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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1997-9-4
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pubmed:abstractText |
mel-18 is a mammalian homolog of Drosophila melanogaster Polycomb group genes. Mice lacking the mel-18 gene show a posterior transformation of the axial skeleton, severe combined immunodeficiency, and a food-passing disturbance in the lower intestine due to hypertrophy of the smooth muscle layer. In this study, the severe combined immunodeficiency observed in mel-18 mutant mice is correlated with the impaired mitotic response of lymphocyte precursors upon interleukin-7 stimulation. Strikingly, the axial skeleton and lymphoid phenotypes are identical in both mel-18 and bmi-1 mutants, indicating that the Mel-18 and Bmi-1 gene products might act in the same genetic cascade. These results suggest that mammalian Polycomb group gene products are involved in cell cycle progression in the immune system.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
|
pubmed:issn |
1074-7613
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
135-46
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9252126-Animals,
pubmed-meshheading:9252126-Bone Marrow Cells,
pubmed-meshheading:9252126-Cell Cycle,
pubmed-meshheading:9252126-Cell Division,
pubmed-meshheading:9252126-DNA-Binding Proteins,
pubmed-meshheading:9252126-Flow Cytometry,
pubmed-meshheading:9252126-Genotype,
pubmed-meshheading:9252126-Hematopoietic Stem Cells,
pubmed-meshheading:9252126-Interleukin-7,
pubmed-meshheading:9252126-Lymphocytes,
pubmed-meshheading:9252126-Mice,
pubmed-meshheading:9252126-Signal Transduction,
pubmed-meshheading:9252126-Zinc Fingers
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pubmed:year |
1997
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pubmed:articleTitle |
The role of mel-18, a mammalian Polycomb group gene, during IL-7-dependent proliferation of lymphocyte precursors.
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pubmed:affiliation |
Core Research for Evolution Science and Technology, Japan Science and Technology Corporation, and Division of Molecular Immunology, Center for Biomedical Science, School of Medicine, Chiba University.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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