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Results: 1 to 20 of 630

1.

Identification of New Mechanisms of Cellular Response to Chemotherapy by Tracking Changes in Post-Translational Modifications by Ubiquitin and Ubiquitin-Like Proteins.

Bonacci T, Audebert S, Camoin L, Baudelet E, Bidaut G, Garcia M, Witzel II, Perkins ND, Borg JP, Iovanna JL, Soubeyran P.

J Proteome Res. 2014 Apr 2. [Epub ahead of print]

PMID:
24654937
[PubMed - as supplied by publisher]
2.

Safety and effects of the vector for the Leber hereditary optic neuropathy gene therapy clinical trial.

Koilkonda RD, Yu H, Chou TH, Feuer WJ, Ruggeri M, Porciatti V, Tse D, Hauswirth WW, Chiodo V, Boye SL, Lewin AS, Neuringer M, Renner L, Guy J.

JAMA Ophthalmol. 2014 Apr 1;132(4):409-20. doi: 10.1001/jamaophthalmol.2013.7630.

PMID:
24457989
[PubMed - indexed for MEDLINE]
3.

Mitochondrial DNA profiling via genomic analysis in mesial temporal lobe epilepsy patients with hippocampal sclerosis.

Gurses C, Azakli H, Alptekin A, Cakiris A, Abaci N, Arikan M, Kursun O, Gokyigit A, Ustek D.

Gene. 2014 Apr 1;538(2):323-7. doi: 10.1016/j.gene.2014.01.030. Epub 2014 Jan 16.

PMID:
24440288
[PubMed - indexed for MEDLINE]
4.

Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations.

Auré K, Dubourg O, Jardel C, Clarysse L, Sternberg D, Fournier E, Laforêt P, Streichenberger N, Petiot P, Gervais-Bernard H, Vial C, Bedat-Millet AL, Drouin-Garraud V, Bouillaud F, Vandier C, Fontaine B, Lombès A.

Neurology. 2013 Nov 19;81(21):1810-8. doi: 10.1212/01.wnl.0000436067.43384.0b. Epub 2013 Oct 23.

PMID:
24153443
[PubMed - indexed for MEDLINE]
5.

Whole-exome sequencing identifies a variant of the mitochondrial MT-ND1 gene associated with epileptic encephalopathy: west syndrome evolving to Lennox-Gastaut syndrome.

Delmiro A, Rivera H, García-Silva MT, García-Consuegra I, Martín-Hernández E, Quijada-Fraile P, de Las Heras RS, Moreno-Izquierdo A, Martín MÁ, Arenas J, Martínez-Azorín F.

Hum Mutat. 2013 Dec;34(12):1623-7. doi: 10.1002/humu.22445. Epub 2013 Oct 10.

PMID:
24105702
[PubMed - indexed for MEDLINE]
6.

Mitochondria and tumors: a new perspective.

Chintha R, Kaipa PR, Sekhar N, Hasan Q.

Indian J Cancer. 2013 Jul-Sep;50(3):206-13. doi: 10.4103/0019-509X.118732.

PMID:
24061460
[PubMed - indexed for MEDLINE]
Free Article
7.

Highly expressed MT-ND3 positively associated with histological severity of hepatic steatosis.

Wang HN, Chen HD, Chen KY, Xiao JF, He K, Xiang GA, Xie X.

APMIS. 2014 May;122(5):443-51. doi: 10.1111/apm.12166. Epub 2013 Sep 11.

PMID:
24020820
[PubMed - indexed for MEDLINE]
8.

Mitochondrial ATP 6 and 8 polymorphisms in irritable bowel syndrome with diarrhea.

Wang WF, Li X, Guo MZ, Chen JD, Yang YS, Peng LH, Wang YH, Zhang CY, Li HH.

World J Gastroenterol. 2013 Jun 28;19(24):3847-53. doi: 10.3748/wjg.v19.i24.3847.

PMID:
23840124
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Mitochondrial cytochrome c oxidase subunit II variations predict adverse prognosis in cytogenetically normal acute myeloid leukaemia.

Silkjaer T, Nyvold CG, Juhl-Christensen C, Hokland P, Nørgaard JM.

Eur J Haematol. 2013 Oct;91(4):295-303. doi: 10.1111/ejh.12166. Epub 2013 Aug 20.

PMID:
23826975
[PubMed - indexed for MEDLINE]
10.

A novel m.6307A>G mutation in the mitochondrial COXI gene in asthenozoospermic infertile men.

Baklouti-Gargouri S, Ghorbel M, Ben Mahmoud A, Mkaouar-Rebai E, Cherif M, Chakroun N, Sellami A, Fakhfakh F, Ammar-Keskes L.

Mol Reprod Dev. 2013 Jul;80(7):581-7. doi: 10.1002/mrd.22197. Epub 2013 Jun 17.

