Davidson MM - Search Results

1

Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 gene.

Akman HO, Davidzon G, Tanji K, Macdermott EJ, Larsen L, Davidson MM, Haller RG, Szczepaniak LS, Lehman TJ, Hirano M, DiMauro S. Akman HO, et al. Among authors: davidson mm. Neuromuscul Disord. 2010 Jun;20(6):397-402. doi: 10.1016/j.nmd.2010.04.004. Epub 2010 May 14. Neuromuscul Disord. 2010. PMID: 20471263 Free PMC article.

2

Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA.

Karadimas CL, Greenstein P, Sue CM, Joseph JT, Tanji K, Haller RG, Taivassalo T, Davidson MM, Shanske S, Bonilla E, DiMauro S. Karadimas CL, et al. Among authors: davidson mm. Neurology. 2000 Sep 12;55(5):644-9. doi: 10.1212/wnl.55.5.644. Neurology. 2000. PMID: 10980727

3

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.

4

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

5

Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes.

Hirano M, Shtilbans A, Mayeux R, Davidson MM, DiMauro S, Knowles JA, Schon EA. Hirano M, et al. Among authors: davidson mm. Proc Natl Acad Sci U S A. 1997 Dec 23;94(26):14894-9. doi: 10.1073/pnas.94.26.14894. Proc Natl Acad Sci U S A. 1997. PMID: 9405710 Free PMC article.

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

Novel cell lines derived from adult human ventricular cardiomyocytes.

Davidson MM, Nesti C, Palenzuela L, Walker WF, Hernandez E, Protas L, Hirano M, Isaac ND. Davidson MM, et al. J Mol Cell Cardiol. 2005 Jul;39(1):133-47. doi: 10.1016/j.yjmcc.2005.03.003. J Mol Cell Cardiol. 2005. PMID: 15913645

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

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.

Taylor RW, Giordano C, Davidson MM, d'Amati G, Bain H, Hayes CM, Leonard H, Barron MJ, Casali C, Santorelli FM, Hirano M, Lightowlers RN, DiMauro S, Turnbull DM. Taylor RW, et al. Among authors: davidson mm. J Am Coll Cardiol. 2003 May 21;41(10):1786-96. doi: 10.1016/s0735-1097(03)00300-0. J Am Coll Cardiol. 2003. PMID: 12767666 Free article.

10

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.

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