GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Online Resource
    Online Resource
    Saint Louis :Elsevier Science & Technology,
    Keywords: Mitosis -- Regulation. ; Meiosis. ; Molecular biology. ; Electronic books.
    Description / Table of Contents: Molecular Regulation of Nuclear Events in Mitosis and Meiosis presents papers from researchers in various fields engaged in the scientific study of molecular mechanisms involved in the control of nuclear events in meiotic and mitotic cell activity. Various articles in the book discuss a wide range of topics such as the development of cytoplasmic activities that control chromosome cycles during maturation of amphibian oocytes; dynamics of the nuclear lamina during mitosis and meiosis; role of protein phosphorylation in xenopus oocyte meiotic maturation; and cell cycle studies of histone modifications. Molecular and cell biologists, oncologists, and biochemists will find the book invaluable.
    Type of Medium: Online Resource
    Pages: 1 online resource (390 pages)
    Edition: 1st ed.
    ISBN: 9781483272702
    DDC: 574.87623
    Language: English
    Note: Front Cover -- Molecular Regulation of Nuclear Events in Mitosis and Meiosis -- Copyright Page -- Table of Contents -- Preface -- Chapter 1. Development of Cytoplasmic Activities That Control Chromosome Cycles during Maturation of Amphibian Oocytes -- I. INTRODUCTION -- II. OOCYTE MATURATION -- III. MATURATION-PROMOTING FACTOR (MPF) -- IV. CYTOSTATIC FACTOR (CSF) -- V. CONCLUDING REMARKS -- ACKNOWLEDGMENTS -- REFERENCES -- Chapter 2. Dynamics of the Nuclear Lamina during Mitosis and Meiosis -- I. INTRODUCTION -- II. DYNAMICS OF THE NUCLEAR LAMINA IN MITOSIS -- III. DYNAMICS OF THE NUCLEAR LAMINA DURING MEIOTIC PROPHASE -- IV. DYNAMICS OF THE NUCLEAR LAMINA DURING EGG MATURATION AND EARLY DEVELOPMENT -- V. COMPARISON OF THE DYNAMICS OF THE NUCLEAR LAMINA DURING MITOSIS AND MEIOSIS -- ACKNOWLEDGMENTS -- REFERENCES -- Chapter 3. Regulation of Nuclear Formation and Breakdown in Cell-Free Extracts of Amphibian Eggs -- I. INTRODUCTION -- IL REGULATION OF PRONUCLEAR FORMATION -- III. REGULATION OF CHROMOSOME CONDENSATION -- IV. THE ROLE OF MPF, Ca2+ IONS, AND PROTEINPHOSPHORYLATION IN CONTROLLING NUCLEAR ENVELOPE BREAKDOWN, CHROMOSOME CONDENSATION, AND SPINDLE ASSEMBLY IN CELL-FREE EXTRACTS -- V. SUMMARY -- ACKNOWLEDGMENTS -- REFERENCES -- Chapter 4. Role of Protein Phosphorylation in Xenopus Oocyte Meiotic Maturation -- I. INTRODUCTION -- II. MATURATION-INHIBITING PHOSPHOPROTEINS (Mp-P) AND cAMP -- III. PROTEIN PHOSPHORYLATION AND MATURATION-PROMOTING FACTOR (MPF) ACTIVITY -- IV. CONCLUSIONS -- ACKNOWLEDGMENTS -- REFERENCES -- Chapter 5. Maintenance of Oocyte Meiotic Arrest by Follicular Fluid Factors -- I. INTRODUCTION -- II. CHARACTERIZATION OF FOLLICULAR FLUID OOCYTE MATURATION INHIBITOR (OMI) BY USE OF ISOLATED MAMMALIAN OOCYTES. , III. HYPOXANTHINE