Aaron DiAntonio

Affiliations: 
Washington University, Saint Louis, St. Louis, MO 
Area:
Drosophila NMJ
Google:
"Aaron DiAntonio"
Mean distance: 13.54 (cluster 32)
 
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Publications

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Lee B, Oh Y, Cho E, et al. (2022) FK506-binding protein-like and FK506-binding protein 8 regulate dual leucine zipper kinase degradation and neuronal responses to axon injury. The Journal of Biological Chemistry. 101647
Bloom AJ, Mao X, Strickland A, et al. (2022) Constitutively active SARM1 variants that induce neuropathy are enriched in ALS patients. Molecular Neurodegeneration. 17: 1
Li Y, Pazyra-Murphy MF, Avizonis D, et al. (2022) Sarm1 activation produces cADPR to increase intra-axonal Ca++ and promote axon degeneration in PIPN. The Journal of Cell Biology. 221
Ko KW, Devault L, Sasaki Y, et al. (2021) Live imaging reveals the cellular events downstream of SARM1 activation. Elife. 10
Wu T, Zhu J, Strickland A, et al. (2021) Neurotoxins subvert the allosteric activation mechanism of SARM1 to induce neuronal loss. Cell Reports. 37: 109872
Eastman S, Smith T, Zaydman MA, et al. (2021) A phytobacterial TIR domain effector manipulates NAD to promote virulence. The New Phytologist
DiAntonio A, Milbrandt J, Figley MD. (2021) The SARM1 TIR NADase: Mechanistic Similarities to Bacterial Phage Defense and Toxin-Antitoxin Systems. Frontiers in Immunology. 12: 752898
Sasaki Y, Zhu J, Shi Y, et al. (2021) Nicotinic acid mononucleotide is an allosteric SARM1 inhibitor promoting axonal protection. Experimental Neurology. 113842
Figley MD, Gu W, Nanson JD, et al. (2021) SARM1 is a metabolic sensor activated by an increased NMN/NAD ratio to trigger axon degeneration. Neuron
Chen YH, Sasaki Y, DiAntonio A, et al. (2021) SARM1 is required in human derived sensory neurons for injury-induced and neurotoxic axon degeneration. Experimental Neurology. 113636
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