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Fine mapping of the human renal oncocytoma-associated translocation (5;11)(q35;q13) breakpoint.
- Source :
-
Cancer genetics and cytogenetics [Cancer Genet Cytogenet] 1997 Jul 15; Vol. 96 (2), pp. 95-101. - Publication Year :
- 1997
-
Abstract
- Recent cytogenetic analysis of a series of human renal oncocytomas revealed the presence of a recurring chromosomal translocation (5;11)(q35;q13) as sole anomaly in a subset of the tumors. The molecular characterization of this translocation was initiated using two primary t(5;11)-positive renal oncocytomas and a panel of somatic cell hybrids derived from one of these tumors, in conjunction with fluorescence in situ hybridization (FISH) and Southern blot analysis. The breakpoint in chromosome band 11q13 could be located within a genomic interval of at maximum 400 Kb immediately centromeric to the BCL1 locus.
- Subjects :
- Chromosome Banding
Chromosome Disorders
Chromosome Mapping
Genetic Markers
Humans
Hybrid Cells
In Situ Hybridization, Fluorescence
Translocation, Genetic
Adenoma, Oxyphilic genetics
Chromosome Aberrations genetics
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 5
Kidney Neoplasms genetics
Subjects
Details
- Language :
- English
- ISSN :
- 0165-4608
- Volume :
- 96
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Cancer genetics and cytogenetics
- Publication Type :
- Academic Journal
- Accession number :
- 9216713
- Full Text :
- https://doi.org/10.1016/s0165-4608(96)00250-6