IN PIG FOLLICULAR FLUID AS THE PRINCIPAL INHIBITOR OF MOUSE OOCYTE MATURATION AND THE PREVENTION OF FOLLICLE STIMULATING HORMONE (FSH) REVERSAL OF cAMP-MAINTAINED MEIOTIC ARREST -- IV. ASSAY FOR AND CHARACTERIZATION OF HUMAN FOLLICULAR FLUID OMI BY USE OF OOCYTES FROM THE AMPHIBIAN , XENOPUS LAEVIS -- V. FAILURE TO INHIBIT XENOPUS OOCYTE MATURATION BY USE OF EXOGENOUS HYPOXANTHINE IN COMBINATION WITH N6,2' -O-DIBUTYRYL-cAMP (Bt2-CYCLIC AMP) -- VI. HOW DO THE INHIBITORY FACTORS PRESENT IN FOLLICULAR FLUID MAINTAIN MEIOTIC ARREST IN OOCYTES? -- VII. CONCLUSIONS -- ACKNOWLEDGMENTS -- REFERENCES -- Chapter 6. Regulation of Chromatin Condensation and Decondensation in Sea Urchin Pronuclei -- I. INTRODUCTION -- II. MITOTIC AND PREMATURE CHROMOSOME CONDENSATION -- III. MALE PRONUCLEAR DECONDENSATION -- IV. CONCLUSIONS -- ADDENDUM -- ACKNOWLEDGMENTS -- REFERENCES -- Chapter 7. Regulation of Mitosis by Nonhistone Protein Factors in Mammalian Cells -- I. INTRODUCTION -- II. THE MITOTIC FACTORS -- III. INHIBITORS OF THE MITOTIC FACTORS -- IV. ROLE OF PROTEIN PHOSPHORYLATION AND DEPHOSPHORYLATION IN THE REGULATION OF NUCLEAR EVENTS ASSOCIATED WITH MITOSIS AND MEIOSIS -- V. CONCLUSIONS -- ACKNOWLEDGMENTS -- REFERENCES -- Chapter 8. Mitosis-Specific Cytoplasmic Protein Kinases -- I. INTRODUCTION -- II. IDENTIFICATION OF PROTEIN KINASES IN CELLULAR EXTRACTS -- III. CELL CYCLE SPECIFICITY OF KINASE ACTIVITIES -- IV. COMPARISON OF KINASE ACTIVITIES WITH PROTEIN KINASES IMPLICATED IN MITOTIC EVENTS -- V. COMPARISON OF KINASE ACTIVITIES WITH MITOTIC FACTORS -- VI. CONCLUSIONS AND PERSPECTIVES -- ACKNOWLEDGMENTS -- REFERENCES -- Chapter 9. Antibodies to Mitosis-Specific Phosphoproteins -- I. INTRODUCTION -- II. MONOCLONAL ANTIBODIES TO CELLS IN MITOSIS -- III. CHARACTERIZATION OF ANTIGENS REACTIVE WITH MPM-1 AND MPM-2. , IV. CYTOLOGICAL LOCALIZATION OF ANTIGENS REACTIVE WITH MPM-1 AND MPM-2 -- V. BIOLOGICAL ACTIVITY OF MPM-1 AND MPM-2 ANTIBODIES -- VI. DISCUSSION -- REFERENCES -- Chapter 10. Mitosis-Specific Protein Phosphorylation Associated with Premature Chromosome Condensation in a ts Cell Cycle Mutant -- I. INTRODUCTION -- II. ISOLATION AND PRELIMINARY CHARACTERIZATIONOF THE tsBN2 CELL LINE -- III. INDUCTION OF PREMATURE CHROMOSOME CONDENSATION (PCC) IN tsBN2 CELLS AT THE NONPERMISSIVE TEMPERATURE -- IV. INDUCTION OF MITOSIS-SPECIFIC PHOSPHORYLATION IN tsBN2 CELLS BY TEMPERATURE SHIFT -- V. NEWLY SYNTHESIZED PROTEIN(S) IN tsBN2 CELLS SHOWING PCC -- VI. DISCUSSION -- ACKNOWLEDGMENTS -- REFERENCES -- Chapter 11. Chromatin Structure and Histone Modifications through Mitosis in Plasmodia of Physarum polycephalum -- I. INTRODUCTION -- II. CHROMATIN STRUCTURE AND ORGANIZATION -- III. CONTROL OF CHROMOSOME CONDENSATION -- IV. CELL CYCLE STUDIES OF HISTONE MODIFICATIONS -- V. HISTONE H1° -- VI. HISTONE H1 KINASES -- VII. DISCUSSION -- ACKNOWLEDGMENTS -- REFERENCES -- Index.
