Malena A - Search Results

1

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. Autophagy. 2016 Nov;12(11):2098-2112. doi: 10.1080/15548627.2016.1226734. Epub 2016 Sep 14. Autophagy. 2016. PMID: 27627835 Free PMC article.

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. 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

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. Among authors: malena a. Brain. 2007 Oct;130(Pt 10):2715-24. doi: 10.1093/brain/awm151. Epub 2007 Jul 11. Brain. 2007. PMID: 17626036

4

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: malena a. 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

5

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: malena a. Hum Mol Genet. 2017 Mar 15;26(6):1087-1103. doi: 10.1093/hmg/ddx019. Hum Mol Genet. 2017. PMID: 28087734 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: malena a. 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

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: malena a. 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

8

Beta-agonist stimulation ameliorates the phenotype of spinal and bulbar muscular atrophy mice and patient-derived myotubes.

Milioto C, Malena A, Maino E, Polanco MJ, Marchioretti C, Borgia D, Pereira MG, Blaauw B, Lieberman AP, Venturini R, Plebani M, Sambataro F, Vergani L, Pegoraro E, Sorarù G, Pennuto M. Milioto C, et al. Among authors: malena a. Sci Rep. 2017 Jan 24;7:41046. doi: 10.1038/srep41046. Sci Rep. 2017. PMID: 28117338 Free PMC article.

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: malena a. Genes (Basel). 2013 Jun 4;4(2):275-92. doi: 10.3390/genes4020275. Genes (Basel). 2013. PMID: 24705164 Free PMC article.

10

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. Acta Neuropathol. 2013 Jul;126(1):109-21. doi: 10.1007/s00401-013-1122-9. Epub 2013 May 4. Acta Neuropathol. 2013. PMID: 23644820

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