such as Denmark, Hungary, Egypt, Iraq, India, Australia and Iran ...

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