Fanin M - Search Results

1

Biochemical and ultrastructural evidence of endoplasmic reticulum stress in LGMD2I.

Boito CA, Fanin M, Gavassini BF, Cenacchi G, Angelini C, Pegoraro E. Boito CA, et al. Among authors: fanin m. Virchows Arch. 2007 Dec;451(6):1047-55. doi: 10.1007/s00428-007-0515-3. Epub 2007 Oct 20. Virchows Arch. 2007. PMID: 17952692

2

TGFBR2 but not SPP1 genotype modulates osteopontin expression in Duchenne muscular dystrophy muscle.

Piva L, Gavassini BF, Bello L, Fanin M, Soraru G, Barp A, Ermani M, Angelini C, Hoffman EP, Pegoraro E. Piva L, et al. Among authors: fanin m. J Pathol. 2012 Oct;228(2):251-9. doi: 10.1002/path.4026. Epub 2012 Aug 28. J Pathol. 2012. PMID: 22431140 Free PMC article.

3

Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology.

Pegoraro E, Cepollaro F, Prandini P, Marin A, Fanin M, Trevisan CP, El-Messlemani AH, Tarone G, Engvall E, Hoffman EP, Angelini C. Pegoraro E, et al. Among authors: fanin m. Am J Pathol. 2002 Jun;160(6):2135-43. doi: 10.1016/s0002-9440(10)61162-5. Am J Pathol. 2002. PMID: 12057917 Free PMC article.

4

Gene expression profiling in dysferlinopathies using a dedicated muscle microarray.

Campanaro S, Romualdi C, Fanin M, Celegato B, Pacchioni B, Trevisan S, Laveder P, De Pittà C, Pegoraro E, Hayashi YK, Valle G, Angelini C, Lanfranchi G. Campanaro S, et al. Among authors: fanin m. Hum Mol Genet. 2002 Dec 15;11(26):3283-98. doi: 10.1093/hmg/11.26.3283. Hum Mol Genet. 2002. PMID: 12471055

5

Loss of calpain-3 autocatalytic activity in LGMD2A patients with normal protein expression.

Fanin M, Nascimbeni AC, Fulizio L, Trevisan CP, Meznaric-Petrusa M, Angelini C. Fanin M, et al. Am J Pathol. 2003 Nov;163(5):1929-36. doi: 10.1016/S0002-9440(10)63551-1. Am J Pathol. 2003. PMID: 14578192 Free PMC article.

6

Molecular and muscle pathology in a series of caveolinopathy patients.

Fulizio L, Nascimbeni AC, Fanin M, Piluso G, Politano L, Nigro V, Angelini C. Fulizio L, et al. Among authors: fanin m. Hum Mutat. 2005 Jan;25(1):82-9. doi: 10.1002/humu.20119. Hum Mutat. 2005. PMID: 15580566

7

The frequency of limb girdle muscular dystrophy 2A in northeastern Italy.

Fanin M, Nascimbeni AC, Fulizio L, Angelini C. Fanin M, et al. Neuromuscul Disord. 2005 Mar;15(3):218-24. doi: 10.1016/j.nmd.2004.11.003. Epub 2005 Jan 28. Neuromuscul Disord. 2005. PMID: 15725583

8

Muscle protein analysis in the detection of heterozygotes for recessive limb girdle muscular dystrophy type 2B and 2E.

Fanin M, Nascimbeni AC, Angelini C. Fanin M, et al. Neuromuscul Disord. 2006 Nov;16(11):792-9. doi: 10.1016/j.nmd.2006.06.010. Epub 2006 Aug 23. Neuromuscul Disord. 2006. PMID: 16934466

9

Expression profiling characterization of laminin alpha-2 positive MDC.

Millino C, Bellin M, Fanin M, Romualdi C, Pegoraro E, Angelini C, Lanfranchi G. Millino C, et al. Among authors: fanin m. Biochem Biophys Res Commun. 2006 Nov 17;350(2):345-51. doi: 10.1016/j.bbrc.2006.09.063. Epub 2006 Sep 25. Biochem Biophys Res Commun. 2006. PMID: 17010933

10

How to tackle the diagnosis of limb-girdle muscular dystrophy 2A.

Fanin M, Nascimbeni AC, Tasca E, Angelini C. Fanin M, et al. Eur J Hum Genet. 2009 May;17(5):598-603. doi: 10.1038/ejhg.2008.193. Epub 2008 Oct 15. Eur J Hum Genet. 2009. PMID: 18854869 Free PMC article.

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