TAIANA, MICHELA MARIA
TAIANA, MICHELA MARIA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith–Wiedemann Syndrome Cell Lines
2024 S. Pileggi, E.A. Colombo, S. Ancona, R. Quadri, C. Bernardelli, P. Colapietro, M. Taiana, L. Fontana, M. Miozzo, E. Lesma, S.M. Sirchia
Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot-Marie-Tooth type 2A
2023 F. Rizzo, S. Bono, M.D. Ruepp, S. Salani, L. Ottoboni, E. Abati, V. Melzi, C. Cordiglieri, S. Pagliarani, R. De Gioia, A. Anastasia, M. Taiana, M. Garbellini, S. Lodato, P. Kunderfranco, D. Cazzato, D. Cartelli, C. Lonati, N. Bresolin, G. Comi, M. Nizzardo, S. Corti
Stathmins and Motor Neuron Diseases: Pathophysiology and Therapeutic Targets
2022 D. Gagliardi, E. Pagliari, M. Meneri, V. Melzi, F. Rizzo, G.P. Comi, S.P. Corti, M.M. Taiana, M. Nizzardo
Molecular analysis of SMARD1 patient-derived cells demonstrates that nonsense-mediated mRNA decay is impaired
2022 M. Taiana, A. Govoni, S. Salani, N. Kleinschmidt, N. Galli, M. Saladini, S.B. Ghezzi, V. Melzi, M. Bersani, R. Del Bo, O. Muehlemann, E. Bertini, V. Sansone, E. Albamonte, S. Messina, F. Mari, E. Cesaroni, L. Porfiri, F.D. Tiziano, G.L. Vita, M. Sframeli, C. Bonanno, N. Bresolin, G. Comi, S. Corti, M. Nizzardo
Morpholino oligomers ameliorates pathological hallmarks in C9orf72 cellular lines and mice
2021 M. Bersani, D. Gagliardi, M. Taiana, F. Biella, M. Nizzardo, S. Corti
Impairment of the neurotrophic signaling hub B-Raf contributes to motoneuron degeneration in spinal muscular atrophy
2021 N. Hensel, F. Cieri, P. Santonicola, I. Tapken, T. Schüning, M. Taiana, E. Pagliari, A. Joseph, S. Fischer, N. Heidrich, H. Brinkmann, S. Kubinski, A.K. Bergmann, M.F. Richter, K. Jung, S. Corti, E. Di Schiavi, P. Claus
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
2021 C. Malacarne, M. Galbiati, E. Giagnorio, P. Cavalcante, F. Salerno, F. Andreetta, C. Cagnoli, M. Taiana, M. Nizzardo, S. Corti, V. Pensato, A. Venerando, C. Gellera, S. Fenu, D. Pareyson, R. Masson, L. Maggi, E. Dalla Bella, G. Lauria, R. Mantegazza, P. Bernasconi, A. Poletti, S. Bonanno, S. Marcuzzo
Changes in pathological phenotype of C9orf72 ALS iPSC-derived lines after treatment with Morpholino oligomers
2020 M. Bersani, M. Taiana, F. Biella, M. Nizzardo, S. Ghezzi, S. Corti
Evaluation of Morpholino oligomers therapeutic efficacy in C9orf72 ALS iPSC-derived lines
2020 M. Bersani, M. Taiana, F. Biella, M. Nizzardo, S. Ghezzi, N. Bresolin, G.P. Comi, S. Corti
Optimization of AAV9 gene therapy for Spinal Muscular Atrophy with respiratory distress Type 1 using in vivo disease models
2020 E. Pagliari, P. Rinchetti, N. Galli, S. Ghezzi, M. Taiana, G. Comi, S. Corti, M. Nizzardo
Current understanding of and emerging treatment options for spinal muscular atrophy with respiratory distress type 1 (SMARD1)
2020 M.G.L. Perego, N. Galli, M. Nizzardo, A. Govoni, M. Taiana, N. Bresolin, G.P. Comi, S. Corti
Synaptotagmin 13 is neuroprotective across motor neuron diseases
2020 M. Nizzardo, M. Taiana, F. Rizzo, J. Aguila Benitez, J. Nijssen, I. Allodi, V. Melzi, N. Bresolin, G.P. Comi, E. Hedlund, S. Corti
Insights into disease mechanisms and potential therapeutics for C9orf72-related amyotrophic lateral sclerosis/frontotemporal dementia
2020 D. Gagliardi, G. Costamagna, M. Taiana, L. Andreoli, F. Biella, M. Bersani, N. Bresolin, G.P. Comi, S. Corti
Spinal muscular atrophy with respiratory distress type 1: Clinical phenotypes, molecular pathogenesis and therapeutic insights
2020 M. Saladini, M. Nizzardo, A. Govoni, M. Taiana, N. Bresolin, G.P. Comi, S. Corti
IGHMBP2 related pathological pathways in Spinal Muscular Atrophy with Respiratory Distress type 1 (SMARD1) in vitro models
2019 N. Galli, M. Taiana, E. Pagliari, S. Ghezzi, G. Comi, S. Corti, M. Nizzardo
Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons
2019 F. Rizzo, M. Nizzardo, S. Vashisht, E. Molteni, V. Melzi, M. Taiana, S. Salani, P. Santonicola, E. Di Schiavi, M. Bucchia, A. Bordoni, I. Faravelli, N. Bresolin, G.P. Comi, U. Pozzoli, S. Corti
R-Loops in Motor Neuron Diseases
2018 M.G.L. Perego, M. Taiana, N. Bresolin, G.P. Comi, S. Corti
Transcriptional role of androgen receptor in the expression of long non-coding RNA Sox2OT in neurogenesis
2017 V. Tosetti, J. Sassone, A.L.M. Ferri, M. Taiana, G. Bedini, S. Nava, G. Brenna, C. Di Resta, D. Pareyson, A.M. Di Giulio, S. Carelli, E.A. Parati, A. Gorio
COL6A5 variants in familial neuropathic chronic itch
2017 F. Martinelli Boneschi, M. Colombi, M. Castori, G. Devigili, R. Eleopra, R.A. Malik, M. Ritelli, N. Zoppi, C. Dordoni, M. Sorosina, P. Grammatico, H. Fadavi, M.M. Gerrits, R. Almomani, C.G. Faber, I.S.J. Merkies, D. Toniolo, M. Cocca, C. Doglioni, S.G. Waxman, S.D. Dib-hajj, M..M. Taiana, J. Sassone, R. Lombardi, D. Cazzato, A. Zauli, S. Santoro, M. Marchi, G. Lauria
Network topology of NaV1.7 mutations in sodium channel-related painful disorders
2017 D. Kapetis, J. Sassone, Y. Yang, B. Galbardi, M.N. Xenakis, R.L. Westra, R. Szklarczyk, P. Lindsey, C.G. Faber, M. Gerrits, I.S.J. Merkies, S.D. Dib-hajj, M. Mantegazza, S.G. Waxman, G. LAURIA PINTER, M.M. Taiana, M. Marchi, R. Lombardi, D. Cazzato, F. Boneschi Martinelli, A. Zauli, F. Clarelli, S. Santoro, I. Lopez, A. Quattrini, J. Hoeijmakers, M. Sopacua, B. De Greef, H.J.M. Smeets, R. Al Momani, J.M. Vanoevelen, I. Eijkenboom, S. Cestãle, O. Chever, R. Malik, M. Tavakoli, D. Ziegler, F. MARTINELLI BONESCHI