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Items: 1 to 20 of 226

1.

Mitochondrial regulation of epigenetics and its role in human diseases.

Minocherhomji S, Tollefsbol TO, Singh KK.

Epigenetics. 2012 Apr;7(4):326-34. doi: 10.4161/epi.19547. Epub 2012 Apr 1. Review.

2.

Genetic insights into OXPHOS defect and its role in cancer.

Chandra D, Singh KK.

Biochim Biophys Acta. 2011 Jun;1807(6):620-5. doi: 10.1016/j.bbabio.2010.10.023. Epub 2010 Nov 11. Review.

3.

Significance of Mitochondria DNA Mutations in Diseases.

Zhu Z, Wang X.

Adv Exp Med Biol. 2017;1038:219-230. doi: 10.1007/978-981-10-6674-0_15. Review.

PMID:
29178079
4.

Mechanisms of mitochondrial diseases.

Ylikallio E, Suomalainen A.

Ann Med. 2012 Feb;44(1):41-59. doi: 10.3109/07853890.2011.598547. Epub 2011 Aug 2.

PMID:
21806499
5.

A novel role for mitochondria in regulating epigenetic modification in the nucleus.

Smiraglia DJ, Kulawiec M, Bistulfi GL, Gupta SG, Singh KK.

Cancer Biol Ther. 2008 Aug;7(8):1182-90. Epub 2008 Aug 1.

6.

A cytoplasmic suppressor of a nuclear mutation affecting mitochondrial functions in Drosophila.

Chen S, Oliveira MT, Sanz A, Kemppainen E, Fukuoh A, Schlicht B, Kaguni LS, Jacobs HT.

Genetics. 2012 Oct;192(2):483-93. doi: 10.1534/genetics.112.143719. Epub 2012 Jul 30.

7.

Role of mtDNA-related mitoepigenetic phenomena in cancer.

Ferreira A, Serafim TL, Sardão VA, Cunha-Oliveira T.

Eur J Clin Invest. 2015 Jan;45 Suppl 1:44-9. doi: 10.1111/eci.12359. Review.

PMID:
25524586
8.

Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency.

Kemp JP, Smith PM, Pyle A, Neeve VC, Tuppen HA, Schara U, Talim B, Topaloglu H, Holinski-Feder E, Abicht A, Czermin B, Lochmüller H, McFarland R, Chinnery PF, Chrzanowska-Lightowlers ZM, Lightowlers RN, Taylor RW, Horvath R.

Brain. 2011 Jan;134(Pt 1):183-95. doi: 10.1093/brain/awq320. Epub 2010 Dec 17.

9.

Mitochondrial disorders due to nuclear OXPHOS gene defects.

Ugalde C, Morán M, Blázquez A, Arenas J, Martín MA.

Adv Exp Med Biol. 2009;652:85-116. doi: 10.1007/978-90-481-2813-6_7. Review.

PMID:
20225021
10.

Human mitochondrial DNA: roles of inherited and somatic mutations.

Schon EA, DiMauro S, Hirano M.

Nat Rev Genet. 2012 Dec;13(12):878-90. doi: 10.1038/nrg3275. Review.

11.

Global genetic determinants of mitochondrial DNA copy number.

Zhang H, Singh KK.

PLoS One. 2014 Aug 29;9(8):e105242. doi: 10.1371/journal.pone.0105242. eCollection 2014.

12.

Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups.

Gómez-Durán A, Pacheu-Grau D, López-Gallardo E, Díez-Sánchez C, Montoya J, López-Pérez MJ, Ruiz-Pesini E.

Hum Mol Genet. 2010 Sep 1;19(17):3343-53. doi: 10.1093/hmg/ddq246. Epub 2010 Jun 21.

PMID:
20566709
13.

Epigenetics, epidemiology and mitochondrial DNA diseases.

Chinnery PF, Elliott HR, Hudson G, Samuels DC, Relton CL.

Int J Epidemiol. 2012 Feb;41(1):177-87. doi: 10.1093/ije/dyr232. Epub 2012 Jan 28. Review.

15.

Mitochondrial DNA mutations and depletion in pediatric medicine.

Spinazzola A.

Semin Fetal Neonatal Med. 2011 Aug;16(4):190-6. doi: 10.1016/j.siny.2011.04.011. Epub 2011 Jun 8. Review.

PMID:
21652274
16.

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
17.
18.

Animal mitochondria: evolution, function, and disease.

Tao M, You CP, Zhao RR, Liu SJ, Zhang ZH, Zhang C, Liu Y.

Curr Mol Med. 2014 Jan;14(1):115-24. Review.

PMID:
24195633
19.

The mitochondrial side of epigenetics.

Castegna A, Iacobazzi V, Infantino V.

Physiol Genomics. 2015 Aug;47(8):299-307. doi: 10.1152/physiolgenomics.00096.2014. Epub 2015 Jun 2. Review.

PMID:
26038395
20.

Mitochondrial and nuclear accumulation of the transcription factor ATFS-1 promotes OXPHOS recovery during the UPR(mt).

Nargund AM, Fiorese CJ, Pellegrino MW, Deng P, Haynes CM.

Mol Cell. 2015 Apr 2;58(1):123-33. doi: 10.1016/j.molcel.2015.02.008. Epub 2015 Mar 12.

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