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  • *Cell Lineage  (1)
  • 25.70.Lm  (1)
  • 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
    ISSN: 1434-601X
    Keywords: 25.70.Gh ; 25.70.Lm
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Inclusive neutron multiplicity distributions were measured by means of 4π liquid-scintillator detectors for Ar and Kr-induced reactions at 44 MeV/nucleon and 32 MeV/nucleon, respectively. For all the systems studied, the observed distributions exhibit a bump structure at large multiplicity, corresponding to highly dissipative collisions. For Ar-induced reactions, the excitation energies necessary to explain the most probable neutron multiplicity associated with these dissipative collisions are estimated, the correspondence between excitation energy and neutron multiplicity being calculated in the framework of the statistical model. The so-obtained values of excitation energies, which are systematically lower than those predicted using the massive-transfer picture, are discussed.
    Type of Medium: Electronic Resource
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