Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 101

1.

Bioenergetics and the epigenome: interface between the environment and genes in common diseases.

Wallace DC.

Dev Disabil Res Rev. 2010;16(2):114-9. doi: 10.1002/ddrr.113. Review.

PMID:
20818725
2.

Energetics, epigenetics, mitochondrial genetics.

Wallace DC, Fan W.

Mitochondrion. 2010 Jan;10(1):12-31. doi: 10.1016/j.mito.2009.09.006. Epub 2009 Sep 29. Review.

3.

Mitochondrial DNA mutations in disease and aging.

Wallace DC.

Environ Mol Mutagen. 2010 Jun;51(5):440-50. doi: 10.1002/em.20586. Review.

PMID:
20544884
5.

Mitochondria, bioenergetics, and the epigenome in eukaryotic and human evolution.

Wallace DC.

Cold Spring Harb Symp Quant Biol. 2009;74:383-93. doi: 10.1101/sqb.2009.74.031. Epub 2009 Dec 2. Review.

6.

Animal models for mitochondrial disease.

Wallace DC.

Methods Mol Biol. 2002;197:3-54. Review.

PMID:
12013805
7.

Colloquium paper: bioenergetics, the origins of complexity, and the ascent of man.

Wallace DC.

Proc Natl Acad Sci U S A. 2010 May 11;107 Suppl 2:8947-53. doi: 10.1073/pnas.0914635107. Epub 2010 May 5.

8.

A mitochondrial bioenergetic etiology of disease.

Wallace DC.

J Clin Invest. 2013 Apr;123(4):1405-12. doi: 10.1172/JCI61398. Epub 2013 Apr 1.

9.

Mouse models for mitochondrial disease.

Wallace DC.

Am J Med Genet. 2001 Spring;106(1):71-93. Review.

PMID:
11579427
10.

Molecular and bioenergetic differences between cells with African versus European inherited mitochondrial DNA haplogroups: implications for population susceptibility to diseases.

Kenney MC, Chwa M, Atilano SR, Falatoonzadeh P, Ramirez C, Malik D, Tarek M, Del Carpio JC, Nesburn AB, Boyer DS, Kuppermann BD, Vawter MP, Jazwinski SM, Miceli MV, Wallace DC, Udar N.

Biochim Biophys Acta. 2014 Feb;1842(2):208-19. doi: 10.1016/j.bbadis.2013.10.016. Epub 2013 Nov 4.

11.

Mitochondrial genome changes and neurodegenerative diseases.

Pinto M, Moraes CT.

Biochim Biophys Acta. 2014 Aug;1842(8):1198-207. doi: 10.1016/j.bbadis.2013.11.012. Epub 2013 Nov 16. Review.

12.

Molecular genetics of mitochondrial disorders.

Wong LJ.

Dev Disabil Res Rev. 2010;16(2):154-62. doi: 10.1002/ddrr.104. Review.

PMID:
20818730
13.

Molecular research technologies in mitochondrial diseases: the microarray approach.

Crimi M, O'Hearn SF, Wallace DC, Comi GP.

IUBMB Life. 2005 Dec;57(12):811-8. Review.

14.

Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency.

Cízková A, Stránecký V, Ivánek R, Hartmannová H, Nosková L, Piherová L, Tesarová M, Hansíková H, Honzík T, Zeman J, Divina P, Potocká A, Paul J, Sperl W, Mayr JA, Seneca S, Houstĕk J, Kmoch S.

BMC Genomics. 2008 Jan 25;9:38. doi: 10.1186/1471-2164-9-38.

15.

Neurodevelopmental manifestations of mitochondrial disease.

Falk MJ.

J Dev Behav Pediatr. 2010 Sep;31(7):610-21. doi: 10.1097/DBP.0b013e3181ef42c1. Review.

16.

Mitochondrial energetics and therapeutics.

Wallace DC, Fan W, Procaccio V.

Annu Rev Pathol. 2010;5:297-348. doi: 10.1146/annurev.pathol.4.110807.092314. Review.

17.

Sequence variants in four candidate genes (NIPSNAP1, GBAS, CHCHD1 and METT11D1) in patients with combined oxidative phosphorylation system deficiencies.

Smits P, Rodenburg RJ, Smeitink JA, van den Heuvel LP.

J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S13-9.

PMID:
24137763
18.

The pathophysiology of mitochondrial disease as modeled in the mouse.

Wallace DC, Fan W.

Genes Dev. 2009 Aug 1;23(15):1714-36. doi: 10.1101/gad.1784909. Review.

19.

Mitochondrial DNA mutations and breast tumorigenesis.

Yadav N, Chandra D.

Biochim Biophys Acta. 2013 Dec;1836(2):336-44. doi: 10.1016/j.bbcan.2013.10.002. Epub 2013 Oct 16. Review.

20.

A mitochondrial paradigm for degenerative diseases and ageing.

Wallace DC.

Novartis Found Symp. 2001;235:247-63; discussion 263-6. Review.

PMID:
11280029
Items per page

Supplemental Content

Write to the Help Desk