Zanna C - Search Results

1

SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder.

Del Dotto V, Ullah F, Di Meo I, Magini P, Gusic M, Maresca A, Caporali L, Palombo F, Tagliavini F, Baugh EH, Macao B, Szilagyi Z, Peron C, Gustafson MA, Khan K, La Morgia C, Barboni P, Carbonelli M, Valentino ML, Liguori R, Shashi V, Sullivan J, Nagaraj S, El-Dairi M, Iannaccone A, Cutcutache I, Bertini E, Carrozzo R, Emma F, Diomedi-Camassei F, Zanna C, Armstrong M, Page M, Stong N, Boesch S, Kopajtich R, Wortmann S, Sperl W, Davis EE, Copeland WC, Seri M, Falkenberg M, Prokisch H, Katsanis N, Tiranti V, Pippucci T, Carelli V. Del Dotto V, et al. Among authors: zanna c. J Clin Invest. 2020 Jan 2;130(1):108-125. doi: 10.1172/JCI128514. J Clin Invest. 2020. PMID: 31550240 Free PMC article.

2

Leber's hereditary optic neuropathy (LHON) pathogenic mutations induce mitochondrial-dependent apoptotic death in transmitochondrial cells incubated with galactose medium.

Ghelli A, Zanna C, Porcelli AM, Schapira AH, Martinuzzi A, Carelli V, Rugolo M. Ghelli A, et al. Among authors: zanna c. J Biol Chem. 2003 Feb 7;278(6):4145-50. doi: 10.1074/jbc.M210285200. Epub 2002 Nov 21. J Biol Chem. 2003. PMID: 12446713 Free article.

3

Apoptotic cell death of cybrid cells bearing Leber's hereditary optic neuropathy mutations is caspase independent.

Zanna C, Ghelli A, Porcelli AM, Carelli V, Martinuzzi A, Rugolo M. Zanna C, et al. Ann N Y Acad Sci. 2003 Dec;1010:213-7. doi: 10.1196/annals.1299.037. Ann N Y Acad Sci. 2003. PMID: 15033723

4

Bioenergetics shapes cellular death pathways in Leber's hereditary optic neuropathy: a model of mitochondrial neurodegeneration.

Carelli V, Rugolo M, Sgarbi G, Ghelli A, Zanna C, Baracca A, Lenaz G, Napoli E, Martinuzzi A, Solaini G. Carelli V, et al. Among authors: zanna c. Biochim Biophys Acta. 2004 Jul 23;1658(1-2):172-9. doi: 10.1016/j.bbabio.2004.05.009. Biochim Biophys Acta. 2004. PMID: 15282189 Free article. Review.

5

Caspase-independent death of Leber's hereditary optic neuropathy cybrids is driven by energetic failure and mediated by AIF and Endonuclease G.

Zanna C, Ghelli A, Porcelli AM, Martinuzzi A, Carelli V, Rugolo M. Zanna C, et al. Apoptosis. 2005 Oct;10(5):997-1007. doi: 10.1007/s10495-005-0742-5. Apoptosis. 2005. PMID: 16151635

6

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes.

Amati-Bonneau P, Valentino ML, Reynier P, Gallardo ME, Bornstein B, Boissière A, Campos Y, Rivera H, de la Aleja JG, Carroccia R, Iommarini L, Labauge P, Figarella-Branger D, Marcorelles P, Furby A, Beauvais K, Letournel F, Liguori R, La Morgia C, Montagna P, Liguori M, Zanna C, Rugolo M, Cossarizza A, Wissinger B, Verny C, Schwarzenbacher R, Martín MA, Arenas J, Ayuso C, Garesse R, Lenaers G, Bonneau D, Carelli V. Amati-Bonneau P, et al. Among authors: zanna c. Brain. 2008 Feb;131(Pt 2):338-51. doi: 10.1093/brain/awm298. Epub 2007 Dec 24. Brain. 2008. PMID: 18158317 Free article.

7

Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus.

La Morgia C, Achilli A, Iommarini L, Barboni P, Pala M, Olivieri A, Zanna C, Vidoni S, Tonon C, Lodi R, Vetrugno R, Mostacci B, Liguori R, Carroccia R, Montagna P, Rugolo M, Torroni A, Carelli V. La Morgia C, et al. Among authors: zanna c. Neurology. 2008 Mar 4;70(10):762-70. doi: 10.1212/01.wnl.0000295505.74234.d0. Epub 2008 Jan 23. Neurology. 2008. PMID: 18216301

8

OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion.

Zanna C, Ghelli A, Porcelli AM, Karbowski M, Youle RJ, Schimpf S, Wissinger B, Pinti M, Cossarizza A, Vidoni S, Valentino ML, Rugolo M, Carelli V. Zanna C, et al. Brain. 2008 Feb;131(Pt 2):352-67. doi: 10.1093/brain/awm335. Brain. 2008. PMID: 18222991

9

Protection against oxidant-induced apoptosis by exogenous glutathione in Leber hereditary optic neuropathy cybrids.

Ghelli A, Porcelli AM, Zanna C, Martinuzzi A, Carelli V, Rugolo M. Ghelli A, et al. Among authors: zanna c. Invest Ophthalmol Vis Sci. 2008 Feb;49(2):671-6. doi: 10.1167/iovs.07-0880. Invest Ophthalmol Vis Sci. 2008. PMID: 18235013

10

The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity.

Ghelli A, Porcelli AM, Zanna C, Vidoni S, Mattioli S, Barbieri A, Iommarini L, Pala M, Achilli A, Torroni A, Rugolo M, Carelli V. Ghelli A, et al. Among authors: zanna c. PLoS One. 2009 Nov 19;4(11):e7922. doi: 10.1371/journal.pone.0007922. PLoS One. 2009. PMID: 19936068 Free PMC article.

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