Cytogenetic evolution patterns in non-Hodgkin's lymphoma.

No abstract is available for this paper.

• Publication year

  1995

• Venue

  Blood

• Publication date

  1995-11-15

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1182/BLOOD.V86.10.3905.BLOODJOURNAL86103905PMID 7579360
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• The Biology of Cancer

  2015cited by this paper
• Some current problems of cancer cytogenetics.

  2009influential reference
• Catalog of Chromosome Aberrations in Cancer

  1996cited by this paper
• Sequential analysis of 43 patients with non-Hodgkin's lymphoma: clinical correlations with cytogenetic, histologic, immunophenotyping, and molecular studies.

  1995cited by this paper
• Chromosomal translocations in human cancer

  1994influential reference
• Translocation (3;21)(q26;q22) in therapy-related myelodysplasia following drugs targeting DNA-topoisomerase II combined with alkylating agents, and in myeloproliferative disorders undergoing spontaneous leukemic transformation.

  1994cited by this paper
• Secondary chromosomal abnormalities in acute leukemias.

  1994cited by this paper
• 6q deletions define distinct clinico-pathologic subsets of non-Hodgkin's lymphoma.

  1993cited by this paper
• The clinical applications of new DNA diagnostic technology on the management of cancer patients.

  1993cited by this paper
• The cytogenetic scenario of chronic myeloid leukemia.

  1993cited by this paper
• Combination of t(14;18) and a Burkitt's type translocation in B-cell malignancies.

  1993cited by this paper
• Deletions involving two distinct regions of 6q in B-cell non-Hodgkin lymphoma.

  1992cited by this paper
• Translocations involving band 3q27 and Ig gene regions in non-Hodgkin's lymphoma.

  1992cited by this paper
• Leukaemic intermediate lymphocytic lymphomas: analysis of twelve cases diagnosed by morphology.

  1992cited by this paper
• Follicular lymphoma with t(8;14)(q24;q32): a distinct clinical and molecular subset of t(8;14)-bearing lymphomas.

  1992cited by this paper
• Cytogenetic analysis of 434 consecutively ascertained specimens of non‐Hodgkin's lymphoma: Correlations between recurrent aberrations, histology, and exposure to cytotoxic treatment

  1991cited by this paper
• Non‐Hodgkin's lymphomas with t(11;14)(q13;q32): a subset of mantle zone/intermediate lymphocytic lymphoma?

  1991cited by this paper
• Sequential karyotypes in non‐Hodgkin lymphoma: Their nature and significance

  1990cited by this paper
• Report of the committee on chromosome changes in neoplasia

  1990cited by this paper
• Report of the committee on chromosome changes in neoplasia.

  1990cited by this paper
• A genetic model for colorectal tumorigenesis.

  1990cited by this paper
• [Natural history of cancer].

  1990influential reference
• Chromosomal and molecular clues to tumor progression.

  1989cited by this paper
• Primary chromosome abnormalities in human neoplasia.

  1989cited by this paper
• The management of patients with adenocarcinoma and poorly differentiated carcinoma of unknown primary site.

  1989cited by this paper
• The t(2;5)(p23;q35): a recurring chromosomal abnormality in Ki-1-positive anaplastic large cell lymphoma.

  1989cited by this paper
• Correlation of secondary cytogenetic abnormalities with histologic appearance in non-Hodgkin's lymphomas bearing t(14;18)(q32;q21).

  1988cited by this paper
• Genetic convergence and divergence in tumor progression.

  1988cited by this paper
• Correlation of chromosome abnormalities with histologic and immunologic characteristics in non-Hodgkin's lymphoma and adult T cell leukemia-lymphoma. Fifth International Workshop on Chromosomes in Leukemia-Lymphoma.

  1987cited by this paper
• Multiple recurrent genomic defects in follicular lymphoma. A possible model for cancer.

  1987cited by this paper
• Intermediate- to high-grade histology of lymphomas carrying t(14;18) is associated with additional nonrandom chromosome changes.

  1987cited by this paper
• Correlation between chromosomal abnormalities and blast phenotype in the blast crisis of Ph-positive CGL.

  1986cited by this paper
• Evolution of tumours and the impact of molecular oncology

  1985cited by this paper
• Prognostic implications of karyotype and morphology in patients with non‐Hodgkin's lymphoma

  1983cited by this paper
• Distinctive chromosomal abnormalities in histologic subtypes of non-Hodgkin's lymphoma.

