Sironi M - Search Results

1

A common genetic variant in FOXP2 is associated with language-based learning (dis)abilities: Evidence from two Italian independent samples.

Mozzi A, Riva V, Forni D, Sironi M, Marino C, Molteni M, Riva S, Guerini FR, Clerici M, Cagliani R, Mascheretti S. Mozzi A, et al. Among authors: sironi m. Am J Med Genet B Neuropsychiatr Genet. 2017 Jul;174(5):578-586. doi: 10.1002/ajmg.b.32546. Epub 2017 Apr 24. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28436202

2

Comparative analysis of the human dystrophin and utrophin gene structures.

Pozzoli U, Sironi M, Cagliani R, Comi GP, Bardoni A, Bresolin N. Pozzoli U, et al. Among authors: sironi m. Genetics. 2002 Feb;160(2):793-8. doi: 10.1093/genetics/160.2.793. Genetics. 2002. PMID: 11861579 Free PMC article.

3

Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot.

Sironi M, Pozzoli U, Cagliani R, Giorda R, Comi GP, Bardoni A, Menozzi G, Bresolin N. Sironi M, et al. Hum Genet. 2003 Mar;112(3):272-88. doi: 10.1007/s00439-002-0881-5. Epub 2002 Dec 19. Hum Genet. 2003. PMID: 12596052

4

Comparative analysis of vertebrate dystrophin loci indicate intron gigantism as a common feature.

Pozzoli U, Elgar G, Cagliani R, Riva L, Comi GP, Bresolin N, Bardoni A, Sironi M. Pozzoli U, et al. Among authors: sironi m. Genome Res. 2003 May;13(5):764-72. doi: 10.1101/gr.776503. Genome Res. 2003. PMID: 12727896 Free PMC article.

5

Silencer elements as possible inhibitors of pseudoexon splicing.

Sironi M, Menozzi G, Riva L, Cagliani R, Comi GP, Bresolin N, Giorda R, Pozzoli U. Sironi M, et al. Nucleic Acids Res. 2004 Mar 19;32(5):1783-91. doi: 10.1093/nar/gkh341. Print 2004. Nucleic Acids Res. 2004. PMID: 15034146 Free PMC article.

6

An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotype.

Cagliani R, Sironi M, Ciafaloni E, Bardoni A, Fortunato F, Prelle A, Serafini M, Bresolin N, Comi GP. Cagliani R, et al. Among authors: sironi m. Hum Genet. 2004 Jun;115(1):13-8. doi: 10.1007/s00439-004-1118-6. Epub 2004 Apr 30. Hum Genet. 2004. PMID: 15118904

7

Over-representation of exonic splicing enhancers in human intronless genes suggests multiple functions in mRNA processing.

Pozzoli U, Riva L, Menozzi G, Cagliani R, Comi GP, Bresolin N, Giorda R, Sironi M. Pozzoli U, et al. Among authors: sironi m. Biochem Biophys Res Commun. 2004 Sep 17;322(2):470-6. doi: 10.1016/j.bbrc.2004.07.144. Biochem Biophys Res Commun. 2004. PMID: 15325254

8

Fixation of conserved sequences shapes human intron size and influences transposon-insertion dynamics.

Sironi M, Menozzi G, Comi GP, Bresolin N, Cagliani R, Pozzoli U. Sironi M, et al. Trends Genet. 2005 Sep;21(9):484-8. doi: 10.1016/j.tig.2005.06.009. Trends Genet. 2005. PMID: 16005101

9

Analysis of intronic conserved elements indicates that functional complexity might represent a major source of negative selection on non-coding sequences.

Sironi M, Menozzi G, Comi GP, Cagliani R, Bresolin N, Pozzoli U. Sironi M, et al. Hum Mol Genet. 2005 Sep 1;14(17):2533-46. doi: 10.1093/hmg/ddi257. Epub 2005 Jul 21. Hum Mol Genet. 2005. PMID: 16037065

10

Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophies.

Cagliani R, Magri F, Toscano A, Merlini L, Fortunato F, Lamperti C, Rodolico C, Prelle A, Sironi M, Aguennouz M, Ciscato P, Uncini A, Moggio M, Bresolin N, Comi GP. Cagliani R, et al. Among authors: sironi m. Hum Mutat. 2005 Sep;26(3):283. doi: 10.1002/humu.9364. Hum Mutat. 2005. PMID: 16100712

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