Chromosomal Alterations: Origin and Significance with Contributions by Numerous Experts - gebunden oder broschiert

EAN (ISBN-13): 9783540578123
ISBN (ISBN-10): 3540578129
Gebundene Ausgabe
Erscheinungsjahr: 1000
Herausgeber: Springer

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ISBN/EAN: 3540578129

ISBN - alternative Schreibweisen:
3-540-57812-9, 978-3-540-57812-3
Alternative Schreibweisen und verwandte Suchbegriffe:
Titel des Buches: alteration

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Daten vom Verlag:

Autor/in: Günter Obe; Adayapalam T. Natarajan
Titel: Chromosomal Alterations - Origin and Significance
Verlag: Springer; Springer Berlin
402 Seiten
Erscheinungsjahr: 1994-07-22
Berlin; Heidelberg; DE
Gedruckt / Hergestellt in Deutschland.
Gewicht: 0,745 kg
Sprache: Englisch
85,55 € (DE)
87,95 € (AT)
106,60 CHF (CH)
Not available, publisher indicates OP

BB; Book; Hardcover, Softcover / Biologie/Mikrobiologie; Zellbiologie (Zytologie); Verstehen; mutation; Chromosomal Aberrations; genetics; cytogenetics; DNA; Chromosom; mutagenicity; chromosome; mutagen; Zytogenetik; Chromosomen; Chromosomenaberrationen; B; Cell Biology; Biomedical and Life Sciences; Zoology; Pharmacology/Toxicology; Human Genetics; Cancer Research; Zoologie und Tierwissenschaften; Pharmakologie; Genetik, Medizin; Onkologie; BC; EA

Radiation-Induced Formation of DNA Double-Strand Breaks in Plasmids and E.coli.- UV-induced pyrimidine monoadducts and their in vivo photofootprints.- Chromatin Structure, Hyperthermia and Repair of UV-Induced DNA Photolesions in Mammalian Cells.- An Inherited Homogeneously Staining Region Derived from a Long-Range Repeat Family in the House Mouse.- Detection of Genetic Imbalances in Tumor Genomes by Fluorescence in situ Hybridization with Tumor Genomic DNA and Subregional DNA Probes.- Fluorescent in situ hybridization (FISH) in cytogenetical studies.- The Use of Premature Chromosome Condensation and Chromosome Painting to Understand Chromosome Exchange Formation.- The Role of DNA Double-Strand-Break Rejoining in Chromosome Damage and Repair.- Investigations of Aberration Origins Using BrdUrd.- Elucidation of Some Factors Involved in the Formation of Chromosomal Aberrations by Inhibiting the Repair Polymerase.- Use of Antitopoisomerase Drugs to Study the Mechanisms of Induction of Chromosomal Damage.- Search for Perturbations induced by X-irradiation in the G2 Phase of Human Lymphocytes.- A Comparison of Radiation-Induced Aberrations in Human Cells Involving Early and Late Replicating X Chromosomes.- Radioprotective Chemicals as Tools for Studying Mechanisms of Radiation-Induced Chromosome Damage in Human Lymphocytes.- Factors Determining the Yields of Radiation-Induced Chromosomal Aberrations as Visualised by Means of Premature Chromosome Condensation in Interphase Cells.- Synergism and adaptive response in the interaction of low dose irradiation with subsequent mutagenic treatment in G2 phase human lymphocytes.- Responses of Radiosensitive Mutant Mammalian Cell Lines to Restriction Endonuclease induced DNA Double-Strand Breaks.- Quantitative Localization of Chromatid Breaks Induced by Alu I in the Long Arms of Chromosomes Number 1 of Chinese Hamster Ovary (CHO) Cells by Microphotometric Scanning.- “Life time” of AluI inside Glycerol-Induced Vesicles in CHO Cells.- Progress in Automatic Dicentric Hunting.- The Micronucleus Assay with Rodent Peripheral Blood and Acridine Orange Supravital Staining.- The Formation of Micronuclei after Exposure to Ionizing Radiation.- Excision Repaired Sites, Chromosome Breaks and Chromosome Loss Measured Simultaneously in Human Lymphocytes using the Cytokinesis Block Micronucleus Assay and Cytosine Arabinoside.- The Potential of FISH for Meiotic Segregation Analysis.- Reliable Chromosome Studies of Human Oocytes and Spermatozoa using the Gradual Fixation-Air Drying (GF-AD) Method.- Nondisjunction by Failures in the Molecular Control of Oocyte Maturation.- Cytogenetic and Molecular Investigations in Chromosomal Instability Syndromes.- Distributions of Spontaneous Chromosomal Aberrations and of Spontaneous and Induced SCE and Micronuclei in Peripheral Lymphocytes from a Human Population.- Does the Genetic Deficiency in ALDH2 Determine the Alcohol-Drinking Behavior and the Induction of Chromosome Alterations in Peripheral Lymphocytes by Alcohol?.- Variability of chromosomal alterations in human peripheral lymphocytes of smokers and nonsmokers.- Chromosome analysis in accidental, occupational and environmental radiation exposure.- New Approaches to Design and Interpretation of in vitro Chromosomal Aberration Tests.- Comments on Short-Term Cytogenetic Assays for Screening of Environmental Chemical Carcinogens.- Localized Chromosomal Aberrations in the Heterochromatic q Arm of the X Chromosome in V79 Chinese hamster cells and the Implications for Industrial in vitro Cytogenetic Screening.- Cytogenetic Studies in Laboratory Animals Exposed by Inhalation to Mainstream Smoke or Environmental Tobacco Smoke.- Evolutionary Aspects of Structural Chromosome Aberrations.