MARCHESI, VERONICA
MARCHESI, VERONICA
Dipartimento di Scienze Farmacologiche e Biomolecolari Rodolfo Paoletti
Aberrant interplay between the mutant androgen receptor and GLI3: highlighting a potential neurodevelopmental weakness in Kennedy’s Disease
2026 M. Cozzi, M.E. Cicardi, L. Cornaggia, P. Pramaggiore, B. Tedesco, V. Ferrari, M. Chierichetti, A. Mohamed, V. Marchesi, A. Brivio, C. Milioto, M. Piccolella, M. Galbiati, P. Rusmini, V. Crippa, D. Bonanomi, A. Provenzani, R. Cristofani, A. Poletti
From proteostatic control to collapse: exploring the ribosome-associated quality control – integrated stress response axis in Myofibrillar myopathy 13
2026 V. Marchesi, V. Ferrari, M. Cozzi, M. Chierichetti, P. Pramaggiore, A. Mohamed, M. Galbiati, P. Rusmini, L. Cornaggia, A. Brivio, M. Piccolella, V. Crippa, R. Cristofani, A. Poletti, B. Tedesco
Shared behaviours of ALS and NEIMY KIF5A mutants: similarities between a neurodegenerative and a neurodevelopmental molecular phenotypes
2026 M. Cozzi, S. Magri, B. Tedesco, V. Ferrari, M. Chierichetti, L. Cornaggia, A. Mohamed, V. Marchesi, M. Piccolella, M. Galbiati, P. Rusmini, V. Crippa, C. Gellera, R. Cristofani, F. Taroni, A. Poletti
Molecular, cellular, and clinical aspects of myofibrillar myopathy caused by HSPB8 frameshift mutations
2026 W. Zhou, V. Marchesi, M. Mcleod, A.J. Kordala, S. Szwec, J.A. Mielcarz, A. Poletti, B. Tedesco
Unveiling novel players in HSPB8 pathology caused by frameshift mutations
2025 B. Tedesco, V. Marchesi, V. Ferrari, M. Cozzi, P. Pramaggiore, R. Cristofani, V. Crippa, P. Rusmini, M. Chierichetti, L. Cornaggia, A. Mohamed, M. Galbiati, M. Piccolella, L. Weiss, V. Kimonis, V. Timmerman, A. Poletti
COMMON AND NOVEL MOLECULAR MECHANISMS OF FRAMESHIFT MUTATIONS CAUSING HSPB8 PATHOLOGY
2025 V. Marchesi, L. Vendredy, S. Peric, V. Ferrari, M. Cozzi, V. Crippa, R. Cristofani, P. Pramaggiore, P. Rusmini, M. Chierichetti, L. Cornaggia, A. Mohamed, M. Galbiati, M. Piccolella, L. Weiss, A. Topf, V. Kimonis, V. Timmerman, A. Poletti, B. Tedesco
Strategies to promote the expression of the androgen receptor AR-A isoform lacking the polyglutamine tract in spinal and bulbar muscular atrophy
2025 B. Tedesco, M. Chierichetti, P. Pramaggiore, V. Ferrari, L. Cornaggia, M. Cozzi, A.A.M. Mohamed, V. Marchesi, M. Piccolella, V. Crippa, P. Rusmini, M. Galbiati, C. Rinaldi, R.M. Cristofani, A. Poletti
Novel HSPB8 mutations in severe early-onset myopathy with involvement of respiratory and cardiac muscles cause proteostasis defects in cell models
2025 B. Tedesco, S. Peric, G.S. Kocak, J. Tan, H. Duong, A. Töpf, V. Rakocevic-Stojanovic, S. Milenkovic, Y. Parkhurst, L. Gibbs, A. Martin-Rios, P.D. Lambiase, O.P. Guttmann, C. Marini-Bettolo, E. Harris, M.B. Harms, V. Ivanovic, V. Marchesi, M. Milone, V. Timmerman, V. Straub, A. Poletti, V. Kimonis