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ACVR1-activating mutation causes neuropathic pain and sensory neuron hyperexcitability in humans.
Yu X, Ton AN, Niu Z, Morales BM, Chen J, Braz J, Lai MH, Barruet E, Liu H, Cheung K, Ali S, Chan T, Bigay K, Ho J, Nikolli I, Hansberry S, Wentworth K, Kriegstein A, Basbaum A, Hsiao EC. Yu X, et al. Among authors: hansberry s. Pain. 2023 Jan 1;164(1):43-58. doi: 10.1097/j.pain.0000000000002656. Epub 2022 Apr 20. Pain. 2023. PMID: 35442931 Free PMC article.
Functional Testing of Bone Morphogenetic Protein (BMP) Pathway Variants Identified on Whole-Exome Sequencing in a Patient with Delayed-Onset Fibrodysplasia Ossificans Progressiva (FOP) Using ACVR1R206H -Specific Human Cellular and Zebrafish Models.
Wentworth KL, Lalonde RL, Groppe JC, Brewer N, Moody T, Hansberry S, Taylor KE, Shore EM, Kaplan FS, Pignolo RJ, Yelick PC, Hsiao EC. Wentworth KL, et al. Among authors: hansberry s. J Bone Miner Res. 2022 Nov;37(11):2058-2076. doi: 10.1002/jbmr.4711. Epub 2022 Nov 15. J Bone Miner Res. 2022. PMID: 36153796 Free PMC article.
Pharmacological PINK1 activation ameliorates Pathology in Parkinson's Disease models.
Chin RM, Rakhit R, Ditsworth D, Wang C, Bartholomeus J, Liu S, Mody A, Laishu A, Eastes A, Tai C, Kim RY, Li J, Hansberry S, Khasnavis S, Rafalski V, Herendeen D, Garda V, Phung J, de Roulet D, Ordureau A, Harper JW, Johnstone S, Stöhr J, Hertz NT. Chin RM, et al. Among authors: hansberry s. bioRxiv [Preprint]. 2023 Feb 15:2023.02.14.528378. doi: 10.1101/2023.02.14.528378. bioRxiv. 2023. PMID: 36824886 Free PMC article. Preprint.
Consolidating the Academic End of a Community-Based Participatory Research Venture to Address Health Disparities.
Arrieta MI, Fisher L, Shaw T, Bryan V, Hudson A, Hansberry S, Eastburn S, Freed CR, Shelley-Tremblay S, Hanks RS, Washington-Lewis C, Roussel L, Dagenais PA, Icenogle M, Slagle ML, Parker LL, Crook E. Arrieta MI, et al. Among authors: hansberry s. J High Educ Outreach Engagem. 2017;21(3):113-134. J High Educ Outreach Engagem. 2017. PMID: 29623008 Free PMC article.