|ANGPTL3 stimulates endothelial cell adhesion and migration via integrin αvβ3 and induces blood vessel formation in vivo|
G Camenisch, MT Pisabarro, D Sherman, J Kowalski, M Nagel, P Hass, ...
Journal of Biological Chemistry 277 (19), 17281-17290, 2002
|The effects of the flipped model of instruction on student engagement and performance in the secondary mathematics classroom.|
Journal of Educators Online 12 (1), 91-115, 2015
|Structural basis of Nav1. 7 inhibition by an isoform-selective small-molecule antagonist|
S Ahuja, S Mukund, L Deng, K Khakh, E Chang, H Ho, S Shriver, C Young, ...
Science 350 (6267), 2015
|Generation of an LFA-1 antagonist by the transfer of the ICAM-1 immunoregulatory epitope to a small molecule|
TR Gadek, DJ Burdick, RS McDowell, MS Stanley, JC Marsters, KJ Paris, ...
Science 295 (5557), 1086-1089, 2002
|USP7 small-molecule inhibitors interfere with ubiquitin binding|
L Kategaya, P Di Lello, L Rougé, R Pastor, KR Clark, J Drummond, ...
Nature 550 (7677), 534-538, 2017
|Potent α4β1 peptide antagonists as potential anti-inflammatory agents|
DY Jackson, C Quan, DR Artis, T Rawson, B Blackburn, M Struble, ...
Journal of medicinal chemistry 40 (21), 3359-3368, 1997
|Strategies to enhance data collection and analysis in qualitative research|
KR Clark, BL Vealé
Radiologic Technology 89 (5), 482CT-485CT, 2018
|Managing multiple generations in the workplace|
Radiologic technology 88 (4), 379-396, 2017
|Examining the effects of the flipped model of instruction on student engagement and performance in the secondary mathematics classroom: An action research study|
Capella University, 2013
|Selective α4β7 integrin antagonists and their potential as antiinflammatory agents|
NJP Dubree, DR Artis, G Castanedo, J Marsters, D Sutherlin, L Caris, ...
Journal of medicinal chemistry 45 (16), 3451-3457, 2002
|Development of a potent, specific CDK8 kinase inhibitor which phenocopies CDK8/19 knockout cells|
MFT Koehler, P Bergeron, EM Blackwood, K Bowman, KR Clark, ...
ACS medicinal chemistry letters 7 (3), 223-228, 2016
|Structural basis for dual-mode inhibition of the ABC transporter MsbA|
H Ho, A Miu, MK Alexander, NK Garcia, A Oh, I Zilberleyb, M Reichelt, ...
Nature 557 (7704), 196-201, 2018
|CDK2/cyclinA inhibitors: targeting the cyclinA recruitment site with small molecules derived from peptide leads|
G Castanedo, K Clark, S Wang, V Tsui, M Wong, J Nicholas, ...
Bioorganic & medicinal chemistry letters 16 (6), 1716-1720, 2006
|Competition between intercellular adhesion molecule‐1 and a small‐molecule antagonist for a common binding site on the αl subunit of lymphocyte function‐associated antigen‐1|
SM Keating, KR Clark, LD Stefanich, F Arellano, CP Edwards, SC Bodary, ...
Protein science 15 (2), 290-303, 2006
|Structure–activity relationships by mass spectrometry: identification of novel MMP-3 inhibitors|
DA Ockey, JL Dotson, ME Struble, JT Stults, JH Bourell, KR Clark, ...
Bioorganic & medicinal chemistry 12 (1), 37-44, 2004
|Design and development of a series of potent and selective type II inhibitors of CDK8|
P Bergeron, MFT Koehler, EM Blackwood, K Bowman, K Clark, ...
ACS medicinal chemistry letters 7 (6), 595-600, 2016
|Motivating students in the 21st century|
ML Sedden, KR Clark
Radiologic Technology 87 (6), 609-616, 2016
|GNE-781, a highly advanced potent and selective bromodomain inhibitor of cyclic adenosine monophosphate response element binding protein, binding protein (CBP)|
FA Romero, J Murray, KW Lai, V Tsui, BK Albrecht, L An, MH Beresini, ...
Journal of Medicinal Chemistry 60 (22), 9162-9183, 2017
|Solid-phase synthesis of dual α4β1/α4β7 integrin antagonists: two scaffolds with overlapping pharmacophores|
GM Castanedo, FC Sailes, NJP Dubree, JB Nicholas, L Caris, K Clark, ...
Bioorganic & medicinal chemistry letters 12 (20), 2913-2917, 2002
|N-Benzoyl amino acids as LFA-1/ICAM inhibitors 1: Amino acid structure–activity relationship|
DJ Burdick, K Paris, K Weese, M Stanley, M Beresini, K Clark, ...
Bioorganic & medicinal chemistry letters 13 (6), 1015-1018, 2003