  1982cited by this paper
• Cytogenetic studies on Burkitt's lymphoma-leukemia.

  1982cited by this paper
• The experimental study of tumor progression: a review.

  1954cited by this paper
• Correlation of Chromosome Abnormalities With Histologic and Immunologic Characteristics in Non-Hodgkin ’ s Lymphoma and Adult

  year unknowncited by this paper
• National cancer institute sponsored study of classifications of non‐hodgkin's lymphomas. Summary and description of a working formulation for clinical usage

  year unknowncited by this paper

• Genetic Abnormalities Detected in Non-Hodgkin Lymphoma

  2021cites this paper
• Relative frequency and clinicopathologic characteristics of MYC-rearranged follicular lymphoma.

  2021cites this paper
• Relapse of follicular lymphoma arising from a non‐t(14;18) clone

  2020cites this paper
• Mature B-Cell Acute Lymphoblastic Leukemia

  2019cites this paper
• Pathogenesis of B-Cell Lymphoma

  2019cites this paper
• Prognostic impact of trisomy 21 in follicular lymphoma

  2018cites this paper
• Genetics in Hematologic Disorders: Implications of Recurring Chromosome Abnormalities and Gene Mutations

  2018cites this paper
• Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia

  2018cites this paper
• Role of MYC in pediatric and adult B-cell lymphoma patients

  2017influential citation
• Follicular lymphoma: State‐of‐the‐art ICML workshop in Lugano 2015

  2017cites this paper
• A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of TP53 in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia

  2016cites this paper
• The PCBP1 gene encoding poly(rc) binding protein i is recurrently mutated in Burkitt lymphoma

  2015cites this paper
• Tandem triplication of the long arm of chromosome 1, trp(1)(q21q32), in two cases with myelodysplastic syndromes

  2015cites this paper
• Sequential karyotyping in Burkitt lymphoma reveals a linear clonal evolution with increase in karyotype complexity and a high frequency of recurrent secondary aberrations

  2015influential citation
• Atlas of Genetics and Cytogenetics in Oncology and Haematology

  2014cites this paper
• Duodenal follicular lymphoma: Comprehensive gene expression analysis with insights into pathogenesis

  2014cites this paper
• Intravascular large B-cell lymphoma manifesting as cholecystitis: report of an Asian variant showing gain of chromosome 18 with concurrent deletion of chromosome 6q.

  2014influential citation
• Molecular pathogenesis of follicular lymphoma.

  2014cites this paper
• t(8;9)(q24;p13) /MYC

  2014cites this paper
• Pathology of follicular lymphoma.

  2014cites this paper
• clinical associations in diffuse large B-cell lymphoma Spectral karyotyping identifies new rearrangements, translocations, and

  2013cites this paper
• center B cells using cDNA arrays Gene expression profiling of follicular lymphoma and normal germinal

  2013cites this paper
• Chapter 9 Role of Cytogenetic Analysis in the Diagnosis and Classification of Hematopoietic Neoplasms

  2013cites this paper
• Caracterització genètica del limfoma esplènic de la zona marginal (LEZM)

  2013cites this paper
• Variants Amplifications in Mantle Cell Lymphoma Are Associated With Blastoid Increased Number of Chromosomal Imbalances and High-Level DNA

  2013cites this paper
• Molecular lesions in childhood and adult acute megakaryoblastic leukaemia

  2012cites this paper
• Lymphoma cytogenetics.

  2011cites this paper
• Synergistic effect of Bcl2, Myc and Ccnd1 transforms mouse primary B cells into malignant cells

  2011cites this paper
• Molecular cytogenetic analysis of chemoresistant non-Hodgkin's lymphoma patients with p53 abnormalities using fluorescence in situ hybridisation and comparative genomic hybridisation.

  2011cites this paper
• Molecular cytogenetic analysis of chemoresistant non-Hodgkin's lymphoma patients with p53 abnormalities using fluorescence in situ hybridisation and comparative genomic hybridisation.

  2011cites this paper
• Follicular lymphoma grade 3B.

  2011cites this paper
• del(13q) in non-Hodgkin's lymphoma

  2011cites this paper
• Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis

  2011cites this paper
• Mature B‐ and T‐cell neoplasms and Hodgkin lymphoma

  2010cites this paper
• Prognostic factors in follicular lymphoma.

