His main research concerns Cell biology, Heterotrimeric G protein, RGS Proteins, G protein-coupled receptor and GTP-Binding Protein alpha Subunits. Mitosis is the focus of his Cell biology research. His study in Heterotrimeric G protein focuses on G beta-gamma complex in particular.
His research on G protein-coupled receptor concerns the broader Biochemistry. His GTP-Binding Protein alpha Subunits research includes themes of Gs alpha subunit, Gi alpha subunit and Thigmotropism. His studies deal with areas such as G12/G13 alpha subunits and G alpha subunit as well as GTPase-activating protein.
Francis S. Willard spends much of his time researching Cell biology, Heterotrimeric G protein, Biochemistry, G protein and G protein-coupled receptor. His study in Cell biology focuses on RGS Proteins, Signal transduction, GTPase, GTPase-activating protein and Effector. He works mostly in the field of RGS Proteins, limiting it down to concerns involving G alpha subunit and, occasionally, High-throughput screening.
His work on G beta-gamma complex and GTP-Binding Protein alpha Subunits as part of general Heterotrimeric G protein study is frequently connected to GTP', therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. His G protein study combines topics from a wide range of disciplines, such as Guanine nucleotide exchange factor, Nucleotide and Second messenger system. Francis S. Willard interconnects Cell surface receptor, Biophysics and Drug discovery in the investigation of issues within G protein-coupled receptor.
Francis S. Willard mainly investigates Receptor, Agonist, G protein-coupled receptor, Pharmacology and Drug discovery. His Receptor research is multidisciplinary, incorporating perspectives in Biophysics and Signal transduction. His G protein-coupled receptor research is multidisciplinary, relying on both Heterotrimeric G protein and G protein.
The Heterotrimeric G protein study combines topics in areas such as Gs alpha subunit, Second messenger system and Gq alpha subunit. His Classical pharmacology study in the realm of Drug discovery interacts with subjects such as Phenotypic screening. His Cell biology study frequently draws connections to adjacent fields such as Peptide sequence.
His primary areas of investigation include Receptor, Type 2 Diabetes Mellitus, Drug discovery, Functional selectivity and Pharmacology. Receptor is a subfield of Biochemistry that he studies. His studies in Type 2 Diabetes Mellitus integrate themes in fields like Metabolic disease, Disease, Molecular Pharmacology and Bioinformatics.
His Drug discovery study integrates concerns from other disciplines, such as Glucagon, Insulin and G protein-coupled receptor. His research investigates the link between Functional selectivity and topics such as Glucagon-like peptide 1 receptor that cross with problems in Extracellular, Biophysics, Transmembrane domain and Protein structure. His research in Pharmacology intersects with topics in Diabetes mellitus and Mechanism of action.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
G-protein signaling: back to the future
C. R. McCudden;M. D. Hains;R. J. Kimple;D. P. Siderovski.
Cellular and Molecular Life Sciences (2005)
The GAPs, GEFs, and GDIs of heterotrimeric G-protein alpha subunits.
David P. Siderovski;Francis S. Willard.
International Journal of Biological Sciences (2005)
A Seven-Transmembrane RGS Protein That Modulates Plant Cell Proliferation
Jin Gui Chen;Francis S. Willard;Jirong Huang;Jiansheng Liang.
Science (2003)
Translation of Polarity Cues into Asymmetric Spindle Positioning in Caenorhabditis elegans Embryos.
Kelly Colombo;Stephan W. Grill;Randall J. Kimple;Francis S. Willard.
Science (2003)
Crystal structure of the human PRMT5:MEP50 complex
Stephen Antonysamy;Zahid Bonday;Robert M. Campbell;Brandon Doyle.
Proceedings of the National Academy of Sciences of the United States of America (2012)
Return of the GDI: The GoLoco Motif in Cell Division
Francis S. Willard;Randall J. Kimple;David P. Siderovski.
Annual Review of Biochemistry (2004)
RIC-8 Is Required for GPR-1/2-Dependent Gα Function during Asymmetric Division of C. elegans Embryos
Katayoun Afshar;Francis S. Willard;Kelly Colombo;Christopher A. Johnston.
Cell (2004)
GTPase acceleration as the rate-limiting step in Arabidopsis G protein-coupled sugar signaling
Christopher A. Johnston;J. Philip Taylor;Yajun Gao;Adam J. Kimple.
Proceedings of the National Academy of Sciences of the United States of America (2007)
Role of the p70S6K pathway in regulating the actin cytoskeleton and cell migration
Leise A Berven;Francis S Willard;Michael F Crouch.
Experimental Cell Research (2004)
Structural diversity in the RGS domain and its interaction with heterotrimeric G protein alpha-subunits.
Meera Soundararajan;Francis S. Willard;Adam J. Kimple;Andrew P. Turnbull.
Proceedings of the National Academy of Sciences of the United States of America (2008)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
West Virginia University
Monash University
Monash University
Monash University
École Polytechnique Fédérale de Lausanne
National Institutes of Health
Pfizer (Germany)
The University of Texas Southwestern Medical Center
University of North Carolina at Chapel Hill
National Institutes of Health
University of Technology Sydney
University of Maryland, College Park
KU Leuven
Nagoya Institute of Technology
Spanish National Research Council
Aix-Marseille University
Heinrich Heine University Düsseldorf
University of South Florida
University of Potsdam
Dalhousie University
Umeå University
Sutter Health
Antoni van Leeuwenhoek Hospital
University of Technology Sydney
University of Toronto
International Institute for Applied Systems Analysis