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Items: 1 to 20 of 88

1.

Mangiferin Accelerates Glycolysis and Enhances Mitochondrial Bioenergetics.

Liu Z, Apontes P, Fomenko EV, Chi N, Schuster VL, Kurland IJ, Pessin JE, Chi Y.

Int J Mol Sci. 2018 Jan 9;19(1). pii: E201. doi: 10.3390/ijms19010201.

2.

Germline Mutations in Cancer Predisposition Genes are Frequent in Sporadic Sarcomas.

Chan SH, Lim WK, Ishak NDB, Li ST, Goh WL, Tan GS, Lim KH, Teo M, Young CNC, Malik S, Tan MH, Teh JYH, Chin FKC, Kesavan S, Selvarajan S, Tan P, Teh BT, Soo KC, Farid M, Quek R, Ngeow J.

Sci Rep. 2017 Sep 6;7(1):10660. doi: 10.1038/s41598-017-10333-x.

3.

A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR).

Zhou M, Wang M, Xue L, Lin Z, He Q, Shi W, Chen Y, Jin X, Li H, Jiang P, Guan MX.

J Biol Chem. 2017 Aug 25;292(34):13934-13946. doi: 10.1074/jbc.M117.787028. Epub 2017 Jul 5.

PMID:
28679533
4.

Plasma metabolomics reveals a diagnostic metabolic fingerprint for mitochondrial aconitase (ACO2) deficiency.

Abela L, Spiegel R, Crowther LM, Klein A, Steindl K, Papuc SM, Joset P, Zehavi Y, Rauch A, Plecko B, Simmons TL.

PLoS One. 2017 May 2;12(5):e0176363. doi: 10.1371/journal.pone.0176363. eCollection 2017.

5.

Salicylic Acid-Dependent Plant Stress Signaling via Mitochondrial Succinate Dehydrogenase.

Belt K, Huang S, Thatcher LF, Casarotto H, Singh KB, Van Aken O, Millar AH.

Plant Physiol. 2017 Apr;173(4):2029-2040. doi: 10.1104/pp.16.00060. Epub 2017 Feb 16.

6.

Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe Encephalopathy.

Ait-El-Mkadem S, Dayem-Quere M, Gusic M, Chaussenot A, Bannwarth S, François B, Genin EC, Fragaki K, Volker-Touw CLM, Vasnier C, Serre V, van Gassen KLI, Lespinasse F, Richter S, Eisenhofer G, Rouzier C, Mochel F, De Saint-Martin A, Abi Warde MT, de Sain-van der Velde MGM, Jans JJM, Amiel J, Avsec Z, Mertes C, Haack TB, Strom T, Meitinger T, Bonnen PE, Taylor RW, Gagneur J, van Hasselt PM, Rötig A, Delahodde A, Prokisch H, Fuchs SA, Paquis-Flucklinger V.

Am J Hum Genet. 2017 Jan 5;100(1):151-159. doi: 10.1016/j.ajhg.2016.11.014. Epub 2016 Dec 15.

7.

The genetics and pathology of mitochondrial disease.

Alston CL, Rocha MC, Lax NZ, Turnbull DM, Taylor RW.

J Pathol. 2017 Jan;241(2):236-250. doi: 10.1002/path.4809. Epub 2016 Nov 2. Review.

8.

Wilson Disease: Epigenetic effects of choline supplementation on phenotype and clinical course in a mouse model.

Medici V, Kieffer DA, Shibata NM, Chima H, Kim K, Canovas A, Medrano JF, Islas-Trejo AD, Kharbanda KK, Olson K, Su RJ, Islam MS, Syed R, Keen CL, Miller AY, Rutledge JC, Halsted CH, LaSalle JM.

Epigenetics. 2016 Nov;11(11):804-818. Epub 2016 Sep 9.

9.

The Assembly Factor SDHAF2 Is Dispensable for Flavination of the Catalytic Subunit of Mitochondrial Complex II in Breast Cancer Cells.

Bezawork-Geleta A, Dong L, Rohlena J, Neuzil J.

J Biol Chem. 2016 Oct 7;291(41):21414-21420. Epub 2016 Sep 1.

10.

Differential susceptibility of mitochondrial complex II to inhibition by oxaloacetate in brain and heart.

Stepanova A, Shurubor Y, Valsecchi F, Manfredi G, Galkin A.

Biochim Biophys Acta. 2016 Sep;1857(9):1561-8. doi: 10.1016/j.bbabio.2016.06.002. Epub 2016 Jun 7.

11.

Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive SDHB mutation with reduced penetrance.

Ardissone A, Invernizzi F, Nasca A, Moroni I, Farina L, Ghezzi D.

Mol Genet Metab Rep. 2015 Dec;5:51-54.

12.

Combined defects in oxidative phosphorylation and fatty acid β-oxidation in mitochondrial disease.

Nsiah-Sefaa A, McKenzie M.

Biosci Rep. 2016 Feb 2;36(2). pii: e00313. doi: 10.1042/BSR20150295. Review.

13.

Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid Cancer.

Yehia L, Niazi F, Ni Y, Ngeow J, Sankunny M, Liu Z, Wei W, Mester JL, Keri RA, Zhang B, Eng C.

Am J Hum Genet. 2015 Nov 5;97(5):661-76. doi: 10.1016/j.ajhg.2015.10.001. Epub 2015 Oct 29.

14.

Succinate Dehydrogenase Loss in Familial Paraganglioma: Biochemistry, Genetics, and Epigenetics.

Her YF, Maher LJ 3rd.

Int J Endocrinol. 2015;2015:296167. doi: 10.1155/2015/296167. Epub 2015 Jul 29. Review.

15.

15 YEARS OF PARAGANGLIOMA: Clinical manifestations of paraganglioma syndromes types 1-5.

Benn DE, Robinson BG, Clifton-Bligh RJ.

Endocr Relat Cancer. 2015 Aug;22(4):T91-103. doi: 10.1530/ERC-15-0268. Review.

16.
17.

Mitochondrial roles in disease: a box full of surprises.

Suomalainen A.

EMBO Mol Med. 2015 Oct;7(10):1245-7. doi: 10.15252/emmm.201505350. No abstract available.

18.

Yeast as a system for modeling mitochondrial disease mechanisms and discovering therapies.

Lasserre JP, Dautant A, Aiyar RS, Kucharczyk R, Glatigny A, Tribouillard-Tanvier D, Rytka J, Blondel M, Skoczen N, Reynier P, Pitayu L, Rötig A, Delahodde A, Steinmetz LM, Dujardin G, Procaccio V, di Rago JP.

Dis Model Mech. 2015 Jun;8(6):509-26. doi: 10.1242/dmm.020438. Review.

19.
20.

Cytochrome c oxidase deficiency accelerates mitochondrial apoptosis by activating ceramide synthase 6.

Schüll S, Günther SD, Brodesser S, Seeger JM, Tosetti B, Wiegmann K, Pongratz C, Diaz F, Witt A, Andree M, Brinkmann K, Krönke M, Wiesner RJ, Kashkar H.

Cell Death Dis. 2015 Mar 12;6:e1691. doi: 10.1038/cddis.2015.62.

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