(Q53885333)

22 May 2018

title

PMS2 involvement in patients suspected of Lynch syndrome. (English)

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22 May 2018

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22 May 2018

Robert Hofstra

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22 May 2018

author name string

Renée C Niessen

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22 May 2018

Jan H Kleibeuker

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22 May 2018

Helga Westers

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22 May 2018

Paul O J Jager

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22 May 2018

Dennie Rozeveld

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22 May 2018

Krista K Bos

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22 May 2018

Wytske Boersma-van Ek

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22 May 2018

Harry Hollema

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22 May 2018

publication date

1 April 2009

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22 May 2018

Genes, Chromosomes and Cancer

published in

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22 May 2018

volume

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22 May 2018

issue

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22 May 2018

page(s)

322-329

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22 May 2018

Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation.

cites work

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7 January 2021

Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer

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7 January 2021

Mutational analysis of the PMS2 gene in sporadic endometrial cancers with microsatellite instability

1 reference

7 January 2021

Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant

1 reference

7 January 2021

Toward new strategies to select young endometrial cancer patients for mismatch repair gene mutation analysis.

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7 January 2021

Long-range PCR facilitates the identification of PMS2-specific mutations.

1 reference

7 January 2021

A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome

1 reference

7 January 2021

Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer

1 reference

7 January 2021

Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome

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7 January 2021

RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference

1 reference

7 January 2021

The added value of PMS2 immunostaining in the diagnosis of hereditary nonpolyposis colorectal cancer

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7 January 2021

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

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7 January 2021

PMS2 mutations in HNPCC

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7 January 2021

Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome).

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7 January 2021

Eukaryotic DNA mismatch repair

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7 January 2021

Hereditary colorectal cancer

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7 January 2021

Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation

1 reference

7 January 2021

Genomic organization of the human PMS2 gene family.

1 reference

7 January 2021

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

1 reference

7 January 2021

Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancer.

1 reference

7 January 2021

Getting rid of the PMS2 pseudogenes: mission impossible?

1 reference

7 January 2021

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations

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7 January 2021

Human PMS2 gene family: origin, molecular evolution, and biological implications

1 reference

7 January 2021

Use of Molecular Tumor Characteristics to Prioritize Mismatch Repair Gene Testing in Early-Onset Colorectal Cancer

1 reference

7 January 2021

Immunohistochemistry identifies carriers of mismatch repair gene defects causing hereditary nonpolyposis colorectal cancer

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7 January 2021

Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations

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7 January 2021

Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer

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7 January 2021

The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)

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7 January 2021

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

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7 January 2021

Familial mutations in PMS2 can cause autosomal dominant hereditary nonpolyposis colorectal cancer

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7 January 2021

Different mutator phenotypes in Mlh1- versus Pms2-deficient mice

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7 January 2021

Identifiers

DOI

10.1002/GCC.20642

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22 May 2018

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22 May 2018