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Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival in ALS: Insights from a Next Generation Sequencing Study of an Italian ALS Cohort.
Scarlino S, Domi T, Pozzi L, Romano A, Pipitone GB, Falzone YM, Mosca L, Penco S, Lunetta C, Sansone V, Tremolizzo L, Fazio R, Agosta F, Filippi M, Carrera P, Riva N, Quattrini A. Scarlino S, et al. Int J Mol Sci. 2020 May 8;21(9):3346. doi: 10.3390/ijms21093346. Int J Mol Sci. 2020. PMID: 32397312 Free PMC article.
Coexistence of variants in TBK1 and in other ALS-related genes elucidates an oligogenic model of pathogenesis in sporadic ALS.
Lattante S, Doronzio PN, Marangi G, Conte A, Bisogni G, Bernardo D, Russo T, Lamberti D, Patrizi S, Apollo FP, Lunetta C, Scarlino S, Pozzi L, Zollino M, Riva N, Sabatelli M. Lattante S, et al. Among authors: scarlino s. Neurobiol Aging. 2019 Dec;84:239.e9-239.e14. doi: 10.1016/j.neurobiolaging.2019.03.010. Epub 2019 Mar 27. Neurobiol Aging. 2019. PMID: 31000212
DDIT4/REDD1/RTP801 is a novel negative regulator of Schwann cell myelination.
Noseda R, Belin S, Piguet F, Vaccari I, Scarlino S, Brambilla P, Martinelli Boneschi F, Feltri ML, Wrabetz L, Quattrini A, Feinstein E, Huganir RL, Bolino A. Noseda R, et al. Among authors: scarlino s. J Neurosci. 2013 Sep 18;33(38):15295-305. doi: 10.1523/JNEUROSCI.2408-13.2013. J Neurosci. 2013. PMID: 24048858 Free PMC article.