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Items: 1 to 20 of 26


The complete mitogenome of a 500-year-old Inca child mummy.

Gómez-Carballa A, Catelli L, Pardo-Seco J, Martinón-Torres F, Roewer L, Vullo C, Salas A.

Sci Rep. 2015 Nov 12;5:16462. doi: 10.1038/srep16462.


Mitochondrial mutations in subjects with psychiatric disorders.

Sequeira A, Rollins B, Magnan C, van Oven M, Baldi P, Myers RM, Barchas JD, Schatzberg AF, Watson SJ, Akil H, Bunney WE, Vawter MP.

PLoS One. 2015 May 26;10(5):e0127280. doi: 10.1371/journal.pone.0127280. eCollection 2015.


Mitochondrial DNA haplogroup confers genetic susceptibility to nasopharyngeal carcinoma in Chaoshanese from Guangdong, China.

Hu SP, Du JP, Li DR, Yao YG.

PLoS One. 2014 Jan 31;9(1):e87795. doi: 10.1371/journal.pone.0087795. eCollection 2014.


Mitochondrial sequence variation in African-American primary open-angle glaucoma patients.

Collins DW, Gudiseva HV, Trachtman BT, Jerrehian M, Gorry T, Merritt WT 3rd, Rhodes AL, Sankar PS, Regina M, Miller-Ellis E, O'Brien JM.

PLoS One. 2013 Oct 1;8(10):e76627. doi: 10.1371/journal.pone.0076627. eCollection 2013.


The role of the mitochondrial ribosome in human disease: searching for mutations in 12S mitochondrial rRNA with high disruptive potential.

Smith PM, Elson JL, Greaves LC, Wortmann SB, Rodenburg RJ, Lightowlers RN, Chrzanowska-Lightowlers ZM, Taylor RW, Vila-Sanjurjo A.

Hum Mol Genet. 2014 Feb 15;23(4):949-67. doi: 10.1093/hmg/ddt490. Epub 2013 Oct 2.


MitoLSDB: a comprehensive resource to study genotype to phenotype correlations in human mitochondrial DNA variations.

K S, Jalali S, Scaria V, Bhardwaj A.

PLoS One. 2013 Apr 9;8(4):e60066. doi: 10.1371/journal.pone.0060066. Print 2013.


Somatic mitochondrial DNA mutations in Chinese patients with osteosarcoma.

Yu M, Wan Y, Zou Q.

Int J Exp Pathol. 2013 Apr;94(2):126-32. doi: 10.1111/iep.12015. Epub 2013 Feb 27.


Mitochondrial DNA variations in Madras motor neuron disease.

Govindaraj P, Nalini A, Krishna N, Sharath A, Khan NA, Tamang R, Gourie-Devi M, Brown RH, Thangaraj K.

Mitochondrion. 2013 Nov;13(6):721-8. doi: 10.1016/j.mito.2013.02.003. Epub 2013 Feb 16.


Toward a mtDNA locus-specific mutation database using the LOVD platform.

Elson JL, Sweeney MG, Procaccio V, Yarham JW, Salas A, Kong QP, van der Westhuizen FH, Pitceathly RD, Thorburn DR, Lott MT, Wallace DC, Taylor RW, McFarland R.

Hum Mutat. 2012 Sep;33(9):1352-8. doi: 10.1002/humu.22118. Epub 2012 Jul 2.


The maintenance of mitochondrial genetic stability is crucial during the oncogenic process.

Iglesias P, Salas A, Costoya JA.

Commun Integr Biol. 2012 Jan 1;5(1):34-8.


Mitochondrial DNA mutation m.10680G > A is associated with Leber hereditary optic neuropathy in Chinese patients.

Zhang AM, Jia X, Guo X, Zhang Q, Yao YG.

J Transl Med. 2012 Mar 9;10:43. doi: 10.1186/1479-5876-10-43.


Mitochondrial DNA haplogroup background affects LHON, but not suspected LHON, in Chinese patients.

Zhang AM, Jia X, Bi R, Salas A, Li S, Xiao X, Wang P, Guo X, Kong QP, Zhang Q, Yao YG.

PLoS One. 2011;6(11):e27750. doi: 10.1371/journal.pone.0027750. Epub 2011 Nov 15.


Is mitochondrial tRNA(phe) variant m.593T>C a synergistically pathogenic mutation in Chinese LHON families with m.11778G>A?

Zhang AM, Bandelt HJ, Jia X, Zhang W, Li S, Yu D, Wang D, Zhuang XY, Zhang Q, Yao YG.

PLoS One. 2011;6(10):e26511. doi: 10.1371/journal.pone.0026511. Epub 2011 Oct 19.


Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution.

Voets AM, van den Bosch BJ, Stassen AP, Hendrickx AT, Hellebrekers DM, Van Laer L, Van Eyken E, Van Camp G, Pyle A, Baudouin SV, Chinnery PF, Smeets HJ.

Mitochondrion. 2011 Nov;11(6):964-72. doi: 10.1016/j.mito.2011.09.003. Epub 2011 Sep 17.


Mitochondrial subversion in cancer.

Chatterjee A, Dasgupta S, Sidransky D.

Cancer Prev Res (Phila). 2011 May;4(5):638-54. doi: 10.1158/1940-6207.CAPR-10-0326. Review.


Evolutionary analyses of entire genomes do not support the association of mtDNA mutations with Ras/MAPK pathway syndromes.

Gómez-Carballa A, Cerezo M, Balboa E, Heredia C, Castro-Feijóo L, Rica I, Barreiro J, Eirís J, Cabanas P, Martínez-Soto I, Fernández-Toral J, Castro-Gago M, Pombo M, Carracedo Á, Barros F, Salas A.

PLoS One. 2011 Apr 19;6(4):e18348. doi: 10.1371/journal.pone.0018348.


Reassessing the role of mitochondrial DNA mutations in autism spectrum disorder.

Álvarez-Iglesias V, Mosquera-Miguel A, Cuscó I, Carracedo Á, Pérez-Jurado LA, Salas A.

BMC Med Genet. 2011 Apr 6;12:50. doi: 10.1186/1471-2350-12-50.


Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C.

Yu D, Jia X, Zhang AM, Li S, Zou Y, Zhang Q, Yao YG.

PLoS One. 2010 Oct 18;5(10):e13426. doi: 10.1371/journal.pone.0013426.


A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss.

Bai Y, Wang Z, Dai W, Li Q, Chen G, Cong N, Guan M, Li H.

BMC Med Genet. 2010 Sep 7;11:129. doi: 10.1186/1471-2350-11-129.

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