ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

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
    Publication Date: 2016-01-06
    Description: A diffusion model for the coordination of DNA replication in 〈i〉Schizosaccharomyces pombe〈/i〉 Scientific Reports, Published online: 5 January 2016; doi:10.1038/srep18757
    Electronic ISSN: 2045-2322
    Topics: Natural Sciences in General
    Published by Springer Nature
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    facet.materialart.
    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2000-09-23
    Description: In this month's essay, Paul Nurse recapitulates the ontogeny of one of the most important theories in the history of biology, the cell theory, which proposes that all forms of life are composed of cells. Along the way, he lays out the wondrous molecular complexities and processes that he and others have discovered in the course of their studies of the lives of cells. In particular, Nurse focuses on the mechanisms and controls of cell reproduction that ultimately allow growth, development, and evolution to occur.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nurse, P -- New York, N.Y. -- Science. 2000 Sep 8;289(5485):1711-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Imperial Cancer Research Fund, London, UK.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11001740" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Apoptosis ; Biological Evolution ; Catalysis ; Cell Biology/*history ; *Cell Cycle ; Cell Division ; *Cell Physiological Phenomena ; DNA Replication ; Energy Metabolism ; Enzymes/metabolism ; Genes ; History, 17th Century ; History, 18th Century ; History, 19th Century ; History, 20th Century ; Humans ; Neoplasms/genetics/pathology ; Organelles/metabolism ; Signal Transduction
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    facet.materialart.
    Unknown
    American Association for the Advancement of Science (AAAS)
    Publication Date: 2001-02-24
    Description: A cell ensures that its genome is replicated only once during its division cycle through a process called licensing. In an enlightening Perspective, Lygerou and Nurse explain how binding of the Geminin protein to Cdt1 blocks the binding of licensing factors to chromatin, inhibiting the onset of S phase (Wohlschlegel et al.).〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lygerou, Z -- Nurse, P -- New York, N.Y. -- Science. 2000 Dec 22;290(5500):2271-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of General Biology, School of Medicine, University of Patras, 26110 Rio, Patras, Greece. z_lygerou@yahoo.com〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11188727" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; *Cell Cycle ; Cell Cycle Proteins/chemistry/*metabolism/pharmacology ; Cell Nucleus/metabolism ; Chromatin/*metabolism ; DNA Damage ; DNA Helicases/metabolism ; *DNA Replication/drug effects ; DNA-Binding Proteins/chemistry/*metabolism ; Evolution, Molecular ; Geminin ; Humans ; Interphase ; Metaphase ; Mitosis ; Models, Biological ; Origin Recognition Complex ; S Phase ; Xenopus ; Xenopus Proteins
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    facet.materialart.
    Unknown
    Nature Publishing Group (NPG)
    Publication Date: 2008-07-25
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nurse, Paul -- England -- Nature. 2008 Jul 24;454(7203):424-6. doi: 10.1038/454424a.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Rockefeller University, 1230 York Avenue, New York, New York 10065, USA. nurse@mail.rockefeller.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18650911" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Science Disciplines/education/*methods/trends ; Humans ; *Information Science/methods/trends ; *Logic ; Models, Biological
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Publication Date: 2009-05-29
