Varaico: Literature-Extracted Genetic Variants

Gene:EGFR
Variant:p.M766T
Back to variants list

EGFR

NM_005228.5:p.M766T

Associated Papers

Multimodal scanning of genetic variants with base and prime editing.

Belli O et al.

Nature Biotechnology, 2025

Predicting Resistance to Small Molecule Kinase Inhibitors.

Nagarajan A et al.

Journal of Chemical Information and Modeling, 2025

Comprehensive mutational scanning of EGFR reveals TKI sensitivities of extracellular domain mutants.

Hayes TK et al.

Nature Communications, 2024

38548752 (PubMed )
Supplement: 41467_2024_45594_MOESM4_ESM.xlsx › All

Structure-Guided Strategies of Targeted Therapies for Patients with EGFR-Mutant Non-Small Cell Lung Cancer.

Du Z et al.

Biomolecules, 2023

36830579 (PubMed )
Supplement: biomolecules-13-00210-s001.zip › biomolecules-2098784-supplementary.xlsx › Table_S8

Comparison of mutation profile between primary phyllodes tumors of the breast and their paired local recurrences.

Mitus J et al.

Polish Journal of Pathology : Official Journal of the Polish Society of Pathologists, 2020

Effects of Single Nucleotide Polymorphisms on the Binding of Afatinib to EGFR: A Potential Patient Stratification Factor Revealed by Modeling Studies.

Kannan S et al.

Journal of Chemical Information and Modeling, 2019

Altered conformational landscape and dimerization dependency underpins the activation of EGFR by αC-β4 loop insertion mutations.

Ruan Z et al.

Proceedings of the National Academy of Sciences of the United States of America, 2018

Computational and Experimental Characterization of Patient Derived Mutations Reveal an Unusual Mode of Regulatory Spine Assembly and Drug Sensitivity in EGFR Kinase.

Ruan Z et al.

Biochemistry, 2017

Structural investigations of T854A mutation in EGFR and identification of novel inhibitors using structure activity relationships.

Goyal S et al.

Bmc Genomics, 2015

The structural impact of cancer-associated missense mutations in oncogenes and tumor suppressors.

Stehr H et al.

Molecular Cancer, 2011

21575214 (PubMed )
Supplement: 1476-4598-10-54-S3.XLS › mutations.txt

Using whole genome amplification (WGA) of low-volume biopsies to assess the prognostic role of EGFR, KRAS, p53, and CMET mutations in advanced-stage non-small cell lung cancer (NSCLC).

Lim EH et al.

Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer, 2009

Comparison of the EGFR resistance mutation profiles generated by EGFR-targeted tyrosine kinase inhibitors and the impact of drug combinations.

Avizienyte E et al.

The Biochemical Journal, 2008

18588508 (PubMed )
Supplement: supplement_1.pdf
Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."