Lenaz G - Search Results

1

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. 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.

2

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: lenaz 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.

3

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: lenaz 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.

4

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: lenaz g. Arch Neurol. 2005 May;62(5):730-6. doi: 10.1001/archneur.62.5.730. Arch Neurol. 2005. PMID: 15883259

5

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. Among authors: lenaz g. Biochem J. 2006 May 1;395(3):493-500. doi: 10.1042/BJ20051748. Biochem J. 2006. PMID: 16402916 Free PMC article.

6

New insights into structure and function of mitochondria and their role in aging and disease.

Lenaz G, Baracca A, Fato R, Genova ML, Solaini G. Lenaz G, et al. Antioxid Redox Signal. 2006 Mar-Apr;8(3-4):417-37. doi: 10.1089/ars.2006.8.417. Antioxid Redox Signal. 2006. PMID: 16677088 Review.

7

Mitochondrial Complex I: structure, function, and implications in neurodegeneration.

Lenaz G, Baracca A, Fato R, Genova ML, Solaini G. Lenaz G, et al. Ital J Biochem. 2006 Sep-Dec;55(3-4):232-53. Ital J Biochem. 2006. PMID: 17274529 Review.

8

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: lenaz 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.

9

The study of the pathogenic mechanism of mitochondrial diseases provides information on basic bioenergetics.

Solaini G, Harris DA, Lenaz G, Sgarbi G, Baracca A. Solaini G, et al. Among authors: lenaz g. Biochim Biophys Acta. 2008 Jul-Aug;1777(7-8):941-5. doi: 10.1016/j.bbabio.2008.04.034. Epub 2008 Apr 30. Biochim Biophys Acta. 2008. PMID: 18486591 Free article.

10

Human NARP mitochondrial mutation metabolism corrected with alpha-ketoglutarate/aspartate: a potential new therapy.

Sgarbi G, Casalena GA, Baracca A, Lenaz G, DiMauro S, Solaini G. Sgarbi G, et al. Among authors: lenaz g. Arch Neurol. 2009 Aug;66(8):951-7. doi: 10.1001/archneurol.2009.134. Arch Neurol. 2009. PMID: 19667215

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