T. Keates

发表

Selective inhibition of BET bromodomains

William B. Smith, S. Knapp, M. McKeown, 2010, Nature.

Histone Recognition and Large-Scale Structural Analysis of the Human Bromodomain Family

A. Gingras, T. Pawson, S. Knapp, 2012, Cell.

Structure of human CDC2-like kinase 2 (CLK2)

S. Knapp, A. Edwards, O. Fedorov, 2010 .

[1,2,4]Triazolo[4,3-a]phthalazines: Inhibitors of Diverse Bromodomains

S. Knapp, O. Fedorov, S. Müller, 2013, Journal of medicinal chemistry.

Bromodomain-peptide displacement assays for interactome mapping and inhibitor discovery.

S. Knapp, O. Fedorov, P. Filippakopoulos, 2011, Molecular bioSystems.

Structural basis for Cul3 protein assembly with the BTB-Kelch family of E3 ubiquitin ligases.

S. Knapp, F. von Delft, O. Gileadi, 2013, The Journal of Biological Chemistry.

Structure of cyclin G-associated kinase (GAK) trapped in different conformations using nanobodies

S. Knapp, S. Muyldermans, A. Joachimiak, 2014, The Biochemical journal.

Property enhancement for hot deformed Fe-Nd-B magnets by modification of composition of the Nd-rich phase

T. Keates, M. Al-Khafaji, M. Leonowicz, 1994 .

Expressing the human proteome for affinity proteomics: optimising expression of soluble protein domains and in vivo biotinylation

S. Müller, C. Allerston, O. Gileadi, 2012 .

Structural basis for Cul3 protein assembly with the BTB-Kelch family of E3 ubiquitin ligases.

S. Knapp, F. von Delft, O. Gileadi, 2013, The Journal of Biological Chemistry.

Expressing the human proteome for affinity proteomics: optimising expression of soluble protein domains and in vivo biotinylation

C. Allerston, O. Gileadi, Martin Hammarström, 2012, New biotechnology.