Sironi M - Search Results

1

Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy.

Felisari G, Martinelli Boneschi F, Bardoni A, Sironi M, Comi GP, Robotti M, Turconi AC, Lai M, Corrao G, Bresolin N. Felisari G, et al. Among authors: sironi m. Neurology. 2000 Aug 22;55(4):559-64. doi: 10.1212/wnl.55.4.559. Neurology. 2000. PMID: 10953192

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. Hum Genet. 2001 Jul;109(1):73-84. doi: 10.1007/s004390100547. Hum Genet. 2001. PMID: 11479738

3

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. 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.

4

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. 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.

5

A CAV3 microdeletion differentially affects skeletal muscle and myocardium.

Cagliani R, Bresolin N, Prelle A, Gallanti A, Fortunato F, Sironi M, Ciscato P, Fagiolari G, Bonato S, Galbiati S, Corti S, Lamperti C, Moggio M, Comi GP. Cagliani R, et al. Among authors: sironi m. Neurology. 2003 Dec 9;61(11):1513-9. doi: 10.1212/01.wnl.0000097320.35982.03. Neurology. 2003. PMID: 14663034

6

Transcriptional activation of the non-muscle, full-length dystrophin isoforms in Duchenne muscular dystrophy skeletal muscle.

Sironi M, Bardoni A, Felisari G, Cagliani R, Robotti M, Comi GP, Moggio M, Bresolin N. Sironi M, et al. J Neurol Sci. 2001 May 1;186(1-2):51-7. doi: 10.1016/s0022-510x(01)00502-0. J Neurol Sci. 2001. PMID: 11412872

7

Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies.

Bardoni A, Felisari G, Sironi M, Comi G, Lai M, Robotti M, Bresolin N. Bardoni A, et al. Among authors: sironi m. Neuromuscul Disord. 2000 Mar;10(3):194-9. doi: 10.1016/s0960-8966(99)00108-x. Neuromuscul Disord. 2000. PMID: 10734267

8

Two dystrophin proteins and transcripts in a mild dystrophinopathic patient.

Cagliani R, Bardoni A, Sironi M, Fortunato F, Prelle A, Felisari G, Bonaglia MC, D'Angelo MG, Moggio M, Bresolin N, Comi GP. Cagliani R, et al. Among authors: sironi m. Neuromuscul Disord. 2003 Jan;13(1):13-6. doi: 10.1016/s0960-8966(02)00192-x. Neuromuscul Disord. 2003. PMID: 12467727

9

Absence of brain Dp140 isoform and cognitive impairment in Becker muscular dystrophy.

Bardoni A, Sironi M, Felisari G, Comi GP, Bresolin N. Bardoni A, et al. Among authors: sironi m. Lancet. 1999 Mar 13;353(9156):897-8. doi: 10.1016/S0140-6736(98)05801-2. Lancet. 1999. PMID: 10093987 No abstract available.

10

A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype.

Sironi M, Corti S, Locatelli F, Cagliani R, Comi GP. Sironi M, et al. Hum Mutat. 2001 Mar;17(3):239. doi: 10.1002/humu.18. Hum Mutat. 2001. PMID: 11241855 No abstract available.

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