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Page 1
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy.
Monfrini E, Straniero L, Bonato S, Monzio Compagnoni G, Bordoni A, Dilena R, Rinchetti P, Silipigni R, Ronchi D, Corti S, Comi GP, Bresolin N, Duga S, Di Fonzo A. Monfrini E, et al. Among authors: rinchetti p. Parkinsonism Relat Disord. 2019 Jun;63:66-72. doi: 10.1016/j.parkreldis.2019.02.045. Epub 2019 Mar 1. Parkinsonism Relat Disord. 2019. PMID: 30850329 Free article.
Systematic elucidation of neuron-astrocyte interaction in models of amyotrophic lateral sclerosis using multi-modal integrated bioinformatics workflow.
Mishra V, Re DB, Le Verche V, Alvarez MJ, Vasciaveo A, Jacquier A, Doulias PT, Greco TM, Nizzardo M, Papadimitriou D, Nagata T, Rinchetti P, Perez-Torres EJ, Politi KA, Ikiz B, Clare K, Than ME, Corti S, Ischiropoulos H, Lotti F, Califano A, Przedborski S. Mishra V, et al. Among authors: rinchetti p. Nat Commun. 2020 Nov 4;11(1):5579. doi: 10.1038/s41467-020-19177-y. Nat Commun. 2020. PMID: 33149111 Free PMC article.
Sumoylation regulates the assembly and activity of the SMN complex.
Riboldi GM, Faravelli I, Kuwajima T, Delestrée N, Dermentzaki G, De Planell-Saguer M, Rinchetti P, Hao LT, Beattie CC, Corti S, Przedborski S, Mentis GZ, Lotti F. Riboldi GM, et al. Among authors: rinchetti p. Nat Commun. 2021 Aug 19;12(1):5040. doi: 10.1038/s41467-021-25272-5. Nat Commun. 2021. PMID: 34413305 Free PMC article.
Brain Calcifications: Genetic, Molecular, and Clinical Aspects.
Monfrini E, Arienti F, Rinchetti P, Lotti F, Riboldi GM. Monfrini E, et al. Among authors: rinchetti p. Int J Mol Sci. 2023 May 19;24(10):8995. doi: 10.3390/ijms24108995. Int J Mol Sci. 2023. PMID: 37240341 Free PMC article. Review.
15 results