  2010cites this paper
• Fatal Mimicry: Oral Melanoma versus Mantle Cell Lymphoma

  2010cites this paper
• Human major histocompatibility complex (MHC)-region gene and haplotype polymorphisms in non-Hodgkin’s lymphoma

  2009cites this paper
• Lymphomas with concurrent BCL2 and MYC translocations: the critical factors associated with survival.

  2009cites this paper
• factors associated with survival translocations : the critical MYC and BCL 2 Lymphomas with concurrent

  2009cites this paper
• Genetic and epigenetic characterization of pediatric high hyperdiploid acute lymphoblastic leukemia

  2009cites this paper
• Medical management update: Non-Hodgkin lymphoma.

  2009cites this paper
• Specific synthetic lethal killing of RAD54B-deficient human colorectal cancer cells by FEN1 silencing

  2009cites this paper
• Gene expression analysis in DLBCL; Identification and characterization of novel proteins

  2008cites this paper
• Specific cytogenetic abnormalities are associated with a significantly inferior outcome in children and adolescents with mature B-cell Non-Hodgkin’s Lymphoma: Results of the FAB/LMB 96 international study

  2008cites this paper
• The spectrum of B-cell non-Hodgkin lymphomas with dual IgH-BCL2 and BCL6 translocations.

  2008cites this paper
• Report of a workshop on malignant lymphoma: a review of molecular and clinical risk profiling

  2008cites this paper
• Prognostic significance of secondary cytogenetic alterations in follicular lymphomas

  2008cites this paper
• Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3.

  2007cites this paper
• Non-Hodgkin lymphoma with t(14;18): clonal evolution patterns and cytogenetic–pathologic–clinical correlations

  2007cites this paper
• Tiling resolution array CGH, expression, and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3

  2007cites this paper
• FISH analysis for the detection of lymphoma-associated chromosomal abnormalities in routine paraffin-embedded tissue.

  2006cites this paper
• A marginal zone phenotype in follicular lymphoma with t(14;18) is associated with secondary cytogenetic aberrations typical of marginal zone lymphoma

  2006cites this paper
• Chapter 2 – Cytogenetic Analysis of Malignant Lymphoma

  2006cites this paper
• Molecular, cytogenetic, and immunophenotypic characterization of follicular lymphoma grade 3B; a separate entity or part of the spectrum of diffuse large B-cell lymphoma or follicular lymphoma?

  2006cites this paper
• Centrosome aberrations in hematological malignancies

  2005cites this paper
• Personal and Occupational Exposure to Organic Solvents and Risk of Non-Hodgkin’s Lymphoma (NHL) in Women (United States)

  2005cites this paper
• Microarray studies of prognostic stratification and transformation of follicular lymphomas.

  2005cites this paper
• 6q- is an early and persistent chromosomal aberration in CD3-CD4+ T-cell clones associated with the lymphocytic variant of hypereosinophilic syndrome.

  2005cites this paper
• Chromosomal aberrations in follicular non-Hodgkin lymphomas of Japanese patients, detected with comparative genomic hybridization and polymerase chain reaction analysis.

  2005cites this paper
• Expression of CD29 on lymphoma cells and/or CD36 on microvascular endothels correlates with high serum LDH level in diffuse large B-cell lymphomas (DLBCLs) and is frequent in de novo CD5-positive DLBCLs.

  2005cites this paper
• Applications of Matrix-CGH (Array-CGH) for Genomic Research and Clinical Diagnostics

  2005cites this paper
• FcγRIIB is differentially expressed during B cell maturation and in B‐cell lymphomas

  2004cites this paper
• FcgammaRIIB is differentially expressed during B cell maturation and in B-cell lymphomas.

  2004cites this paper
• Delineation of a minimal region of deletion at 6q16.3 in follicular lymphoma and construction of a bacterial artificial chromosome contig spanning a 6‐megabase region of 6q16–q21

  2004cites this paper
• Aberrations involving 13q12 approximately q14 are frequent secondary events in childhood acute lymphoblastic leukemia.

  2004cites this paper
• Homogeneous immunophenotype and paucity of secondary genomic aberrations are distinctive features of endemic but not of sporadic Burkitt's lymphoma and diffuse large B‐cell lymphoma with MYC rearrangement

  2004cites this paper
• Automated array-based genomic profiling in chronic lymphocytic leukemia: development of a clinical tool and discovery of recurrent genomic alterations.

  2004cites this paper
• Chromosomal abnormalities of 200 Chinese patients with non-Hodgkin's lymphoma in Taiwan: with special reference to T-cell lymphoma.

