Vergani L - Search Results

1

Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues.

Rinaldi F, Terracciano C, Pisani V, Massa R, Loro E, Vergani L, Di Girolamo S, Angelini C, Gourdon G, Novelli G, Botta A. Rinaldi F, et al. Among authors: vergani l. Neurobiol Dis. 2012 Jan;45(1):264-71. doi: 10.1016/j.nbd.2011.08.010. Epub 2011 Aug 18. Neurobiol Dis. 2012. PMID: 21872659 Free article.

2

Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients.

Gambardella S, Rinaldi F, Lepore SM, Viola A, Loro E, Angelini C, Vergani L, Novelli G, Botta A. Gambardella S, et al. Among authors: vergani l. J Transl Med. 2010 May 20;8:48. doi: 10.1186/1479-5876-8-48. J Transl Med. 2010. PMID: 20487562 Free PMC article.

3

The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients.

Botta A, Rinaldi F, Catalli C, Vergani L, Bonifazi E, Romeo V, Loro E, Viola A, Angelini C, Novelli G. Botta A, et al. Among authors: vergani l. J Med Genet. 2008 Oct;45(10):639-46. doi: 10.1136/jmg.2008.058909. Epub 2008 Jul 8. J Med Genet. 2008. PMID: 18611984

4

MBNL142 and MBNL143 gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases.

Botta A, Malena A, Tibaldi E, Rocchi L, Loro E, Pena E, Cenci L, Ambrosi E, Bellocchi MC, Pagano MA, Novelli G, Rossi G, Monaco HL, Gianazza E, Pantic B, Romeo V, Marin O, Brunati AM, Vergani L. Botta A, et al. Among authors: vergani l. Cell Death Dis. 2013 Aug 15;4(8):e770. doi: 10.1038/cddis.2013.291. Cell Death Dis. 2013. PMID: 23949219 Free PMC article.

5

Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells.

Loro E, Rinaldi F, Malena A, Masiero E, Novelli G, Angelini C, Romeo V, Sandri M, Botta A, Vergani L. Loro E, et al. Among authors: vergani l. Cell Death Differ. 2010 Aug;17(8):1315-24. doi: 10.1038/cdd.2010.33. Epub 2010 Apr 30. Cell Death Differ. 2010. PMID: 20431600

6

Disruption of skeletal muscle mitochondrial network genes and miRNAs in amyotrophic lateral sclerosis.

Russell AP, Wada S, Vergani L, Hock MB, Lamon S, Léger B, Ushida T, Cartoni R, Wadley GD, Hespel P, Kralli A, Soraru G, Angelini C, Akimoto T. Russell AP, et al. Among authors: vergani l. Neurobiol Dis. 2013 Jan;49:107-17. doi: 10.1016/j.nbd.2012.08.015. Epub 2012 Sep 4. Neurobiol Dis. 2013. PMID: 22975021

7

Altered Ca2+ homeostasis and endoplasmic reticulum stress in myotonic dystrophy type 1 muscle cells.

Botta A, Malena A, Loro E, Del Moro G, Suman M, Pantic B, Szabadkai G, Vergani L. Botta A, et al. Among authors: vergani l. Genes (Basel). 2013 Jun 4;4(2):275-92. doi: 10.3390/genes4020275. Genes (Basel). 2013. PMID: 24705164 Free PMC article.

8

Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts.

Pantic B, Borgia D, Giunco S, Malena A, Kiyono T, Salvatori S, De Rossi A, Giardina E, Sangiuolo F, Pegoraro E, Vergani L, Botta A. Pantic B, et al. Among authors: vergani l. Exp Cell Res. 2016 Mar 1;342(1):39-51. doi: 10.1016/j.yexcr.2016.02.013. Epub 2016 Feb 19. Exp Cell Res. 2016. PMID: 26905645

9

Infantile lipid storage myopathy with nocturnal hypoventilation shows abnormal low-affinity muscle carnitine uptake in vitro.

Vergani L, Angelini C. Vergani L, et al. Neuromuscul Disord. 1999 Jul;9(5):320-2. doi: 10.1016/s0960-8966(98)00131-x. Neuromuscul Disord. 1999. PMID: 10407853

10

Activities of mitochondrial complexes correlate with nNOS amount in muscle from ALS patients.

Sorarù G, Vergani L, Fedrizzi L, D'Ascenzo C, Polo A, Bernazzi B, Angelini C. Sorarù G, et al. Among authors: vergani l. Neuropathol Appl Neurobiol. 2007 Apr;33(2):204-11. doi: 10.1111/j.1365-2990.2006.00791.x. Neuropathol Appl Neurobiol. 2007. PMID: 17359361

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