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Items: 14

1.

Therapeutic effect of green tea extract on alcohol induced hepatic mitochondrial DNA damage in albino wistar rats.

Reddyvari H, Govatati S, Matha SK, Korla SV, Malempati S, Pasupuleti SR, Bhanoori M, Nallanchakravarthula V.

J Adv Res. 2017 May;8(3):289-295. doi: 10.1016/j.jare.2017.02.002. Epub 2017 Feb 24.

2.

Digital PCR methods improve detection sensitivity and measurement precision of low abundance mtDNA deletions.

Belmonte FR, Martin JL, Frescura K, Damas J, Pereira F, Tarnopolsky MA, Kaufman BA.

Sci Rep. 2016 Apr 28;6:25186. doi: 10.1038/srep25186.

3.

Pearson marrow pancreas syndrome in patients suspected to have Diamond-Blackfan anemia.

Gagne KE, Ghazvinian R, Yuan D, Zon RL, Storm K, Mazur-Popinska M, Andolina L, Bubala H, Golebiowska S, Higman MA, Kalwak K, Kurre P, Matysiak M, Niewiadomska E, Pels S, Petruzzi MJ, Pobudejska-Pieniazek A, Szczepanski T, Fleming MD, Gazda HT, Agarwal S.

Blood. 2014 Jul 17;124(3):437-40. doi: 10.1182/blood-2014-01-545830. Epub 2014 Apr 15.

4.

Complex-I defect with minimal manifestations.

Finsterer J, Melichart M, Wöhrer A.

Arch Med Sci. 2014 Feb 24;10(1):200-2. doi: 10.5114/aoms.2014.40747. Epub 2014 Feb 23. No abstract available.

5.

Disease progression in patients with single, large-scale mitochondrial DNA deletions.

Grady JP, Campbell G, Ratnaike T, Blakely EL, Falkous G, Nesbitt V, Schaefer AM, McNally RJ, Gorman GS, Taylor RW, Turnbull DM, McFarland R.

Brain. 2014 Feb;137(Pt 2):323-34. doi: 10.1093/brain/awt321. Epub 2013 Nov 25.

6.

Mitochondrial DNA deletions in Alzheimer's brains: a review.

Phillips NR, Simpkins JW, Roby RK.

Alzheimers Dement. 2014 May;10(3):393-400. doi: 10.1016/j.jalz.2013.04.508. Epub 2013 Jul 11. Review.

7.

Mitochondrial disease in childhood: mtDNA encoded.

Saneto RP, Sedensky MM.

Neurotherapeutics. 2013 Apr;10(2):199-211. doi: 10.1007/s13311-012-0167-0. Review.

8.

Mitochondrial genome variations in advanced stage endometriosis: a study in South Indian population.

Govatati S, Tipirisetti NR, Perugu S, Kodati VL, Deenadayal M, Satti V, Bhanoori M, Shivaji S.

PLoS One. 2012;7(7):e40668. doi: 10.1371/journal.pone.0040668. Epub 2012 Jul 17.

9.

Mitochondrial DNA deletions are associated with non-B DNA conformations.

Damas J, Carneiro J, Gonçalves J, Stewart JB, Samuels DC, Amorim A, Pereira F.

Nucleic Acids Res. 2012 Sep;40(16):7606-21. doi: 10.1093/nar/gks500. Epub 2012 May 31.

10.

Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

Lakshmanan LN, Gruber J, Halliwell B, Gunawan R.

PLoS One. 2012;7(4):e35271. doi: 10.1371/journal.pone.0035271. Epub 2012 Apr 18.

11.

Physiology and pathophysiology of mitochondrial DNA.

Li H, Liu D, Lu J, Bai Y.

Adv Exp Med Biol. 2012;942:39-51. doi: 10.1007/978-94-007-2869-1_2. Review.

12.

Endocrine manifestations related to inherited metabolic diseases in adults.

Vantyghem MC, Dobbelaere D, Mention K, Wemeau JL, Saudubray JM, Douillard C.

Orphanet J Rare Dis. 2012 Jan 28;7:11. doi: 10.1186/1750-1172-7-11. Review.

13.

Novel large-range mitochondrial DNA deletions and fatal multisystemic disorder with prominent hepatopathy.

Bianchi M, Rizza T, Verrigni D, Martinelli D, Tozzi G, Torraco A, Piemonte F, Dionisi-Vici C, Nobili V, Francalanci P, Boldrini R, Callea F, Santorelli FM, Bertini E, Carrozzo R.

Biochem Biophys Res Commun. 2011 Nov 18;415(2):300-4. doi: 10.1016/j.bbrc.2011.10.049. Epub 2011 Oct 18.

14.

On the sequence-directed nature of human gene mutation: the role of genomic architecture and the local DNA sequence environment in mediating gene mutations underlying human inherited disease.

Cooper DN, Bacolla A, Férec C, Vasquez KM, Kehrer-Sawatzki H, Chen JM.

Hum Mutat. 2011 Oct;32(10):1075-99. doi: 10.1002/humu.21557. Epub 2011 Sep 2. Review.

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