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MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations

Journal of medical genetics, 2010-01, Vol.47 (1), p.22-29

2010

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Autocrine induction of invasion and metastasis by tumor-associated trypsin inhibitor in human colon cancer cells

Oncogene, 2008-07, Vol.27 (29), p.4024-4033

2008

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The LAZ3(BCL-6) oncoprotein recruits a SMRT/mSIN3A/histone deacetylase containing complex to mediate transcriptional repression

Nucleic acids research, 1998-10, Vol.26 (20), p.4645-4651

1998

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Recurrent genomic aberrations combined with deletions of various tumour suppressor genes may deregulate the G1 S transition in CD4+CD56+ haematodermic neoplasms and contribute to the aggressiveness of the disease

Leukemia, 2009-04, Vol.23 (4), p.698-707

2009

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Corepressor SMRT Binds the BTB/POZ Repressing Domain of the LAZ3/BCL6 Oncoprotein

Proceedings of the National Academy of Sciences - PNAS, 1997-09, Vol.94 (20), p.10762-10767

1997

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LAZ3, a novel zinc-finger encoding gene, is disrupted by recurring chromosome 3q27 translocations in human lymphomas

Nature genetics, 1993-09, Vol.5 (1), p.66-70

1993

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Nonrandom 4p13 rearrangements of the RhoH/TTF gene, encoding a GTP-binding protein, in non-Hodgkin's lymphoma and multiple myeloma

Oncogene, 2000-04, Vol.19 (16), p.2023-2032

2000

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Genotype–phenotype correlation of 30 patients with Smith-Magenis syndrome (SMS) using comparative genome hybridisation array: cleft palate in SMS is associated with larger deletions

Journal of medical genetics, 2007-08, Vol.44 (8), p.537-540

2007

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Overexpressed BCL6 (LAZ3) oncoprotein triggers apoptosis, delays S phase progression and associates with replication foci

Oncogene, 1999-09, Vol.18 (36), p.5063-5075

1999

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A novel modulator domain of Ets transcription factors

Genes & development, 1992-06, Vol.6 (6), p.965-974

1992

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LAZ3 Rearrangements in Non-Hodgkin’s Lymphoma: Correlation With Histology, Immunophenotype, Karyotype, and Clinical Outcome in 217 Patients

Blood, 1994-05, Vol.83 (9), p.2423-2427

1994

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Small deletions occur in highly conserved regions of the LAZ3/BCL6 major translocation cluster in one case of non-Hodgkin's lymphoma without 3q27 translocation

Oncogene, 1997-02, Vol.14 (7), p.849-855

1997

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Splicing with inverted order of exons occurs proximal to large introns

The EMBO journal, 1992-03, Vol.11 (3), p.1095-1098

1992

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Waved aCGH: to smooth or not to smooth

Nucleic acids research, 2010-04, Vol.38 (7), p.e94-e94

2010

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High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2αB gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21

Blood, 2000-10, Vol.96 (8), p.2862-2869

2000

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A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma

The journal of clinical endocrinology and metabolism, 1999-05, Vol.84 (5), p.1700-1704

1999

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Therostasin, a Novel Clotting Factor Xa Inhibitor from the Rhynchobdellid Leech, Theromyzon tessulatum

The Journal of biological chemistry, 2000-10, Vol.275 (42), p.32701-32707

2000

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The BTB/POZ domain targets the LAZ3/BCL6 oncoprotein to nuclear dots and mediates homomerisation in vivo

Oncogene, 1995-12, Vol.11 (12), p.2689-2697

1995

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Analysis of LAZ3 (BCL-6) Status in B-Cell Non-Hodgkin's Lymphomas: Results of Rearrangement and Gene Expression Studies and a Mutational Analysis of Coding Region Sequences

Blood, 1995-05, Vol.85 (10), p.2877-2884

1995

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The B cell transcriptional coactivator BOB1/OBF1 gene fuses to the LAZ3/BCL6 gene by t(3;11)(q27;q23.1) chromosomal translocation in a B cell leukemia line (Karpas 231)

