نتایج جستجو برای: chromosomal sensitivity

تعداد نتایج: 380653  

2015
Yun Gao Steven Setiawan Theng Way-Champ Mah Caroline G. L. Lee

Pleiotropic pro-inflammatory cytokines, TNF-α and IFN-γ (TI), play important yet diverse roles in cell survival, proliferation, and death. Recent evidence highlights FAT10 as a downstream molecule in the pathway of inflammation-induced tumorigenesis through mediating the effect of cytokines in causing numerical CIN and protecting cells from cytokines-induced cell death. cDNA microarray analysis...

Journal: :Cancer research 2005
Yehudit Birger Frédéric Catez Takashi Furusawa Jae-Hwan Lim Marta Prymakowska-Bosak Katherine L West Yuri V Postnikov Diana C Haines Michael Bustin

We report that loss of HMGN1, a nucleosome-binding protein that alters the compaction of the chromatin fiber, increases the cellular sensitivity to ionizing radiation and the tumor burden of mice. The mortality and tumor burden of ionizing radiation-treated Hmgn1-/- mice is higher than that of their Hmgn1+/+ littermates. Hmgn1-/- fibroblasts have an altered G2-M checkpoint activation and are hy...

2012
Eriko Kage-Nakadai Hiroyuki Kobuna Osamu Funatsu Muneyoshi Otori Keiko Gengyo-Ando Sawako Yoshina Sayaka Hori Shohei Mitani

BACKGROUND Transgenic strains of Caenorhabditis elegans are typically generated by injecting DNA into the germline to form multi-copy extrachromosomal arrays. These transgenes are semi-stable and their expression is silenced in the germline. Mos1 transposon or microparticle bombardment methods have been developed to create single- or low-copy chromosomal integrated lines. Here we report an alte...

2017
Chunhua Yin Jiaqi Li Quan He Sisun Liu Linsheng He

Cervical cancer is one of the most prevalent malignancies in women, which has human papillomavirus infection as the major risk factor. Here we report the establishment of a new HPV-negative cervical cancer cell line and characterization of genetic alterations relevant to the pathogenesis of cervical cancer. A new cervical cancer cell line was established by extensive culture and natural selecti...

Journal: :Oncology reports 2007
Tibor Szarvas Ilona Kovalszky Katalin Bedi Attila Szendroi Attila Majoros Péter Riesz Tibor Füle Viktória László András Kiss Imre Romics

The accumulation of genetic alterations plays a role in the evolution of bladder cancer. These changes can be detected in the urine by DNA analysis of the cells exfoliated from the bladder wall enabling us to detect bladder cancer. The urine supernatant, besides the urine sediment, contains DNA, however in a much smaller amount. The origin of DNA in these two fractions is probably different. Ou...

2014
S. K. Arya A. Mukherjee

Sensitivity of common onion (Allium cepa L.) and faba bean (Vicia faba L.) to cadmium (Cd) stress was investigated using genotoxicity endpoints. Simultaneously, the antioxidative stress enzymes (guaiacol peroxidise and catalase) and lipid peroxidation [malonaldehyde (MDA) content] were investigated in the plants exposed to Cd in solution. The endpoints screened for genotoxicity included chromos...

Journal: :Forensic science international. Genetics 2011
Heather E LaSalle George Duncan Bruce McCord

The goal of this paper was to examine and compare two different commercially available approaches to the determination of the relative quantities of autosomal and Y chromosomal DNA using real-time PCR. One, Quantifiler(®) Duo, utilizes a TaqMan(®) assay with single copy probes for both autosomal human and Y quantification. The other method, Plexor HY(®) utilizes a primer quenching assay with mu...

Gourabi H Kalantari H Mohseni Meybodi A,

Background: Constitutional chromosome abnormalities are among the major contributors to the genetic causes of reproductive disorders. Despite all of worldwide efforts have been made so far, the prognosis for mosaic X chromosome aberration below 30% of unemployed has yet to be established. The purpose of this study was to assess the quantity and quiddity of chromosomal aberrations that may negat...

M. Salehi

Chromosomal abnormalities are major causes of infertility, miscarriage and birth of handicapped progeny. In human live births, the prevalence of a chromosome aberration is ?0.5% and, of these, 0.1–0.3% correspond to structural chromosome rearrangements such as translocations, inversions, insertions and deletions .Our proband is an infant who had died 4 hours after birth due to a variety of abno...

Ajinkya Jadhav, Krutika Patil, Premkumar Torane, Rukaiya Ansari, Vidya Bhairi, Yamini Jadhav,

Triploidy is a lethal chromosomal abnormality. Foetuses with triploid condition have a tendency to die in early conception and very few survive to term. In this study, we report the prenatal diagnosis of fetal triploidy with unexpected chromosomal translocation. A 27 years old women was referred to our clinical cytogenetic department due to history of previous conceptus with intrauterine growth...

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