E. Park

发表

Structure and mechanism of activity-based inhibition of the EGF-Receptor by Mig 6

Nayoung K. D. Kim, R. Beroukhim, S. Ficarro, 2016 .

Structure of a Bud6/Actin Complex Reveals a Novel WH2-like Actin Monomer Recruitment Motif.

M. Eck, B. Goode, E. Park, 2015, Structure.

Discovery of a Highly Potent and Broadly Effective Epidermal Growth Factor Receptor and HER2 Exon 20 Insertion Mutant Inhibitor

P. Jänne, N. Gray, H. Choi, 2018, Angewandte Chemie.

Discovery of a Highly Potent and Broadly Effective Epidermal Growth Factor Receptor and HER2 Exon 20 Insertion Mutant Inhibitor.

P. Jänne, N. Gray, H. Choi, 2018, Angewandte Chemie.

Mutant-Selective Allosteric EGFR Degraders are Effective Against a Broad Range of Drug-Resistant Mutations.

P. Jänne, N. Gray, M. Eck, 2020, Angewandte Chemie.

Structural, Biochemical, and Clinical Characterization of Epidermal Growth Factor Receptor (EGFR) Exon 20 Insertion Mutations in Lung Cancer

Geoffrey R. Oxnard, Ross A. Soo, Matthew Meyerson, 2013, Science Translational Medicine.

Structural, biochemical, and clinical characterization of Epidermal Growth Factor Receptor (EGFR) exon 20 insertion mutations in lung cancer (Science Translational Medicine (2014) 6, (225er1))

M. Meyerson, M. Hanna, L. Sequist, 2014 .

Architecture of autoinhibited and active BRAF/MEK1/14-3-3 complexes

S. Ficarro, J. Marto, M. Eck, 2019, Nature.

PH domain-mediated autoinhibition and oncogenic activation of Akt

P. Cole, M. Eck, H. Arthanari, 2022, bioRxiv.

Cryo-EM structure of a RAS/RAF recruitment complex

Anna M. Schmoker, M. Eck, S. Rawson, 2022, bioRxiv.

Mutant‐Selective Allosteric EGFR Degraders are Effective Against a Broad Range of Drug‐Resistant Mutations

P. Jänne, N. Gray, M. Eck, 2020, Angewandte Chemie.

Leveraging Gas-Phase Fragmentation Pathways for Improved Identification and Selective Detection of Targets Modified by Covalent Probes.

N. Gray, S. Ficarro, Tinghu Zhang, 2016, Analytical chemistry.