Occurrence of TEL-AML1 fusion resulting from (12;21) translocation in human early B-lineage leukemia cell lines

Fusion of PDGF receptor β to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation

1994 • 1,211 citations

Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia.

1995 • 738 citations

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 • 566 citations

The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion

1995 • 563 citations

High frequency of t(12;21) in childhood B-lineage acute lymphoblastic leukemia

1995 • 454 citations

TEL/AML-1 dimerizes and is associated with a favorable outcome in childhood acute lymphoblastic leukemia

1996 • 306 citations

The novel activation of ABL by fusion to an ets-related gene, TEL.

1995 • 289 citations

The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia

1996 • 258 citations

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 • 235 citations

t( 12;21): A new recurrent translocation in acute lymphoblastic leukemia

1994 • 229 citations

Frequent loss of heterozygosity at the TEL gene locus in acute lymphoblastic leukemia of childhood

1995 • 132 citations

Genomic organization of TEL: the human ETS-variant gene 6.

1996 • 114 citations

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 • 112 citations

TEL and KIP1 define the smallest region of deletions on 12p13 in hematopoietic malignancies

1995 • 103 citations

Detection and quantification of TEL/AML1 fusion transcripts by polymerase chain reaction in childhood acute lymphoblastic leukemia.

1996 • 101 citations

Fluorescence in situ hybridization mapping of translocations and deletions involving the short arm of human chromosome 12 in malignant hematologic diseases

1994 • 90 citations

TEL-AML1 fusion RNA as a new target to detect minimal residual disease in pediatric B-cell precursor acute lymphoblastic leukemia

1996 • 86 citations

Recurrent chromosomal translocations and fusion genes in leukemia-lymphoma cell lines.

1995 • 85 citations

High incidence of TEL/AML1 fusion resulting from a cryptic t(12;21) in childhood B-lineage acute lymphoblastic leukemia in Taiwan.

1996 • 83 citations

TEL/AML1 fusion gene is a rare event in adult acute lymphoblastic leukemia.

1996 • 76 citations

Mutational analysis of the candidate tumor suppressor genes TEL and KIP1 in childhood acute lymphoblastic leukemia.

1996 • 67 citations

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 • 57 citations

The der(21)t(12;21) chromosome is always formed in a 12;21 translocation associated with childhood acute lymphoblastic leukaemia

1996 • 54 citations

The TEL gene and human leukemia

1996 • 54 citations

Identification of cytogenetically undetected 12p13 translocations and associated deletions with fluorescence in situ hybridization

1995 • 42 citations

Lack of TEL-AML1 fusion transcript resulting from a cryptic t(12;21) in adult B lineage acute lymphoblastic leukemia in Taiwan.

1996 • 25 citations

Epidemiological research on the influence of maternal and paternal external exposure factors on the incidence of congenital leukaemia

1996 • 2 citations

Deleted Work

1955 • 0 citations