New insights into form and function of fibronectin splice variants von White, ES, Baralle, FE, Muro, AF

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An age-related reduction of brain TBPH/TDP-43 levels precedes the onset of locomotion defects in a Drosophila ALS model von Cragnaz, L, Klima, R, De Conti, L, Romano, G, Feiguin, F, Buratti, E, Baralle, M, Baralle, F.E

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High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis von Corrado, Lucia, Ratti, A., Gellera, C., Buratti, E., Castellotti, B., Carlomagno, Y., Ticozzi, N., Mazzini, L., Testa, L., Taroni, F., Baralle, F. E., Silani, V., D'Alfonso, S.

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Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9 von Buratti, E, Baralle, F E

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HnRNP A1 controls a splicing regulatory circuit promoting mesenchymal-to-epithelial transition von Bonomi, Serena, di Matteo, Anna, Buratti, Emanuele, Cabianca, Daphne S, Baralle, Francisco E, Ghigna, Claudia, Biamonti, Giuseppe

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Functional mapping of the interaction between TDP-43 and hnRNP A2 in vivo von D'Ambrogio, Andrea, Buratti, Emanuele, Stuani, Cristiana, Guarnaccia, Corrado, Romano, Maurizio, Ayala, Youhna M, Baralle, Francisco E

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Functional characterization of the common c.-32-13T>G mutation of GAA gene: identification of potential therapeutic agents von Dardis, Andrea, Zanin, Irene, Zampieri, Stefania, Stuani, Cristiana, Pianta, Annalisa, Romanello, Milena, Baralle, Francisco E, Bembi, Bruno, Buratti, Emanuele

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Regulated Splicing of the Fibronectin EDA Exon Is Essential for Proper Skin Wound Healing and Normal Lifespan von Muro, Andrés F., Chauhan, Anil K., Gajovic, Srecko, Iaconcig, Alessandra, Porro, Fabiola, Stanta, Giorgio, Baralle, Francisco E.

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Functional Analysis of cis-Acting Elements Regulating the Alternative Splicing of Human CFTR Exon 9 von Niksic, Martina, Romano, Maurizio, Buratti, Emanuele, Pagani, Franco, Baralle, Francisco E.

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Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping von Buratti, Emanuele, Dörk, Thilo, Zuccato, Elisabetta, Pagani, Franco, Romano, Maurizio, Baralle, Francisco E.

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A new type of mutation causes a splicing defect in ATM von Baralle, Francisco E, Pagani, Franco, Buratti, Emanuele, Stuani, Cristiana, Bendix, Regina, Dörk, Thilo

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New type of disease causing mutations: the example of the composite exonic regulatory elements of splicing in CFTR exon 12 von Pagani, Franco, Stuani, Cristiana, Tzetis, Maria, Kanavakis, Emmanuel, Efthymiadou, Alexandra, Doudounakis, Stavros, Casals, Teresa, Baralle, Francisco E.

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Investigating dysfunctional RNA processing in TDP-43 mouse mutants von Sivakumar, P, Humphrey, J, Ule, A, Bodo, C, Emmett, W, Ricketts, T, Oliveira, H, Wang, E, Housman, D, Greensmith, L, Buratti, E, Baralle, F, Plagnol, V, Acevedo-Arozena, A, Fisher, E.M.C, Fratta, P

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Coupling of Transcription with Alternative Splicing: RNA Pol II Promoters Modulate SF2/ASF and 9G8 Effects on an Exonic Splicing Enhancer von Cramer, Paula, Cáceres, Javier F, Cazalla, Demián, Kadener, Sebastián, Muro, Andrés F, Baralle, Francisco E, Kornblihtt, Alberto R

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An Intronic Polypyrimidine-rich Element Downstream of the Donor Site Modulates Cystic Fibrosis Transmembrane Conductance Regulator Exon 9 Alternative Splicing von Zuccato, Elisabetta, Buratti, Emanuele, Stuani, Cristiana, Baralle, Francisco E., Pagani, Franco

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Depletion of TDP-43 affects Drosophila motoneurons terminal synapsis and locomotive behavior von Feiguin, Fabian, Godena, Vinay K., Romano, Giulia, D’Ambrogio, Andrea, Klima, Raffaella, Baralle, Francisco E.

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Another step forward for SELEXive splicing von Buratti, Emanuele, Baralle, Francisco E.

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Functional properties and evolutionary splicing constraints on a composite exonic regulatory element of splicing in CFTR exon 12 von Haque, Ariful, Buratti, Emanuele, Baralle, Francisco E

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Functional Association between Promoter Structure and Transcript Alternative Splicing von Cramer, Paula, Pesce, C. Gustavo, Baralle, Francisco E., Kornblihtt, Alberto R.

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Identification of a mutation that perturbs NF1 gene splicing using genomic DNA samples and a minigene assay von Baralle, M, Baralle, D, Conti, L. De, Mattocks, C, Whittaker, J, Knezevich, A, Ffrench-Constant, C, Baralle, F.E

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