Pozzoli U - Search Results

1

From early stress to 12-month development in very preterm infants: Preliminary findings on epigenetic mechanisms and brain growth.

Fumagalli M, Provenzi L, De Carli P, Dessimone F, Sirgiovanni I, Giorda R, Cinnante C, Squarcina L, Pozzoli U, Triulzi F, Brambilla P, Borgatti R, Mosca F, Montirosso R. Fumagalli M, et al. Among authors: pozzoli u. PLoS One. 2018 Jan 5;13(1):e0190602. doi: 10.1371/journal.pone.0190602. eCollection 2018. PLoS One. 2018. PMID: 29304146 Free PMC article.

2

Evolution of ocular clinical and electrophysiological findings in pediatric Bardet-Biedl syndrome.

Spaggiari E, Salati R, Nicolini P, Borgatti R, Pozzoli U, Polenghi F. Spaggiari E, et al. Among authors: pozzoli u. Int Ophthalmol. 1999;23(2):61-7. doi: 10.1023/a:1026560721525. Int Ophthalmol. 1999. PMID: 11196121

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

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.

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

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

8

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.

9

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

10

Influence of the serotonin transporter promoter gene and shyness on children's cerebral responses to facial expressions.

Battaglia M, Ogliari A, Zanoni A, Citterio A, Pozzoli U, Giorda R, Maffei C, Marino C. Battaglia M, et al. Among authors: pozzoli u. Arch Gen Psychiatry. 2005 Jan;62(1):85-94. doi: 10.1001/archpsyc.62.1.85. Arch Gen Psychiatry. 2005. PMID: 15630076

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