Secondary mutation in a coding mononucleotide tract in MSH6 causes loss of immunoexpression of MSH6 in colorectal carcinomas with MLH1/PMS2 deficiency.
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Clinical problems of colorectal cancer and endometrial cancer cases with unknown cause of tumor mismatch repair deficiency (suspected Lynch syndrome)Immunohistochemistry and microsatellite instability analysis in molecular subtyping of colorectal carcinoma based on mismatch repair competency.Molecular genetics of microsatellite-unstable colorectal cancer for pathologists.Comparison of the Mismatch Repair System between Primary and Metastatic Colorectal Cancers Using Immunohistochemistry.Intratumoral heterogeneity of intrahepatic cholangiocarcinoma.Endoscopic biopsies from gastrointestinal carcinomas and their suitability for molecular analysis: a review of the literature and recommendations for clinical practice and research.Evaluation of colorectal cancers for Lynch syndrome: practical molecular diagnostics for surgical pathologists.Targeted sequencing of 36 known or putative colorectal cancer susceptibility genes.Immunohistochemical null-phenotype for mismatch repair proteins in colonic carcinoma associated with concurrent MLH1 hypermethylation and MSH2 somatic mutations.Differences in Microsatellite Instability Profiles between Endometrioid and Colorectal Cancers: A Potential Cause for False-Negative Results?
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Secondary mutation in a coding mononucleotide tract in MSH6 causes loss of immunoexpression of MSH6 in colorectal carcinomas with MLH1/PMS2 deficiency.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 24 August 2012
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Secondary mutation in a coding ...... mas with MLH1/PMS2 deficiency.
@en
Secondary mutation in a coding ...... mas with MLH1/PMS2 deficiency.
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type
label
Secondary mutation in a coding ...... mas with MLH1/PMS2 deficiency.
@en
Secondary mutation in a coding ...... mas with MLH1/PMS2 deficiency.
@nl
prefLabel
Secondary mutation in a coding ...... mas with MLH1/PMS2 deficiency.
@en
Secondary mutation in a coding ...... mas with MLH1/PMS2 deficiency.
@nl
P2093
P2860
P1433
P1476
Secondary mutation in a coding ...... mas with MLH1/PMS2 deficiency.
@en
P2093
C Richard Boland
David S Klimstra
Efsevia Vakiani
Hangjun Wang
Jeanine Ruggeri
Jinru Shia
Laura H Tang
Liying Zhang
Moshe Shike
P2860
P2888
P304
P356
10.1038/MODPATHOL.2012.138
P50
P577
2012-08-24T00:00:00Z