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Computational Analysis of KRAS Mutations: Implications for Different Effects on the KRAS p.G12D and p.G13D Mutations

Overview of attention for article published in PLOS ONE, February 2013
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Title
Computational Analysis of KRAS Mutations: Implications for Different Effects on the KRAS p.G12D and p.G13D Mutations
Published in
PLOS ONE, February 2013
DOI 10.1371/journal.pone.0055793
Pubmed ID
Authors

Chih-Chieh Chen, Tze-Kiong Er, Yen-Yi Liu, Jenn-Kang Hwang, Maria Jesus Barrio, Maximiliano Rodrigo, Enrique Garcia-Toro, Marta Herreros-Villanueva

Abstract

The issue of whether patients diagnosed with metastatic colorectal cancer who harbor KRAS codon 13 mutations could benefit from the addition of anti-epidermal growth factor receptor therapy remains under debate. The aim of the current study was to perform computational analysis to investigate the structural implications of the underlying mutations caused by c.38G>A (p.G13D) on protein conformation.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 140 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 2 1%
Denmark 1 <1%
South Africa 1 <1%
Unknown 136 97%

Demographic breakdown

Readers by professional status Count As %
Researcher 28 20%
Student > Ph. D. Student 27 19%
Student > Master 21 15%
Student > Bachelor 13 9%
Other 9 6%
Other 12 9%
Unknown 30 21%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 34 24%
Agricultural and Biological Sciences 31 22%
Medicine and Dentistry 14 10%
Chemistry 13 9%
Pharmacology, Toxicology and Pharmaceutical Science 6 4%
Other 6 4%
Unknown 36 26%