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Items: 1 to 20 of 538

1.

The mitochondrial TMEM177 associates with COX20 during COX2 biogenesis.

Lorenzi I, Oeljeklaus S, Aich A, Ronsör C, Callegari S, Dudek J, Warscheid B, Dennerlein S, Rehling P.

Biochim Biophys Acta. 2018 Feb;1865(2):323-333. doi: 10.1016/j.bbamcr.2017.11.010. Epub 2017 Nov 16.

2.

Frequency of primary mutations of Leber's hereditary optic neuropathy patients in North Indian population.

Mishra A, Devi S, Saxena R, Gupta N, Kabra M, Chowdhury MR.

Indian J Ophthalmol. 2017 Nov;65(11):1156-1160. doi: 10.4103/ijo.IJO_380_17.

3.

Mitochondrial genetics and therapeutic overview of Leber's hereditary optic neuropathy.

Manickam AH, Michael MJ, Ramasamy S.

Indian J Ophthalmol. 2017 Nov;65(11):1087-1092. doi: 10.4103/ijo.IJO_358_17. Review.

4.

A Map of Human Mitochondrial Protein Interactions Linked to Neurodegeneration Reveals New Mechanisms of Redox Homeostasis and NF-κB Signaling.

Malty RH, Aoki H, Kumar A, Phanse S, Amin S, Zhang Q, Minic Z, Goebels F, Musso G, Wu Z, Abou-Tok H, Meyer M, Deineko V, Kassir S, Sidhu V, Jessulat M, Scott NE, Xiong X, Vlasblom J, Prasad B, Foster LJ, Alberio T, Garavaglia B, Yu H, Bader GD, Nakamura K, Parkinson J, Babu M.

Cell Syst. 2017 Dec 27;5(6):564-577.e12. doi: 10.1016/j.cels.2017.10.010. Epub 2017 Nov 8.

PMID:
29128334
5.

RNA-binding activity of TRIM25 is mediated by its PRY/SPRY domain and is required for ubiquitination.

Choudhury NR, Heikel G, Trubitsyna M, Kubik P, Nowak JS, Webb S, Granneman S, Spanos C, Rappsilber J, Castello A, Michlewski G.

BMC Biol. 2017 Nov 8;15(1):105. doi: 10.1186/s12915-017-0444-9.

6.

Identification of an ND4 Mutation in Leber Hereditary Optic Neuropathy.

Lu Q, Guo Y, Yi J, Deng X, Yang Z, Yuan X, Deng H.

Optom Vis Sci. 2017 Dec;94(12):1090-1094. doi: 10.1097/OPX.0000000000001147.

PMID:
29116953
7.

XRCC5 cooperates with p300 to promote cyclooxygenase-2 expression and tumor growth in colon cancers.

Zhang Z, Zheng F, Yu Z, Hao J, Chen M, Yu W, Guo W, Chen Y, Huang W, Duan Z, Deng W.

PLoS One. 2017 Oct 19;12(10):e0186900. doi: 10.1371/journal.pone.0186900. eCollection 2017.

8.

Tailoring naringenin conjugates with amplified and triple antiplatelet activity profile: Rational design, synthesis, human plasma stability and in vitro evaluation.

Stylos E, Chatziathanasiadou MV, Tsiailanis A, Kellici TF, Tsoumani M, Kostagianni AD, Deligianni M, Tselepis AD, Tzakos AG.

Biochim Biophys Acta. 2017 Nov;1861(11 Pt A):2609-2618. doi: 10.1016/j.bbagen.2017.08.018. Epub 2017 Aug 24.

PMID:
28844979
9.

Leber's Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India.

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

Invest Ophthalmol Vis Sci. 2017 Aug 1;58(10):3923-3930. doi: 10.1167/iovs.16-20695.

PMID:
28768321
10.

Architecture of the human interactome defines protein communities and disease networks.

Huttlin EL, Bruckner RJ, Paulo JA, Cannon JR, Ting L, Baltier K, Colby G, Gebreab F, Gygi MP, Parzen H, Szpyt J, Tam S, Zarraga G, Pontano-Vaites L, Swarup S, White AE, Schweppe DK, Rad R, Erickson BK, Obar RA, Guruharsha KG, Li K, Artavanis-Tsakonas S, Gygi SP, Harper JW.

Nature. 2017 May 25;545(7655):505-509. doi: 10.1038/nature22366. Epub 2017 May 17.

11.

