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Items: 1 to 20 of 40

1.

Cardiomyopathy-associated mutation in the ADP/ATP carrier reveals translation-dependent regulation of cytochrome c oxidase activity.

Ogunbona OB, Baile MG, Claypool SM.

Mol Biol Cell. 2018 Jun 15;29(12):1449-1464. doi: 10.1091/mbc.E17-12-0700. Epub 2018 Apr 24.

2.

Krüppel-like factor 4 (KLF4) induces mitochondrial fusion and increases spare respiratory capacity of human glioblastoma cells.

Wang S, Shi X, Wei S, Ma D, Oyinlade O, Lv SQ, Ying M, Zhang YA, Claypool SM, Watkins P, Xia S.

J Biol Chem. 2018 Apr 27;293(17):6544-6555. doi: 10.1074/jbc.RA117.001323. Epub 2018 Mar 5.

PMID:
29507094
3.

Multitiered and Cooperative Surveillance of Mitochondrial Phosphatidylserine Decarboxylase 1.

Ogunbona OB, Onguka O, Calzada E, Claypool SM.

Mol Cell Biol. 2017 Aug 11;37(17). pii: e00049-17. doi: 10.1128/MCB.00049-17. Print 2017 Sep 1.

4.

The Mammalian Malonyl-CoA Synthetase ACSF3 Is Required for Mitochondrial Protein Malonylation and Metabolic Efficiency.

Bowman CE, Rodriguez S, Selen Alpergin ES, Acoba MG, Zhao L, Hartung T, Claypool SM, Watkins PA, Wolfgang MJ.

Cell Chem Biol. 2017 Jun 22;24(6):673-684.e4. doi: 10.1016/j.chembiol.2017.04.009. Epub 2017 May 4.

5.

Human adenine nucleotide translocases physically and functionally interact with respirasomes.

Lu YW, Acoba MG, Selvaraju K, Huang TC, Nirujogi RS, Sathe G, Pandey A, Claypool SM.

Mol Biol Cell. 2017 Jun 1;28(11):1489-1506. doi: 10.1091/mbc.E17-03-0195. Epub 2017 Apr 12.

6.

Rapid degradation of mutant SLC25A46 by the ubiquitin-proteasome system results in MFN1/2-mediated hyperfusion of mitochondria.

Steffen J, Vashisht AA, Wan J, Jen JC, Claypool SM, Wohlschlegel JA, Koehler CM.

Mol Biol Cell. 2017 Mar 1;28(5):600-612. doi: 10.1091/mbc.E16-07-0545. Epub 2017 Jan 5.

7.

Erratum. Impaired Cardiolipin Biosynthesis Prevents Hepatic Steatosis and Diet-Induced Obesity. Diabetes 2016;65:3289-3300.

Cole LK, Mejia EM, Vandel M, Sparagna GC, Claypool SM, Dyck-Chan L, Klein J, Hatch GM.

Diabetes. 2017 Jan;66(1):231. doi: 10.2337/db17-er01a. Epub 2016 Nov 17. No abstract available.

8.

Natural and Induced Mitochondrial Phosphate Carrier Loss: DIFFERENTIAL DEPENDENCE OF MITOCHONDRIAL METABOLISM AND DYNAMICS AND CELL SURVIVAL ON THE EXTENT OF DEPLETION.

Seifert EL, Gál A, Acoba MG, Li Q, Anderson-Pullinger L, Golenár T, Moffat C, Sondheimer N, Claypool SM, Hajnóczky G.

J Biol Chem. 2016 Dec 9;291(50):26126-26137. Epub 2016 Oct 25.

9.

Impaired Cardiolipin Biosynthesis Prevents Hepatic Steatosis and Diet-Induced Obesity.

Cole LK, Mejia EM, Vandel M, Sparagna GC, Claypool SM, Dyck-Chan L, Klein J, Hatch GM.

Diabetes. 2016 Nov;65(11):3289-3300. Epub 2016 Aug 5. Erratum in: Diabetes. 2017 Jan;66(1):231.

