Functional analysis of rare variants in mismatch repair proteins augments results from computation-based predictive methods-Reference-Cited by-同舟云学术

Functional analysis of rare variants in mismatch repair proteins augments results from computation-based predictive methods

Published:2017-05-11 Issue:7 Volume:18 Page:519-533
ISSN:1538-4047
Container-title:Cancer Biology & Therapy
language:en
Short-container-title:Cancer Biology & Therapy

Author:

Arora Sanjeevani¹,Huwe Peter J.¹,Sikder Rahmat¹,Shah Manali¹,Browne Amanda J.²,Lesh Randy¹,Nicolas Emmanuelle¹,Deshpande Sanat²,Hall Michael J.³,Dunbrack Roland L.¹,Golemis Erica A.¹

Affiliation:

1. Molecular Therapeutics Program, Fox Chase Cancer Center, Philadelphia, PA, USA

2. Immersion Science Program, Fox Chase Cancer Center, Philadelphia, PA, USA

3. Department of Clinical Genetics, Fox Chase Cancer Center, Philadelphia, PA, USA

Publisher

Informa UK Limited

Subject

Cancer Research,Pharmacology,Oncology,Molecular Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/15384047.2017.1326439

Reference69 articles.

1. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

2. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

3. Milestones of Lynch syndrome: 1895–2015

4. Functional characterization ofMLH1missense variants identified in lynch syndrome patients

5. Endonucleolytic Function of MutLα in Human Mismatch Repair

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