    Description: Many eukaryotic cell types undergo size-dependent cell cycle transitions controlled by the ubiquitous cyclin-dependent kinase Cdk1 (refs 1-4). The proteins that control Cdk1 activity are well described but their links with mechanisms monitoring cell size remain elusive. In the fission yeast Schizosaccharomyces pombe, cells enter mitosis and divide at a defined and reproducible size owing to the regulated activity of Cdk1 (refs 2, 3). Here we show that the cell polarity protein kinase Pom1, which localizes to cell ends, regulates a signalling network that contributes to the control of mitotic entry. This network is located at cortical nodes in the middle of interphase cells, and these nodes contain the Cdk1 inhibitor Wee1, the Wee1-inhibitory kinases Cdr1 (also known as Nim1) and Cdr2, and the anillin-like protein Mid1. Cdr2 establishes the hierarchical localization of other proteins in the nodes, and receives negative regulatory signals from Pom1. Pom1 forms a polar gradient extending from the cell ends towards the cell middle and acts as a dose-dependent inhibitor of mitotic entry, working through the Cdr2 pathway. As cells elongate, Pom1 levels decrease at the cell middle, leading to mitotic entry. We propose that the Pom1 polar gradient and the medial cortical nodes generate information about cell size and coordinate this with mitotic entry by regulating Cdk1 through Pom1, Cdr2, Cdr1 and Wee1.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Moseley, James B -- Mayeux, Adeline -- Paoletti, Anne -- Nurse, Paul -- England -- Nature. 2009 Jun 11;459(7248):857-60. doi: 10.1038/nature08074. Epub 2009 May 27.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉The Rockefeller University, New York, New York 10065, USA. jmoseley@rockefeller.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/19474789" target="_blank"〉PubMed〈/a〉
    Keywords: CDC2 Protein Kinase/antagonists & inhibitors/metabolism ; Cell Cycle Proteins/antagonists & inhibitors/metabolism ; *Cell Polarity ; Interphase ; *Mitosis ; Nuclear Proteins/antagonists & inhibitors/metabolism ; Phosphorylation ; Protein Kinases/*metabolism ; Protein Transport ; Protein-Serine-Threonine Kinases/metabolism ; Protein-Tyrosine Kinases/antagonists & inhibitors/metabolism ; Schizosaccharomyces/*cytology/*metabolism ; Schizosaccharomyces pombe Proteins/antagonists & inhibitors/metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Publication Date: 1990-12-14
    Description: The onset of M phase requires the activation of the pp34 protein kinase in all eukaryotes thus far examined. In Schizosaccharomyces pombe, pp34 is phosphorylated on Tyr15, and dephosphorylation of this residue regulates the initiation of mitosis. In this study, it is shown that dephosphorylation of Tyr15 triggered activation of the pp34-cyclin complex from fission yeast, that a human protein-tyrosine phosphatase can catalyze this event both in vitro and in vivo, and that activation of fission yeast pp34 does not require threonine dephosphorylation. The complementary DNA that encoded the tyrosine phosphatase replaced the mitotic activator p80cdc25, closely associating the cdc25(+)-activating pathway with tyrosine dephosphorylation of pp34.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Gould, K L -- Moreno, S -- Tonks, N K -- Nurse, P -- New York, N.Y. -- Science. 1990 Dec 14;250(4987):1573-6.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry, University of Oxford, United Kingdom.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/1703321" target="_blank"〉PubMed〈/a〉
    Keywords: *Cell Cycle Proteins ; Cyclins/metabolism ; Enzyme Activation ; Fungal Proteins/*metabolism ; Humans ; *Mitosis ; Mutation ; Phosphoprotein Phosphatases/genetics/*metabolism ; Phosphorylation ; Phosphotyrosine ; Protein Kinases/*metabolism ; Protein Tyrosine Phosphatases ; Schizosaccharomyces/genetics/*metabolism ; Transformation, Genetic ; Tyrosine/analogs & derivatives/metabolism ; *ras-GRF1
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Publication Date: 2005-07-09
    Description: Fission yeast (Schizosaccharomyces pombe) cells grow longitudinally in a manner dependent on a polarized distribution of their interphase microtubules. We found that this distribution required sliding of microtubules toward the cell center along preexisting microtubules. This sliding was mediated by the minus end-directed kinesin motor Klp2, which helped microtubules to become properly organized with plus ends predominantly oriented toward the cell ends and minus ends toward the cell center. Thus, interphase microtubules in the fission yeast require motor activities for their proper organization.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Carazo-Salas, Rafael E -- Antony, Claude -- Nurse, Paul -- New York, N.Y. -- Science. 2005 Jul 8;309(5732):297-300.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cell Cycle Laboratory, 44 Lincoln's Inn Fields, Cancer Research UK, London Research Institute, WC2A 1PX, UK. carazo01@cancer.org.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/16002618" target="_blank"〉PubMed〈/a〉