The Association between the C5263T Mutation in the Mitochondrial ND2 Gene and Coronary Heart Disease among Young Chinese Han People.

Han GX, Xia L, Li SS, Jin QH, Song Y, Shen H, Wang LL, Kong LJ, Li TS, Zhu HY.

Biomed Environ Sci. 2017 Apr;30(4):280-287. doi: 10.3967/bes2017.037.

12.

Human mitochondrial cytochrome c oxidase assembly factor COX18 acts transiently as a membrane insertase within the subunit 2 maturation module.

Bourens M, Barrientos A.

J Biol Chem. 2017 May 12;292(19):7774-7783. doi: 10.1074/jbc.M117.778514. Epub 2017 Mar 22.

PMID:
28330871
13.

Mitochondrial variations in the MT-ND4 and MT-TL1 genes are associated with male infertility.

Ni F, Zhou Y, Zhang WX, Wang XM, Song XM, Jiang H.

Syst Biol Reprod Med. 2017 Feb;63(1):2-6. doi: 10.1080/19396368.2016.1256451. Epub 2016 Dec 14.

PMID:
27973917
14.

Novel mutation of ND4 gene identified by targeted next-generation sequencing in patient with Leigh syndrome.

Xu B, Li X, Du M, Zhou C, Fang H, Lyu J, Yang Y.

J Hum Genet. 2017 Feb;62(2):291-297. doi: 10.1038/jhg.2016.127. Epub 2016 Oct 20.

PMID:
27761019
15.

Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study.

Dankowski T, Schröder T, Möller S, Yu X, Ellinghaus D, Bär F, Fellermann K, Lehnert H, Schreiber S, Franke A, Sina C, Ibrahim SM, König IR.

BMC Gastroenterol. 2016 Oct 3;16(1):118.

16.

Defining the Protein-Protein Interaction Network of the Human Protein Tyrosine Phosphatase Family.

Li X, Tran KM, Aziz KE, Sorokin AV, Chen J, Wang W.

Mol Cell Proteomics. 2016 Sep;15(9):3030-44. doi: 10.1074/mcp.M116.060277. Epub 2016 Jul 18.

17.

An organelle-specific protein landscape identifies novel diseases and molecular mechanisms.

Boldt K, van Reeuwijk J, Lu Q, Koutroumpas K, Nguyen TM, Texier Y, van Beersum SE, Horn N, Willer JR, Mans DA, Dougherty G, Lamers IJ, Coene KL, Arts HH, Betts MJ, Beyer T, Bolat E, Gloeckner CJ, Haidari K, Hetterschijt L, Iaconis D, Jenkins D, Klose F, Knapp B, Latour B, Letteboer SJ, Marcelis CL, Mitic D, Morleo M, Oud MM, Riemersma M, Rix S, Terhal PA, Toedt G, van Dam TJ, de Vrieze E, Wissinger Y, Wu KM, Apic G, Beales PL, Blacque OE, Gibson TJ, Huynen MA, Katsanis N, Kremer H, Omran H, van Wijk E, Wolfrum U, Kepes F, Davis EE, Franco B, Giles RH, Ueffing M, Russell RB, Roepman R; UK10K Rare Diseases Group.

Nat Commun. 2016 May 13;7:11491. doi: 10.1038/ncomms11491.

18.

HSP90 Inhibition Suppresses PGE2 Production via Modulating COX-2 and 15-PGDH Expression in HT-29 Colorectal Cancer Cells.

Mohammadi A, Yaghoobi MM, Gholamhoseinian Najar A, Kalantari-Khandani B, Sharifi H, Saravani M.

Inflammation. 2016 Jun;39(3):1116-23. doi: 10.1007/s10753-016-0343-1.

PMID:
27075590
19.

The Effect on Cognition of Mitochondrial Respiratory System Proteins in Peripheral Blood Mononuclear Cells in the Course of Lung Cancer.

Michalak S, Rybacka-Mossakowska J, Gazdulska J, Gołda-Gocka I, Ramlau R.

Adv Exp Med Biol. 2016;911:45-52. doi: 10.1007/5584_2016_221.

PMID:
26987334
20.

COX-1 and COX-2 polymorphisms in susceptibility to cerebral palsy in very preterm infants.

Kapitanović Vidak H, Catela Ivković T, Vidak Z, Kapitanović S.

Mol Neurobiol. 2017 Mar;54(2):930-938. doi: 10.1007/s12035-016-9713-9. Epub 2016 Jan 19.

PMID:
26781425

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