A complex pattern of recurrent chromosomal losses and gains in T-cell prolymphocytic leukemia.

Integrated genomic sequencing reveals mutational landscape of T-cell prolymphocytic leukemia. Blood (2014) 1.36

TCR-dependent transformation of mature memory phenotype T cells in mice. J Clin Invest (2011) 1.13

Genomic profiling of peripheral T-cell lymphoma, unspecified, and anaplastic large T-cell lymphoma delineates novel recurrent chromosomal alterations. Am J Pathol (2004) 1.08

Molecular allelokaryotyping of T-cell prolymphocytic leukemia cells with high density single nucleotide polymorphism arrays identifies novel common genomic lesions and acquired uniparental disomy. Haematologica (2009) 0.99

High TCL1 expression and intact T-cell receptor signaling define a hyperproliferative subset of T-cell prolymphocytic leukemia. Blood (2007) 0.98

Chromosomal gains at 9q characterize enteropathy-type T-cell lymphoma. Am J Pathol (2002) 0.98

Recurrent JAK1 and JAK3 somatic mutations in T-cell prolymphocytic leukemia. Leukemia (2013) 0.93

Dysregulated TCL1 requires the germinal center and genome instability for mature B-cell transformation. Blood (2006) 0.86

Intestinal γδ T-cell lymphomas are most frequently of type II enteropathy-associated T-cell type. Hum Pathol (2013) 0.81

Redundant and nonredundant functions of ATM and H2AX in αβ T-lineage lymphocytes. J Immunol (2012) 0.80

Pediatric T-cell prolymphocytic leukemia with an isolated 12(p13) deletion and aberrant CD117 expression. Exp Hematol Oncol (2012) 0.80

Do novo del(9)(p13) in a childhood T-cell prolymphocytic leukemia as sole abnormality. Exp Hematol Oncol (2014) 0.75

Challenging perspectives on the cellular origins of lymphoma. Open Biol (2016) 0.75

Burrowing through the Heterogeneity: Review of Mouse Models of PTCL-NOS. Front Oncol (2016) 0.75

LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1. Science (2003) 19.77

Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer. Nature (1998) 7.55

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study. J Med Genet (1997) 6.85

Regulation of autophagy by the inositol trisphosphate receptor. Cell Death Differ (2007) 4.12

EWS and ATF-1 gene fusion induced by t(12;22) translocation in malignant melanoma of soft parts. Nat Genet (1993) 2.72

Chromosomes in Ewing's sarcoma. I. An evaluation of 85 cases of remarkable consistency of t(11;22)(q24;q12). Cancer Genet Cytogenet (1988) 2.42

Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints. Genes Chromosomes Cancer (1992) 2.31

Quantitative HOX expression in chromosomally defined subsets of acute myelogenous leukemia. Leukemia (2002) 2.29

Rituximab in CD20 positive multiple myeloma. Leukemia (2007) 2.11

Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome. Proc Natl Acad Sci U S A (1989) 2.06

Candidate tumor-suppressor genes MTS1 (p16INK4A) and MTS2 (p15INK4B) display frequent homozygous deletions in primary cells from T- but not from B-cell lineage acute lymphoblastic leukemias. Blood (1994) 2.01

Are complicated forms of celiac disease cryptic T-cell lymphomas? Blood (1998) 1.87

The human protooncogene product p33pim is expressed during fetal hematopoiesis and in diverse leukemias. Proc Natl Acad Sci U S A (1989) 1.86

The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence. Genomics (1991) 1.76

An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome. Hum Mol Genet (1993) 1.75

Systematic analysis of 95 reciprocal translocations of autosomes. Hum Genet (1978) 1.59

Expression and prognostic significance of survivin in de novo acute myeloid leukaemia. Br J Haematol (2000) 1.56

The clinicopathological features of extensive small intestinal CD4 T cell infiltration. Gut (1999) 1.54

Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization. Hum Genet (1993) 1.51

High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2 alpha B gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21. Blood (2000) 1.50

Rapid development of myelopathy after HTLV-I infection acquired by transfusion during cardiac transplantation. N Engl J Med (1990) 1.46

A t(8;14)(q24;q11) translocation in a T-cell leukemia (L1-ALL) with c-myc and TcR-alpha chain locus rearrangements. Int J Cancer (1986) 1.43

Translocation involving chromosome 22 in Ewing's sarcoma. A cytogenetic study of four fresh tumors. Cancer Genet Cytogenet (1984) 1.42

Activation of the human homologue of the Drosophila sina gene in apoptosis and tumor suppression. Proc Natl Acad Sci U S A (1996) 1.40

The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 families. Hum Genet (1983) 1.40

