Analysis of KRAS G12 / G13 in colorectal cancer using an economical digital PCR assay that unequivocally differentiates missense and synonymous alleles-Reference-Cited by-同舟云学术

Analysis of KRAS G12 / G13 in colorectal cancer using an economical digital PCR assay that unequivocally differentiates missense and synonymous alleles

Published:2021-07-26 Issue:11 Volume:99 Page:2554-2569
ISSN:0008-4034
Container-title:The Canadian Journal of Chemical Engineering
language:en
Short-container-title:Can J Chem Eng

Author:

Bidshahri Roza¹²,Fakhfakh Kareem¹³,McNeil Kelly⁴,Won Jennifer R.⁵,Wolber Robert⁵⁶,Hughesman Curtis⁷,Haynes Charles¹²³⁸

Affiliation:

1. Michael Smith Laboratories University of British Columbia Vancouver British Columbia Canada

2. Biomedical Engineering Program University of British Columbia Vancouver British Columbia Canada

3. Department of Chemical and Biological Engineering University of British Columbia Vancouver British Columbia Canada

4. Department of Genetics and Molecular Diagnostics British Columbia Cancer Agency Vancouver British Columbia Canada

5. Canadian Immunohistochemistry Quality Control, Department of Pathology and Laboratory Medicine University of British Columbia Vancouver British Columbia Canada

6. Department of Pathology Lion's Gate Hospital North Vancouver British Columbia Canada

7. Cancer Genetics and Genomics Lab British Columbia Cancer Agency Vancouver British Columbia Canada

8. Genome Sciences and Technology Program Vancouver British Columbia Canada

Publisher

Wiley

Subject

General Chemical Engineering

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjce.24243

Reference62 articles.

1. Colorectal Cancer Epidemiology: Incidence, Mortality, Survival, and Risk Factors

2. Effects of KRAS, BRAF, NRAS, and PIK3CA mutations on the efficacy of cetuximab plus chemotherapy in chemotherapy-refractory metastatic colorectal cancer: a retrospective consortium analysis

3. Genetic prognostic and predictive markers in colorectal cancer

4. KRAS, BRAF, PIK3CA, and PTEN mutations: implications for targeted therapies in metastatic colorectal cancer

5. Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)

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