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  • 1
    Publikationsdatum: 2022-11-04
    Beschreibung: Recalling IOC-Resolution XXX-3 and in accordance with 207 EX/Dec.5.II.A, this report provides a summary of a recently completed evaluation, namely: Internal Oversight Service (IOS) Evaluation of the Strategic positioning of the Intergovernmental Oceanographic Commission (IOC-UNESCO).
    Beschreibung: Item 9 of the provisional agenda of the Executive Board of UNESCO (212 EX/9). OPENASFA INPUT
    Beschreibung: Published
    Beschreibung: Non Refereed
    Schlagwort(e): International Oceanographic Commission of UNESCO ; Strategic position ; IOC-UNESCO ; Evaluation ; Scientific programmes ; Oceanography
    Repository-Name: AquaDocs
    Materialart: Report
    Format: 9pp.
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Publikationsdatum: 2022-11-02
    Beschreibung: Among the approximately 10,000 beneficial species of marine phytoplankton in the world’s oceans today, some 200 taxa can harm human society through the production of toxins that threaten seafood security and human health. These toxins are also responsible for wild or aquaculture fish-kills, may interfere with recreation-al use of coastal or inland waters, or cause economic losses. Non-toxic microalgae attaining high biomass can also cause Harmful Algal Blooms (HABs) by producing seawater discolorations, anoxia or mucilage that negatively affect the environment and human activities. The most frequently asked questions about harmful algal blooms are if they are increasing and expand-ing worldwide, and what are the mechanisms behind this perceived escalation. These questions have been addressed in several review papers concerning HAB trends at various scales, where evidences of expansion, intensification and increased impacts of harmful algal blooms have been gathered from a selection of examples that have gained high prominence in the scientific world and in society 1,2,3,4. Eutrophication, human-mediated introduction of alien harmful species, climatic variability, and aquaculture have all been mentioned as possible causes of HAB trends at various spatial and temporal scales 5,6. Over the last 40 years, the capacity and monitoring efforts to detect harmful species and harmful events have significantly increased, thus increasing the reporting of harmful events across the world’s seas. The resulting information is mostly scattered in the ever growing literature, with data from statutory monitoring programs often not published in peer review journals, while an extensive and detailed overview of the huge amount of information on harmful species, their spatial and temporal distribution and the trends of HABs they have caused has never been attempted so far. This lack of a synthesis of the relevant data has hampered a sound global assessment of the present status of phenomena related to harmful algae. Following the lead of the International Panel for Climate Change (IPCC) consensus reporting mechanism, and to complement the World Ocean Assessment, the need has been expressed for a Global HAB Status Report compiling an overview of Harmful Algal Bloom events and their societal impacts; providing a worldwide appraisal of the occurrence of toxin-producing microalgae; aimed towards the long term goal of assessing the status and probability of change in HAB frequencies, intensities, and range resulting from environmental changes at the local and global scale. This initiative was launched in April 2013 in Paris by the IOC Intergovernmental Panel on HABs (IOC/IPHAB), and has been pursued with the support of the Government of Flanders and hosted within the IOC International Oceanographic Date Exchange Programme (IODE) in partnership with ICES, PICES and IAEA. As a first step towards a global HAB status assessment, a Special Issue of the journal Harmful Algae (vol. 102, February 2021) has been published comprising 12 papers 7-18 each presenting an overview of toxic and non-toxic HABs in a specific area of the world’s seas. The regional overviews build on existing literature and exploit the information gathered in two relevant data-bases, both incorporated into the Ocean Biodiversity Information System (OBIS).
    Beschreibung: Government of Flanders
    Beschreibung: OPENASFA INPUT This Global HAB Status Report summary was prepared based on the special issue Global HAB Status reporting, vol. 102 (Feb. 2021) of the Harmful Algae (Elsevier Journal)
    Beschreibung: Published
    Beschreibung: Refereed
    Schlagwort(e): Harmful Algae Bloom ; Status Report ; HAB ; IODE ; International Oceanographic Data and Information Exchange ; Ocean Biodiversity Information System ; OBIS ; Harmful species ; PICES ; ICES ; IAEA
    Repository-Name: AquaDocs
    Materialart: Report
    Format: 14pp.
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    facet.materialart.
