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Results: 1 to 20 of 96

1.

The molecular era of the mitochondrial calcium uniporter.

Kamer KJ, Mootha VK.

Nat Rev Mol Cell Biol. 2015 Sep;16(9):545-53. doi: 10.1038/nrm4039. Epub 2015 Aug 19.

PMID:
26285678
2.

FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy.

Fassone E, Duncan AJ, Taanman JW, Pagnamenta AT, Sadowski MI, Holand T, Qasim W, Rutland P, Calvo SE, Mootha VK, Bitner-Glindzicz M, Rahman S.

Hum Mol Genet. 2015 Jul 15;24(14):4183. doi: 10.1093/hmg/ddv164. Epub 2015 May 28. No abstract available.

PMID:
26022995
3.

IGF2BP2/IMP2-Deficient mice resist obesity through enhanced translation of Ucp1 mRNA and Other mRNAs encoding mitochondrial proteins.

Dai N, Zhao L, Wrighting D, Krämer D, Majithia A, Wang Y, Cracan V, Borges-Rivera D, Mootha VK, Nahrendorf M, Thorburn DR, Minichiello L, Altshuler D, Avruch J.

Cell Metab. 2015 Apr 7;21(4):609-21. doi: 10.1016/j.cmet.2015.03.006.

PMID:
25863250
4.

Effects of sodium benzoate, a widely used food preservative, on glucose homeostasis and metabolic profiles in humans.

Lennerz BS, Vafai SB, Delaney NF, Clish CB, Deik AA, Pierce KA, Ludwig DS, Mootha VK.

Mol Genet Metab. 2015 Jan;114(1):73-9. doi: 10.1016/j.ymgme.2014.11.010. Epub 2014 Nov 15.

PMID:
25497115
5.

Directed evolution of APEX2 for electron microscopy and proximity labeling.

Lam SS, Martell JD, Kamer KJ, Deerinck TJ, Ellisman MH, Mootha VK, Ting AY.

Nat Methods. 2015 Jan;12(1):51-4. doi: 10.1038/nmeth.3179. Epub 2014 Nov 24.

6.

Biochemical characterization of pathogenic mutations in human mitochondrial methionyl-tRNA formyltransferase.

Sinha A, Köhrer C, Weber MH, Masuda I, Mootha VK, Hou YM, RajBhandary UL.

J Biol Chem. 2014 Nov 21;289(47):32729-41. doi: 10.1074/jbc.M114.610626. Epub 2014 Oct 6.

PMID:
25288793
7.

Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy.

Ajroud-Driss S, Fecto F, Ajroud K, Lalani I, Calvo SE, Mootha VK, Deng HX, Siddique N, Tahmoush AJ, Heiman-Patterson TD, Siddique T.

Neurogenetics. 2015 Jan;16(1):1-9. doi: 10.1007/s10048-014-0421-1. Epub 2014 Sep 6.

PMID:
25193783
8.

Proteomic mapping of the human mitochondrial intermembrane space in live cells via ratiometric APEX tagging.

Hung V, Zou P, Rhee HW, Udeshi ND, Cracan V, Svinkina T, Carr SA, Mootha VK, Ting AY.

Mol Cell. 2014 Jul 17;55(2):332-41. doi: 10.1016/j.molcel.2014.06.003. Epub 2014 Jul 4.

9.

Expansion of biological pathways based on evolutionary inference.

Li Y, Calvo SE, Gutman R, Liu JS, Mootha VK.

Cell. 2014 Jul 3;158(1):213-25. doi: 10.1016/j.cell.2014.05.034.

10.

Reconstitution of the mitochondrial calcium uniporter in yeast.

Kovács-Bogdán E, Sancak Y, Kamer KJ, Plovanich M, Jambhekar A, Huber RJ, Myre MA, Blower MD, Mootha VK.

Proc Natl Acad Sci U S A. 2014 Jun 17;111(24):8985-90. doi: 10.1073/pnas.1400514111. Epub 2014 Jun 2.

11.

The uniporter: from newly identified parts to function.

Kamer KJ, Sancak Y, Mootha VK.

Biochem Biophys Res Commun. 2014 Jul 11;449(4):370-2. doi: 10.1016/j.bbrc.2014.04.143. Epub 2014 May 9. No abstract available.

PMID:
24814702
12.

Functional genomic analysis of human mitochondrial RNA processing.

Wolf AR, Mootha VK.

Cell Rep. 2014 May 8;7(3):918-31. doi: 10.1016/j.celrep.2014.03.035. Epub 2014 Apr 18.

13.

Next generation sequencing with copy number variant detection expands the phenotypic spectrum of HSD17B4-deficiency.

Lieber DS, Hershman SG, Slate NG, Calvo SE, Sims KB, Schmahmann JD, Mootha VK.

BMC Med Genet. 2014 Mar 6;15:30. doi: 10.1186/1471-2350-15-30.

14.

A systematic survey of lipids across mouse tissues.

Jain M, Ngoy S, Sheth SA, Swanson RA, Rhee EP, Liao R, Clish CB, Mootha VK, Nilsson R.

Am J Physiol Endocrinol Metab. 2014 Apr 15;306(8):E854-68. doi: 10.1152/ajpendo.00371.2013. Epub 2014 Feb 11.

15.

MICU1 and MICU2 play nonredundant roles in the regulation of the mitochondrial calcium uniporter.

Kamer KJ, Mootha VK.

EMBO Rep. 2014 Mar;15(3):299-307. doi: 10.1002/embr.201337946. Epub 2014 Feb 6.

16.

Metabolic enzyme expression highlights a key role for MTHFD2 and the mitochondrial folate pathway in cancer.

Nilsson R, Jain M, Madhusudhan N, Sheppard NG, Strittmatter L, Kampf C, Huang J, Asplund A, Mootha VK.

Nat Commun. 2014;5:3128. doi: 10.1038/ncomms4128.

17.

Medicine. A common pathway for a rare disease?

Vafai SB, Mootha VK.

Science. 2013 Dec 20;342(6165):1453-4. doi: 10.1126/science.1248449. No abstract available.

PMID:
24357304
18.

CLYBL is a polymorphic human enzyme with malate synthase and β-methylmalate synthase activity.

Strittmatter L, Li Y, Nakatsuka NJ, Calvo SE, Grabarek Z, Mootha VK.

Hum Mol Genet. 2014 May 1;23(9):2313-23. doi: 10.1093/hmg/ddt624. Epub 2013 Dec 11.

19.

EMRE is an essential component of the mitochondrial calcium uniporter complex.

Sancak Y, Markhard AL, Kitami T, Kovács-Bogdán E, Kamer KJ, Udeshi ND, Carr SA, Chaudhuri D, Clapham DE, Li AA, Calvo SE, Goldberger O, Mootha VK.

Science. 2013 Dec 13;342(6164):1379-82. doi: 10.1126/science.1242993. Epub 2013 Nov 14.

20.

Meclizine inhibits mitochondrial respiration through direct targeting of cytosolic phosphoethanolamine metabolism.

Gohil VM, Zhu L, Baker CD, Cracan V, Yaseen A, Jain M, Clish CB, Brookes PS, Bakovic M, Mootha VK.

J Biol Chem. 2013 Dec 6;288(49):35387-95. doi: 10.1074/jbc.M113.489237. Epub 2013 Oct 19.

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