Expression of TEL-AML1 Fusion Transcripts and Response to Induction Therapy in Standard Risk Acute Lymphoblastic Leukemia
暂无分享,去创建一个
P S Gaynon | H. Sather | F. Uckun | P. Gaynon | P. Hokland | F M Uckun | C. Navara | N. Pallisgaard | N Pallisgaard | P Hokland | C Navara | R Narla | H Sather | N Heerema | R. Narla | N. Heerema | Nyla Heerema
[1] M. Greaves,et al. Prenatal origin of acute lymphoblastic leukaemia in children , 1999, The Lancet.
[2] P S Gaynon,et al. Prognostic impact of trisomies of chromosomes 10, 17, and 5 among children with acute lymphoblastic leukemia and high hyperdiploidy (> 50 chromosomes). , 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[3] O. Hrusak,et al. TEL/AML1 positivity in childhood ALL: average or better prognosis? , 1999, Leukemia.
[4] P. Marynen,et al. The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia. , 1996, Blood.
[5] N. Heerema,et al. Expression of BCR-ABL, E2A-PBX1, and MLL-AF4 fusion transcripts in newly diagnosed children with acute lymphoblastic leukemia: a Children's Cancer Group initiative. , 1997, Leukemia & lymphoma.
[6] J. Whang‐Peng. Chromosomal abnormalities in acute lymphoblastic leukemia: structural and numerical changes in 234 cases. , 1981, Cancer genetics and cytogenetics.
[7] S. Raimondi. Current Status of Cytogenetic Research in Childhood Acute Lymphoblastic Leukemia , 1993 .
[8] J. Downing,et al. TEL gene rearrangement in acute lymphoblastic leukemia: a new genetic marker with prognostic significance. , 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[9] F. Uckun,et al. Immunophenotype-karyotype associations in human acute lymphoblastic leukemia. , 1989, Blood.
[10] N. Heerema,et al. Clinical significance of translocation t(1;19) in childhood acute lymphoblastic leukemia in the context of contemporary therapies: a report from the Children's Cancer Group. , 1998, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[11] C. Pui,et al. Uniform approach to risk classification and treatment assignment for children with acute lymphoblastic leukemia. , 1996, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[12] J. Downing,et al. Case-control study suggests a favorable impact of TEL rearrangement in patients with B-lineage acute lymphoblastic leukemia treated with antimetabolite-based therapy: a Pediatric Oncology Group study. , 1997, Blood.
[13] P S Gaynon,et al. CLINICAL OBSERVATIONS, INTERVENTIONS, AND THERAPEUTIC TRIALS Association of Chromosome Arm 9p Abnormalities With Adverse Risk in Childhood Acute Lymphoblastic Leukemia: A Report From the Children's Cancer Group , 2016 .
[14] Jianxiang Wang,et al. Transformation properties of the ETO gene, fusion partner in t(8:21) leukemias. , 1997, Cancer research.
[15] C. Bloomfield,et al. Chromosomal abnormalities in acute lymphoblastic leukemia. , 1981, Cancer research.
[16] P. Hokland,et al. Rapid and sensitive minimal residual disease detection in acute leukemia by quantitative real‐time RT‐PCR exemplified by t(12;21) TEL‐AML1 fusion transcript , 1999, Genes, chromosomes & cancer.
[17] D. Gilliland,et al. TEL is one of the targets for deletion on 12p in many cases of childhood B-lineage acute lymphoblastic leukemia , 1997, Leukemia.
[18] H. Sather,et al. Clinical features and treatment outcome of childhood T-lineage acute lymphoblastic leukemia according to the apparent maturational stage of T-lineage leukemic blasts: a Children's Cancer Group study. , 1997, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[19] D C Ward,et al. Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[20] H. Cavé,et al. ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia , 1997, Leukemia.
[21] E. Macintyre,et al. High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia. , 1995, Blood.
[22] E. Macintyre,et al. Fluorescence in situ hybridization analysis of masked (8;21)(q22;q22) translocations. , 1999, Cancer genetics and cytogenetics.
[23] P. Marynen,et al. TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13). , 1995, Blood.
[24] T. Golub,et al. Oligomerization of the ABL tyrosine kinase by the Ets protein TEL in human leukemia , 1996, Molecular and cellular biology.
