Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0023470,
umls-concept:C0027022,
umls-concept:C0040715,
umls-concept:C0205182,
umls-concept:C0332120,
umls-concept:C0332281,
umls-concept:C0599718,
umls-concept:C0599813,
umls-concept:C0599893,
umls-concept:C1314939,
umls-concept:C1419782,
umls-concept:C1521692,
umls-concept:C1521991,
umls-concept:C1522702,
umls-concept:C1708726,
umls-concept:C1880022,
umls-concept:C2699782
|
pubmed:issue |
8
|
pubmed:dateCreated |
1997-11-12
|
pubmed:abstractText |
A reciprocal chromosome translocation between 13q12 and 8p11 is the consistent cytogenetic abnormality seen in a nonspecific myeloproliferative disorder that is associated with T-cell leukemia/lymphoma and peripheral blood eosinophilia. Detailed molecular analyses of the translocation breakpoints associated with this rearrangement have not been reported to date. We have now generated somatic cell hybrids from a newly described patient with this specific structural rearrangement and analyzed the breakpoints on the derivative chromosomes. We have shown that the breakpoint on chromosome 13 lies within a 300- to 500-kb region defined by the KIAA177 gene and D13S1123 marker. In addition, we have identified a 1.2-Mb YAC, 959A4, that crosses the translocation breakpoint on the short arm of chromosome 8 in this patient. The location of this breakpoint in 8p11 is distinct from the t(8;16) and t(8;22) translocations associated with M4/M5 myeloid leukemias, and suggests that three distinct loci located within 8p11 are involved in the pathogenesis of myeloid neoplasias.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0006-4971
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
90
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
3136-41
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:9376595-Adult,
pubmed-meshheading:9376595-Cells, Cultured,
pubmed-meshheading:9376595-Chromosome Mapping,
pubmed-meshheading:9376595-Chromosomes, Human, Pair 13,
pubmed-meshheading:9376595-Chromosomes, Human, Pair 8,
pubmed-meshheading:9376595-Humans,
pubmed-meshheading:9376595-In Situ Hybridization, Fluorescence,
pubmed-meshheading:9376595-Leukemia, Myeloid,
pubmed-meshheading:9376595-Male,
pubmed-meshheading:9376595-Polymerase Chain Reaction,
pubmed-meshheading:9376595-Translocation, Genetic
|
pubmed:year |
1997
|
pubmed:articleTitle |
Molecular characterization of the t(8;13)(p11;q12) translocation associated with an atypical myeloproliferative disorder: evidence for three discrete loci involved in myeloid leukemias on 8p11.
|
pubmed:affiliation |
Department of Neurosciences, Cleveland Clinic Foundation, OH 44195, USA.
|
pubmed:publicationType |
Journal Article,
Case Reports
|