Vergani L - Search Results

1

A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function.

Spinazzi M, Cazzola S, Bortolozzi M, Baracca A, Loro E, Casarin A, Solaini G, Sgarbi G, Casalena G, Cenacchi G, Malena A, Frezza C, Carrara F, Angelini C, Scorrano L, Salviati L, Vergani L. Spinazzi M, et al. Among authors: vergani l. Hum Mol Genet. 2008 Nov 1;17(21):3291-302. doi: 10.1093/hmg/ddn225. Epub 2008 Aug 4. Hum Mol Genet. 2008. PMID: 18678599

2

Inhibition of mitochondrial fission favours mutant over wild-type mitochondrial DNA.

Malena A, Loro E, Di Re M, Holt IJ, Vergani L. Malena A, et al. Among authors: vergani l. Hum Mol Genet. 2009 Sep 15;18(18):3407-16. doi: 10.1093/hmg/ddp281. Epub 2009 Jun 27. Hum Mol Genet. 2009. PMID: 19561330

3

Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients.

Borgia D, Malena A, Spinazzi M, Desbats MA, Salviati L, Russell AP, Miotto G, Tosatto L, Pegoraro E, Sorarù G, Pennuto M, Vergani L. Borgia D, et al. Among authors: vergani l. Hum Mol Genet. 2017 Mar 15;26(6):1087-1103. doi: 10.1093/hmg/ddx019. Hum Mol Genet. 2017. PMID: 28087734 Free PMC article.

4

Cultured muscle cells display defects of mitochondrial myopathy ameliorated by anti-oxidants.

Vergani L, Malena A, Sabatelli P, Loro E, Cavallini L, Magalhaes P, Valente L, Bragantini F, Carrara F, Leger B, Poulton J, Russell AP, Holt IJ. Vergani L, et al. Brain. 2007 Oct;130(Pt 10):2715-24. doi: 10.1093/brain/awm151. Epub 2007 Jul 11. Brain. 2007. PMID: 17626036

5

Mitochondrial quality control: Cell-type-dependent responses to pathological mutant mitochondrial DNA.

Malena A, Pantic B, Borgia D, Sgarbi G, Solaini G, Holt IJ, Spinazzola A, Perissinotto E, Sandri M, Baracca A, Vergani L. Malena A, et al. Among authors: vergani l. Autophagy. 2016 Nov;12(11):2098-2112. doi: 10.1080/15548627.2016.1226734. Epub 2016 Sep 14. Autophagy. 2016. PMID: 27627835 Free PMC article.

6

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

7

Androgen-dependent impairment of myogenesis in spinal and bulbar muscular atrophy.

Malena A, Pennuto M, Tezze C, Querin G, D'Ascenzo C, Silani V, Cenacchi G, Scaramozza A, Romito S, Morandi L, Pegoraro E, Russell AP, Sorarù G, Vergani L. Malena A, et al. Among authors: vergani l. Acta Neuropathol. 2013 Jul;126(1):109-21. doi: 10.1007/s00401-013-1122-9. Epub 2013 May 4. Acta Neuropathol. 2013. PMID: 23644820

8

Development and characterization of polyspecific anti-mitochondrion antibodies for proteomics studies on in toto tissue homogenates.

Loro E, Gianazza E, Cazzola S, Malena A, Wait R, Begum S, Brizio C, Dabbeni-Sala F, Vergani L. Loro E, et al. Among authors: vergani l. Electrophoresis. 2009 Apr;30(8):1329-41. doi: 10.1002/elps.200800576. Electrophoresis. 2009. PMID: 19382133

9

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.

10

Spinal and bulbar muscular atrophy: skeletal muscle pathology in male patients and heterozygous females.

Sorarù G, D'Ascenzo C, Polo A, Palmieri A, Baggio L, Vergani L, Gellera C, Moretto G, Pegoraro E, Angelini C. Sorarù G, et al. Among authors: vergani l. J Neurol Sci. 2008 Jan 15;264(1-2):100-5. doi: 10.1016/j.jns.2007.08.012. Epub 2007 Sep 12. J Neurol Sci. 2008. PMID: 17854832

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