Philip J Thomas

Reduced histone deacetylase 7 activity restores function to misfolded CFTR in cystic fibrosis.

John R Yates, Gerard Manning, Yoshihiro Matsumura, 2010, Nature chemical biology.

Direct Binding of the Corrector VX-809 to Human CFTR NBD1: Evidence of an Allosteric Coupling between the Binding Site and the NBD1:CL4 Interface

Zhengrong Yang, Julie D Forman-Kay, J. Forman-Kay, 2017, Molecular Pharmacology.

Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene

George P Patrinos, Rachel Karchin, David L. Masica, 2013, Nature Genetics.

Cooperative, ATP-dependent Association of the Nucleotide Binding Cassettes during the Catalytic Cycle of ATP-binding Cassette Transporters*

John F Hunt, J. Hunt, L. Millen, 2002, The Journal of Biological Chemistry.

Active nuclear import and passive nuclear export are the primary determinants of TDP-43 localization

Yuh Min Chook, Y. Chook, P. Thomas, 2018, Scientific Reports.

Side chain and backbone contributions of Phe508 to CFTR folding

Chad A Brautigam, M. Machius, P. Thomas, 2005, Nature Structural &Molecular Biology.

NMR evidence for differential phosphorylation‐dependent interactions in WT and ΔF508 CFTR

Julie D Forman-Kay, J. Forman-Kay, V. Kanelis, 2010, The EMBO journal.

ATP binding to the motor domain from an ABC transporter drives formation of a nucleotide sandwich dimer.

John F Hunt, J. Hunt, N. Karpowich, 2002, Molecular cell.