Articles with public access mandates - Laura Gasparini - Fondazione Telethon, ItalyLearn more
NoteFor this mandate, articles should be available from specific locations.
Not available based on mandate: 1
Oct-1 recruitment to the nuclear envelope in adult-onset autosomal dominant leukodystrophy
M Columbaro, E Mattioli, NM Maraldi, M Ortolani, L Gasparini, MR D'Apice, ...
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1832 (3), 411-420, 2013
Available based on mandate: 5
A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD)
E Giorgio, D Robyr, M Spielmann, E Ferrero, E Di Gregorio, D Imperiale, ...
Human molecular genetics 24 (11), 3143-3154, 2015
Lamin B1 overexpression increases nuclear rigidity in autosomal dominant leukodystrophy fibroblasts
D Ferrera, C Canale, R Marotta, N Mazzaro, M Gritti, M Mazzanti, ...
The FASEB Journal 28 (9), 3906, 2014
Lamin B1 protein is required for dendrite development in primary mouse cortical neurons
C Giacomini, S Mahajani, R Ruffilli, R Marotta, L Gasparini
Molecular biology of the cell 27 (1), 35-47, 2016
Messenger RNA processing is altered in autosomal dominant leukodystrophy
A Bartoletti-Stella, L Gasparini, C Giacomini, P Corrado, R Terlizzi, ...
Human molecular genetics 24 (10), 2746-2756, 2015
Mice overexpressing lamin B1 in oligodendrocytes recapitulate the age-dependent motor signs, but not the early autonomic cardiovascular dysfunction of autosomal-dominant …
VL Martire, S Alvente, S Bastianini, C Berteotti, C Bombardi, ...
Experimental neurology 301, 1-12, 2018
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