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  • 1
    Keywords: Forschungsbericht
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource ([8] S., 33,1 KB)
    Language: German
    Note: Förderkennzeichen BMBF 01GN0527 , Unterschiede zwischen der elektronischen Ressource und dem gedruckten Dokument können nicht ausgeschlossen werden. - Auch als gedr. Ausg. vorhanden , Systemvoraussetzungen: Acrobat reader.
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  • 2
    Keywords: Forschungsbericht
    Type of Medium: Online Resource
    Pages: Online Ressource, 14 p. = 41,5 Kb., text
    Edition: [Elektronische Ressource]
    Series Statement: Verbundprojekt Etablierung eines in vitro-Modells neuronaler Zellen / Projektkoordinator: Anna M. Wobus ... Teilprojekt 1
    Language: German
    Note: On the front page: Teilprojekt 1; Teilprojekt 2: Funktionelle Charakterisierung ES-Zell-differenzierter Neuronen (Universität Köln). - Contract BMBF 0311473. - Differences between the printed and electronic version of the document are possible. - nBibliography p. 10 - 12 , Also available as printed version , Systemvoraussetzungen: Acrobat Reader.
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 752 (1995), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1460-9568
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Besides other mechanisms, the influx of Ca2+ into embryonic neurons controls growth and differentiation processes. To study the expression and regulation of voltage-gated Ca2+ channels during early neurogenesis, we measured whole-cell Ca2+ currents (Ica) in neurons developing from pluripotent embryonic stem cells. Various receptor agonists, including somatostatin and baclofen, reversibly inhibited ICa in embryonic stem cell-derived neurons. The effects of somatostatin and baclofen were abolished by pretreatment of cells with pertussis toxin and mimicked by intracellular infusion of guanosine 5′-O-(3-thiotriphosphate), suggesting the involvement of pertussis toxin-sensitive G proteins in Ica inhibition. Investigations at different stages of neuronal differentiation showed that somatostatin efficiently suppressed L- and N-type Ca2+ channels in immature as well as mature neurons. In contrast, inhibition of L- and N-type channels by baclofen was rarely observed at the early stage. In terminally differentiated neurons, responses to baclofen were as prominent as those to somatostatin but were confined to N-type Ca2+ channels. The stage-dependent sensitivity of voltage-gated Ca2+ channels to somatostatin and baclofen was not due to differential expression of Gαo isoforms, as revealed by reverse transcription-polymerase chain reaction and immunofluorescence microscopy. These findings demonstrate that specific neurotransmitters such as somatostatin regulate voltage-gated Ca2+ channels via G proteins during the early stages of neurogenesis, thus providing a mechanism for the epigenetic control of neuronal differentiation.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 33 (1977), S. 1212-1213 
    ISSN: 1420-9071
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The antibiotic netropsin was found to induce an increase of the aberration frequency of up to 10% and a decondensation and elongation of centromeric regions of the chromosomes in mouse ascites tumour cells cultivated in vitro.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-041X
    Keywords: Mouse embryonic stem cells ; Differentiation ; Cardiomyocytes ; Skeletal muscle cells ; Retinoic acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Pluripotent embryonic stem cells (ES cells) differentiating via embryo-like aggregates (embryoid bodies) into derivatives of the primary germ layers were used as a model system to investigate the time- and concentration dependent effects of retinoic acid (RA) on the in vitro differentiation pattern. When ES cells, cultivated normally under conditions resulting in cardiomyocyte differentiation, were treated during the first 2 days of embryoid body formation with high RA concentrations (10−9 to 10−7 M) a strong inhibition of cardiogenesis was found. ES cells differentiating as embryoid bodies and treated with the same RA concentration between the 5th and 7th day resulted in a slight induction of cardiogenesis. In contrast, incubation of embryoid bodies with 10−8 and 10−7 M RA between the 2nd and 5th day of embryoid body development resulted in a total inhibition of cardiogenesis but in an induction of myogenesis. This was demonstrated by indirect immunofluorescence and, as shown by reverse transcription- polymerase chain reaction (RT-PCR), by the time- and concentration-dependent inhibition of transcription of cardiac-specific α- and β-cardiac myosin heavy chain (MHC) genes, and the induction of transcription of skeletal muscle-specific myogenin. In addition, using the whole-cell patch-clamp technique, these skeletal myocytes were functionally characterized by the expression of tissue-specific Ca2+ channels and nicotinic cholinoceptors. In summary, a specific effect of RA on ES cell differentiation in the embryoid body resulting in a switch from cardiogenesis to myogenesis and an induction of neuronal cells was found.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1432-041X
