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Items: 1 to 20 of 657

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.

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
5.

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
6.

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.

7.

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.

8.

FASTKD1 and FASTKD4 have opposite effects on expression of specific mitochondrial RNAs, depending upon their endonuclease-like RAP domain.

Boehm E, Zaganelli S, Maundrell K, Jourdain AA, Thore S, Martinou JC.

Nucleic Acids Res. 2017 Jun 2;45(10):6135-6146. doi: 10.1093/nar/gkx164.

9.

Protein interaction screening identifies SH3RF1 as a new regulator of FAT1 protein levels.

de Bock CE, Hughes MR, Snyder K, Alley S, Sadeqzadeh E, Dun MD, McNagny KM, Molloy TJ, Hondermarck H, Thorne RF.

FEBS Lett. 2017 Feb;591(4):667-678. doi: 10.1002/1873-3468.12569. Epub 2017 Feb 16.

PMID:
28129444
10.

[The role of MT-ND1 m.3635G>A mutation in Leber's hereditary optic neuropathy].

Zhang J, Zhang Z, Fu R, Ji Y, Jiang P, Tong Y, Qu J, Guan M.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Dec 10;33(6):747-751. Chinese.

PMID:
27984598
11.

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
12.

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
13.

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.

14.

MtDNA T4216C variation in multiple sclerosis: a systematic review and meta-analysis.

Andalib S, Emamhadi M, Yousefzadeh-Chabok S, Salari A, Sigaroudi AE, Vafaee MS.

Acta Neurol Belg. 2016 Dec;116(4):439-443. Epub 2016 Jul 25. Review.

PMID:
27457485
15.

Previously Unclassified Mutation of mtDNA m.3472T>C: Evidence of Pathogenicity in Leber's Hereditary Optic Neuropathy.

Sheremet NL, Nevinitsyna TA, Zhorzholadze NV, Ronzina IA, Itkis YS, Krylova TD, Tsygankova PG, Malakhova VA, Zakharova EY, Tokarchuk AV, Panteleeva AA, Karger EM, Lyamzaev KG, Avetisov SE.

Biochemistry (Mosc). 2016 Jul;81(7):748-54. doi: 10.1134/S0006297916070117.

16.

Mitochondrial respiratory chain disorders in the Old Order Amish population.

Ghaloul-Gonzalez L, Goldstein A, Walsh Vockley C, Dobrowolski SF, Biery A, Irani A, Ibarra J, Morton DH, Mohsen AW, Vockley J.

Mol Genet Metab. 2016 Aug;118(4):296-303. doi: 10.1016/j.ymgme.2016.06.005. Epub 2016 Jun 16.

PMID:
27344355
17.

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
18.

Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy.

Ji Y, Liang M, Zhang J, Zhu L, Zhang Z, Fu R, Liu X, Zhang M, Fu Q, Zhao F, Tong Y, Sun Y, Jiang P, Guan MX.

Invest Ophthalmol Vis Sci. 2016 May 1;57(6):2377-89. doi: 10.1167/iovs.16-19243.

PMID:
27177320
19.

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.

20.

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

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