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Structure (London, England : 1993)|May 6, 2014
Structural basis for phosphorylation-dependent recruitment of Tel2 to Hsp90 by Pih1Mohinder Pal, Marc Morgan, Sarah E L Phelps, et al.
The EMBO Journal|March 25, 2004
Structural basis for recruitment of the ATPase activator Aha1 to the Hsp90 chaperone machineryPhilippe Meyer, Chrisostomos Prodromou, Chunyan Liao, et al.
Journal of Medicinal Chemistry|February 6, 2004
Structural basis for the synthesis of indirubins as potent and selective inhibitors of glycogen synthase kinase-3 and cyclin-dependent kinasesPanagiotis Polychronopoulos, Prokopios Magiatis, Alexios-Leandros Skaltsounis, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 28, 2010
Inhibition of Hsp90 with resorcylic acid macrolactones: synthesis and binding studiesJames E H Day, Swee Y Sharp, Martin G Rowlands, et al.
Journal of Medicinal Chemistry|March 25, 2008
Molecular characterization of macbecin as an Hsp90 inhibitorChristine J Martin, Sabine Gaisser, Iain R Challis, et al.
Nature Communications|August 2, 2018
Author Correction: RPAP3 provides a flexible scaffold for coupling HSP90 to the human R2TP co-chaperone complexFabrizio Martino, Mohinder Pal, Hugo Muñoz-Hernández, et al.
Nature Communications|April 18, 2018
RPAP3 provides a flexible scaffold for coupling HSP90 to the human R2TP co-chaperone complexFabrizio Martino, Mohinder Pal, Hugo Muñoz-Hernández, et al.
Cell|March 24, 2004
Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAFPaul T C Wan, Mathew J Garnett, S Mark Roe, et al.
ACS Chemical Biology|September 22, 2011
Targeting the Hsp90 molecular chaperone with novel macrolactams. Synthesis, structural, binding, and cellular studiesJames E H Day, Swee Y Sharp, Martin G Rowlands, et al.
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