Source:http://linkedlifedata.com/resource/pubmed/id/11054073
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2000-11-9
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pubmed:abstractText |
Monosomy 7 is the most frequent chromosome abnormality among patients with secondary myelodysplastic syndrome (MDS). We used fluorescence in situ hybridization (FISH) and fluorescence-activated cell sorting (FACS) in order to clarify the lineage involvement. Four patients, three with de novo MDS and one with secondary MDS, were enrolled in this study. Monosomy 7 was observed in pluripotent stem cells (CD34(+)Thy-1(+)), and in B (CD34(+)CD19(+)) and T/natural killer (NK) progenitors (CD34(+)CD7(+)). The number of abnormal cells of B (CD19(+)) and T (CD3(+)) cells was below the cut-off value, but approximately 60% of the NK cells (CD3-CD56(+)) contained monosomy 7 in three of the patients.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0007-1048
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
110
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
876-9
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:11054073-Aged,
pubmed-meshheading:11054073-Aged, 80 and over,
pubmed-meshheading:11054073-Antigens, CD34,
pubmed-meshheading:11054073-B-Lymphocytes,
pubmed-meshheading:11054073-Chromosomes, Human, Pair 7,
pubmed-meshheading:11054073-Female,
pubmed-meshheading:11054073-Flow Cytometry,
pubmed-meshheading:11054073-Hematopoietic Stem Cells,
pubmed-meshheading:11054073-Humans,
pubmed-meshheading:11054073-Immunophenotyping,
pubmed-meshheading:11054073-In Situ Hybridization, Fluorescence,
pubmed-meshheading:11054073-Killer Cells, Natural,
pubmed-meshheading:11054073-Male,
pubmed-meshheading:11054073-Middle Aged,
pubmed-meshheading:11054073-Monosomy,
pubmed-meshheading:11054073-Myelodysplastic Syndromes
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pubmed:year |
2000
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pubmed:articleTitle |
Involvement of natural killer cells in patients with myelodysplastic syndrome carrying monosomy 7 revealed by the application of fluorescence in situ hybridization to cells collected by means of fluorescence-activated cell sorting.
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pubmed:affiliation |
Third Department of Internal Medicine, Akita University School of Medicine, Akita, Japan. ikuo@med.akita-u.ac.jp
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pubmed:publicationType |
Journal Article
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