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Alison Donnelly Axtman

University of North Carolina (UNC) at Chapel Hill - Structural Genomics Consortium

Chapel Hill, NC

United States

University of North Carolina (UNC) at Chapel Hill - Division of Chemical Biology and Medicinal Chemistry

102 Ridge Road

Chapel Hill, NC 27514

United States

SCHOLARLY PAPERS

4

DOWNLOADS

158

TOTAL CITATIONS

4

Scholarly Papers (4)

1.

A Brain-Penetrant PIKfyve Inhibitor Reverses Experimental Neuropathic Pain via Inhibition of Sodium Channels

Number of pages: 21 Posted: 19 Apr 2024
University of Florida, University of North Carolina (UNC) at Chapel Hill - Structural Genomics Consortium, University of Florida, University of Florida, University of Florida and University of North Carolina (UNC) at Chapel Hill - Structural Genomics Consortium
Downloads 51 (1,052,702)

Abstract:

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PIKfyve, pain, chemical probe, PIKfyve inhibitor, SGC-PIKFYVE-1, sodium channels, nociceptive behavior, Sensory Neurons, Pharmacokinetics

2.

Development of a Potent and Selective Chemical Probe for the Pleiotropic Kinase CK2

Number of pages: 84 Posted: 30 Nov 2020
University of North Carolina (UNC) at Chapel Hill - Division of Chemical Biology and Medicinal Chemistry, University of North Carolina (UNC) at Chapel Hill - Division of Chemical Biology and Medicinal Chemistry, University of North Carolina (UNC) at Chapel Hill - Division of Chemical Biology and Medicinal Chemistry, Goethe University Frankfurt - Institute of Pharmaceutical Chemistry, Goethe University Frankfurt - Institute of Pharmaceutical Chemistry, Goethe University Frankfurt - Structural Genomics Consortium, Western University - Department of Biochemistry, Western University - Department of Biochemistry, Western University - Department of Biochemistry, Goethe University Frankfurt - Institute of Pharmaceutical Chemistry and University of North Carolina (UNC) at Chapel Hill - Structural Genomics Consortium
Downloads 46 (1,109,210)
Citation 4

Abstract:

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kinase, IDG, CK2, small molecule, nanoBRET, chemical probe, Cancer, crystal structure, proliferation

3.

Identification and optimization of first-in-class RNA helicase inhibitors

Number of pages: 33 Posted: 09 Jan 2026
University of Missouri, affiliation not provided to SSRN, affiliation not provided to SSRN, affiliation not provided to SSRN, Goethe University Frankfurt - Structural Genomics Consortium, Nanjing University of Science and Technology, affiliation not provided to SSRN, affiliation not provided to SSRN, York University, University of Toronto, University of Toronto, University of Toronto, University of Toronto, York University, affiliation not provided to SSRN, affiliation not provided to SSRN, University of Toronto, affiliation not provided to SSRN, University of Missouri - Columbia and University of North Carolina (UNC) at Chapel Hill - Structural Genomics Consortium
Downloads 40 (1,183,237)

Abstract:

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RNA helicases, MDA5, LGP2, DDX1, inhibitor, structure-based virtual screening, hit-to-lead optimization, HDX-MS

4.

Modulation of Tau Tubulin Kinases ((TTBK1 and TTBK2) Impacts Ciliogenesis

Number of pages: 107 Posted: 19 May 2022
University of North Carolina (UNC) at Chapel Hill - Structural Genomics Consortium, University of North Carolina (UNC) at Chapel Hill - Human Pluripotent Stem Cell Core, Goethe University Frankfurt - Institute of Pharmaceutical Chemistry, University of North Carolina (UNC) at Chapel Hill - Structural Genomics Consortium, University of North Carolina (UNC) at Chapel Hill - Department of Pharmacology, University of North Carolina (UNC) at Chapel Hill, School of Medicine, Department of Neuroscience, University of North Carolina (UNC) at Chapel Hill - Structural Genomics Consortium, University of North Carolina (UNC) at Chapel Hill - Structural Genomics Consortium, University of North Carolina (UNC) at Chapel Hill - Human Pluripotent Stem Cell Core and University of North Carolina (UNC) at Chapel Hill - Structural Genomics Consortium
Downloads 21 (1,436,435)

Abstract:

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kinase, IDG, TTBK1, TTBK2, small molecule, NanoBRET, crystal structure, cilia, induced pluripotent stem cells, ciliogenesis