نتایج جستجو برای: induced mutation

تعداد نتایج: 1234912  

2004
K. B. Anjaria B. S. Rao

The potentiating effect of tumour promoter anthralin on gamma radiation and 4-Nitroquinoline 1oxide (4-NQO) induced gene conversion and back mutation was studied using diploid yeast Saccharomyces cerevisiae D7. Cells were exposed to 20-400 Gy of gamma radiation and plated on media without anthralin or containing 0.0510 mg/ml of anthralin. In another set of experiments, cells were treated with 0...

Journal: :Mutagenesis 2008
Akshay K Ahuja Ruth C Barber Robert J Hardwick Michael M Weil Paula C Genik David J Brenner Yuri E Dubrova

Using single-molecule polymerase chain reaction, the frequency of spontaneous and radiation-induced mutation at an expanded simple tandem repeat (ESTR) locus was studied in DNA samples extracted from sperm and bone marrow of Atm knockout (Atm(+/-)) heterozygous male mice. The frequency of spontaneous mutation in sperm and bone marrow in Atm(+/-) males did not significantly differ from that in w...

Journal: :Cancer research 2007
Laurent Miccoli Karen L-A Burr Peter Hickenbotham Errol C Friedberg Jaime F Angulo Yuri E Dubrova

Spontaneous and induced mutation rates at two expanded simple tandem repeat (ESTR) loci were studied in the germ line of xeroderma pigmentosum group C (Xpc) knockout mice defective in global genome nucleotide excision repair. Spontaneous and radiation-induced mutation rates in homozygous Xpc(-/-) males were significantly higher than those in isogenic wild-type (Xpc(+/+)) and heterozygous (Xpc(+...

Journal: :Toxicology in vitro : an international journal published in association with BIBRA 1991
H Stopper M Metzler

In addition to hormonal activity, genetic damage has been proposed as an important factor in oestrogen-mediated carcinogenesis. However, as short-term tests for oestrogens usually fail to show DNA mutations, lesions other than classic nuclear DNA mutation have to be considered. Oestrogen-induced mitochondrial damage was studied in the yeast Saccharomyces cerevisiae. Stilbene-type, but not stero...

Journal: :Stem cells 2012
Junfeng Ji Siemon H Ng Vivek Sharma Dante Neculai Samer Hussein Michelle Sam Quang Trinh George M Church John D McPherson Andras Nagy Nizar N Batada

Mutations in human induced pluripotent stem cells (iPSCs) pose a risk for their clinical use due to preferential reprogramming of mutated founder cell and selection of mutations during maintenance of iPSCs in cell culture. It is unknown, however, if mutations in iPSCs are due to stress associated with oncogene expression during reprogramming. We performed whole exome sequencing of human foreski...

Journal: :Carcinogenesis 1996
Y Omori V Krutovskikh N Mironov H Tsuda H Yamasaki

Cx32 is a major gap junction protein of the liver and is often aberrantly expressed in liver tumours. We have studied mutation of the Cx32 gene during chemically induced hepatocarcinogenesis. DNA from 12 rat liver tumours induced by diethylnitrosamine or N-ethyl-N-hydroxyethylnitrosamine (EHEN) was analysed by the PCR/SSCP method. One tumour induced by EHEN harboured a G--> A transition mutatio...

A. Karami, A. Khalilpoor F. Biramijamal M. Eshraghi M. Ghanei S. Arjmand

Objective Mustard gas (MG) is a poisoning chemical, mutagenic and carcinogenic alkylating agent. It is used during World War I and also Iran-Iraq conflict. The p53 tumor suppressor gene is involved in the pathogenesis of malignant disease. The aim of this study is to determine possible mutation in p53 gene of lung sample from mustard gas exposed patients. Material and Methods Twelve lung bio...

Jalali, Hossein, Mahdavi, Mohammad Reza , Shekarriz, Ramin,

Background and purpose: 5-Flourouracil (5-FU) is one of the most common chemical drugs used in chemotherapy of patients with cancers. Dihydropyrimidine dehydrogenase (DPD) is a critical enzyme in the catabolism of 5-FU. More than 80% of the administered 5-FU is catabolized by DPD. c.1905+1G>A mutation on DPD gene is the most important mutation associated with DPD enzymatic deficiency which lead...

abdi rad, isa, bagheri, morteza, Kavosi, Negin, khadem vatani, kamal, Mohammad Zad, Mir Hossein Seyed, rahimi, Behzad, Rostamzadeh, Alireza,

Background & Aims: Recent studies have shown that some of the MEFV gene mutations are common in patients with coronary artery disease. The present study was designed to investigate the presence or absence of E148Q mutation in exon 2 of MEFV gene in patients with premature coronary artery disease. Materials & Methods: In this study, 90 patients with coronary artery disease were voluntarily sele...

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