Source:http://linkedlifedata.com/resource/pubmed/id/17321333
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2007-2-26
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pubmed:abstractText |
A reciprocal t(X;12)(p11;p13) was found as the sole clonal abnormality in biphenotypic leukemia with myeloid and B-lymphoid differentiation. With fluorescence in situ hybridization analysis, the ETV6 gene (previously TEL) was found to be translocated intact to the derivative X chromosome; no MLL and BCR/ABL rearrangements were found. The patient achieved complete remission after induction chemotherapy. To our knowledge, this cytogenetic aberration has not been reported previously as a sole abnormality in hematological malignancies. Its presence may suggest an important role in the pathogenesis of biphenotypic leukemia.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0165-4608
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
173
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
159-63
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pubmed:meshHeading |
pubmed-meshheading:17321333-Acute Disease,
pubmed-meshheading:17321333-Chromosome Banding,
pubmed-meshheading:17321333-Chromosome Painting,
pubmed-meshheading:17321333-Chromosomes, Human, Pair 12,
pubmed-meshheading:17321333-Chromosomes, Human, X,
pubmed-meshheading:17321333-Female,
pubmed-meshheading:17321333-Humans,
pubmed-meshheading:17321333-Karyotyping,
pubmed-meshheading:17321333-Leukemia,
pubmed-meshheading:17321333-Lymphocytes,
pubmed-meshheading:17321333-Middle Aged,
pubmed-meshheading:17321333-Myeloid Cells,
pubmed-meshheading:17321333-Translocation, Genetic
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pubmed:year |
2007
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pubmed:articleTitle |
Translocation (X;12)(p11;p13) as a sole abnormality in biphenotypic acute leukemia.
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pubmed:affiliation |
Laboratory of Health Physics and Environmental Hygiene, National Center for Scientific Research (NCSR) Demokritos, 15310 Aghia Paraskevi, Athens, Greece. pmanola@ipta.demokritos.gr
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pubmed:publicationType |
Journal Article,
Case Reports
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