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Items: 1 to 20 of 427

1.

Genetic variants in ATP6 and ND3 mitochondrial genes are not associated with aggressive prostate cancer in Mexican-Mestizo men with overweight or obesity.

Canto P, Benítez Granados J, Martínez Ramírez MA, Reyes E, Feria-Bernal G, García-García E, Tejeda ME, Zavala E, Tapia A, Rojano-Mejía D, Méndez JP.

Aging Male. 2016 Sep;19(3):187-191. Epub 2016 May 17.

PMID:
27187822
2.

Impaired Cellular Bioenergetics Causes Mitochondrial Calcium Handling Defects in MT-ND5 Mutant Cybrids.

McKenzie M, Duchen MR.

PLoS One. 2016 Apr 25;11(4):e0154371. doi: 10.1371/journal.pone.0154371. eCollection 2016.

3.

Mitochondrial ND3 G10398A mutation: a biomarker for breast cancer.

Yu Y, Lv F, Lin H, Qian G, Jiang YS, Pang LX, Wang YP, Wang XF, Kang YM, Li CB, Liu Q, Xu JZ, You W.

Genet Mol Res. 2015 Dec 21;14(4):17426-31. doi: 10.4238/2015.December.21.12.

5.

A Dynamic Protein Interaction Landscape of the Human Centrosome-Cilium Interface.

Gupta GD, Coyaud É, Gonçalves J, Mojarad BA, Liu Y, Wu Q, Gheiratmand L, Comartin D, Tkach JM, Cheung SW, Bashkurov M, Hasegan M, Knight JD, Lin ZY, Schueler M, Hildebrandt F, Moffat J, Gingras AC, Raught B, Pelletier L.

Cell. 2015 Dec 3;163(6):1484-99. doi: 10.1016/j.cell.2015.10.065.

6.

Characterization of the Cardiac Overexpression of HSPB2 Reveals Mitochondrial and Myogenic Roles Supported by a Cardiac HspB2 Interactome.

Grose JH, Langston K, Wang X, Squires S, Mustafi SB, Hayes W, Neubert J, Fischer SK, Fasano M, Saunders GM, Dai Q, Christians E, Lewandowski ED, Ping P, Benjamin IJ.

PLoS One. 2015 Oct 14;10(10):e0133994. doi: 10.1371/journal.pone.0133994. eCollection 2015.

7.

Mitochondrial NADH Dehydrogenase Subunit 3 Polymorphism Associated with an Earlier Age at Onset in Male Machado-Joseph disease Patients.

Chen S, Gan SR, Cai PP, Ni W, Zhou Q, Dong Y, Wang N, Wu ZY.

CNS Neurosci Ther. 2016 Jan;22(1):38-42. doi: 10.1111/cns.12443. Epub 2015 Sep 4.

PMID:
26336829
8.

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.

9.

The BioPlex Network: A Systematic Exploration of the Human Interactome.

Huttlin EL, Ting L, Bruckner RJ, Gebreab F, Gygi MP, Szpyt J, Tam S, Zarraga G, Colby G, Baltier K, Dong R, Guarani V, Vaites LP, Ordureau A, Rad R, Erickson BK, Wühr M, Chick J, Zhai B, Kolippakkam D, Mintseris J, Obar RA, Harris T, Artavanis-Tsakonas S, Sowa ME, De Camilli P, Paulo JA, Harper JW, Gygi SP.

Cell. 2015 Jul 16;162(2):425-40. doi: 10.1016/j.cell.2015.06.043.

10.

Quantitative detection of circulating tumor-derived mitochondrial NADH subunit variants as a potential prognostic biomarker for oral cancer.

Uzawa K, Kasamatsu A, Baba T, Kimura Y, Nakashima D, Higo M, Sakamoto Y, Ogawara K, Shiiba M, Tanzawa H.

Int J Oncol. 2015 Sep;47(3):1077-83. doi: 10.3892/ijo.2015.3083. Epub 2015 Jul 15.

PMID:
26179426
11.

Polymorphisms in the mitochondrially encoded ATP synthase 8 gene are associated with susceptibility to bullous pemphigoid in the German population.