A human homolog of the S. cerevisiae HIR1 and HIR2 transcriptional repressors cloned from the DiGeorge syndrome critical region. Hum Mol Genet (1995) 1.39

High frequencies of inversions and translocations of chromosomes 7 and 14 in ataxia telangiectasia. Mutat Res (1980) 1.38

High human T-cell lymphotropic virus type I proviral DNA load with polyclonal integration in peripheral blood mononuclear cells of French West Indian, Guianese, and African patients with tropical spastic paraparesis. Blood (1990) 1.37

Cancer risk in heterozygotes for ataxia-telangiectasia. Int J Cancer (2001) 1.32

Drastic rise of intracellular adenosine(5')tetraphospho(5')adenosine correlates with onset of DNA synthesis in eukaryotic cells. Eur J Biochem (1984) 1.31

Breast cancer risk in ataxia telangiectasia (AT) heterozygotes: haplotype study in French AT families. Br J Cancer (1999) 1.30

Cell surface phenotype and human T lymphotropic virus type 1 antigen expression in 12 T cell lines derived from peripheral blood and cerebrospinal fluid of West Indian, Guyanese and African patients with tropical spastic paraparesis. J Gen Virol (1990) 1.29

Human T cell gamma genes are frequently rearranged in B-lineage acute lymphoblastic leukemias but not in chronic B cell proliferations. J Exp Med (1987) 1.28

DiGeorge syndrome and related syndromes associated with 22q11.2 deletions. A review. Ann Genet (1995) 1.28

Interstitial 22q11 microdeletion excluding the ADU breakpoint in a patient with DiGeorge syndrome. Hum Mol Genet (1995) 1.27

Hybrid T cell receptor genes formed by interlocus recombination in normal and ataxia-telangiectasis lymphocytes. J Exp Med (1990) 1.27

[Chromosome 8 : complete trisomy and segmental trisomies]. Ann Genet (1977) 1.22

Haploinsufficiency of the IKZF1 (IKAROS) tumor suppressor gene cooperates with BCR-ABL in a transgenic model of acute lymphoblastic leukemia. Leukemia (2010) 1.22

Regulation of transcription of the human T cell antigen receptor delta chain gene. A T lineage-specific enhancer element is located in the J delta 3-C delta intron. J Exp Med (1990) 1.22

Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses. Genes Chromosomes Cancer (2000) 1.21

DNA replication-dependent formation of joint DNA molecules in Physarum polycephalum. Mol Cell (2001) 1.20

A model for tumor suppression using H-1 parvovirus. Proc Natl Acad Sci U S A (1993) 1.20

Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity. Hum Mol Genet (1995) 1.20

Peripheral selection of V delta 1+ cells with restricted T cell receptor delta gene junctional repertoire in the peripheral blood of healthy donors. J Exp Med (1993) 1.20

hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities. J Pathol (2007) 1.20

Evaluation of MDM2 and CDK4 amplification by real-time PCR on paraffin wax-embedded material: a potential tool for the diagnosis of atypical lipomatous tumours/well-differentiated liposarcomas. J Pathol (2004) 1.19

NF-kappaB inhibition sensitizes to starvation-induced cell death in high-risk myelodysplastic syndrome and acute myeloid leukemia. Oncogene (2007) 1.19

Transgenic mice for MTCP1 develop T-cell prolymphocytic leukemia. Blood (1998) 1.18

Cell-specific expression of a profilin gene family. DNA Cell Biol (1990) 1.17

The MTCP-1/c6.1B gene encodes for a cytoplasmic 8 kD protein overexpressed in T cell leukemia bearing a t(X;14) translocation. Oncogene (1994) 1.17

MicroRNA-206 expression levels correlate with clinical behaviour of rhabdomyosarcomas. Br J Cancer (2010) 1.16

Persistent polyclonal B lymphocytosis with binucleated lymphocytes: a study of 25 cases. Groupe Français d'Hématologie Cellulaire. Br J Haematol (1999) 1.16

The cell cycle of lymphocytes in Fanconi anemia. Hum Genet (1982) 1.16

Oligoclonal expansion of CD8+ CD57+ T cells with restricted T-cell receptor beta chain variability after bone marrow transplantation. Blood (1994) 1.15

MTCP-1: a novel gene on the human chromosome Xq28 translocated to the T cell receptor alpha/delta locus in mature T cell proliferations. Oncogene (1993) 1.14

Cyclin D2 dysregulation by chromosomal translocations to TCR loci in T-cell acute lymphoblastic leukemias. Leukemia (2006) 1.12

[De novo trisomy 4p by 4p isochromosome]. Ann Genet (1976) 1.11

No germline ATM mutation in a series of 16T-cell prolymphocytic leukemias. Blood (2000) 1.11

