Michela Taiana

发表

Neutralization of Schwann Cell-Secreted VEGF Is Protective to In Vitro and In Vivo Experimental Diabetic Neuropathy

G. Lauria, J. Sassone, R. Lombardi, 2014, PloS one.

Mutant SOD1 accumulation in sensory neurons does not associate with endoplasmic reticulum stress features: Implications for differential vulnerability of sensory and motor neurons to SOD1 toxicity

G. Lauria, J. Sassone, M. Taiana, 2016, Neuroscience Letters.

Revealing the involvement of miR-376a, miR-432 and miR-451a in infantile ascending hereditary spastic paralysis by microRNA profiling in iPSCs

S. Corti, S. Franceschetti, A. Gambardella, 2018 .

ALS mouse model SOD1G93A displays early pathology of sensory small fibers associated to accumulation of a neurotoxic splice variant of peripherin.

G. Lauria, C. Bendotti, J. Sassone, 2016, Human molecular genetics.

Alpha-lipoic acid prevents mitochondrial damage and neurotoxicity in experimental chemotherapy neuropathy

G. Lauria, F. Taroni, P. Podini, 2008, Experimental Neurology.

Insights into disease mechanisms and potential therapeutics for C9orf72-related amyotrophic lateral sclerosis/frontotemporal dementia

N. Bresolin, G. Comi, S. Corti, 2020, Ageing Research Reviews.

Transcriptional role of androgen receptor in the expression of long non-coding RNA Sox2OT in neurogenesis

Davide Pareyson, Jenny Sassone, Michela Taiana, 2017, PloS one.

Network topology of NaV1.7 mutations in sodium channel-related painful disorders

Filippo Martinelli-Boneschi, Andrea Zauli, Ronald L. Westra, 2017, BMC Systems Biology.

COL6A5 variants in familial neuropathic chronic itch

S. Dib-Hajj, S. Waxman, M. Cocca, 2017, Brain : a journal of neurology.

Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons

S. Salani, F. Rizzo, N. Bresolin, 2019, Brain : a journal of neurology.

Schwann cells mediate the impairment of neurite growth by increased VEGF secretion in DRG neurons exposed to hyperglycemia

Taiana, Michela Taiana, Renato Mantegazza, 2012 .

Synaptotagmin 13 is neuroprotective across motor neuron diseases

F. Rizzo, N. Bresolin, G. Comi, 2020, Acta Neuropathologica.

Morphometry of dermal nerve fibers in human skin

G. Lauria, J. Casanova-Mollá, G. Lauria, 2011, Neurology.

Stathmins and Motor Neuron Diseases: Pathophysiology and Therapeutic Targets

F. Rizzo, G. Comi, S. Corti, 2022, Biomedicines.

Current understanding of and emerging treatment options for spinal muscular atrophy with respiratory distress type 1 (SMARD1)

N. Bresolin, G. Comi, S. Corti, 2020, Cellular and Molecular Life Sciences.

R-Loops in Motor Neuron Diseases

N. Bresolin, G. Comi, S. Corti, 2018, Molecular Neurobiology.

Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot–Marie–Tooth type 2A

S. Salani, F. Rizzo, S. Corti, 2023, Cellular and Molecular Life Sciences.

Side and time variability of intraepidermal nerve fiber density

G. Lauria, R. Eleopra, J. Sassone, 2015, Neurology.

Dysregulation of Muscle-Specific MicroRNAs as Common Pathogenic Feature Associated with Muscle Atrophy in ALS, SMA and SBMA: Evidence from Animal Models and Human Patients

S. Corti, C. Gellera, D. Pareyson, 2021, International journal of molecular sciences.

Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons

S. Salani, F. Rizzo, N. Bresolin, 2019, Brain : a journal of neurology.

Impairment of the neurotrophic signaling hub B-Raf contributes to motoneuron degeneration in spinal muscular atrophy

S. Corti, P. Claus, A. Bergmann, 2021, Proceedings of the National Academy of Sciences.