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Frontiers in Molecular Biosciences|May 27, 2021
Lipid Droplets in the Pathogenesis of Hereditary Spastic ParaplegiaNimesha Tadepalle, Elena I RugarliNeuron|June 17, 2026
Limiting neurodegeneration in ALS: A phosphatase paves the wayElena I Rugarli, Thomas LangerThe EMBO Journal|February 23, 2012
Mitochondrial quality control: a matter of life and death for neuronsElena I Rugarli, Thomas LangerBiochimica Et Biophysica Acta|August 12, 2009
Emerging roles of mitochondrial proteases in neurodegenerationPaola Martinelli, Elena I RugarliCritical Reviews in Biochemistry and Molecular Biology|February 12, 2019
A concert of RNA-binding proteins coordinates mitochondrial functionDésirée Schatton, Elena I RugarliBMC Biology|July 11, 2008
A cryptic promoter in the first exon of the SPG4 gene directs the synthesis of the 60-kDa spastin isoformGiuseppe Mancuso, Elena I RugarliTrends in Molecular Medicine|May 2, 2006
Translating m-AAA protease function in mitochondria to hereditary spastic paraplegiaElena I Rugarli, Thomas LangerHuman Molecular Genetics|January 26, 2002
Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamicsAlessia Errico, Andrea Ballabio, Elena I RugarliPlos One|May 8, 2012
Alternative splicing of Spg7, a gene involved in hereditary spastic paraplegia, encodes a variant of paraplegin targeted to the endoplasmic reticulumGiuseppe Mancuso, Esther Barth, Pietro Crivello, et al.Human Molecular Genetics|July 23, 2004
Spastin interacts with the centrosomal protein NA14, and is enriched in the spindle pole, the midbody and the distal axonAlessia Errico, Pamela Claudiani, Marilena D'Addio, et al.Pageof 6