Leukemia, 1996-04, Vol.10 (4), p.579-587

1996

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Genomic structure and assignment of the RhoH/TTF small GTPase gene (ARHH) to 4p13 by in situ hybridization

Genomics (San Diego, Calif.), 1997-07, Vol.43 (1), p.89-94

1997

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Cloning of a breakpoint cluster region at band 3q27 involved in human non-Hodgkin's lymphoma

Genes chromosomes & cancer, 1993-11, Vol.8 (3), p.149-154

1993

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Dysregulation and overexpression of HMGA2 in myelofibrosis with myeloid metaplasia

Genes chromosomes & cancer, 2004-01, Vol.39 (1), p.82-87

2004

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Detection of minimal residual disease in chronic myeloid leukemia patients after bone marrow transplantation by polymerase chain reaction

Leukemia, 1990, Vol.4 (1), p.1-5

1990

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Recurrent genomic aberrations combined with deletions of various tumour suppressor genes may deregulate the G1 S transition in CD4+CD56+ haematodermic neoplasms and contribute to the aggressiveness of the disease

Leukemia, 2009-04, Vol.23 (4), p.825-826

2009

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MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations

Autocrine induction of invasion and metastasis by tumor-associated trypsin inhibitor in human colon cancer cells

The LAZ3(BCL-6) oncoprotein recruits a SMRT/mSIN3A/histone deacetylase containing complex to mediate transcriptional repression

Recurrent genomic aberrations combined with deletions of various tumour suppressor genes may deregulate the G1 S transition in CD4+CD56+ haematodermic neoplasms and contribute to the aggressiveness of the disease

Corepressor SMRT Binds the BTB/POZ Repressing Domain of the LAZ3/BCL6 Oncoprotein

LAZ3, a novel zinc-finger encoding gene, is disrupted by recurring chromosome 3q27 translocations in human lymphomas

Nonrandom 4p13 rearrangements of the RhoH/TTF gene, encoding a GTP-binding protein, in non-Hodgkin's lymphoma and multiple myeloma

Genotype–phenotype correlation of 30 patients with Smith-Magenis syndrome (SMS) using comparative genome hybridisation array: cleft palate in SMS is associated with larger deletions

Overexpressed BCL6 (LAZ3) oncoprotein triggers apoptosis, delays S phase progression and associates with replication foci

A novel modulator domain of Ets transcription factors

LAZ3 Rearrangements in Non-Hodgkin’s Lymphoma: Correlation With Histology, Immunophenotype, Karyotype, and Clinical Outcome in 217 Patients

Small deletions occur in highly conserved regions of the LAZ3/BCL6 major translocation cluster in one case of non-Hodgkin's lymphoma without 3q27 translocation

Splicing with inverted order of exons occurs proximal to large introns

Waved aCGH: to smooth or not to smooth

High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2αB gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21

A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma

Therostasin, a Novel Clotting Factor Xa Inhibitor from the Rhynchobdellid Leech, Theromyzon tessulatum

The BTB/POZ domain targets the LAZ3/BCL6 oncoprotein to nuclear dots and mediates homomerisation in vivo

Analysis of LAZ3 (BCL-6) Status in B-Cell Non-Hodgkin's Lymphomas: Results of Rearrangement and Gene Expression Studies and a Mutational Analysis of Coding Region Sequences

The B cell transcriptional coactivator BOB1/OBF1 gene fuses to the LAZ3/BCL6 gene by t(3;11)(q27;q23.1) chromosomal translocation in a B cell leukemia line (Karpas 231)

Genomic structure and assignment of the RhoH/TTF small GTPase gene (ARHH) to 4p13 by in situ hybridization

Cloning of a breakpoint cluster region at band 3q27 involved in human non-Hodgkin's lymphoma

Dysregulation and overexpression of HMGA2 in myelofibrosis with myeloid metaplasia

Detection of minimal residual disease in chronic myeloid leukemia patients after bone marrow transplantation by polymerase chain reaction

Recurrent genomic aberrations combined with deletions of various tumour suppressor genes may deregulate the G1 S transition in CD4+CD56+ haematodermic neoplasms and contribute to the aggressiveness of the disease

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