Davidson MM - Search Results

1

Cellular and molecular studies in muscle and cultures from patients with multiple mitochondrial DNA deletions.

Carrozzo R, Davidson MM, Walker WF, Hirano M, Miranda AF. Carrozzo R, et al. Among authors: davidson mm. J Neurol Sci. 1999 Nov 15;170(1):24-31. doi: 10.1016/s0022-510x(99)00193-8. J Neurol Sci. 1999. PMID: 10540032 Free article.

2

Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation.

Giordano C, Pallotti F, Walker WF, Checcarelli N, Musumeci O, Santorelli F, d'Amati G, Schon EA, DiMauro S, Hirano M, Davidson MM. Giordano C, et al. Among authors: davidson mm. Biochem Biophys Res Commun. 2002 Apr 26;293(1):521-9. doi: 10.1016/S0006-291X(02)00256-5. Biochem Biophys Res Commun. 2002. PMID: 12054632

3

Evidence for nuclear modifier gene in mitochondrial cardiomyopathy.

Davidson MM, Walker WF, Hernandez-Rosa E, Nesti C. Davidson MM, et al. J Mol Cell Cardiol. 2009 Jun;46(6):936-42. doi: 10.1016/j.yjmcc.2009.02.011. Epub 2009 Feb 21. J Mol Cell Cardiol. 2009. PMID: 19233192 Free PMC article.

4

Long-term analysis of differentiation in human myoblasts repopulated with mitochondria harboring mtDNA mutations.

Sobreira C, King MP, Davidson MM, Park H, Koga Y, Miranda AF. Sobreira C, et al. Among authors: davidson mm. Biochem Biophys Res Commun. 1999 Dec 9;266(1):179-86. doi: 10.1006/bbrc.1999.1758. Biochem Biophys Res Commun. 1999. PMID: 10581186 Free article.

5

Dihydrorhodamine 123 identifies impaired mitochondrial respiratory chain function in cultured cells harboring mitochondrial DNA mutations.

Sobreira C, Davidson M, King MP, Miranda AF. Sobreira C, et al. J Histochem Cytochem. 1996 Jun;44(6):571-9. doi: 10.1177/44.6.8666742. J Histochem Cytochem. 1996. PMID: 8666742

6

Mitochondria in neuromuscular disorders.

DiMauro S, Bonilla E, Davidson M, Hirano M, Schon EA. DiMauro S, et al. Biochim Biophys Acta. 1998 Aug 10;1366(1-2):199-210. doi: 10.1016/s0005-2728(98)00113-3. Biochim Biophys Acta. 1998. PMID: 9714805 Free article. Review.

7

Mitochondria and the heart.

Hirano M, Davidson M, DiMauro S. Hirano M, et al. Curr Opin Cardiol. 2001 May;16(3):201-10. doi: 10.1097/00001573-200105000-00008. Curr Opin Cardiol. 2001. PMID: 11357017 Review.

8

Copper supplementation restores cytochrome c oxidase activity in cultured cells from patients with SCO2 mutations.

Salviati L, Hernandez-Rosa E, Walker WF, Sacconi S, DiMauro S, Schon EA, Davidson MM. Salviati L, et al. Among authors: davidson mm. Biochem J. 2002 Apr 15;363(Pt 2):321-7. doi: 10.1042/0264-6021:3630321. Biochem J. 2002. PMID: 11931660 Free PMC article.

9

Biochemical analysis of respiratory function in cybrid cell lines harbouring mitochondrial DNA mutations.

Pallotti F, Baracca A, Hernandez-Rosa E, Walker WF, Solaini G, Lenaz G, Melzi D'Eril GV, Dimauro S, Schon EA, Davidson MM. Pallotti F, et al. Among authors: davidson mm. Biochem J. 2004 Dec 1;384(Pt 2):287-93. doi: 10.1042/BJ20040561. Biochem J. 2004. PMID: 15324306 Free PMC article.

10

Mitochondrial damage mediates genotoxicity of arsenic in mammalian cells.

Liu SX, Davidson MM, Tang X, Walker WF, Athar M, Ivanov V, Hei TK. Liu SX, et al. Among authors: davidson mm. Cancer Res. 2005 Apr 15;65(8):3236-42. doi: 10.1158/0008-5472.CAN-05-0424. Cancer Res. 2005. PMID: 15833855

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