    Keywords: Mouse embryonic stem cells ; Differentiation ; Cardiomyocytes ; Skeletal muscle cells ; Retinoic acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Pluripotent embryonic stem cells (ES cells) differentiating via embryo-like aggregates (embryoid bodies) into derivatives of the primary germ layers were used as a model system to investigate the time- and concentration dependent effects of retinoic acid (RA) on the in vitro differentiation pattern. When ES cells, cultivated normally under conditions resulting in cardiomyocyte differentiation, were treated during the first 2 days of embryoid body formation with high RA concentrations (10−9 to 10−7 M) a strong inhibition of cardiogenesis was found. ES cells differentiating as embryoid bodies and treated with the same RA concentration between the 5th and 7th day resulted in a slight induction of cardiogenesis. In contrast, incubation of embryoid bodies with 10−8 and 10−7 M RA between the 2nd and 5th day of embryoid body development resulted in a total inhibition of cardiogenesis but in an induction of myogenesis. This was demonstrated by indirect immunofluorescence and, as shown by reverse transcription- polymerase chain reaction (RT-PCR), by the time- and concentration-dependent inhibition of transcription of cardiac-specific α- andβ-cardiac myosin heavy chain (MHC) genes, and the induction of transcription of skeletal muscle-specificmyogenin. In addition, using the whole-cell patch-clamp technique, these skeletal myocytes were functionally characterized by the expression of tissue-specific Ca2+ channels and nicotinic cholinoceptors. In summary, a specific effect of RA on ES cell differentiation in the embryoid body resulting in a switch from cardiogenesis to myogenesis and an induction of neuronal cells was found.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 49 (1977), S. 249-252 
    ISSN: 1432-2242
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-0778
    Keywords: cardiogenesis ; cell differentiation ; gene expression ; mouse embryonic stem cells ; myogenesis ; neurogenesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract Embryonic stem cells, totipotent cells of the early mouse embryo, were established as permanent cell lines of undifferentiated cells. ES cells provide an important cellular system in developmental biology for the manipulation of preselected genes in mice by using the gene targeting technology. Embryonic stem cells, when cultivated as embryo-like aggregates, so-called ‘embryoid bodies’, are able to differentiate in vitro into derivatives of all three primary germ layers, the endoderm, ectoderm and mesoderm. We established differentiation protocols for the in vitro development of undifferentiated embryonic stem cells into differentiated cardiomyocytes, skeletal muscle, neuronal, epithelial and vascular smooth muscle cells. During differentiation, tissue-specific genes, proteins, ion channels, receptors and action potentials were expressed in a developmentally controlled pattern. This pattern closely recapitulates the developmental pattern during embryogenesis in the living organism. In vitro, the controlled developmental pattern was found to be influenced by differentiation and growth factor molecules or by xenobiotics. Furthermore, the differentiation system has been used for genetic analyses by ‘gain of function’ and ‘loss of function’ approaches in vitro.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Reproduktionsmedizin 16 (2000), S. 37-42 
    ISSN: 1434-808X
    Keywords: Schlüsselwörter ; Menschliche embryonale Stammzellen •¶Pluripotenz • Zellkerntransfer • Klonieren • Gewebetransplantation ; Key words ; Human embryonic stem cells • Pluripotency • Nuclear transfer • Therapeutic cloning • Tissue transplantation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Technological advances in the last two years in mammalian nuclear transfer techniques and the establishment of human embryonic stem cell lines formed the background of the International Workshop on „Embryonic Stem Cells and Nuclear Transfer Strategies“ organized at the Gene Center, Munich, September 1999. The aim of the meeting was to bring together scientists working in the stem cell field and those working on somatic nuclear transfer techniques to discuss the present status and prospects of both technologies for basic and applied research and future use in medicine and livestock breeding. „Biology of Embryonic Stem Cells“, „Nuclear Transfer Strategies“, and „Stem Cell Differentiation – Cell Therapy“ were the main topics of the meeting. It became clear that we are far from understanding the processes involved in stem cell self-renewal and differentiation and the mechanisms resulting in reprogramming of nuclei from somatic cells after transfer into enucleated oocytes. However, data were presented that showed the enormous potential of the embryonic stem cell technology for tissue transplantation in the future. Before any use of this technology in combination with any cloning technology for human cell therapy will be possible, further research including animal models and stem cell differentiation approaches in culture (i. e., identification of differentiation factors, selective differentiation strategies, reporter gene assays) is necessary to understand the basic principles of pluripotent stem cell differentiation and the mechanisms involved in reprogramming somatic cell nuclei.
    Notes: Zusammenfassung Am 9. und 10. September 1999 fand im Genzentrum München ein internationaler Workshop zum Thema ,,Stem cells and nuclear transfer strategies – present state and future prospects“ statt. Organisatoren und Chairmen waren Anna M. Wobus (IPK Gatersleben), Eckhard Wolf (Genzentrum München) und Henning M. Beier (Anatomie und Reproduktionsbiologie der RWTH Aachen). International anerkannte Experten hielten folgende Vorträge: Jonathan Van Blerkom (Boulder, Co/USA) ,,The oocyte – the ultimate stem cell“, Austin Smith (Edinburgh/UK) ,,Control of stem cell pluripotency and differentiation“, Hans R. Schöler (Philadelphia, Pa/USA) ,,Oct-4 expression in ES cells and early embryogenesis“, Keith H. S. Campbell (Roslin/UK) ,,Viable offspring derived from fetal and adult mammalian cells – applications and progress“, Jose B. Cibelli (Worcester, Mass./USA) ,,Genetic modification by somatic cell nuclear transplantation“, Oliver Brüstle (Bonn) ,,Transplantation of embryonic stem cell-derived neural precursors“, Anthony D. Ho (Heidelberg) ,,Symmetry of division of haematopoietic stem cells“, Axel Haverich (Hannover) ,,Modern strategies of cell and tissue repair – Requirements of transplantation therapy“. Bei diesem Workshop wurde eine Fülle von wissenschaftlichen Daten präsentiert, die das enorme Potential der embryonalen Stammzelltechnologie für die zukünftige Gewebetransplantation deutlich machte. Über 150 Wissenschaftler aus Deutschland, Europa und den USA nahmen an diesem Workshop teil.
    Type of Medium: Electronic Resource
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