Morosetti R - Search Results

1

The ER-bound RING finger protein 5 (RNF5/RMA1) causes degenerative myopathy in transgenic mice and is deregulated in inclusion body myositis.

Delaunay A, Bromberg KD, Hayashi Y, Mirabella M, Burch D, Kirkwood B, Serra C, Malicdan MC, Mizisin AP, Morosetti R, Broccolini A, Guo LT, Jones SN, Lira SA, Puri PL, Shelton GD, Ronai Z. Delaunay A, et al. Among authors: morosetti r. PLoS One. 2008 Feb 13;3(2):e1609. doi: 10.1371/journal.pone.0001609. PLoS One. 2008. PMID: 18270596 Free PMC article.

2

Increased aging in primary muscle cultures of sporadic inclusion-body myositis.

Morosetti R, Broccolini A, Sancricca C, Gliubizzi C, Gidaro T, Tonali PA, Ricci E, Mirabella M. Morosetti R, et al. Neurobiol Aging. 2010 Jul;31(7):1205-14. doi: 10.1016/j.neurobiolaging.2008.08.011. Epub 2008 Sep 26. Neurobiol Aging. 2010. PMID: 18823681

3

Hereditary inclusion-body myopathy: clues on pathogenesis and possible therapy.

Broccolini A, Gidaro T, Morosetti R, Mirabella M. Broccolini A, et al. Among authors: morosetti r. Muscle Nerve. 2009 Sep;40(3):340-9. doi: 10.1002/mus.21385. Muscle Nerve. 2009. PMID: 19618441 Review.

4

Hereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle.

Broccolini A, Gidaro T, Morosetti R, Sancricca C, Mirabella M. Broccolini A, et al. Among authors: morosetti r. Acta Myol. 2011 Oct;30(2):91-5. Acta Myol. 2011. PMID: 22106710 Free PMC article. Review.

5

Mesoangioblasts of inclusion-body myositis: a twofold tool to study pathogenic mechanisms and enhance defective muscle regeneration.

Morosetti R, Gliubizzi C, Broccolini A, Sancricca C, Mirabella M. Morosetti R, et al. Acta Myol. 2011 Jun;30(1):24-8. Acta Myol. 2011. PMID: 21842589 Free PMC article. Review.

6

alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy.

Broccolini A, Gliubizzi C, Pavoni E, Gidaro T, Morosetti R, Sciandra F, Giardina B, Tonali P, Ricci E, Brancaccio A, Mirabella M. Broccolini A, et al. Among authors: morosetti r. Neuromuscul Disord. 2005 Feb;15(2):177-84. doi: 10.1016/j.nmd.2004.10.001. Epub 2004 Dec 10. Neuromuscul Disord. 2005. PMID: 15694140

7

Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis.

Broccolini A, Gidaro T, Morosetti R, Gliubizzi C, Servidei T, Pescatori M, Tonali PA, Ricci E, Mirabella M. Broccolini A, et al. Among authors: morosetti r. J Neurochem. 2006 Feb;96(3):777-89. doi: 10.1111/j.1471-4159.2005.03584.x. Epub 2006 Jan 9. J Neurochem. 2006. PMID: 16405511 Free article.

8

Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle.

Broccolini A, Gidaro T, De Cristofaro R, Morosetti R, Gliubizzi C, Ricci E, Tonali PA, Mirabella M. Broccolini A, et al. Among authors: morosetti r. J Neurochem. 2008 May;105(3):971-81. doi: 10.1111/j.1471-4159.2007.05208.x. Epub 2007 Dec 24. J Neurochem. 2008. PMID: 18182043 Free article.

9

TWEAK in inclusion-body myositis muscle: possible pathogenic role of a cytokine inhibiting myogenesis.

Morosetti R, Gliubizzi C, Sancricca C, Broccolini A, Gidaro T, Lucchini M, Mirabella M. Morosetti R, et al. Am J Pathol. 2012 Apr;180(4):1603-13. doi: 10.1016/j.ajpath.2011.12.027. Epub 2012 Feb 4. Am J Pathol. 2012. PMID: 22314077

10

NCAM is hyposialylated in hereditary inclusion body myopathy due to GNE mutations.

Ricci E, Broccolini A, Gidaro T, Morosetti R, Gliubizzi C, Frusciante R, Di Lella GM, Tonali PA, Mirabella M. Ricci E, et al. Among authors: morosetti r. Neurology. 2006 Mar 14;66(5):755-8. doi: 10.1212/01.wnl.0000200956.76449.3f. Neurology. 2006. PMID: 16534119

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