(Q57742646)

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Non-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in theMSH2 gene

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scholarly article

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Non-Hodgkin lymphoma related to hereditary nonpolyposis colorectal cancer in a patient with a novel heterozygous complex deletion in theMSH2 gene (English)

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cancer research

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colorectal cancer

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colorectal carcinoma

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non-Hodgkin lymphoma

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Ester Castellsagué

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E. Castellsagué

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M. Pineda

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I. Blanco

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S. González

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4

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G. Llort

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E. Musulén

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T. Frebourg

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S. Baert-Desurmont

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G. Capellá

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publication date

2008

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Genes, Chromosomes and Cancer

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47

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4

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326-332

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The role of microsatellite instability in gastric low- and high-grade lymphoma development

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Genetic analysis of mouse embryonic stem cells bearing Msh3 and Msh2 single and compound mutations

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7 January 2021

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Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutations

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Microsatellite instability in primary neoplasms from HIV+ patients

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Complex gene rearrangements caused by serial replication slippage

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Combined use of MLPA and nonfluorescent multiplex PCR analysis by high performance liquid chromatography for the detection of genomic rearrangements

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Phenotype associated with recessively inherited mutations in DNA mismatch repair (MMR) genes.

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7 January 2021

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Microsatellite instability in a pleomorphic rhabdomyosarcoma in a patient with hereditary non-polyposis colorectal cancer

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Screening for genomic rearrangements of the MMR genes must be included in the routine diagnosis of HNPCC.

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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The mutator pathway is a feature of immunodeficiency-related lymphomas

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Standardized approach for microsatellite instability detection in colorectal carcinomas.

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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New developments in Lynch syndrome (hereditary nonpolyposis colorectal cancer) and mismatch repair gene testing

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Non-Hodgkin's lymphoma in a patient with probable hereditary nonpolyposis colon cancer: report of a case and review of the literature

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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A novel germline mutation of MSH2 in a hereditary nonpolyposis colorectal cancer patient with liposarcoma

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Ikaros is a mutational target for lymphomagenesis in Mlh1-deficient mice.

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7 January 2021

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Mismatch repair gene expression in malignant lymphoproliferative disorders of B-cell origin

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Distinct patterns of germ-line deletions inMLH1 andMSH2: the implication of Alu repetitive element in the genetic etiology of Lynch syndrome (HNPCC)

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Genetic instability is associated with histological transformation of follicle center lymphoma

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Cancer risk in 348 French MSH2 or MLH1 gene carriers

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Stability of BAT26 in tumours of hereditary nonpolyposis colorectal cancer patients with MSH2 intragenic deletion

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Genomic rearrangements in MSH2, MLH1 or MSH6 are rare in HNPCC patients carrying point mutations

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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MSH2 deficient mice are viable and susceptible to lymphoid tumours

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Association of a Duodenal Follicular Lymphoma and Hereditary Nonpolyposis Colorectal Cancer

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Familial T-cell non-Hodgkin lymphoma caused by biallelic MSH2 mutations

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Prostate cancer is part of the hereditary non-polyposis colorectal cancer (HNPCC) tumor spectrum

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPA.

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Molecular characterization of the spectrum of genomic deletions in the mismatch repair genesMSH2,MLH1,MSH6, andPMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC)

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Breast cancer in an MSH2 gene mutation carrier

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Different mutator phenotypes in Mlh1- versus Pms2-deficient mice

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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Gene conversion is a frequent mechanism of inactivation of the wild-type allele in cancers from MLH1/MSH2 deletion carriers.

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https://api.crossref.org/works/10.1002%2FGCC.20536

7 January 2021

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10.1002/GCC.20536

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