Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 12

1.

Multi-dimensional Roles of Ketone Bodies in Fuel Metabolism, Signaling, and Therapeutics.

Puchalska P, Crawford PA.

Cell Metab. 2017 Feb 7;25(2):262-284. doi: 10.1016/j.cmet.2016.12.022. Review.

PMID:
28178565
2.

Metabolic Alterations in Developing Brain After Injury: Knowns and Unknowns.

McKenna MC, Scafidi S, Robertson CL.

Neurochem Res. 2015 Dec;40(12):2527-43. doi: 10.1007/s11064-015-1600-7. Epub 2015 Jul 7. Review.

3.

Cardiomyocyte-specific deficiency of ketone body metabolism promotes accelerated pathological remodeling.

Schugar RC, Moll AR, André d'Avignon D, Weinheimer CJ, Kovacs A, Crawford PA.

Mol Metab. 2014 Aug 13;3(7):754-69. doi: 10.1016/j.molmet.2014.07.010. eCollection 2014 Oct.

4.

Impact of peripheral ketolytic deficiency on hepatic ketogenesis and gluconeogenesis during the transition to birth.

Cotter DG, Ercal B, d'Avignon DA, Dietzen DJ, Crawford PA.

J Biol Chem. 2013 Jul 5;288(27):19739-49. doi: 10.1074/jbc.M113.454868. Epub 2013 May 20.

5.

Ketone body metabolism and cardiovascular disease.

Cotter DG, Schugar RC, Crawford PA.

Am J Physiol Heart Circ Physiol. 2013 Apr 15;304(8):H1060-76. doi: 10.1152/ajpheart.00646.2012. Epub 2013 Feb 8. Review.

6.

Successful adaptation to ketosis by mice with tissue-specific deficiency of ketone body oxidation.

Cotter DG, Schugar RC, Wentz AE, d'Avignon DA, Crawford PA.

Am J Physiol Endocrinol Metab. 2013 Feb 15;304(4):E363-74. doi: 10.1152/ajpendo.00547.2012. Epub 2012 Dec 11.

7.
8.

Altered systemic ketone body metabolism in advanced heart failure.

Janardhan A, Chen J, Crawford PA.

Tex Heart Inst J. 2011;38(5):533-8.

9.

Obligate role for ketone body oxidation in neonatal metabolic homeostasis.

Cotter DG, d'Avignon DA, Wentz AE, Weber ML, Crawford PA.

J Biol Chem. 2011 Mar 4;286(9):6902-10. doi: 10.1074/jbc.M110.192369. Epub 2011 Jan 5.

10.

Succinyl CoA: 3-oxoacid CoA transferase (SCOT): human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient.

Kassovska-Bratinova S, Fukao T, Song XQ, Duncan AM, Chen HS, Robert MF, Pérez-Cerdá C, Ugarte M, Chartrand C, Vobecky S, Kondo N, Mitchell GA.

Am J Hum Genet. 1996 Sep;59(3):519-28.

11.
12.

Food intolerance in humans.

Herman RH, Hagler L.

West J Med. 1979 Feb;130(2):95-116. Review. No abstract available.

Supplemental Content

Support Center