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Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes. UK Cancer Cytogenetics Group (UKCCG).
Bench, A J; Nacheva, E P; Hood, T L; Holden, J L; French, L; Swanton, S; Champion, K M; Li, J; Whittaker, P; Stavrides, G; Hunt, A R; Huntly, B J; Campbell, L J; Bentley, D R; Deloukas, P; Green, A R.
Afiliación
  • Bench AJ; University of Cambridge, Department of Haematology, Cambridge Institute for Medical Research, UK.
Oncogene ; 19(34): 3902-13, 2000 Aug 10.
Article en En | MEDLINE | ID: mdl-10952764
Deletion of the long arm of chromosome 20 represents the most common chromosomal abnormality associated with the myeloproliferative disorders (MPDs) and is also found in other myeloid malignancies including myelodysplastic syndromes (MDS) and acute myeloid leukaemia (AML). Previous studies have identified a common deleted region (CDR) spanning approximately 8 Mb. We have now used G-banding, FISH or microsatellite PCR to analyse 113 patients with a 20q deletion associated with a myeloid malignancy. Our results define a new MPD CDR of 2.7 Mb, an MDS/AML CDR of 2.6 Mb and a combined 'myeloid' CDR of 1.7 Mb. We have also constructed the most detailed physical map of this region to date--a bacterial clone map spanning 5 Mb of the chromosome which contains 456 bacterial clones and 202 DNA markers. Fifty-one expressed sequences were localized within this contig of which 37 lie within the MPD CDR and 20 within the MDS/AML CDR. Of the 16 expressed sequences (six genes and 10 unique ESTs) within the 'myeloid' CDR, five were expressed in both normal bone marrow and purified CD34 positive cells. These data identify a set of genes which are both positional and expression candidates for the target gene(s) on 20q.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Cromosomas Humanos Par 20 / Deleción Cromosómica / Mapeo Contig / Trastornos Mieloproliferativos Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Oncogene Asunto de la revista: BIOLOGIA MOLECULAR / NEOPLASIAS Año: 2000 Tipo del documento: Article Pais de publicación: Reino Unido
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Cromosomas Humanos Par 20 / Deleción Cromosómica / Mapeo Contig / Trastornos Mieloproliferativos Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Oncogene Asunto de la revista: BIOLOGIA MOLECULAR / NEOPLASIAS Año: 2000 Tipo del documento: Article Pais de publicación: Reino Unido