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 30 (1991), S. 7754-7758 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Biochemistry 28 (1989), S. 6943-6949 
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 1520-4995
    Source: ACS Legacy Archives
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Molecular biology reports 6 (1980), S. 115-118 
    ISSN: 1573-4978
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract It has been previously demonstrated that nucleosome repeat lengths change during avian erythroid development and that repeat lengths correlate with histone H5 levels. Chromatin condensation also occurs during this process. In order to further investigate the relationship between histone H5 and/or chromatin condensation and nucleosome structure, repeat lengths were examined duringin vitro differentiation of mouse erythroleukemia cells in which chromation condensation occurs but in which histone H5 is absent. Our finding that repeat lengths do not change during this process supports the hypothesis that H5 plays a role in the mechanism which determines nucleosome repeat lengths.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Bioscience reports 9 (1989), S. 623-633 
    ISSN: 1573-4935
    Keywords: cell fusion ; erythrocyte membrane ; phospholipid asymmetry ; phospholipid packing ; phosphatidylserine ; polyethylene glycol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Phospholipid packing has been suggested as a relevant variable in the control of membrane fusion events. To test this possibility in a model system, a comparison was made of the fusability of erythrocytes with a normal asymmetric transbilayer distribution of plasma membrane phospholipids (tightly packed exterior lipids) and erythrocytes with a symmetric transbilayer distribution of phospholipids (more loosely packed exterior lipids), using polyethylene glycol as fusogen. Not only were lipid-symmetric cells more readily fused, but fusions of mixtures of lipid-symmetric and lipid-asymmetric cells indicated that both fusing partners must have a symmetric distribution for fusion to be enhanced. Lipid-symmetric cells may fuse more readily because loose packing of the exterior lipids enhances hydrophobic interactions between cells. Alternatively, enhanced membrane fluidity may facilitate intramembranous particle clustering, previously implicated as a potentiator of fusion. Finally, exposure of phosphatidylserine on the surface of lipid-symmetric erythrocytes may be responsible for their enhanced fusion.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 126 (1986), S. 53-59 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Staining of sickle cells with the fluorescent probes chlortetracycline (a Ca2+probe) and diindocarbocyanine (a general membrane probe) revealed the presence of Ca2+-containing vesicles which are not found in normal erythrocytes. These vesicles increase in number upon deoxygenation, and are apparently formed by endocytosis, as judged by the use of the extracellular fluorescent probe lucifer yellow. The presence of vesicles is not restricted to any particular morphological or density class of cells in the general population.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Cellular Physiology 123 (1985), S. 209-214 
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: Using phospholipase digestion and the fluorescent probe merocyanine 540 the maintenance of phospholipid asymmetry in the plasma membrane of human erythrocyte ghosts was investigated. Digestion with phospholipase A2 indicated that ghosts prepare in the presence of Mg++ as the only divalent cation retained the normal phospholipid asymmetry characteristic of intact erythrocytes. These ghosts, like normal erythrocytes, also failed to stain with merocyanine 540. However, the presence of as little as 5-10 μM Ca++ during ghost preparation resulted in ghosts in which lipid asymmetry had been abolished, as indicated by phospholipase digestion. Moreover, these ghosts stained with merocyanine 540. In contrast to ghosts, intact erythrocytes treated with ionophore required millimolar levels of Ca++ ions to disrupt membrane lipid asymmetry. To discover the reason for this difference in behavior between ghosts and intact cells, ghosts were prepared from preswollen cells using only small volumes of buffer for lysis. These experiments demonstrated that as the cellular contents of erythrocytes are diluted, the asymmetric arrangement of phospholipids becomes more sensitive to disruption by Ca++.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...