    Unbekannt
    UNESCO | Paris, France
    Publikationsdatum: 2022-09-30
    Beschreibung: In 2017, the UN General Assembly declared the UN Decade of Ocean Science for Sustainable Development (2021-2030). It has entrusted IOC-UNESCO with the design and delivery of the Decade to ensure that ocean science is indeed underpinning sustainable ocean management and the 2030 Sustainable Development Agenda more broadly. Fulfilling its mandate as trustee of the Ocean Decade, as well as delivering on a growing list of additional roles, in an oceanographic space that is both expanding and increasingly crowded, establishes an important opportunity but also an overarching challenge for IOC-UNESCO. In the context of the upcoming UN Decade of the Ocean, the IOC-UNESCO agreed with the Internal Oversight Service (IOS) on the merit of conducting an evaluation of its strategic positioning within the UN system and the broader landscape of ocean-related actors and programmes, taking into account relevant enabling policy frameworks to which the work of the Commission responds.
    Beschreibung: OPENASFA INPUT Published by UNESCO's Internal Oversight Service.
    Beschreibung: Published
    Beschreibung: Not Known
    Schlagwort(e): Evaluation ; International Oceanographic Commission of UNESCO ; Oceanography ; Scientific programmes
    Repository-Name: AquaDocs
    Materialart: Report
    Format: 2pp.
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
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    Unbekannt
    UNESCO | Paris, France
    Publikationsdatum: 2022-09-30
    Beschreibung: Environmental DNA expeditions in UNESCO World Heritage Marine Sites: engaging citizen-scientists for biodiversity conservation of UNESCO sites.
    Beschreibung: Government of Flanders
    Beschreibung: OPENASFA INPUT
    Beschreibung: Published
    Schlagwort(e): Biodiversity ; Environmental DNA ; eDNA ; Marine environment ; Water analysis ; Oceanographic data ; OBIS ; Open Science ; Community participation ; Research projects ; World Heritage List
    Repository-Name: AquaDocs
    Materialart: Other
    Format: 2pp.
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Publikationsdatum: 2022-06-17
    Beschreibung: Sea wave monitoring is key in many applications in oceanography such as the validation of weather and wave models. Conventional in situ solutions are based on moored buoys whose measurements are often recognized as a standard. However, being exposed to a harsh environment, they are not reliable, need frequent maintenance, and the datasets feature many gaps. To overcome the previous limitations, we propose a system including a buoy, a micro-seismic measuring station, and a machine learning algorithm. The working principle is based on measuring the micro-seismic signals generated by the sea waves. Thus, the machine learning algorithm will be trained to reconstruct the missing buoy data from the micro-seismic data. As the micro-seismic station can be installed indoor, it assures high reliability while the machine learning algorithm provides accurate reconstruction of the missing buoy data. In this work, we present the methods to process the data, develop and train the machine learning algorithm, and assess the reconstruction accuracy. As a case of study, we used experimental data collected in 2014 from the Northern Tyrrhenian Sea demonstrating that the data reconstruction can be done both for significant wave height and wave period. The proposed approach was inspired from Data Science, whose methods were the foundation for the new solutions presented in this work. For example, estimating the period of the sea waves, often not discussed in previous works, was relatively simple with machine learning. In conclusion, the experimental results demonstrated that the new system can overcome the reliability issues of the buoy keeping the same accuracy.