[25] T. Golub,et al. Involvement of the TEL gene in hematologic malignancy by diverse molecular genetic mechanisms. , 1996, Current topics in microbiology and immunology.
[26] M. Schrappe,et al. Acute lymphoblastic leukemia of childhood: identification of two distinct regions of deletion on the short arm of chromosome 12 in the region of TEL and KIP1. , 1996, Blood.
[27] S. Shurtleff,et al. TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis. , 1995, Leukemia.
[28] M. Greaves,et al. Fetal origins of the TEL-AML1 fusion gene in identical twins with leukemia. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[29] J. Rowley,et al. TEL-AML1 translocations with TEL and CDKN2 inactivation in acute lymphoblastic leukemia cell lines , 1996 .
[30] H P Koeffler,et al. TEL/AML-1 dimerizes and is associated with a favorable outcome in childhood acute lymphoblastic leukemia. , 1996, Blood.
[31] A. Borkhardt,et al. Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion , 1999, Genes, chromosomes & cancer.
[32] J. Downing,et al. 12p Abnormalities and the TEL Gene (ETV6) in Childhood Acute Lymphoblastic Leukemia , 1997 .
[33] N. Heerema,et al. Treatment outcome and prognostic factors for infants with acute lymphoblastic leukemia treated on two consecutive trials of the Children's Cancer Group. , 1999, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[34] James M. Roberts,et al. TEL and KIP1 define the smallest region of deletions on 12p13 in hematopoietic malignancies. , 1995, Blood.
[35] P. Riegman,et al. 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. , 1995, Oncogene.
[36] J. Rowley. The role of chromosome translocations in leukemogenesis. , 1999, Seminars in hematology.
[37] C. Reynolds,et al. Frequent loss of heterozygosity at the TEL gene locus in acute lymphoblastic leukemia of childhood. , 1995, Blood.
[38] T. Gu,et al. Core-binding factor: a central player in hematopoiesis and leukemia. , 1999, Cancer research.
[39] Todd R. Golub,et al. Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation , 1994, Cell.
[40] H. Sather,et al. Early response to therapy and outcome in childhood acute lymphoblastic leukemia , 1997, Cancer.
[41] M. Greaves,et al. Protracted and variable latency of acute lymphoblastic leukemia after TEL-AML1 gene fusion in utero. , 1999, Blood.
[42] N. Heerema,et al. Clinical significance of Philadelphia chromosome positive pediatric acute lymphoblastic leukemia in the context of contemporary intensive therapies , 1998, Cancer.
[43] P S Gaynon,et al. Prognostic significance of cytogenetic abnormalities of chromosome arm 12p in childhood acute lymphoblastic leukemia , 2000, Cancer.
[44] G. Morgan,et al. Molecular quantitation of minimal residual disease in acute myeloid leukemia with t(8;21) can identify patients in durable remission and predict clinical relapse. , 2000, Blood.
[45] N. Heerema,et al. Clinical significance of MLL-AF4 fusion transcript expression in the absence of a cytogenetically detectable t(4;11)(q21;q23) chromosomal translocation. , 1998, Blood.
[46] J. Downing,et al. Low frequency of TEL-AML1 in relapsed acute lymphoblastic leukemia supports a favorable prognosis for this genetic subgroup , 1999, Leukemia.
[47] J. Rowley,et al. Correlation between the ETV6/CBFA2 (TEL/AMLI) fusion gene and karyotypic abnormalities in children with B‐cell precursor acute lymphoblastic leukemia , 1996, Genes, chromosomes & cancer.
[48] J. Weissenbach,et al. Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1. , 1995, Blood.
[49] G. Basso,et al. The common TEL/AML1 rearrangement does not represent a frequent event in acute lymphoblastic leukaemia occurring in children with Down syndrome , 1997, Leukemia.
[50] Peter J. Schaap,et al. Molecular characterization of the , 1997 .
[51] Iscn. International System for Human Cytogenetic Nomenclature , 1978 .
[52] P. Marynen,et al. Molecular characterization of 12p abnormalities in hematologic malignancies: deletion of KIP1, rearrangement of TEL, and amplification of CCND2. , 1996, Blood.