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| BASE EXCISION REPAIR, 68
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Kivie Moldave, Department of Molecular Biology and Biochemistry, University of California, Irvine, California, U.S.A.
Sankar Mitra, University of Texas Medical Branch, Galveston, U.S.A.
Amanda McCullough, University of Texas Medical Branch, Galveston, U.S.A.
R. Lloyd, University of Texas Medical Branch, Galveston, U.S.A.
Samuel Wilson, NIEHS, NIH, Research Triangle Park, North Carolina, U.S.A.
Description
This volume of Progress in Nucleic Acid Research and Molecular Biology represents research discussed during the DNA Base
Excision Repair Workshop. This compilation of articles focuses on several recent observations highlighting the complexity of the base
excision repair (BER) process in DNA repair. Focusing on the various facets of BER research, this book is a timely and highly beneficial
reference for investigators in the DNA repair field. It will also aid scientists not directly involved in repair studies to obtain a
comprehensive understanding of the current state of knowledge in the field.
Progress in Nucleic Acid Research and Molecular
Biology provides a forum for discussion of new discoveries, approaches, and ideas in molecular biology. It contains contributions
from leaders in their fields and abundant references.
Audience
Researchers in biochemistry, molecular biology, genetics, and cell biology.
Contents
Preface.
Keynote Address: Past, Present, and Future Aspects of Base Excision Repair.
Multiple Pathways for DNA Base Excision
Repair:
Foreward.
The Switch Mechanism among Multiple BER Pathways.
Yeast Base Excision Repair: Interconnections and Networks.
BER, MGMT, and MMR in Defense Against
Alkylation-Induced Genotoxicity and Apoptosis.
Gene Targeting in the Mouse for Elucidating
the Role of BER:
Foreward.
Mammalian DNA b-Polymerase in Base Excision Repair
of Alkylation Damage.
Regulation of Intracellular
Localization of Human MTH1, OGG1 and MYH Proteins for Repair of Oxidative DNA Damage.
Repair of 8-Oxoguanine and OGG1-Incised Apurinic
Sites In a CHO Cell Line.
Mammalian OGG1/MMH Gene Plays a Major Role for Repair of the 8-hydroxyguanine Lesion in DNA.
Complexities
of BER:
Foreward.
Molecular Mechanism of PCNA-Dependent Base Excision Repair.
Factors Influencing the Removal of Thymine Glycol
from DNA in y-Irradiated Human Cells.
Completion of Base Excision Repair by Mammalian
DNA Ligases.
Uracil-Initiated Base Excision DNA
Repair Synthesis Fidelity In Human Colon Adenocarcinoma LoVo and Escherichia coli Cell Extracts.
DNA Glycosylases:
Specificity and Mechanisms:
Foreward.
Multiple DNA Glycosylases for Repair of 8-Oxoguanine and Their Potential In Vivo
Functions.
DNA Substrates Containing Defined Oxidative Base Lesions and
Their Application to Study Substrate Specificities of Base Excision
Repair Enzymes.
Mechanism of Action of E. coli Formamidopyrimidine N-Glycosylase: Role of K155 in Substrate Binding and Product
Release.
Thymine DNA Glycosylase.
Mitochondrial BER:
Foreward.
Crystallizing Thoughts about DNA Base Excision Repair.
DNA Damage Recognition, and Repair Pathway Coordination Revealed by the Structural Biochemistry of DNA Repair Enzymes.
Potential Double
Flipping Mechanism by E. coli MutY.
Properties and Functions of Human Uracil-DNA Glycosylase From the UNG Gene.
Index.
| Bibliographic details |
Hardbound, 403 pages, publication date: AUG-2001
ISBN-13: 978-0-12-540068-8
ISBN-10: 0-12-540068-3
Imprint: ACADEMIC PRESS
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EUR 106.95
GBP 90.99
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Last update: 3 Oct 2009
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