  2004cites this paper
• Aberrations involving 13q12∼q14 are frequent secondary events in childhood acute lymphoblastic leukemia

  2004cites this paper
• DNA microarray analysis in malignant lymphomas

  2003cites this paper
• ALK-positive diffuse large B-cell lymphoma is associated with Clathrin-ALK rearrangements: report of 6 cases.

  2003cites this paper
• Gene Expression Profile of Serial Samples of Transformed B-Cell Lymphomas

  2003cites this paper
• Analysis of chromosomal copy number changes and oncoprotein expression in primary central nervous system lymphomas: frequent loss of chromosome arm 6q

  2003cites this paper
• Identification of chromosomal copy number changes associated with transformation of follicular lymphoma to diffuse large B-cell lymphoma.

  2003cites this paper
• Cytogenetic study of non-Hodgkin lymphoma from South India. histologic and geographic correlations.

  2003cites this paper
• Characterization of the recurrent translocation t(1;1)(p36.3;q21.1–2) in non‐Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis

  2003cites this paper
• ALK-positive diffuse large B-cell lymphoma is associated with Clathrin-ALK rearrangements: report of six cases

  2003cites this paper
• Interphase cytogenetic characterization of aberrations in the long arm of chromosome 1 in B-cell lymphoid malignancies.

  2003cites this paper
• Abnormalities on 1q and 7q are associated with poor outcome in sporadic Burkitt's lymphoma. A cytogenetic and comparative genomic hybridization study

  2003cites this paper
• Centrosome aberrations as a possible mechanism for chromosomal instability in non-Hodgkin's lymphoma

  2003cites this paper
• Chromosome aberrations in canine multicentric lymphomas detected with comparative genomic hybridisation and a panel of single locus probes

  2003cites this paper
• Interphase cytogenetics of hematological neoplasms under the perspective of the novel WHO classification.

  2003cites this paper
• Case of acute lymphoblastic leukemia presenting with t(14;18)/BCL2, t(8;14)/cMYC, and t(1;2)/FCGR2B

  2003cites this paper
• Multicolour fluorescence in situ hybridization analysis of t(14;18)‐positive follicular lymphoma and correlation with gene expression data and clinical outcome

  2003cites this paper
• Follicular lymphoma lacking the t(14;18)(q32;q21): identification of two disease subtypes

  2003cites this paper
• Cytogenetic evolution of follicular lymphoma.

  2003cites this paper
• Multicolor Karyotyping and Clinicopathological Analysis of Three Intravascular Lymphoma Cases

  2003cites this paper
• Niedrigmaligne B-Zell-Lymphome

  2003cites this paper
• Hochmaligne B-Zell-Lymphome

  2003cites this paper
• Splenic Marginal Zone Lymphomas Presenting with Splenomegaly and Typical Immunophenotype Are Characterized by Allelic Loss in 7q31–32

  2003cites this paper
• Uncovering novel inter‐ and intrachromosomal chromosome 1 aberrations in follicular lymphomas by using an innovative multicolor banding technique

  2002cites this paper
• Spectral karyotyping identifies new rearrangements, translocations, and clinical associations in diffuse large B-cell lymphoma.

  2002cites this paper
• Properties of the mantle cell and mantle cell lymphoma

  2002cites this paper
• Mantle Cell Lymphoma with 8q24 Chromosomal Abnormalities: a Report of 5 Cases with Blastoid Features

  2002cites this paper
• Cytomorphologic, immunohistochemical, and cytogenetic profiles of follicular lymphoma: 2 types of follicular lymphoma grade 3.

  2002cites this paper
• Hemizygous deletions in the HLA region account for loss of heterozygosity in the majority of diffuse large B‐cell lymphomas of the testis and the central nervous system

  2002cites this paper
• Fc receptor homologs (FcRH1-5) extend the Fc receptor family.

  2002cites this paper
• Late appearance of the 11q22.3-23.1 deletion involving the ATM locus in B-cell chronic lymphocytic leukemia and related disorders. Clinico-biological significance.

  2002cites this paper
• Clinicopathologic correlations of genomic gains and losses in follicular lymphoma.

  2002cites this paper
• M-FISH cytogenetic Analysis of Non-Hodgkin Lymphomas with t(14;18)(q32;q21) and add(1)(p36) as a Secondary Abnormality Shows that the Extra Material Often Comes from Chromosome Arm 17q

  2002cites this paper