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Vehmeyer, Katalin
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Vehmeyer, Katalin
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Vehmeyer, Katalin
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Vehmeyer, K.
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2001Journal Article [["dc.bibliographiccitation.firstpage","955"],["dc.bibliographiccitation.issue","11"],["dc.bibliographiccitation.journal","Leukemia Research"],["dc.bibliographiccitation.lastpage","959"],["dc.bibliographiccitation.volume","25"],["dc.contributor.author","Vehmeyer, K."],["dc.contributor.author","Haase, Detlef"],["dc.contributor.author","Alves, Frauke"],["dc.date.accessioned","2018-11-07T08:29:43Z"],["dc.date.available","2018-11-07T08:29:43Z"],["dc.date.issued","2001"],["dc.description.abstract","The colony-forming capacity of the peripheral blood stem/progenitor cells (PBSC) in different forms of myelodysplastic syndrome (MDS) was investigated. In most cases of refractory anemia (RA) the colony growth of PBSC was definitely reduced as compared to the controls. However, in RA with unfavorable chromosomal aberrations, in refractory anemia with ringed sideroblasts (RARS) and in advanced stages of MDS such as refractory anemia with excess blasts (RAEB) and refractory anemia in transformation (RAEB-t), the number of myeloid progenitor cells increased up to 100-fold. In chronic myelomonocytic leukemia (CMML), the increase was even more marked, up to 350-fold. Although the number of PBSC was strongly elevated, these cells were not able to restore hematopoiesis in vivo. In conclusion, the increase of circulating colony-forming cells (CFC) seems to be associated with disease progression, and thus, the evaluation of PBSC could be an important parameter in the diagnosis of MDS. (C) 2001 Elsevier Science Ltd. All rights reserved."],["dc.identifier.doi","10.1016/S0145-2126(01)00064-9"],["dc.identifier.isi","000171788800004"],["dc.identifier.pmid","11597730"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/16720"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Pergamon-elsevier Science Ltd"],["dc.relation.issn","0145-2126"],["dc.title","Increased peripheral stem cell pool in MDS: an indication of disease progression?"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details DOI PMID PMC WOS2001Conference Abstract [["dc.bibliographiccitation.issue","11"],["dc.bibliographiccitation.journal","Blood"],["dc.bibliographiccitation.volume","98"],["dc.contributor.author","Haase, Detlef"],["dc.contributor.author","Steffens, Rainer"],["dc.contributor.author","Alves, Frauke"],["dc.contributor.author","Lorenz, T."],["dc.contributor.author","Vehmeyer, K."],["dc.date.accessioned","2018-11-07T11:23:56Z"],["dc.date.available","2018-11-07T11:23:56Z"],["dc.date.issued","2001"],["dc.format.extent","356A"],["dc.identifier.isi","000172134101503"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/56293"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Amer Soc Hematology"],["dc.publisher.place","Washington"],["dc.relation.issn","0006-4971"],["dc.title","Cytogenetic characterization of stroma cells in MDS and comparison with myeloid cells."],["dc.type","conference_abstract"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]Details WOS