Defective splicing, disease and therapy: searching for master checkpoints in exon definition

por Buratti, Emanuele, Baralle, Marco, Baralle, Francisco E.
Publicado 2006

Complex splicing control of the human Thrombopoietin gene by intronic G runs

por Marcucci, Roberto, Baralle, Francisco E., Romano, Maurizio
Publicado 2007

Reduced splicing efficiency induced by synonymous substitutions may generate a substrate for natural selection of new splicing isoforms: the case of CFTR exon 12

por Raponi, Michela, Baralle, Francisco E., Pagani, Franco
Publicado 2007

Functional properties and evolutionary splicing constraints on a composite exonic regulatory element of splicing in CFTR exon 12

por Haque, Ariful, Buratti, Emanuele, Baralle, Francisco E.
Publicado 2010

Mutually exclusive splicing regulates the Na(v) 1.6 sodium channel function through a combinatorial mechanism that involves three distinct splicing regulatory elements and their li...

por Zubović, Lorena, Baralle, Marco, Baralle, Francisco E.
Publicado 2012

Brain-specific promoter and polyadenylation sites of the β-adducin pre-mRNA generate an unusually long 3′-UTR

por Costessi, Luisa, Devescovi, Giulia, Baralle, Francisco E., Muro, Andrés F.
Publicado 2006

SR protein-mediated inhibition of CFTR exon 9 inclusion: molecular characterization of the intronic splicing silencer

por Buratti, Emanuele, Stuani, Cristiana, De Prato, Greta, Baralle, Francisco E.
Publicado 2007

RNA structure is a key regulatory element in pathological ATM and CFTR pseudoexon inclusion events

por Buratti, Emanuele, Dhir, Ashish, Lewandowska, Marzena A., Baralle, Francisco E.
Publicado 2007

Characterizing TDP-43 interaction with its RNA targets

por Bhardwaj, Amit, Myers, Michael P., Buratti, Emanuele, Baralle, Francisco E.
Publicado 2013

TDP-43 loss of cellular function through aggregation requires additional structural determinants beyond its C-terminal Q/N prion-like domain

por Budini, Mauricio, Romano, Valentina, Quadri, Zainuddin, Buratti, Emanuele, Baralle, Francisco E.
Publicado 2015

Functional studies on the ATM intronic splicing processing element

por Lewandowska, Marzena A., Stuani, Cristiana, Parvizpur, Alireza, Baralle, Francisco E., Pagani, Franco
Publicado 2005

Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene

por Mercado, Pablo Arrisi, Ayala, Youhna M., Romano, Maurizio, Buratti, Emanuele, Baralle, Francisco E.
Publicado 2005

Dissecting the splicing mechanism of the Drosophila editing enzyme; dADAR

por Marcucci, Roberto, Romano, Maurizio, Feiguin, Fabian, O'Connell, Mary A., Baralle, Francisco E.
Publicado 2009

Exon First Nucleotide Mutations in Splicing: Evaluation of In Silico Prediction Tools

por Grodecká, Lucie, Lockerová, Pavla, Ravčuková, Barbora, Buratti, Emanuele, Baralle, Francisco E., Dušek, Ladislav, Freiberger, Tomáš
Publicado 2014

Glial TDP-43 regulates axon wrapping, GluRIIA clustering and fly motility by autonomous and non-autonomous mechanisms

por Romano, Giulia, Appocher, Chiara, Scorzeto, Michele, Klima, Raffaella, Baralle, Francisco E., Megighian, Aram, Feiguin, Fabian
Publicado 2015

HnRNP A1 controls a splicing regulatory circuit promoting mesenchymal-to-epithelial transition

por Bonomi, Serena, di Matteo, Anna, Buratti, Emanuele, Cabianca, Daphne S., Baralle, Francisco E., Ghigna, Claudia, Biamonti, Giuseppe
Publicado 2013

Regulated splicing of the fibronectin EDA exon is essential for proper skin wound healing and normal lifespan

por Muro, Andrés F., Chauhan, Anil K., Gajovic, Srecko, Iaconcig, Alessandra, Porro, Fabiola, Stanta, Giorgio, Baralle, Francisco E.
Publicado 2003

Functional mapping of the interaction between TDP-43 and hnRNP A2 in vivo

por D’Ambrogio, Andrea, Buratti, Emanuele, Stuani, Cristiana, Guarnaccia, Corrado, Romano, Maurizio, Ayala, Youhna M., Baralle, Francisco E.
Publicado 2009

A novel anti-aldolase C antibody specifically interacts with residues 85–102 of the protein

por Langellotti, Simona, Romano, Maurizio, Guarnaccia, Corrado, Granata, Vincenzo, Orrù, Stefania, Zagari, Adriana, Baralle, Francisco E, Salvatore, Francesco
Publicado 2014

A novel Drosophila model of TDP-43 proteinopathies: N-terminal sequences combined with the Q/N domain induce protein functional loss and locomotion defects

por Langellotti, Simona, Romano, Valentina, Romano, Giulia, Klima, Raffaella, Feiguin, Fabian, Cragnaz, Lucia, Romano, Maurizio, Baralle, Francisco E.
Publicado 2016