10.

Defining functional classes of Barth syndrome mutation in humans.

Lu YW, Galbraith L, Herndon JD, Lu YL, Pras-Raves M, Vervaart M, Van Kampen A, Luyf A, Koehler CM, McCaffery JM, Gottlieb E, Vaz FM, Claypool SM.

Hum Mol Genet. 2016 May 1;25(9):1754-70. doi: 10.1093/hmg/ddw046. Epub 2016 Feb 16.

11.

Phosphatidylethanolamine Metabolism in Health and Disease.

Calzada E, Onguka O, Claypool SM.

Int Rev Cell Mol Biol. 2016;321:29-88. doi: 10.1016/bs.ircmb.2015.10.001. Epub 2015 Oct 31. Review.

12.

Specific degradation of phosphatidylglycerol is necessary for proper mitochondrial morphology and function.

Pokorná L, Čermáková P, Horváth A, Baile MG, Claypool SM, Griač P, Malínský J, Balážová M.

Biochim Biophys Acta. 2016 Jan;1857(1):34-45. doi: 10.1016/j.bbabio.2015.10.004. Epub 2015 Oct 19.

13.

Metalloprotease OMA1 Fine-tunes Mitochondrial Bioenergetic Function and Respiratory Supercomplex Stability.

Bohovych I, Fernandez MR, Rahn JJ, Stackley KD, Bestman JE, Anandhan A, Franco R, Claypool SM, Lewis RE, Chan SS, Khalimonchuk O.

Sci Rep. 2015 Sep 14;5:13989. doi: 10.1038/srep13989.

14.

Phosphatidylserine decarboxylase 1 autocatalysis and function does not require a mitochondrial-specific factor.

Onguka O, Calzada E, Ogunbona OB, Claypool SM.

J Biol Chem. 2015 May 15;290(20):12744-52. doi: 10.1074/jbc.M115.641118. Epub 2015 Mar 31.

15.

Disorders of phospholipid metabolism: an emerging class of mitochondrial disease due to defects in nuclear genes.

Lu YW, Claypool SM.

Front Genet. 2015 Feb 3;6:3. doi: 10.3389/fgene.2015.00003. eCollection 2015. Review.

16.

Tafazzins from Drosophila and mammalian cells assemble in large protein complexes with a short half-life.

Xu Y, Malhotra A, Claypool SM, Ren M, Schlame M.

Mitochondrion. 2015 Mar;21:27-32. doi: 10.1016/j.mito.2015.01.002. Epub 2015 Jan 15.

17.

Acyl-CoA thioesterase-2 facilitates mitochondrial fatty acid oxidation in the liver.

Moffat C, Bhatia L, Nguyen T, Lynch P, Wang M, Wang D, Ilkayeva OR, Han X, Hirschey MD, Claypool SM, Seifert EL.

J Lipid Res. 2014 Dec;55(12):2458-70. doi: 10.1194/jlr.M046961. Epub 2014 Aug 11.

18.

Unremodeled and remodeled cardiolipin are functionally indistinguishable in yeast.

Baile MG, Sathappa M, Lu YW, Pryce E, Whited K, McCaffery JM, Han X, Alder NN, Claypool SM.

J Biol Chem. 2014 Jan 17;289(3):1768-78. doi: 10.1074/jbc.M113.525733. Epub 2013 Nov 27.

19.

The topology and regulation of cardiolipin biosynthesis and remodeling in yeast.

Baile MG, Lu YW, Claypool SM.

Chem Phys Lipids. 2014 Apr;179:25-31. doi: 10.1016/j.chemphyslip.2013.10.008. Epub 2013 Nov 1. Review.

20.

The Taz1p transacylase is imported and sorted into the outer mitochondrial membrane via a membrane anchor domain.

Herndon JD, Claypool SM, Koehler CM.

Eukaryot Cell. 2013 Dec;12(12):1600-8. doi: 10.1128/EC.00237-13. Epub 2013 Sep 27.

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