Cytogenetic abnormalities in acute lymphoblastic leukemia;Alteraciones cromosómicas en la leucemia linfobiástica aguda

Anales Espanoles de Pediatria

Volumn 55, Issue 1, 2001, Pages 45-52

  Martin Ramos M L ^a   Fernandez Martinez F J ^a   Barreiro Miranda, E ^a  

^a HOSPITAL UNIVERSITARIO 12 DE OCTUBRE   (Spain)

Author keywords

Acute lymphoblastic leukemia; Cytogenetics; Prognosis

Indexed keywords

ACUTE LEUKEMIA; ACUTE LYMPHOBLASTIC LEUKEMIA; CHILD; CHILDHOOD LEUKEMIA; CHROMOSOME 11Q; CHROMOSOME 12; CHROMOSOME 19P; CHROMOSOME 6Q; CHROMOSOME DELETION; CHROMOSOME INVERSION; CHROMOSOME TRANSLOCATION; CYTOGENETICS; HUMAN; KARYOTYPE; PHILADELPHIA 1 CHROMOSOME; PLOIDY; PROGNOSIS; REVIEW;

CHILD; CHROMOSOME ABERRATIONS; HUMANS; LEUKEMIA, LYMPHOCYTIC, ACUTE, L1; PLOIDIES; PROGNOSIS;

EID: 17444433323     PISSN: 03024342     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (36)

1. Current status of cytogenetic research in childhood acute lymphoblastic leukemia
2. Childhood leukemias
3. Trisomy of leukemic cell chromosomes 4 and 10 identifies children with B-progenitor cell acute lymphoblastic leukemia with a very low risk of treatment failure
4. Hyperdiploid (47-50) acute lymphoblastic leukemia in children
5. Clinical presentation, karyotypic characterization, and treatment autcome of childhood acute lymphoblastic leukemia with a near-haploid or hypodiploid < 45 line
6. Cytogenetic abnormalities in childhood acute lymphoblastic leukemia correlates with clinical features and treatment outcome
7. Prognostic implications of chromosomal findings in acute lymphoblastic leukemia at diagnosis
8. Centric and pericentric chromosome rearrangements in hematopoietic malignancies
9. Philadelphia chromosome positive childhood acute lymphoblastic leukemia: Clinical and cytogenetic characteristics and treatment outcome: A Pediatric Oncology Group Study
10. Translocation t(9;22) is associated with extremely poor prognosis in intensively treated children with acute lymphoblastic leukemia
11. The management of patients with leukemia: The role of cytogenetics in this molecular era
12. Collaborative study of karyotypes in childhood acute lymphoblastic leukemia
13. Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias
14. Human acute leukemia cell line with the t(4;11) chromosomal rearrangement exhibits B lineage and monocytic characteristics
15. Unifirm approch to risk classification and treatment assignment to children with acute lymphoblastic leukemia
16. Immunologic, cytogenetic, and clinical characterization of childhood acute lymphoblastic leukemia with the t(1;9)(q23;p13) or its derivative
17. Fusion with EA2 converts the Pbxl homeodomain protein into a constitutive transcriptional activator in human leukemias carrying the (1;19)
18. Poor prognosis of children with pre-B acute lymphoblastic leukemia is associated with the t(1;19)(q23,p13)
19. Chromosomal translocations involving the E2A gene in acute lymphoblastic leukemia: Clinical features and molecular pathogenesis
20. t(8;14) translocation in a Burkitt's type of lymphoblastic leukemia
21. Molecular basis of human B cell neoplasia
22. High survival rate in advanced-stage-B-cell lymphomas and leukemias without CNS involvement with a short intensive polychemotherapy: Results from the French Paediatric Oncology Society of a randomised trial of 216 children
23. Aplicaciones de la fluorescencia con hibridación in situ (FISH) en la leucemia linfoblástica aguda
24. Heterogeneity of presenting features and their relation to treatment outcome in 120 clildren with T-cell acute lymphoblastic leukemia
25. Chromosomes and causation of human cancer and leukemia XXVI, Berding studies in acute lymphoblastic leukemia
26. Abnormalities of the long arm of chromosome 6 in childhood acute lymphoblastic leukemia
27. Large-scale molecular mapping of human c-myb: c-myb proto-oncogene is not involved in 6q- abnormalities of lymphoid tumors
28. Localization the estrogen receptor locus (ESR) to chromosome 6q25.1 by FISH and a simple post-FISH banding technique
29. Nonrandom abnormalities of chromosome 9p in childhood acute lymphoblastic leukemia: Association with, high-risk clinical features
30. Chromosomal localization of human leukocyte, fibroblast, and immune interferon genes by means of in situ hybridization
31. INK4B) display frequent homozygous deletions in primary cells from T-but not from B-cell lineage acute lymphoblastic leukemias
32. Nonrandom involvement of the 12p12 breakpoint in chromosome abnormalities of childhood acute lymphoblastic leukemia
33. Translocation (12;22)(p13;q11) in myeloproliferative disorders results in fusion of the ETS-like Tel gene on 12p13 to the MN1 gene on 22q11
34. The fusion of TEL and ABL in human acute lymphoblastic leukemia is a rare event
35. t(12;21): A new recurrent translocation in acute lymphoblastic leukemia