Mapping of a Physarum chromosomal origin of replication tightly linked to a developmentally-regulated profilin gene. Nucleic Acids Res (1992) 1.11

Inactivation of the ATM gene in T-cell prolymphocytic leukemias. Blood (1998) 1.10

Prevalence and distribution of ringed sideroblasts in primary myelodysplastic syndromes. J Clin Pathol (1983) 1.09

Processing in the external transcribed spacer of ribosomal RNA from Physarum polycephalum. Nucleic Acids Res (1986) 1.09

Segmental chromosomal alterations lead to a higher risk of relapse in infants with MYCN-non-amplified localised unresectable/disseminated neuroblastoma (a SIOPEN collaborative study). Br J Cancer (2011) 1.09

Crystal structure of p14TCL1, an oncogene product involved in T-cell prolymphocytic leukemia, reveals a novel beta-barrel topology. Structure (1998) 1.09

Cytogenetic studies in acute promyelocytic leukemia: a survey of secondary chromosomal abnormalities. Genes Chromosomes Cancer (1991) 1.09

Interstitial deletion of the short arm of chromosome 20 in arteriohepatic dysplasia (Alagille syndrome). J Pediatr (1990) 1.08

Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormality. Hum Genet (1987) 1.08

Genomic alterations of the p19ARF encoding exons in T-cell acute lymphoblastic leukemia. Blood (1998) 1.07

Multiple tumor-suppressor gene 1 inactivation is the most frequent genetic alteration in T-cell acute lymphoblastic leukemia. Blood (1996) 1.06

Down-regulation of human granzyme B expression by glucocorticoids. Dexamethasone inhibits binding to the Ikaros and AP-1 regulatory elements of the granzyme B promoter. J Biol Chem (1998) 1.06

Leiomyosarcomas and most malignant fibrous histiocytomas share very similar comparative genomic hybridization imbalances: an analysis of a series of 27 leiomyosarcomas. Lab Invest (2001) 1.06

A clinical, molecular and cytogenetic study of 12 cases of human herpesvirus 8 associated primary effusion lymphoma in HIV-infected patients. Hematol J (2001) 1.06

Immunological classification of acute myeloblastic leukemias: relevance to patient outcome. Leukemia (2003) 1.05

Prognostic significance of FLT3 internal tandem repeat in patients with de novo acute myeloid leukemia treated with reinforced courses of chemotherapy. Leukemia (2002) 1.05

Use of oligonucleotide probes directed against T cell antigen receptor gamma delta variable-(diversity)-joining junctional sequences as a general method for detecting minimal residual disease in acute lymphoblastic leukemias. J Clin Invest (1990) 1.04

TCL1 oncogene expression in AIDS-related lymphomas and lymphoid tissues. Proc Natl Acad Sci U S A (1999) 1.03

Structural Organization of the WD repeat protein-encoding gene HIRA in the DiGeorge syndrome critical region of human chromosome 22. Genome Res (1996) 1.03

Secondary nonrandom chromosomal abnormalities of band 13q34 in Burkitt lymphoma-leukemia. Genes Chromosomes Cancer (1989) 1.03

Clonal expansion of lymphocytes bearing the gamma delta T-cell receptor in a patient with large granular lymphocyte disorder. Blood (1989) 1.03

Immunophenotype of adult acute lymphoblastic leukemia, clinical parameters, and outcome: an analysis of a prospective trial including 562 tested patients (LALA87). French Group on Therapy for Adult Acute Lymphoblastic Leukemia. Blood (1994) 1.03

Cytogenetic studies on 519 consecutive de novo acute nonlymphocytic leukemias. Cancer Genet Cytogenet (1987) 1.02

Chromosomes in Ewing's sarcoma. II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16). Cancer Genet Cytogenet (1988) 1.02

Acute myelodysplasia with myelofibrosis: a report of eight cases. Br J Haematol (1981) 1.01

Multiple chromosomal mechanisms generate an EWS/FLI1 or an EWS/ERG fusion gene in Ewing tumors. Cancer Genet Cytogenet (1997) 1.01

Invariant temporal order of replication of the four actin gene loci during the naturally synchronous mitotic cycles of Physarum polycephalum. Proc Natl Acad Sci U S A (1984) 1.00

Aplastic anemia and paroxysmal nocturnal hemoglobinuria: search for a pathogenetic link. Blood (1995) 1.00

Unicolor and bicolor in situ hybridization in the diagnosis of peripheral neuroepithelioma and related tumors. Genes Chromosomes Cancer (1992) 1.00

Acquisition of granzyme B and Fas ligand proteins by human keratinocytes contributes to epidermal cell defense. J Immunol (1997) 0.99

Site-specific initiation of DNA replication within the non-transcribed spacer of Physarum rDNA. Nucleic Acids Res (1995) 0.99