Hirose M, Schilf P, Benoit S, Eming R, Gläser R, Homey B, Kunz M, Nebel A, Peitsch WK, Pföhler C, Sárdy M, Schreiber S, Zillikens D, Schmidt E, Ibrahim SM; German AIBD Genetic Study Group..

Exp Dermatol. 2015 Sep;24(9):715-7. doi: 10.1111/exd.12732. Epub 2015 May 26. No abstract available.

PMID:
25941154
12.

An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase.

Hinttala R, Sasarman F, Nishimura T, Antonicka H, Brunel-Guitton C, Schwartzentruber J, Fahiminiya S, Majewski J, Faubert D, Ostergaard E, Smeitink JA, Shoubridge EA.

Hum Mol Genet. 2015 Jul 15;24(14):4103-13. doi: 10.1093/hmg/ddv149. Epub 2015 Apr 24.

13.

Mitochondrial complex I and V gene polymorphisms associated with breast cancer in mizo-mongloid population.

Thapa S, Lalrohlui F, Ghatak S, Zohmingthanga J, Lallawmzuali D, Pautu JL, Senthil Kumar N.

Breast Cancer. 2016 Jul;23(4):607-16. doi: 10.1007/s12282-015-0611-1. Epub 2015 Apr 21.

PMID:
25896597
14.

Mitochondrial genetic variants identified to be associated with posttraumatic stress disorder.

Flaquer A, Baumbach C, Ladwig KH, Kriebel J, Waldenberger M, Grallert H, Baumert J, Meitinger T, Kruse J, Peters A, Emeny R, Strauch K.

Transl Psychiatry. 2015 Mar 10;5:e524. doi: 10.1038/tp.2015.18.

15.

A novel mutation MT-COIII m.9267G>C and MT-COI m.5913G>A mutation in mitochondrial genes in a Tunisian family with maternally inherited diabetes and deafness (MIDD) associated with severe nephropathy.

Tabebi M, Mkaouar-Rebai E, Mnif M, Kallabi F, Ben Mahmoud A, Ben Saad W, Charfi N, Keskes-Ammar L, Kamoun H, Abid M, Fakhfakh F.

Biochem Biophys Res Commun. 2015 Apr 10;459(3):353-60. doi: 10.1016/j.bbrc.2015.01.151. Epub 2015 Feb 19.

PMID:
25701779
16.

Human mitochondrial COX1 assembly into cytochrome c oxidase at a glance.

Dennerlein S, Rehling P.

J Cell Sci. 2015 Mar 1;128(5):833-7. doi: 10.1242/jcs.161729. Epub 2015 Feb 6. Review.

17.

Systematic identification of molecular links between core and candidate genes in breast cancer.

Arroyo R, Suñé G, Zanzoni A, Duran-Frigola M, Alcalde V, Stracker TH, Soler-López M, Aloy P.

J Mol Biol. 2015 Mar 27;427(6 Pt B):1436-50. doi: 10.1016/j.jmb.2015.01.014. Epub 2015 Jan 29.

PMID:
25640309
18.

Alteration of structure and function of ATP synthase and cytochrome c oxidase by lack of Fo-a and Cox3 subunits caused by mitochondrial DNA 9205delTA mutation.

Hejzlarová K, Kaplanová V, Nůsková H, Kovářová N, Ješina P, Drahota Z, Mráček T, Seneca S, Houštěk J.

Biochem J. 2015 Mar 15;466(3):601-11. doi: 10.1042/BJ20141462.

PMID:
25588698
19.

Accurately mapping the location of the binding site for the interaction between hepatitis B virus X protein and cytochrome c oxidase III.

Li D, Ding J, Chen Z, Chen Y, Lin N, Chen F, Wang X.

Int J Mol Med. 2015 Feb;35(2):319-24. doi: 10.3892/ijmm.2014.2018. Epub 2014 Dec 2.

20.

Nuclear and cytoplasmic p53 suppress cell invasion by inhibiting respiratory complex-I activity via Bcl-2 family proteins.

Kim EM, Park JK, Hwang SG, Kim WJ, Liu ZG, Kang SW, Um HD.

Oncotarget. 2014 Sep 30;5(18):8452-65.

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