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Dominant NARS1 mutations causing axonal Charcot-Marie-Tooth disease expand NARS1-associated diseases.
Beijer D, Marte S, Li JC, De Ridder W, Chen JZ, Tadenev ALD, Miers KE, Deconinck T, Macdonell R, Marques W Jr, De Jonghe P, Pratt SL, Meyer-Schuman R, Züchner S, Antonellis A, Burgess RW, Baets J. Beijer D, et al. Among authors: tadenev ald. Brain Commun. 2024 Mar 8;6(2):fcae070. doi: 10.1093/braincomms/fcae070. eCollection 2024. Brain Commun. 2024. PMID: 38495304
Testing SIPA1L2 as a modifier of CMT1A using mouse models.
Murray GC, Hines TJ, Tadenev ALD, Xu I, Züchner S, Burgess RW. Murray GC, et al. Among authors: tadenev ald. J Neuropathol Exp Neurol. 2024 Apr 19;83(5):318-330. doi: 10.1093/jnen/nlae020. J Neuropathol Exp Neurol. 2024. PMID: 38472136
Misregulation of mitochondria-lysosome contact dynamics in Charcot-Marie-Tooth Type 2B disease Rab7 mutant sensory peripheral neurons.
Wong YC, Jayaraj ND, Belton TB, Shum GC, Ball HE, Ren D, Tadenev ALD, Krainc D, Burgess RW, Menichella DM. Wong YC, et al. Among authors: tadenev ald. Proc Natl Acad Sci U S A. 2023 Oct 31;120(44):e2313010120. doi: 10.1073/pnas.2313010120. Epub 2023 Oct 25. Proc Natl Acad Sci U S A. 2023. PMID: 37878717 Free PMC article.
An allelic series of spontaneous Rorb mutant mice exhibit a gait phenotype, changes in retina morphology and behavior, and gene expression signatures associated with the unfolded protein response.
Murray GC, Bubier JA, Zinder OJ, Harris B, Clark J, Christopher MC, Hanley C, Tjong H, Li M, Ngan CY, Reinholdt L, Burgess RW, Tadenev ALD. Murray GC, et al. Among authors: tadenev ald. G3 (Bethesda). 2023 Aug 9;13(8):jkad131. doi: 10.1093/g3journal/jkad131. G3 (Bethesda). 2023. PMID: 37300435 Free PMC article.
24 results