PMID:
23712756
[PubMed - indexed for MEDLINE]
11.

Haplogroup heterogeneity of LHON patients carrying the m.14484T>C mutation in India.

Khan NA, Govindaraj P, Soumittra N, Srilekha S, Ambika S, Vanniarajan A, Meena AK, Uppin MS, Sundaram C, Taly AB, Bindu PS, Gayathri N, Thangaraj K.

Invest Ophthalmol Vis Sci. 2013 Jun 10;54(6):3999-4005. doi: 10.1167/iovs.13-11925.

PMID:
23674761
[PubMed - indexed for MEDLINE]
Free Article
12.

Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men.

Baklouti-Gargouri S, Ghorbel M, Ben Mahmoud A, Mkaouar-Rebai E, Cherif M, Chakroun N, Sellami A, Fakhfakh F, Ammar-Keskes L.

Mol Biol Rep. 2013 Aug;40(8):4705-12. doi: 10.1007/s11033-013-2566-7. Epub 2013 May 6.

PMID:
23645088
[PubMed - indexed for MEDLINE]
13.

POU domain transcription factor BRN2 is crucial for expression of ASCL1, ND1 and neuroendocrine marker molecules and cell growth in small cell lung cancer.

Ishii J, Sato H, Sakaeda M, Shishido-Hara Y, Hiramatsu C, Kamma H, Shimoyamada H, Fujiwara M, Endo T, Aoki I, Yazawa T.

Pathol Int. 2013 Mar;63(3):158-68. doi: 10.1111/pin.12042.

PMID:
23530560
[PubMed - indexed for MEDLINE]
14.

An inherited heteroplasmic mutation in mitochondrial gene COI in a patient with prostate cancer alters reactive oxygen, reactive nitrogen and proliferation.

Arnold RS, Sun Q, Sun CQ, Richards JC, O'Hearn S, Osunkoya AO, Wallace DC, Petros JA.

Biomed Res Int. 2013;2013:239257. doi: 10.1155/2013/239257. Epub 2012 Dec 27.

PMID:
23509693
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

T4216C mutation in NADH dehydrogenase I gene is associated with recurrent pregnancy loss.

Colagar AH, Mosaieby E, Seyedhassani SM, Mohajerani M, Arasteh A, Kamalidehghan B, Houshmand M.

Mitochondrial DNA. 2013 Oct;24(5):610-2. doi: 10.3109/19401736.2013.772150. Epub 2013 Mar 6.

PMID:
23464625
[PubMed - indexed for MEDLINE]
16.

Protein interactions of the transcription factor Hoxa1.

Lambert B, Vandeputte J, Remacle S, Bergiers I, Simonis N, Twizere JC, Vidal M, Rezsohazy R.

BMC Dev Biol. 2012 Oct 22;12:29. doi: 10.1186/1471-213X-12-29.

PMID:
23088713
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Possible association of a novel missense mutation A6375G in the mitochondrial cytochrome C oxidase I gene with asthenospermia in the Tunisian population.

Baklouti-Gargouri S, Ghorbel M, Chamkha I, Mkaouar-Rebai E, Sellami A, Chakroun N, Fakhfakh F, Ammar-Keskes L.

Genet Test Mol Biomarkers. 2012 Nov;16(11):1298-302. doi: 10.1089/gtmb.2012.0052. Epub 2012 Oct 2.

PMID:
23030649
[PubMed - indexed for MEDLINE]
18.

Charting the landscape of tandem BRCT domain-mediated protein interactions.

Woods NT, Mesquita RD, Sweet M, Carvalho MA, Li X, Liu Y, Nguyen H, Thomas CE, Iversen ES Jr, Marsillac S, Karchin R, Koomen J, Monteiro AN.

Sci Signal. 2012 Sep 18;5(242):rs6.

PMID:
22990118
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Mitochondrial respiratory chain enzyme assay and DNA analysis in peripheral blood leukocytes for the etiological study of Chinese children with Leigh syndrome due to complex I deficiency.

Ma YY, Wu TF, Liu YP, Wang Q, Li XY, Zhang Y, Song JQ, Wang YJ, Yang YL.

Mitochondrial DNA. 2013 Feb;24(1):67-73. doi: 10.3109/19401736.2012.717932. Epub 2012 Sep 5.

PMID:
22947169
[PubMed - indexed for MEDLINE]
20.

Amyloid-β peptide binds to cytochrome C oxidase subunit 1.

Hernandez-Zimbron LF, Luna-Muñoz J, Mena R, Vazquez-Ramirez R, Kubli-Garfias C, Cribbs DH, Manoutcharian K, Gevorkian G.

PLoS One. 2012;7(8):e42344. doi: 10.1371/journal.pone.0042344. Epub 2012 Aug 21.

PMID:
22927926
[PubMed - indexed for MEDLINE]
Free PMC Article

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