Sgarbi G - Search Results

1

Oxidative stress in the denervated muscle.

Abruzzo PM, di Tullio S, Marchionni C, Belia S, Fanó G, Zampieri S, Carraro U, Kern H, Sgarbi G, Lenaz G, Marini M. Abruzzo PM, et al. Among authors: sgarbi g. Free Radic Res. 2010 May;44(5):563-76. doi: 10.3109/10715761003692487. Free Radic Res. 2010. PMID: 20298122

2

T-Cell reactivity to the P2C nonstructural protein of a diabetogenic strain of coxsackievirus B4.

Varela-Calvino R, Sgarbi G, Arif S, Peakman M. Varela-Calvino R, et al. Among authors: sgarbi g. Virology. 2000 Aug 15;274(1):56-64. doi: 10.1006/viro.2000.0446. Virology. 2000. PMID: 10936088 Free article.

3

Enhanced activity of the plasma membrane oxidoreductase in circulating lymphocytes from insulin-dependent diabetes mellitus patients.

Lenaz G, Paolucci U, Fato R, D'Aurelio M, Parenti Castelli G, Sgarbi G, Biagini G, Ragni L, Salardi S, Cacciari E. Lenaz G, et al. Among authors: sgarbi g. Biochem Biophys Res Commun. 2002 Feb 8;290(5):1589-92. doi: 10.1006/bbrc.2002.6392. Biochem Biophys Res Commun. 2002. PMID: 11820804

4

Rhodamine 123 as a probe of mitochondrial membrane potential: evaluation of proton flux through F(0) during ATP synthesis.

Baracca A, Sgarbi G, Solaini G, Lenaz G. Baracca A, et al. Among authors: sgarbi g. Biochim Biophys Acta. 2003 Sep 30;1606(1-3):137-46. doi: 10.1016/s0005-2728(03)00110-5. Biochim Biophys Acta. 2003. PMID: 14507434 Free article.

5

Bioenergetics of mitochondrial diseases associated with mtDNA mutations.

Lenaz G, Baracca A, Carelli V, D'Aurelio M, Sgarbi G, Solaini G. Lenaz G, et al. Among authors: sgarbi g. Biochim Biophys Acta. 2004 Jul 23;1658(1-2):89-94. doi: 10.1016/j.bbabio.2004.03.013. Biochim Biophys Acta. 2004. PMID: 15282179 Free article. Review.

6

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: sgarbi g. 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.

7

Severe impairment of complex I-driven adenosine triphosphate synthesis in leber hereditary optic neuropathy cybrids.

Baracca A, Solaini G, Sgarbi G, Lenaz G, Baruzzi A, Schapira AH, Martinuzzi A, Carelli V. Baracca A, et al. Among authors: sgarbi g. Arch Neurol. 2005 May;62(5):730-6. doi: 10.1001/archneur.62.5.730. Arch Neurol. 2005. PMID: 15883259

8

Inefficient coupling between proton transport and ATP synthesis may be the pathogenic mechanism for NARP and Leigh syndrome resulting from the T8993G mutation in mtDNA.

Sgarbi G, Baracca A, Lenaz G, Valentino LM, Carelli V, Solaini G. Sgarbi G, et al. Biochem J. 2006 May 1;395(3):493-500. doi: 10.1042/BJ20051748. Biochem J. 2006. PMID: 16402916 Free PMC article.

9

Evaluating mitochondrial membrane potential in cells.

Solaini G, Sgarbi G, Lenaz G, Baracca A. Solaini G, et al. Among authors: sgarbi g. Biosci Rep. 2007 Jun;27(1-3):11-21. doi: 10.1007/s10540-007-9033-4. Biosci Rep. 2007. PMID: 17497220 Review.

10

Biochemical phenotypes associated with the mitochondrial ATP6 gene mutations at nt8993.

Baracca A, Sgarbi G, Mattiazzi M, Casalena G, Pagnotta E, Valentino ML, Moggio M, Lenaz G, Carelli V, Solaini G. Baracca A, et al. Among authors: sgarbi g. Biochim Biophys Acta. 2007 Jul;1767(7):913-9. doi: 10.1016/j.bbabio.2007.05.005. Epub 2007 May 18. Biochim Biophys Acta. 2007. PMID: 17568559 Free article.

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