نتایج جستجو برای: miscoding

تعداد نتایج: 222  

Journal: :Cancer research 1996
J Nair H Sone M Nagao A Barbin H Bartsch

Formation of etheno-DNA adducts in the liver was investigated in Long Evans cinnamon (LEC) rats, a Long Evans strain with hereditary abnormal copper metabolism, which develop spontaneous hepatitis and later hepatocellular carcinoma. Using an ultrasensitive immunoaffinity/32P-postlabeling assay (J. Nair et al., Carcinogenesis, 16: 613-617, 1995), the etheno adducts 1,N6-ethenodeoxyadenosine (eps...

2006
Dana T. Minnick Martina L. Veigl David Sedwick

The mutational specificity of the alkylating agent l-3-bis-(2-chloroethyl)-l-nitrosourea (BCNU) »as analyzed at the endogenous hemizygous (alenine phosphoribosyl transferase gene of the Chinese hamster ovary cell line D422. A 1-h treatment of the Chinese hamster ovary cells with 50 UM BCNU resulted in a toxicity level of 62% and induced mutation at this target with a frequency of 32.1 mutants/...

2014
Natallia Shved Cordula Haas Christina Papageorgopoulou Guelfirde Akguel Katja Paulsen Abigail Bouwman Christina Warinner Frank Rühli Oliver Schildgen

Mummified human tissues are of great interest in forensics and biomolecular archaeology. The aim of this study was to analyse post mortem DNA alterations in soft tissues in order to improve our knowledge of the patterns of DNA degradation that occur during salt mummification. In this study, the lower limb of a female human donor was amputated within 24 h post mortem and mummified using a proces...

Journal: :Nucleic Acids Research 2006
Giovanni Maga Igor Shevelev Giuseppe Villani Silvio Spadari Ulrich Hübscher

DNA polymerase lambda (pol lambda) is a member of the X family DNA polymerases and is endowed with multiple enzymatic activities. In this work we investigated the in vitro miscoding properties of full-length, human pol lambda either in the absence or in the presence of the human auxiliary proteins proliferating cell nuclear antigen (PCNA) and replication protein A (RP-A). Our data suggested tha...

Journal: :The Biochemical journal 2003
Agnieszka M Maciejewska Katarzyna D Lichota Jarosław T Kuśmierek

Assuming that the efficiency of the incorporation of 5-methyl-2'-deoxyisocytosine-5' triphosphate (dMiCTP) and dTTP opposite isoguanine (iG) is a measure of the proportion of the keto and enol tautomers of iG in the Thermus aquaticus DNA polymerase active centre, we studied the influence of temperature and iG-neighbouring bases in the template on base-pairing of iG. On the basis of experiments ...

Journal: :Journal of Carcinogenesis 2006
Gulam Waris Haseeb Ahsan

Oxygen derived species such as superoxide radical, hydrogen peroxide, singlet oxygen and hydroxyl radical are well known to be cytotoxic and have been implicated in the etiology of a wide array of human diseases, including cancer. Various carcinogens may also partly exert their effect by generating reactive oxygen species (ROS) during their metabolism. Oxidative damage to cellular DNA can lead ...

Journal: :Mechanisms of Ageing and Development 2015
Jennifer Baur Maria Moreno-Villanueva Tobias Kötter Thilo Sindlinger Alexander Bürkle Michael R. Berthold Michael Junk

Databases are an organized collection of data and necessary to investigate a wide spectrum of research questions. For data evaluation analyzers should be aware of possible data quality problems that can compromise results validity. Therefore data cleaning is an essential part of the data management process, which deals with the identification and correction of errors in order to improve data qu...

2013
Eleonora Turco Ilenia Ventura Anna Minoprio Maria Teresa Russo Paola Torreri Paolo Degan Sara Molatore Guglielmina Nadia Ranzani Margherita Bignami Filomena Mazzei

The MUTYH DNA-glycosylase is indirectly engaged in the repair of the miscoding 7,8-dihydro-8-oxo-2'-deoxyguanine (8-oxodG) lesion by removing adenine erroneously incorporated opposite the oxidized purine. Inherited biallelic mutations in the MUTYH gene are responsible for a recessive syndrome, the MUTYH-associated polyposis (MAP), which confers an increased risk of colorectal cancer. In this st...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Jiqiang Ling Hervé Roy Daoming Qin Mary Anne T Rubio Juan D Alfonzo Kurt Fredrick Michael Ibba

Human mitochondrial tRNA (hmt-tRNA) mutations are associated with a variety of diseases including mitochondrial myopathies, diabetes, encephalopathies, and deafness. Because the current understanding of the precise molecular mechanisms of these mutations is limited, there is no efficient method to treat their associated mitochondrial diseases. Here, we use a variety of known mutations in hmt-tR...

2012
Cathrine Fladeby Erik Sebastian Vik Jon K. Laerdahl Christine Gran Neurauter Julie E. Heggelund Eirik Thorgaard Pernille Strøm-Andersen Magnar Bjørås Bjørn Dalhus Ingrun Alseth

Loss of amino groups from adenines in DNA results in the formation of hypoxanthine (Hx) bases with miscoding properties. The primary enzyme in Escherichia coli for DNA repair initiation at deaminated adenine is endonuclease V (endoV), encoded by the nfi gene, which cleaves the second phosphodiester bond 3' of an Hx lesion. Endonuclease V orthologs are widespread in nature and belong to a family...

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