Pozzoli U - Search Results

1

The dystrophin gene is alternatively spliced throughout its coding sequence.

Sironi M, Cagliani R, Pozzoli U, Bardoni A, Comi GP, Giorda R, Bresolin N. Sironi M, et al. Among authors: pozzoli u. FEBS Lett. 2002 Apr 24;517(1-3):163-6. doi: 10.1016/s0014-5793(02)02613-3. FEBS Lett. 2002. PMID: 12062429 Free article.

2

Analysis of splicing parameters in the dystrophin gene: relevance for physiological and pathogenetic splicing mechanisms.

Sironi M, Pozzoli U, Cagliani R, Comi GP, Bardoni A, Bresolin N. Sironi M, et al. Among authors: pozzoli u. Hum Genet. 2001 Jul;109(1):73-84. doi: 10.1007/s004390100547. Hum Genet. 2001. PMID: 11479738

3

Electrophysiological analysis of cognitive slowing in subjects with mitochondrial encephalomyopathy.

Montirosso R, Brambilla D, Felisari G, Sclaunich F, Filipponi E, Pozzoli U, Bresolin N. Montirosso R, et al. Among authors: pozzoli u. J Neurol Sci. 2002 Feb 15;194(1):3-9. doi: 10.1016/s0022-510x(01)00664-5. J Neurol Sci. 2002. PMID: 11809159 Clinical Trial.

4

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. Genetics. 2002 Feb;160(2):793-8. doi: 10.1093/genetics/160.2.793. Genetics. 2002. PMID: 11861579 Free PMC article.

5

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. Among authors: pozzoli u. Hum Genet. 2003 Mar;112(3):272-88. doi: 10.1007/s00439-002-0881-5. Epub 2002 Dec 19. Hum Genet. 2003. PMID: 12596052

6

Trans-acting factors may cause dystrophin splicing misregulation in BMD skeletal muscles.

Sironi M, Cagliani R, Comi GP, Pozzoli U, Bardoni A, Giorda R, Bresolin N. Sironi M, et al. Among authors: pozzoli u. FEBS Lett. 2003 Feb 27;537(1-3):30-4. doi: 10.1016/s0014-5793(03)00066-8. FEBS Lett. 2003. PMID: 12606026 Free article.

7

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. Genome Res. 2003 May;13(5):764-72. doi: 10.1101/gr.776503. Genome Res. 2003. PMID: 12727896 Free PMC article.

8

The 129 codon polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjects.

Del Bo R, Comi GP, Giorda R, Crimi M, Locatelli F, Martinelli-Boneschi F, Pozzoli U, Castelli E, Bresolin N, Scarlato G. Del Bo R, et al. Among authors: pozzoli u. J Neurol. 2003 Jun;250(6):688-92. doi: 10.1007/s00415-003-1057-5. J Neurol. 2003. PMID: 12796830

9

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. Among authors: pozzoli u. 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.

10

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. 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

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