    Beschreibung: Assist in Gravitation and Instrumentation srl Istituto Nazionale di Geofisica e Vulcanologia
    Beschreibung: Published
    Beschreibung: 798167
    Beschreibung: 4A. Oceanografia e clima
    Beschreibung: JCR Journal
    Schlagwort(e): sea swell ; machine learning ; ocean waves ; micro-seismic data ; sea state ; sea wave period ; buoy ; Marine Science ; Oceanography
    Repository-Name: Istituto Nazionale di Geofisica e Vulcanologia (INGV)
    Materialart: article
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Publikationsdatum: 1996-12-20
    Beschreibung: The human Kv1.5 potassium channel (hKv1.5) contains proline-rich sequences identical to those that bind to Src homology 3 (SH3) domains. Direct association of the Src tyrosine kinase with cloned hKv1.5 and native hKv1.5 in human myocardium was observed. This interaction was mediated by the proline-rich motif of hKv1.5 and the SH3 domain of Src. Furthermore, hKv1.5 was tyrosine phosphorylated, and the channel current was suppressed, in cells coexpressing v-Src. These results provide direct biochemical evidence for a signaling complex composed of a potassium channel and a protein tyrosine kinase.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Holmes, T C -- Fadool, D A -- Ren, R -- Levitan, I B -- F32 NS009952/NS/NINDS NIH HHS/ -- New York, N.Y. -- Science. 1996 Dec 20;274(5295):2089-91.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Biochemistry and Volen Center for Complex Systems, Brandeis University, Waltham, MA 02254, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8953041" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amino Acid Sequence ; Cell Line ; Cloning, Molecular ; Humans ; Kv1.5 Potassium Channel ; Molecular Sequence Data ; Myocardium/chemistry ; Oncogene Protein pp60(v-src)/metabolism ; Patch-Clamp Techniques ; Phosphorylation ; Phosphotyrosine/metabolism ; Potassium Channels/chemistry/*metabolism ; *Potassium Channels, Voltage-Gated ; Recombinant Fusion Proteins/metabolism ; Signal Transduction ; Transfection ; src Homology Domains/*physiology ; src-Family Kinases/chemistry/*metabolism
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
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    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1996-12-20
    Beschreibung: Adipocyte differentiation is an important component of obesity and other metabolic diseases. This process is strongly inhibited by many mitogens and oncogenes. Several growth factors that inhibit fat cell differentiation caused mitogen-activated protein (MAP) kinase-mediated phosphorylation of the dominant adipogenic transcription factor peroxisome proliferator-activated receptor gamma (PPARgamma) and reduction of its transcriptional activity. Expression of PPARgamma with a nonphosphorylatable mutation at this site (serine-112) yielded cells with increased sensitivity to ligand-induced adipogenesis and resistance to inhibition of differentiation by mitogens. These results indicate that covalent modification of PPARgamma by serum and growth factors is a major regulator of the balance between cell growth and differentiation in the adipose cell lineage.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Hu, E -- Kim, J B -- Sarraf, P -- Spiegelman, B M -- R37DK31405/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 1996 Dec 20;274(5295):2100-3.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Dana-Farber Cancer Institute and Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8953045" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): 3T3 Cells ; Adipocytes/*cytology/metabolism ; Animals ; Blood ; Calcium-Calmodulin-Dependent Protein Kinases/antagonists & inhibitors/*metabolism ; Cell Differentiation ; Cell Line ; Enzyme Inhibitors/pharmacology ; Epidermal Growth Factor/pharmacology ; Flavonoids/pharmacology ; Insulin/pharmacology ; Ligands ; Mice ; Mitogens/pharmacology ; Mutation ; Phosphorylation ; Rats ; Receptors, Cytoplasmic and Nuclear/chemistry/genetics/*metabolism ; Tetradecanoylphorbol Acetate/pharmacology ; Transcription Factors/chemistry/genetics/*metabolism ; Transcription, Genetic/drug effects ; Transfection
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1996-12-20
