Bresolin N - Search Results

1

OASes and STING: adaptive evolution in concert.

Mozzi A, Pontremoli C, Forni D, Clerici M, Pozzoli U, Bresolin N, Cagliani R, Sironi M. Mozzi A, et al. Among authors: bresolin n. Genome Biol Evol. 2015 Mar 9;7(4):1016-32. doi: 10.1093/gbe/evv046. Genome Biol Evol. 2015. PMID: 25752600 Free PMC article.

2

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: bresolin n. Neuromuscul Disord. 2000 Mar;10(3):194-9. doi: 10.1016/s0960-8966(99)00108-x. Neuromuscul Disord. 2000. PMID: 10734267

3

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: bresolin n. Neurology. 2000 Aug 22;55(4):559-64. doi: 10.1212/wnl.55.4.559. Neurology. 2000. PMID: 10953192

4

Intraarterial injection of muscle-derived CD34(+)Sca-1(+) stem cells restores dystrophin in mdx mice.

Torrente Y, Tremblay JP, Pisati F, Belicchi M, Rossi B, Sironi M, Fortunato F, El Fahime M, D'Angelo MG, Caron NJ, Constantin G, Paulin D, Scarlato G, Bresolin N. Torrente Y, et al. Among authors: bresolin n. J Cell Biol. 2001 Jan 22;152(2):335-48. doi: 10.1083/jcb.152.2.335. J Cell Biol. 2001. PMID: 11266450 Free PMC article.

5

Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuria.

Cagliani R, Comi GP, Tancredi L, Sironi M, Fortunato F, Giorda R, Bardoni A, Moggio M, Prelle A, Bresolin N, Scarlato G. Cagliani R, et al. Among authors: bresolin n. Neuromuscul Disord. 2001 May;11(4):389-94. doi: 10.1016/s0960-8966(00)00207-8. Neuromuscul Disord. 2001. PMID: 11369190

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. Among authors: bresolin n. 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

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

8

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: bresolin n. 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.

9

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

10

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: bresolin n. 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.

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