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Items: 1 to 20 of 106

1.

Mitochondrial dysfunction in autism.

Giulivi C, Zhang YF, Omanska-Klusek A, Ross-Inta C, Wong S, Hertz-Picciotto I, Tassone F, Pessah IN.

JAMA. 2010 Dec 1;304(21):2389-96. doi: 10.1001/jama.2010.1706.

2.

Alterations in mitochondrial DNA copy number and the activities of electron transport chain complexes and pyruvate dehydrogenase in the frontal cortex from subjects with autism.

Gu F, Chauhan V, Kaur K, Brown WT, LaFauci G, Wegiel J, Chauhan A.

Transl Psychiatry. 2013 Sep 3;3:e299. doi: 10.1038/tp.2013.68.

3.

Bisphenol A induces oxidative stress and mitochondrial dysfunction in lymphoblasts from children with autism and unaffected siblings.

Kaur K, Chauhan V, Gu F, Chauhan A.

Free Radic Biol Med. 2014 Nov;76:25-33. doi: 10.1016/j.freeradbiomed.2014.07.030. Epub 2014 Aug 4.

PMID:
25101517
4.

Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control Study.

Wong S, Napoli E, Krakowiak P, Tassone F, Hertz-Picciotto I, Giulivi C.

Pediatrics. 2016 Apr;137(4). pii: e20151888. doi: 10.1542/peds.2015-1888. Epub 2016 Mar 31. Erratum in: Pediatrics. 2016 Aug;138(2):null.

5.

Elevated mitochondrial DNA copy number in peripheral blood cells is associated with childhood autism.

Chen S, Li Z, He Y, Zhang F, Li H, Liao Y, Wei Z, Wan G, Xiang X, Hu M, Xia K, Chen X, Tang J.

BMC Psychiatry. 2015 Mar 17;15:50. doi: 10.1186/s12888-015-0432-y.

6.

Brief report: High frequency of biochemical markers for mitochondrial dysfunction in autism: no association with the mitochondrial aspartate/glutamate carrier SLC25A12 gene.

Correia C, Coutinho AM, Diogo L, Grazina M, Marques C, Miguel T, Ataíde A, Almeida J, Borges L, Oliveira C, Oliveira G, Vicente AM.

J Autism Dev Disord. 2006 Nov;36(8):1137-40.

PMID:
17151801
7.

Mitochondrial dysfunction in patients with hypotonia, epilepsy, autism, and developmental delay: HEADD syndrome.

Fillano JJ, Goldenthal MJ, Rhodes CH, Marín-García J.

J Child Neurol. 2002 Jun;17(6):435-9.

PMID:
12174964
8.

Failed upregulation of TFAM protein and mitochondrial DNA in oxidatively deficient fibers of chronic obstructive pulmonary disease locomotor muscle.

Konokhova Y, Spendiff S, Jagoe RT, Aare S, Kapchinsky S, MacMillan NJ, Rozakis P, Picard M, Aubertin-Leheudre M, Pion CH, Bourbeau J, Hepple RT, Taivassalo T.

Skelet Muscle. 2016 Feb 18;6:10. doi: 10.1186/s13395-016-0083-9. eCollection 2016.

9.

Mitochondrial dysfunction in autism.

Legido A, Jethva R, Goldenthal MJ.

Semin Pediatr Neurol. 2013 Sep;20(3):163-75. doi: 10.1016/j.spen.2013.10.008. Epub 2013 Oct 29. Review.

PMID:
24331358
10.

Lymphocytic mitochondrial DNA deletions, biochemical folate status and hepatocellular carcinoma susceptibility in a case-control study.

Wu MY, Kuo CS, Lin CY, Lu CL, Syu Huang RF.

Br J Nutr. 2009 Sep;102(5):715-21. doi: 10.1017/S0007114509243054. Epub 2009 Mar 31.

PMID:
19331700
11.

Impaired mitochondrial function is abrogated by dexrazoxane in doxorubicin-treated childhood acute lymphoblastic leukemia survivors.

Lipshultz SE, Anderson LM, Miller TL, Gerschenson M, Stevenson KE, Neuberg DS, Franco VI, LiButti DE, Silverman LB, Vrooman LM, Sallan SE; Dana-Farber Cancer Institute Acute Lymphoblastic Leukemia Consortium.

Cancer. 2016 Mar 15;122(6):946-53. doi: 10.1002/cncr.29872. Epub 2016 Jan 13.

13.

Clinical characterization and mitochondrial DNA sequence variations in Leber hereditary optic neuropathy.

Kumar M, Kaur P, Kumar M, Saxena R, Sharma P, Dada R.

Mol Vis. 2012;18:2687-99. Epub 2012 Nov 12.

14.

An investigation of mitochondrial haplogroups in autism.

Kent L, Gallagher L, Elliott HR, Mowbray C, Chinnery PF.

Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):987-9.

PMID:
18161860
15.
16.

Identification of novel mitochondrial mutations in Leber's hereditary optic neuropathy.

Kumar M, Tanwar M, Saxena R, Sharma P, Dada R.

Mol Vis. 2010 Apr 30;16:782-92.

17.

Role of Mitochondrial DNA Copy Number Alteration in Human Renal Cell Carcinoma.

Lin CS, Lee HT, Lee MH, Pan SC, Ke CY, Chiu AW, Wei YH.

Int J Mol Sci. 2016 May 25;17(6). pii: E814. doi: 10.3390/ijms17060814.

18.

Mitochondrial disease in autism spectrum disorder patients: a cohort analysis.

Weissman JR, Kelley RI, Bauman ML, Cohen BH, Murray KF, Mitchell RL, Kern RL, Natowicz MR.

PLoS One. 2008;3(11):e3815. doi: 10.1371/journal.pone.0003815. Epub 2008 Nov 26.

19.

Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunction.

Raha S, Merante F, Shoubridge E, Myint AT, Tein I, Benson L, Johns T, Robinson BH.

Hum Mutat. 1999;13(3):245-54.

PMID:
10090480
20.

Mutagenesis of mitochondrial DNA in Fuchs endothelial corneal dystrophy.

Czarny P, Seda A, Wielgorski M, Binczyk E, Markiewicz B, Kasprzak E, Jiménez-García MP, Grabska-Liberek I, Pawlowska E, Blasiak J, Szaflik J, Szaflik JP.

Mutat Res. 2014 Feb;760:42-7. doi: 10.1016/j.mrfmmm.2013.12.001. Epub 2013 Dec 26.

PMID:
24374226

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