PINOTTI, Mirko

PINOTTI, Mirko  

Dipartimento di Scienze della vita e biotecnologie  

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Titolo Data di pubblicazione Autore(i) File
A Compensatory U1snRNA Partially Rescues FAH Splicing and Protein Expression in a Splicing-Defective Mouse Model of Tyrosinemia Type I 2020 Balestra, Dario; Scalet, Daniela; Ferrarese, Mattia; Lombardi, Silvia; Ziliotto, Nicole; C. Croes..., Chrystal; Petersen, Naomi; Bosma, Piter; Riccardi, Federico; Pagani, Franco; Pinotti, Mirko; van de Graaf, Stan F. J.
A factor X variant with engineered activation peptide as innovative by-passing agent for haemophilia 2022 Tonetto, E.; Tarantino, R.; Testa, M. F.; Peretto, L.; Bernardi, F.; Pinotti, M.; Branchini, A. file con accesso da definire
A frequent human coagulation Factor VII mutation (A294V, c152) in loop 140s affects the interaction with activators, tissue factor and substrates. 2002 Toso, Raffaella; Pinotti, Mirko; High, Ka; Pollak, Es; Bernardi, Francesco file con accesso da definire
A naturally occurring mutation in ATP synthase subunit c is associated with increased damage following hypoxia/reoxygenation in STEMI patients 2021 Morciano, G.; Pedriali, G.; Bonora, M.; Pavasini, R.; Mikus, E.; Calvi, S.; Bovolenta, M.; Lebied...zinska-Arciszewska, M.; Pinotti, M.; Albertini, A.; Wieckowski, M. R.; Giorgi, C.; Ferrari, R.; Galluzzi, L.; Campo, G.; Pinton, P.
A new type 1 von Willebrand Disease (VWD) characterized by increased clearance of von Willebrand Factor (VWF) due to the heterozygous p.P1127S mutation: clinical phenotype and pathogenic mechanisms 2022 M. Sacco, M. Tardugno; De Cristofaro, R.; Lancellotti, S.; Bernardi, F.; Pinotti, M.; Branchini, ...A.; Giusti, B.; Castaman, G. file con accesso da definire
A next-generation rFVIIa fusion protein with enhanced half-life as a novel by-passing tool in hemophilia 2020 Branchini, Alessio; Ferrarese, Mattia; Nilsen, Jeannette; Bern, Malin; Davidson, Robert J.; Camir...e, Rodney M.; Roopenian, Derry C.; Sandlie, Inger; Lombardi, Silvia; Terje Andersen, Jan; Pinotti, Mirko
A recoded view on the F9 p.Cys178Ter pathogenic mechanism 2020 Branchini, A.; Pinotti, M.
A strategy with chaperone-like compounds to restore expression of factor IX variants affected by frequent missense mutations causing hemophilia B 2018 Pignani, Silvia; Todaro, Alice; Ferrarese, Mattia; Marchi, Saverio; Lombardi, Silvia; Balestra, D...ario; Pinton, Paolo; Bernardi, Francesco; Pinotti, Mirko; Branchini, Alessio
A unique exon specific U1snRNA rescues different haemophilia B - causing splicing-defective factor IX variants in mice 2015 Balestra, Dario; Scalet, Daniela; Pagani, Franco; Bernardi, Francesco; Pinotti, Mirko file con accesso da definire
A very rare simultaneous presence of a ring chromosome 13 and a splicing site mutation on Factor X gene 2013 M., Menegatti; Balestra, Dario; B., Fabrizzi; R., Asselta; Pinotti, Mirko; F., Peyvandi file con accesso da definire
Aberrant splicing reverts a potentially lethal coagulation deficiency caused by a +1g/t splicing mutation 2011 Cavallari, Nicola; Balestra, Dario; Rizzotto, Lara; Maestri, Iva; A., Chamsunri; Bernardi, France...sco; Pinotti, Mirko file con accesso da definire
Activation of a cryptic splice site in a potentially lethal coagulation defect accounts for a functional protein variant 2012 Cavallari, Nicola; Balestra, Dario; Branchini, Alessio; Maestri, Iva; Chuamsunrit, A; Sasanakul, ...W; Mariani, G; Pagani, F; Bernardi, Francesco; Pinotti, Mirko file con accesso da definire
Activation of Endoplasmic Reticulum Stress and Unfolded Protein Response in Congenital Factor VII Deficiency 2018 Andersen, Elisabeth; Chollet, Maria Eugenia; Myklebust, Christiane Filion; Pinotti, Mirko; Bernar...di, Francesco; Chuansumrit, Ampaiwan; Skarpen, Ellen; Sandset, Per Morten; Skretting, Grethe
Acute Coronaric Syndroms and FVII polymorphisms: different effects in the same gene 2001 Ferrara, Rossella; Mastrorilli, Francesca; Bressan, Sabrina; Ferraresi, Paolo; Gemmati, Donato; T...ognazzo, Silvia; Pinotti, Mirko; Scapoli, Gian Luigi; Bernardi, Francesco; Ferrari, Roberto file con accesso da definire
Akt-mediated phosphorylation of MICU1 regulates mitochondrial Ca 2+ levels and tumor growth 2019 Marchi, Saverio; Corricelli, Mariangela; Branchini, Alessio; Vitto, VERONICA ANGELA MARIA; Missir...oli, Sonia; Morciano, Giampaolo; Perrone, Mariasole; Ferrarese, Mattia; Giorgi, Carlotta; Pinotti, Mirko; Galluzzi, Lorenzo; Kroemer, Guido; Pinton, Paolo
Altered mRNA processing and FVIII biosynthesis/function as determinants of phenotype variability in the frequent Arg2016Trp Haemophilia A patients. 2014 Donadon, Irving; Pinotti, Mirko file con accesso da definire
An advanced method for the small-scale production of high-quality minicircle DNA 2021 Mitdank, Hardy; Sama, Simko; Tröger, Meike; Testa, Maria Francesca; Ferrarese, Mattia; Balestra, ...Dario; Pinotti, Mirko; Weng, Alexander file con accesso da definire
An Altered Splicing Registry Explains the Differential ExSpeU1-Mediated Rescue of Splicing Mutations Causing Haemophilia A 2019 Balestra, Dario; Maestri, Iva; Branchini, Alessio; Ferrarese, Mattia; Bernardi, Francesco; Pinott...i, Mirko
An engineered factor X variant as a novel by-passing agent for hemophilia 2022 Tonetto, Elena; Testa, Maria Francesca; Tarantino, Rebecca; Peretto, Laura; Pinotti, Mirko; Branc...hini, Alessio file con accesso da definire
An engineered human albumin enhances half-life and transmucosal delivery when fused to protein-based biologics 2020 Bern, M.; Nilsen, J.; Ferrarese, M.; Sand, K. M. K.; Gjolberg, T. T.; Lode, H. E.; Davidson, R. J....; Camire, R. M.; Baekkevold, E. S.; Foss, S.; Grevys, A.; Dalhus, B.; Wilson, J.; Hoydahl, L. S.; Christianson, G. J.; Roopenian, D. C.; Schlothauer, T.; Michaelsen, T. E.; Moe, M. C.; Lombardi, S.; Pinotti, M.; Sandlie, I.; Branchini, A.; Andersen, J. T.