Deletions of D13S25, D13S319 and RB-1 mapping to 13q14.3 in T-cell prolymphocytic leukaemia

British Journal of Haematology

Volumn 114, Issue 2, 2001, Pages 327-332

  Brito Babapulle, V ^a,b   Baou, M ^a   Matutes, E ^a   Morilla, R ^a   Atkinson, S ^a   Catovsky, D ^a  

^a INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^b ROYAL MARSDEN HOSPITAL   (United Kingdom)

Author keywords

13q14.3 deletions; B CLL; Suppressor genes; T PLL; Trisomy 12

Indexed keywords

ADULT; AGED; ARTICLE; ATAXIA TELANGIECTASIA; B CELL LEUKEMIA; CHROMOSOME 13Q; CHROMOSOME DELETION; CHROMOSOME INVERSION; CHROMOSOME LOSS; CHRONIC LYMPHATIC LEUKEMIA; CLINICAL ARTICLE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE LOCUS; GENE MAPPING; GENETIC MARKER; HUMAN; MALE; MULTIPLE MYELOMA; NONHODGKIN LYMPHOMA; PRIORITY JOURNAL; PROLYMPHOCYTIC LEUKEMIA; T CELL LEUKEMIA; TELOMERE; TUMOR SUPPRESSOR GENE;

ADULT; AGED; AGED, 80 AND OVER; FEMALE; GENE DELETION; GENES, RETINOBLASTOMA; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INVERSION, CHROMOSOME; KARYOTYPING; LEUKEMIA, B-CELL, CHRONIC; LEUKEMIA, PROLYMPHOCYTIC; LEUKEMIA, T-CELL; MALE; MIDDLE AGED; TRISOMY;

EID: 0034892389     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.2001.02935.x     Document Type: Article

References (21)

1. Assignment of 48 ESTs to chromosome 13 band 13q14.3 and expression pattern for ESTs located in the core region deleted in B-CLL
2. Construction of a 780-kb PAC,BAC, and cosmid contig encompassing the minimal critical deletion involved in B-Cell chronic lymphocytic leukemia at 13q14.3
3. Inversion and tandem translocation involving chromosome 14q11 and 14q32 in T-prolymphocytic leukemia and T-cell leukemia in patients with ataxia telangiectasia
4. The D13S25 locus mapping to 13q14.3 is deleted in T-prolymphocytic leukaemia
5. Frequent monoallelic loss of D13S319 in multiple myeloma patients shown by interphase fluorescence in situ hybridisation
6. Detailed molecular delineation of 13q14.3 loss in B-Cell chronic lymphocytic leukemia
7. 13q14 deletion in non-Hodgkin's lymphoma: Correlation with clinicopathologic features
8. Recurrent molecular deletion of the 12p13 region centromeric to ETV6/TEL, in T-cell prolymphocytic leukemia
9. Cytogenetics of chronic lymphocytic leukemia
10. A cosmid and cDNA fine physical map of a 13q14 region frequently lost in B-cell chronic lymphocytic leukemia and the identification of a new tumour suppressor gene, Leu5
11. Cloning of two candidate tumour suppressor genes within a 10kb region on chromosome 13q14, frequently deleted in chronic lymphocytic leukemia
12. Abnormalities of chromosome 8, 11, 14, and X in T-prolymphocytic leukaemia studied by fluorescence in-situ hybridisation
13. Cytogenetic and molecular characterization of a patient with simultaneous B-cell chronic lymphocytic leukemia and peripheral T-cell lymphoma
14. Clinical and laboratory features of 78 cases of T-prolymphocytic leukemia
15. A biological role for deletions in chromosomal band 13q14 in mantle cell and peripheral T-cell lymphoma
16. Unusual breakpoint distribution on chromosome 8p11 in T-prolymphocytic leukemia
17. Expressed sequences as candidates for a novel tumour suppressor gene at band 13q14 in B-cell chronic lymphocytic leukemia and mantle cell lymphoma
18. Identification of TCL-1 locus involved in T-cell neoplasia
19. Clustering of missense mutations in the ataxia telangiectasia gene in sporadic T-cell leukemia
20. ATM is usually rearranged in T-cell prolymphocytic leukemia
21. Deletion of 13q14 remains an independent adverse prognostic variable in multiple myeloma despite its frequent detection by interphase fluorescence in situ hybridisation