Pagani F - Search Results

1

Therapeutic activity of modified U1 core spliceosomal particles.

Rogalska ME, Tajnik M, Licastro D, Bussani E, Camparini L, Mattioli C, Pagani F. Rogalska ME, et al. Among authors: pagani f. Nat Commun. 2016 Apr 4;7:11168. doi: 10.1038/ncomms11168. Nat Commun. 2016. PMID: 27041075 Free PMC article.

2

A new type of mutation causes a splicing defect in ATM.

Pagani F, Buratti E, Stuani C, Bendix R, Dörk T, Baralle FE. Pagani F, et al. Nat Genet. 2002 Apr;30(4):426-9. doi: 10.1038/ng858. Epub 2002 Mar 11. Nat Genet. 2002. PMID: 11889466

3

Can a 'patch' in a skipped exon make the pre-mRNA splicing machine run better?

Buratti E, Baralle FE, Pagani F. Buratti E, et al. Among authors: pagani f. Trends Mol Med. 2003 Jun;9(6):229-32; discussion 233-4. doi: 10.1016/s1471-4914(03)00072-8. Trends Mol Med. 2003. PMID: 12829008

4

Genomic variants in exons and introns: identifying the splicing spoilers.

Pagani F, Baralle FE. Pagani F, et al. Nat Rev Genet. 2004 May;5(5):389-96. doi: 10.1038/nrg1327. Nat Rev Genet. 2004. PMID: 15168696 Review. No abstract available.

5

Functional studies on the ATM intronic splicing processing element.

Lewandowska MA, Stuani C, Parvizpur A, Baralle FE, Pagani F. Lewandowska MA, et al. Among authors: pagani f. Nucleic Acids Res. 2005 Jul 19;33(13):4007-15. doi: 10.1093/nar/gki710. Print 2005. Nucleic Acids Res. 2005. PMID: 16030351 Free PMC article.

6

Influence of Friedreich ataxia GAA noncoding repeat expansions on pre-mRNA processing.

Baralle M, Pastor T, Bussani E, Pagani F. Baralle M, et al. Among authors: pagani f. Am J Hum Genet. 2008 Jul;83(1):77-88. doi: 10.1016/j.ajhg.2008.06.018. Am J Hum Genet. 2008. PMID: 18597733 Free PMC article.

7

Therapeutic strategy to rescue mutation-induced exon skipping in rhodopsin by adaptation of U1 snRNA.

Tanner G, Glaus E, Barthelmes D, Ader M, Fleischhauer J, Pagani F, Berger W, Neidhardt J. Tanner G, et al. Among authors: pagani f. Hum Mutat. 2009 Feb;30(2):255-63. doi: 10.1002/humu.20861. Hum Mutat. 2009. PMID: 18837008

8

A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome.

Crotti L, Lewandowska MA, Schwartz PJ, Insolia R, Pedrazzini M, Bussani E, Dagradi F, George AL Jr, Pagani F. Crotti L, et al. Among authors: pagani f. Heart Rhythm. 2009 Feb;6(2):212-8. doi: 10.1016/j.hrthm.2008.10.044. Epub 2008 Nov 6. Heart Rhythm. 2009. PMID: 19187913

9

Regulation of TMEM16A chloride channel properties by alternative splicing.

Ferrera L, Caputo A, Ubby I, Bussani E, Zegarra-Moran O, Ravazzolo R, Pagani F, Galietta LJ. Ferrera L, et al. Among authors: pagani f. J Biol Chem. 2009 Nov 27;284(48):33360-8. doi: 10.1074/jbc.M109.046607. Epub 2009 Oct 9. J Biol Chem. 2009. PMID: 19819874 Free PMC article.

10

Intron cleavage affects processing of alternatively spliced transcripts.

Pastor T, Dal Mas A, Talotti G, Bussani E, Pagani F. Pastor T, et al. Among authors: pagani f. RNA. 2011 Aug;17(8):1604-13. doi: 10.1261/rna.2514811. Epub 2011 Jun 14. RNA. 2011. PMID: 21673105 Free PMC article.

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