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Donald E. Awrey
Observed names:
Awrey, Donald E.,
D E Awrey,
D. E. Awrey,
D.E. Awrey,
Don Awrey,
Don E. Awrey,
Donald Awrey,
Donald E. Awrey
show all 8
Institutions:
University Health Network,
Princess Margaret Cancer Centre,
MaRS,
Campbell Family Institute for Breast Cancer Research
Observed institutions:
University Health Network,
University of Toronto,
Princess Margaret Cancer Centre,
MaRS,
Campbell Family Institute for Breast Cancer Research,
Donnelly Centre for Cellular and Biomolecular Research,
University of California, Berkeley,
McMaster University
show all 8
OpenAlex ID:
A5109083161
Functional Characterization of CFI-400945, a Polo-like Kinase 4 Inhibitor, as a Potential Anticancer Agent
2014
·
Jacqueline M. Mason
, Dan Chi-Chia Lin
, et al.
·
Cancer Cell
·
202
PDF
The Discovery of Polo-Like Kinase 4 Inhibitors: Identification of (1R,2S)-2-(3-((E)-4-(((cis)-2,6-Dimethylmorpholino)methyl)styryl)-1H-indazol-6-yl)-5′-methoxyspiro[cyclopropane-1,3′-indolin]-2′-one (CFI-400945) as a Potent, Orally Active Antitumor Agent
2014
·
Peter B. Sampson
, Yong Liu
, et al.
·
Journal of Medicinal Chemistry
·
181
Screening for Ligands Using a Generic and High-Throughput Light-Scattering-Based Assay
2006
·
Guillermo A. Senisterra
, Eugene Markin
, et al.
·
SLAS DISCOVERY
·
129
PDF
The Acute Myeloid Leukemia-Associated Protein, Dek, Forms a Splicing-Dependent Interaction with Exon-Product Complexes
2000
·
Tim McGarvey
, Emanuel Rosonina
, et al.
·
The Journal of Cell Biology
·
128
PDF
Mode of Action, In Vitro Activity, and In Vivo Efficacy of AFN-1252, a Selective Antistaphylococcal FabI Inhibitor
2012
·
Nachum Kaplan
, Monique Albert
, et al.
·
Antimicrobial Agents and Chemotherapy
·
122
The Discovery of Polo-Like Kinase 4 Inhibitors: Design and Optimization of Spiro[cyclopropane-1,3′[3H]indol]-2′(1′H)-ones as Orally Bioavailable Antitumor Agents
2014
·
Peter B. Sampson
, Yong Liu
, et al.
·
Journal of Medicinal Chemistry
·
117
Transcription Elongation through DNA Arrest Sites
1997
·
Donald E. Awrey
, Rodney G. Weilbaecher
, et al.
·
Journal of Biological Chemistry
·
112
PDF
Hyperphosphorylation of Glucosyl C6 Carbons and Altered Structure of Glycogen in the Neurodegenerative Epilepsy Lafora Disease
2013
·
Felix Nitschke
, Peixiang Wang
, et al.
·
Cell Metabolism
·
92
PDF
Discovery of Pyrazolo[1,5-a]pyrimidine TTK Inhibitors: CFI-402257 is a Potent, Selective, Bioavailable Anticancer Agent
2016
·
Yong Liu
, Radoslaw Laufer
, et al.
·
ACS Medicinal Chemistry Letters
·
90
The Discovery of PLK4 Inhibitors: (E)-3-((1H-Indazol-6-yl)methylene)indolin-2-ones as Novel Antiproliferative Agents
2013
·
Radoslaw Laufer
, Bryan Forrest
, et al.
·
Journal of Medicinal Chemistry
·
79
Yeast Transcript Elongation Factor (TFIIS), Structure and Function
1998
·
Donald E. Awrey
, Nell Shimasaki
, et al.
·
Journal of Biological Chemistry
·
72
Yeast Transcript Elongation Factor (TFIIS), Structure and Function
1998
·
Valerie K. Olmsted
, Donald E. Awrey
, et al.
·
Journal of Biological Chemistry
·
58
PDF
Growth of recombinant fibroblasts in alginate microcapsules
1994
·
P. L. Chang
, G. Hortelano
, et al.
·
Biotechnology and Bioengineering
·
58
Purified yeast RNA polymerase II reads through intrinsic blocks to elongation in response to the yeast TFIIS analogue, P37.
1994
·
K.R. Christie
, D.E. Awrey
, et al.
·
Journal of Biological Chemistry
·
58
The Discovery of Orally Bioavailable Tyrosine Threonine Kinase (TTK) Inhibitors: 3-(4-(heterocyclyl)phenyl)-1H-indazole-5-carboxamides as Anticancer Agents
2015
·
Yong Liu
, Yunhui Lang
, et al.
·
Journal of Medicinal Chemistry
·
57
The Membrane Glycoprotein gp150 Is Encoded by the lagC Gene and Mediates Cell–Cell Adhesion by Heterophilic Binding during Dictyostelium Development
2000
·
Jun Wang
, Liansheng Hou
, et al.
·
Developmental Biology
·
52
PDF
In vitro characterization of mutant yeast RNA polymerase II with reduced binding for elongation factor TFIIS.
1996
·
J Wu
, D E Awrey
, et al.
·
Proceedings of the National Academy of Sciences
·
50
Elongation factor TFIIS contains three structural domains: solution structure of domain II.
1996
·
P E Morin
, D E Awrey
, et al.
·
Proceedings of the National Academy of Sciences
·
48
Discovery of inhibitors of the mitotic kinase TTK based on N-(3-(3-sulfamoylphenyl)-1H-indazol-5-yl)-acetamides and carboxamides
2014
·
Radoslaw Laufer
, Grace Ng
, et al.
·
Bioorganic & Medicinal Chemistry
·
42
Permeability of alginate microcapsules to secretory recombinant gene products
1996
·
D. E. Awrey
, M. Tse
, et al.
·
Biotechnology and Bioengineering
·
40
Intrinsic Transcript Cleavage in Yeast RNA Polymerase II Elongation Complexes
2003
·
Rodney G. Weilbaecher
, Donald E. Awrey
, et al.
·
Journal of Biological Chemistry
·
37
Systematic Characterization of the Protein Interaction Network and Protein Complexes in Saccharomyces cerevisiae Using Tandem Affinity Purification and Mass Spectrometry
2009
·
Mohan Babu
, Nevan J. Krogan
, et al.
·
Methods in molecular biology
·
36
In vitroactivity (MICs and rate of kill) of AFN-1252, a novel FabI inhibitor, in the presence of serum and in combination with other antibiotics
2013
·
Nachum Kaplan
, Donald Awrey
, et al.
·
Journal of Chemotherapy
·
35
PDF
Design and optimization of (3-aryl-1H-indazol-6-yl)spiro[cyclopropane-1,3′-indolin]-2′-ones as potent PLK4 inhibitors with oral antitumor efficacy
2016
·
Sze-Wan Li
, Yong Liu
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
33
Involvement of a Triton-insoluble Floating Fraction inDictyostelium Cell-Cell Adhesion
2001
·
Tony J.C. Harris
, Donald E. Awrey
, et al.
·
Journal of Biological Chemistry
·
31
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Works count:
36
Citation count:
2,055
H-index:
26
I10-index:
29
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