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  • 1
    Publication Date: 2008-06-24
    Description: The heart is formed from cardiogenic progenitors expressing the transcription factors Nkx2-5 and Isl1 (refs 1 and 2). These multipotent progenitors give rise to cardiomyocyte, smooth muscle and endothelial cells, the major lineages of the mature heart. Here we identify a novel cardiogenic precursor marked by expression of the transcription factor Wt1 and located within the epicardium-an epithelial sheet overlying the heart. During normal murine heart development, a subset of these Wt1(+) precursors differentiated into fully functional cardiomyocytes. Wt1(+) proepicardial cells arose from progenitors that express Nkx2-5 and Isl1, suggesting that they share a developmental origin with multipotent Nkx2-5(+) and Isl1(+) progenitors. These results identify Wt1(+) epicardial cells as previously unrecognized cardiomyocyte progenitors, and lay the foundation for future efforts to harness the cardiogenic potential of these progenitors for cardiac regeneration and repair.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2574791/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2574791/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zhou, Bin -- Ma, Qing -- Rajagopal, Satish -- Wu, Sean M -- Domian, Ibrahim -- Rivera-Feliciano, Jose -- Jiang, Dawei -- von Gise, Alexander -- Ikeda, Sadakatsu -- Chien, Kenneth R -- Pu, William T -- P50 HL074734/HL/NHLBI NIH HHS/ -- P50 HL074734-05/HL/NHLBI NIH HHS/ -- England -- Nature. 2008 Jul 3;454(7200):109-13. doi: 10.1038/nature07060. Epub 2008 Jun 22.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Harvard Stem Cell Institute and Department of Cardiology, Children's Hospital Boston, 300 Longwood Avenue, Boston, Massachusetts 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/18568026" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; *Cell Lineage ; Gene Expression Regulation, Developmental ; Green Fluorescent Proteins/genetics/metabolism ; Heart/*embryology ; Homeodomain Proteins/genetics/metabolism ; Mice ; Myocytes, Cardiac/*cytology/metabolism ; Pericardium/*cytology/embryology/metabolism ; Stem Cells/*cytology/metabolism ; Transcription Factors/genetics/metabolism ; WT1 Proteins/genetics/metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 1995-06-30
    Description: CD25 expression occurs early in thymocyte differentiation. The mechanism of induction of CD25 before T cell receptor rearrangement and the importance of this mechanism for T cell development are unknown. In a thymus reconstitution assay, tumor necrosis factor alpha (TNF-alpha) and interleukin-1 alpha (IL-1 alpha), two cytokines produced within the thymic microenvironment, induced CD25 expression on early immature thymocytes. Either TNF-alpha or IL-1 alpha was necessary for further thymocyte maturation and CD4+CD8+ differentiation. In irradiated mice reconstituted with CD117+CD25+ thymocytes, commitment to the T cell lineage was marked by the loss of precursor multipotency.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Zuniga-Pflucker, J C -- Jiang, D -- Lenardo, M J -- New York, N.Y. -- Science. 1995 Jun 30;268(5219):1906-9.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7541554" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cell Differentiation ; Cells, Cultured ; Hematopoietic Stem Cells/*cytology/immunology ; Interleukin-1/pharmacology/*physiology ; Interleukin-7/pharmacology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Mice, SCID ; Organ Culture Techniques ; Proto-Oncogene Proteins/biosynthesis ; Proto-Oncogene Proteins c-kit ; Receptor Protein-Tyrosine Kinases/biosynthesis ; Receptors, Colony-Stimulating Factor/biosynthesis ; Receptors, Interleukin-2/*biosynthesis ; Stromal Cells/physiology ; T-Lymphocyte Subsets/cytology/immunology ; T-Lymphocytes/*cytology/immunology ; Thymus Gland/cytology/*embryology/immunology ; Tumor Necrosis Factor-alpha/pharmacology/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    ISSN: 1434-601X
    Keywords: 21.10.−k ; 07.75. + h ; 25.70.NP ; 27.30. + t ; 27.40. + z
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract After magnetic separation, identification through time of flight and δE×E measurements has allowed the observation of the new nuclei,29F,35,36Mg,38,39Al,40,41Si,43,44P,45,46,47S;46,47,48,49Cl;49,50,51Ar from the interaction of a48Ca beam of 55 MeV/u with tantalum targets.
    Type of Medium: Electronic Resource
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