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Titlebook: DNA Repair Mechanisms and Their Biological Implications in Mammalian Cells; Muriel W. Lambert,Jacques Laval Book 1989 Springer Science+Bus

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書(shū)目名稱(chēng)DNA Repair Mechanisms and Their Biological Implications in Mammalian Cells
編輯Muriel W. Lambert,Jacques Laval
視頻videohttp://file.papertrans.cn/261/260178/260178.mp4
叢書(shū)名稱(chēng)NATO Science Series A:
圖書(shū)封面Titlebook: DNA Repair Mechanisms and Their Biological Implications in Mammalian Cells;  Muriel W. Lambert,Jacques Laval Book 1989 Springer Science+Bus
描述This volume contains edited contributions from the speakers at the NATO Advanced Research Workshop on "DNA Repair Mechanisms and Their Biological Implications in Mammalian Cells" held October 1-6, 1988, at the Abbaye Royale de Fontevraud, Fontevraud France. The meeting was dedicated to Paul Howard-Flanders (Yale University, New Haven, CT. , 1919-1988), whose seminal con- tributions to the DNA repair field include the cO-discovery of the excision repair pathway, the elucidation of post-repli- cation repair in E. coli, the isolation of the lexA and recC mutants, and his extensive work on the enzymology of RecA. A plethora of recent developments in DNA repair mechan- isms and related processes in mammalian cells have advanced our understanding of this field in a number of different areas and have given new emphasis to the ways these systems both resemble DNA repair processes in other groups of organisms in some respects yet are strikingly different from them in others. Within the past decade there have been a number of international conferences on DNA damage and repair mechanisms but none has been focused on these processes in mammalian cells.
出版日期Book 1989
關(guān)鍵詞DNA; DNA damage; Nucleotide; Purine; Pyrimidine; biological; cells; computed tomography (CT); development; en
版次1
doihttps://doi.org/10.1007/978-1-4684-1327-4
isbn_softcover978-1-4684-1329-8
isbn_ebook978-1-4684-1327-4
copyrightSpringer Science+Business Media New York 1989
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https://doi.org/10.1007/978-3-319-58121-7icipate in the excision of AP sites. In fact, we know a single class of AP endonucleases; these enzymes hydrolyze the C.-O-P bond 5′ to AP sites and the resulting nicks are limited by 3′-OH and 5′-phosphate ends.
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Book 1989ications in Mammalian Cells" held October 1-6, 1988, at the Abbaye Royale de Fontevraud, Fontevraud France. The meeting was dedicated to Paul Howard-Flanders (Yale University, New Haven, CT. , 1919-1988), whose seminal con- tributions to the DNA repair field include the cO-discovery of the excision
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Art, Literature, and Passions of the Skiesormal human cells are Mex. but may become Mex. following transformation .. Thus, the phenotype is important from the practical viewpoint of chemotherapy, as well as a more fundamental one of understanding the events which occur during cellular transformation.
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Investigation of Sequence Specificity in DNA Alkylation and Repair Using Oligodeoxynucleotide Substrethylguanine from DNA and is usually referred to as 3-alkyladenine DNA glycosylase (Margison and Pegg, 1981; Gallagher and Brent, 1984; Male, et al., 1985, 1987). This glycosylase clearly plays a major role in the loss of the N-alkyl purines, which make up the bulk of the DNA base adducts.
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Women, Subject Choice and Employment,at the C8 position. These observations suggest that the Fapy-DNA glycosylase may have a broad substrate specificity which includes all imidazole ring-opened purines modified at the N7 or C8 position in DNA.
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