Genetic Testing for Hereditary Nonpolyposis Colorectal Cancer (HNPCC)-Reference-Cited by-同舟云学术

Genetic Testing for Hereditary Nonpolyposis Colorectal Cancer (HNPCC)

Published:2009-04 Issue:1 Volume:61 Page:
ISSN:1934-8266
Container-title:Current Protocols in Human Genetics
language:en
Short-container-title:Current Protocols in Human Genetics

Author:

Hegde Madhuri R.¹,Roa Benjamin B.²

Affiliation:

1. Emory University Atlanta Georgia

2. Myriad Genetic Laboratories Salt Lake City Utah

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142905.hg1012s61

Reference36 articles.

1. Characterization of two novel adenomatous polyposis coli (APC) gene mutations in patients with familial adenomatous polyposis (FAP)

2. A National Cancer Institute workshop on microsatellite instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal cancer;Boland C.R.;Cancer Res.,1998

3. Microsatellite instability in colorectal-cancer patients with suspected genetic predisposition

4. Immunohistochemical detection of mismatch repair gene proteins as a useful tool for the identification of colorectal carcinoma with the mutator phenotype

5. Molecular analysis of APC mutations in familial adenomatous polyposis and sporadic colon carcinomas

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1. Spectrum of mutations in genes associated with familial colorectal cancer syndrome (MLH1, MSH2, PMS2, MSH6, and APC): A not so common hereditary cancer syndrome in Indian population;Indian Journal of Gastroenterology;2020-11-16

2. Butyrate Inhibits Indices of Colorectal Carcinogenesis via Enhancing α‐Ketoglutarate‐Dependent DNA Demethylation of Mismatch Repair Genes;Molecular Nutrition & Food Research;2018-04-26

3. Hereditary Nonpolyposis Colorectal Cancer and Lynch Syndrome;Molecular Pathology in Clinical Practice;2016

4. Microsatellite Instability Detection by High-Resolution Melting Analysis;Clinical Chemistry;2010-11-01

5. DNA Polymerases as Potential Therapeutic Targets for Cancers Deficient in the DNA Mismatch Repair Proteins MSH2 or MLH1;Cancer Cell;2010-03