    Beschreibung: Epidermal growth factor receptor (EGFR) signaling was analyzed in mammalian cells conditionally defective for receptor-mediated endocytosis. EGF-dependent cell proliferation was enhanced in endocytosis-defective cells. However, early EGF-dependent signaling events were not uniformly up-regulated. A subset of signal transducers required the normal endocytic trafficking of EGFR for full activation. Thus, endocytic trafficking of activated EGFR plays a critical role not only in attenuating EGFR signaling but also in establishing and controlling specific signaling pathways.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Vieira, A V -- Lamaze, C -- Schmid, S L -- CA58689/CA/NCI NIH HHS/ -- CA69099/CA/NCI NIH HHS/ -- New York, N.Y. -- Science. 1996 Dec 20;274(5295):2086-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cell Biology, The Scripps Research Institute, La Jolla, CA 92037, USA. slschmid@scripps.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8953040" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): *Adaptor Proteins, Signal Transducing ; *Adaptor Proteins, Vesicular Transport ; Calcium-Calmodulin-Dependent Protein Kinases/metabolism ; Cell Division/drug effects ; Cell Membrane/metabolism ; Clathrin/*physiology ; Coated Pits, Cell-Membrane/physiology ; Dynamins ; *Endocytosis ; Enzyme Activation ; Epidermal Growth Factor/metabolism/pharmacology ; GTP Phosphohydrolases/physiology ; HeLa Cells ; Humans ; Isoenzymes/metabolism ; Phosphatidylinositol 3-Kinases ; Phospholipase C gamma ; Phosphorylation ; Phosphotransferases (Alcohol Group Acceptor)/metabolism ; Phosphotyrosine/metabolism ; Proteins/metabolism ; Receptor, Epidermal Growth Factor/*metabolism ; Shc Signaling Adaptor Proteins ; *Signal Transduction ; Type C Phospholipases/metabolism
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
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    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1996-12-06
    Beschreibung: The functions of the low-affinity p75 nerve growth factor receptor (p75(NGFR)) in the central nervous system were explored in vivo. In normal mice, approximately 25 percent of the cholinergic basal forebrain neurons did not express TrkA and died between postnatal day 6 and 15. This loss did not occur in p75(NGFR)-deficient mice or in normal mice systemically injected with a p75(NGFR)-inhibiting peptide. Control, but not p75(NGFR)-deficient, mice also had fewer cholinergic striatal interneurons. Apparently, p75(NGFR) mediates apoptosis of these developing neurons in the absence of TrkA, and modulation of p75(NGFR) can promote neuronal survival. Cholinergic basal forebrain neurons are involved in learning and memory.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Van der Zee, C E -- Ross, G M -- Riopelle, R J -- Hagg, T -- New York, N.Y. -- Science. 1996 Dec 6;274(5293):1729-32.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Anatomy and Neurobiology, Tupper Building, Dalhousie University, Halifax, Nova Scotia B3H 4H7, Canada. thagg@is.dal.ca〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8939868" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Animals ; *Apoptosis ; Cell Survival ; Choline O-Acetyltransferase/metabolism ; DNA Fragmentation ; Interneurons/cytology ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Neostriatum/cytology ; Neurons/*cytology/enzymology ; Oligopeptides/pharmacology ; Parasympathetic Nervous System/*cytology ; Phosphorylation ; Prosencephalon/*cytology ; Proto-Oncogene Proteins/metabolism ; Purkinje Cells/cytology ; Receptor Protein-Tyrosine Kinases/metabolism ; Receptor, Nerve Growth Factor ; Receptor, trkA ; Receptors, Nerve Growth Factor/deficiency/metabolism/*physiology
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    facet.materialart.
    Unbekannt
    American Association for the Advancement of Science (AAAS)
    Publikationsdatum: 1996-11-15
    Beschreibung: The initiation of anaphase and exit from mitosis require the activation of a proteolytic system that ubiquitinates and degrades cyclin B. The regulated component of this system is a large ubiquitin ligase complex, termed the anaphase-promoting complex (APC) or cyclosome. Purified Xenopus laevis APC was found to be composed of eight major subunits, at least four of which became phosphorylated in mitosis. In addition to CDC27, CDC16, and CDC23, APC contained a homolog of Aspergillus nidulans BIME, a protein essential for anaphase. Because mutation of bimE can bypass the interphase arrest induced by either nimA mutation or unreplicated DNA, it appears that ubiquitination catalyzed by APC may also negatively regulate entry into mitosis.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Peters, J M -- King, R W -- Hoog, C -- Kirschner, M W -- New York, N.Y. -- Science. 1996 Nov 15;274(5290):1199-201.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/8895470" target="_blank"〉PubMed〈/a〉
    Schlagwort(e): Amino Acid Sequence ; *Anaphase ; Animals ; Aspergillus/chemistry/cytology/metabolism ; Cell Cycle Proteins/*chemistry/metabolism ; Cyclins/metabolism ; Electrophoresis, Polyacrylamide Gel ; Fungal Proteins/analysis/*chemistry/genetics/metabolism ; Ligases/*chemistry/metabolism ; *Mitosis ; Molecular Sequence Data ; Mutation ; Ovum ; Phosphorylation ; Ubiquitin-Protein Ligases ; Xenopus laevis
    Print ISSN: 0036-8075
    Digitale ISSN: 1095-9203
    Thema: Biologie , Chemie und Pharmazie , Informatik , Medizin , Allgemeine Naturwissenschaft , Physik
    Standort Signatur Erwartet Verfügbarkeit
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