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Plos One|September 27, 2007
Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPsFrancesca Gabanella, Matthew E R Butchbach, Luciano Saieva, et al.The Journal of Biological Chemistry|January 26, 2006
Gemin8 is a novel component of the survival motor neuron complex and functions in small nuclear ribonucleoprotein assemblyClaudia Carissimi, Luciano Saieva, Jennifer Baccon, et al.Cell|October 16, 2012
SMN is required for sensory-motor circuit function in DrosophilaWendy L Imlach, Erin S Beck, Ben Jiwon Choi, et al.Genes & Development|July 18, 2018
Dysregulation of Mdm2 and Mdm4 alternative splicing underlies motor neuron death in spinal muscular atrophyMeaghan Van Alstyne, Christian M Simon, S Pablo Sardi, et al.Cell Reports|December 19, 2019
Stasimon Contributes to the Loss of Sensory Synapses and Motor Neuron Death in a Mouse Model of Spinal Muscular AtrophyChristian M Simon, Meaghan Van Alstyne, Francesco Lotti, et al.Cell Reports|December 17, 2013
SMN is essential for the biogenesis of U7 small nuclear ribonucleoprotein and 3'-end formation of histone mRNAsSarah Tisdale, Francesco Lotti, Luciano Saieva, et al.Nature Neuroscience|April 2, 2021
Gain of toxic function by long-term AAV9-mediated SMN overexpression in the sensorimotor circuitMeaghan Van Alstyne, Ivan Tattoli, Nicolas Delestrée, et al.Molecular and Cellular Biology|November 1, 2011
A role for SMN exon 7 splicing in the selective vulnerability of motor neurons in spinal muscular atrophyMatteo Ruggiu, Vicki L McGovern, Francesco Lotti, et al.Biorxiv : the Preprint Server for Biology|July 3, 2026
A p53-ΔNp73 signaling axis drives selective motor neuron degeneration in spinal muscular atrophyMaria J Carlini, Xuemei Hu, Leonie Sowoidnich, et al.Human Molecular Genetics|March 31, 2009
A SMN missense mutation complements SMN2 restoring snRNPs and rescuing SMA miceEileen Workman, Luciano Saieva, Tessa L Carrel, et al.Pageof 6