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Items: 1 to 20 of 140

1.

A European Mitochondrial Haplotype Identified in Ancient Phoenician Remains from Carthage, North Africa.

Matisoo-Smith EA, Gosling AL, Boocock J, Kardailsky O, Kurumilian Y, Roudesli-Chebbi S, Badre L, Morel JP, Sebaï LL, Zalloua PA.

PLoS One. 2016 May 25;11(5):e0155046. doi: 10.1371/journal.pone.0155046. eCollection 2016.

2.

Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss.

Balali M, Kamalidehghan B, Farhadi M, Ahmadipour F, Ashkezari MD, Hemami MR, Arabzadeh H, Falah M, Meng GY, Houshmand M.

Ther Clin Risk Manag. 2016 Jan 28;12:117-28. doi: 10.2147/TCRM.S90581. eCollection 2016.

3.

A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease.

Rajakulendran S, Pitceathly RD, Taanman JW, Costello H, Sweeney MG, Woodward CE, Jaunmuktane Z, Holton JL, Jacques TS, Harding BN, Fratter C, Hanna MG, Rahman S.

PLoS One. 2016 Jan 6;11(1):e0145500. doi: 10.1371/journal.pone.0145500. eCollection 2016.

4.

The role of mitochondrial tRNA mutations in lung cancer.

Wang L, Chen ZJ, Zhang YK, Le HB.

Int J Clin Exp Med. 2015 Aug 15;8(8):13341-6. eCollection 2015.

5.

High glucose uptake unexpectedly is accompanied by high levels of the mitochondrial ß-F1-ATPase subunit in head and neck squamous cell carcinoma.

Huebbers CU, Adam AC, Preuss SF, Schiffer T, Schilder S, Guntinas-Lichius O, Schmidt M, Klussmann JP, Wiesner RJ.

Oncotarget. 2015 Nov 3;6(34):36172-84. doi: 10.18632/oncotarget.5459.

6.

Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort.

Li Y, Beckman KB, Caberto C, Kazma R, Lum-Jones A, Haiman CA, Le Marchand L, Stram DO, Saxena R, Cheng I.

PLoS One. 2015 Sep 4;10(9):e0136796. doi: 10.1371/journal.pone.0136796. eCollection 2015.

7.

Increased Incidence of Mitochondrial Cytochrome C Oxidase 1 Gene Mutations in Patients with Primary Ovarian Insufficiency.

Zhen X, Wu B, Wang J, Lu C, Gao H, Qiao J.

PLoS One. 2015 Jul 30;10(7):e0132610. doi: 10.1371/journal.pone.0132610. eCollection 2015.

8.

Mitochondrial DNA Haplogroups and the Risk of Sporadic Parkinson's Disease in Han Chinese.

Chen YF, Chen WJ, Lin XZ, Zhang QJ, Cai JP, Liou CW, Wang N.

Chin Med J (Engl). 2015 Jul 5;128(13):1748-54. doi: 10.4103/0366-6999.159348.

9.

Carriers of Mitochondrial DNA Macrohaplogroup N Lineages Reached Australia around 50,000 Years Ago following a Northern Asian Route.

Fregel R, Cabrera V, Larruga JM, Abu-Amero KK, González AM.

PLoS One. 2015 Jun 8;10(6):e0129839. doi: 10.1371/journal.pone.0129839. eCollection 2015.

10.

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

Hagen CM, Aidt FH, Havndrup O, Hedley PL, Jensen MK, Kanters JK, Pham TT, Bundgaard H, Christiansen M.

PLoS One. 2015 Apr 29;10(4):e0124540. doi: 10.1371/journal.pone.0124540. eCollection 2015.

11.

Ancient inland human dispersals from Myanmar into interior East Asia since the Late Pleistocene.

Li YC, Wang HW, Tian JY, Liu LN, Yang LQ, Zhu CL, Wu SF, Kong QP, Zhang YP.

Sci Rep. 2015 Mar 26;5:9473. doi: 10.1038/srep09473.

12.

Maternal ancestry and population history from whole mitochondrial genomes.

Kivisild T.

Investig Genet. 2015 Mar 10;6:3. doi: 10.1186/s13323-015-0022-2. eCollection 2015.

13.

Estimates of continental ancestry vary widely among individuals with the same mtDNA haplogroup.

Emery LS, Magnaye KM, Bigham AW, Akey JM, Bamshad MJ.

Am J Hum Genet. 2015 Feb 5;96(2):183-93. doi: 10.1016/j.ajhg.2014.12.015. Epub 2015 Jan 22.

14.

Systematic analysis of the clinical and biochemical characteristics of maternally inherited hypertension in Chinese Han families associated with mitochondrial.

Liu Y, Zhu Q, Zhu C, Wang X, Yang J, Yin T, Gao J, Li Z, Ma Q, Guan M, Li Y, Chen Y.

BMC Med Genomics. 2014 Dec 24;7:73. doi: 10.1186/s12920-014-0073-x.

15.

Results of Mitochondrial DNA Sequence Analysis in Patients with Clinically Diagnosed Leber's Hereditary Optic Neuropathy.

Gürkan H, Ozal SA, Esgin H.

Balkan Med J. 2012 Sep;29(3):306-9. doi: 10.5152/balkanmedj.2012.015. Epub 2012 Sep 1.

16.

Mitochondrial genomic variation associated with higher mitochondrial copy number: the Cache County Study on Memory Health and Aging.

Ridge PG, Maxwell TJ, Foutz SJ, Bailey MH, Corcoran CD, Tschanz JT, Norton MC, Munger RG, O'Brien E, Kerber RA, Cawthon RM, Kauwe JS.

BMC Bioinformatics. 2014;15 Suppl 7:S6. doi: 10.1186/1471-2105-15-S7-S6. Epub 2014 May 28.

17.

Molecular characterization of a Chinese family carrying a novel C4329A mutation in mitochondrial tRNAIle and tRNAGln genes.

Liu Y, Li Y, Gao J, Zhu C, Lan Y, Yang J, Li Z, Guan M, Chen Y.

BMC Med Genet. 2014 Jul 23;15:84. doi: 10.1186/1471-2350-15-84.

18.

The impact of mitochondrial DNA and nuclear genes related to mitochondrial functioning on the risk of Parkinson's disease.

Gaweda-Walerych K, Zekanowski C.

Curr Genomics. 2013 Dec;14(8):543-59. doi: 10.2174/1389202914666131210211033.

19.

Characterization of mitochondrial haplogroups in a large population-based sample from the United States.

Mitchell SL, Goodloe R, Brown-Gentry K, Pendergrass SA, Murdock DG, Crawford DC.

Hum Genet. 2014 Jul;133(7):861-8. doi: 10.1007/s00439-014-1421-9. Epub 2014 Feb 1.

20.

Mitochondrial NADH dehydrogenase polymorphisms are associated with breast cancer in Poland.

Grzybowska-Szatkowska L, Slaska B.

J Appl Genet. 2014 May;55(2):173-81. doi: 10.1007/s13353-013-0190-9. Epub 2014 Jan 11.

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