    Keywords: Benzimidazoles/pharmacology ; Carbamates/pharmacology ; Cell Polarity ; Gene Deletion ; Hydroxyurea/pharmacology ; *Interphase ; Microscopy, Electron ; Microtubule-Associated Proteins/genetics/*metabolism ; Microtubules/*physiology/ultrastructure ; Molecular Motor Proteins/genetics/*metabolism ; Movement ; Recombinant Fusion Proteins/metabolism ; Schizosaccharomyces/*cytology/metabolism/ultrastructure ; Schizosaccharomyces pombe Proteins/genetics/*metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Publication Date: 2003-06-07
    Description: In most eukaryotes cytokinesis is brought about by a contractile actin ring located at the division plane. Here, in fission yeast the actin ring was found to be required to generate late-mitotic microtubular structures located at the division plane, and these in turn maintained the medial position of the actin ring. When these microtubular structures were disrupted, the actin ring migrated away from the cell middle in a membrane traffic-dependent manner, resulting in asymmetrical cell divisions that led to genomic instability. We propose that these microtubular structures contribute to a checkpoint control that retains the equatorial position of the ring when progression through cytokinesis is delayed.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Pardo, Mercedes -- Nurse, Paul -- New York, N.Y. -- Science. 2003 Jun 6;300(5625):1569-74.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cell Cycle Laboratory, Cancer Research UK London Research Institute, 44 Lincoln's Inn Fields, London WC2A 3PX, UK. mercedes.pardo@cancer.org.uk〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/12791993" target="_blank"〉PubMed〈/a〉
    Keywords: Actins/*physiology ; Anaphase ; Benzimidazoles/pharmacology ; Bicyclo Compounds, Heterocyclic/pharmacology ; *Carbamates ; Cell Cycle Proteins/physiology ; Cell Division/*physiology ; Cell Nucleus/physiology ; Cytoskeletal Proteins/physiology ; Interphase ; Microtubule-Organizing Center/physiology/ultrastructure ; Microtubules/*physiology/ultrastructure ; Mitosis ; Mutation ; Recombinant Fusion Proteins/metabolism ; Schizosaccharomyces/cytology/genetics/*physiology ; Schizosaccharomyces pombe Proteins/genetics/metabolism/physiology ; Temperature ; Thiazoles/pharmacology ; Thiazolidines ; Tubulin/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Publication Date: 2010-12-24
    Description: Control of eukaryotic cell proliferation involves an extended regulatory network, the complexity of which has made it difficult to understand the basic principles of the cell cycle. To investigate the core engine of the mitotic cycle we have generated a minimal control network in fission yeast that efficiently sustains cellular reproduction. Here we demonstrate that orderly progression through the major events of the cell cycle can be driven by oscillation of an engineered monomolecular cyclin-dependent protein kinase (CDK) module lacking much of the canonical regulation. We show further that the CDK oscillator acts as the primary organizer of the cell cycle, imposing timing and directionality to a system of two CDK activity thresholds that define independent cell cycle phases. We propose that this simple core architecture forms the basic control of the eukaryotic cell cycle.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Coudreuse, Damien -- Nurse, Paul -- 093917/Wellcome Trust/United Kingdom -- England -- Nature. 2010 Dec 23;468(7327):1074-9. doi: 10.1038/nature09543.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Yeast Genetics and Cell Biology, The Rockefeller University, 1230 York Avenue, New York, New York 10065, USA. dcoudreuse@rockefeller.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21179163" target="_blank"〉PubMed〈/a〉
    Keywords: *Biological Clocks ; Cell Cycle/*physiology ; Cell Proliferation ; Cyclin-Dependent Kinases/*metabolism ; DNA/metabolism ; Schizosaccharomyces/*cytology/*enzymology/genetics ; Schizosaccharomyces pombe Proteins/metabolism ; Time Factors
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Publication Date: 2010-07-24
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Nurse, Paul -- 093917/Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2010 Jul 23;329(5990):380-1. doi: 10.1126/science.329.5990.380.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/20651129" target="_blank"〉PubMed〈/a〉
    Keywords: Academies and Institutes/economics/*organization & administration ; *Biomedical Research/economics ; Budgets ; Great Britain ; History, 20th Century ; History, 21st Century ; Nobel Prize ; Research Support as Topic ; Societies, Scientific/*organization & administration ; Translational Medical Research
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...