Te Brinke H - Search Results

1

Increased protein propionylation contributes to mitochondrial dysfunction in liver cells and fibroblasts, but not in myotubes.

Lagerwaard B, Pougovkina O, Bekebrede AF, Te Brinke H, Wanders RJA, Nieuwenhuizen AG, Keijer J, de Boer VCJ. Lagerwaard B, et al. Among authors: te brinke h. J Inherit Metab Dis. 2021 Mar;44(2):438-449. doi: 10.1002/jimd.12296. Epub 2020 Aug 17. J Inherit Metab Dis. 2021. PMID: 32740932 Free PMC article.

2

Characterization of L-aminocarnitine, an inhibitor of fatty acid oxidation.

Chegary M, Te Brinke H, Doolaard M, Ijlst L, Wijburg FA, Wanders RJ, Houten SM. Chegary M, et al. Among authors: te brinke h. Mol Genet Metab. 2008 Apr;93(4):403-10. doi: 10.1016/j.ymgme.2007.11.001. Epub 2008 Feb 20. Mol Genet Metab. 2008. PMID: 18077198

3

Pyruvate dehydrogenase kinase 4 expression is synergistically induced by AMP-activated protein kinase and fatty acids.

Houten SM, Chegary M, Te Brinke H, Wijnen WJ, Glatz JF, Luiken JJ, Wijburg FA, Wanders RJ. Houten SM, et al. Among authors: te brinke h. Cell Mol Life Sci. 2009 Apr;66(7):1283-94. doi: 10.1007/s00018-009-9066-x. Cell Mol Life Sci. 2009. PMID: 19224132

4

Functional redundancy of mitochondrial enoyl-CoA isomerases in the oxidation of unsaturated fatty acids.

van Weeghel M, te Brinke H, van Lenthe H, Kulik W, Minkler PE, Stoll MS, Sass JO, Janssen U, Stoffel W, Schwab KO, Wanders RJ, Hoppel CL, Houten SM. van Weeghel M, et al. Among authors: te brinke h. FASEB J. 2012 Oct;26(10):4316-26. doi: 10.1096/fj.12-206326. Epub 2012 Jul 10. FASEB J. 2012. PMID: 22782973

5

Carnitine palmitoyltransferase 2 and carnitine/acylcarnitine translocase are involved in the mitochondrial synthesis and export of acylcarnitines.

Violante S, Ijlst L, Te Brinke H, Tavares de Almeida I, Wanders RJ, Ventura FV, Houten SM. Violante S, et al. Among authors: te brinke h. FASEB J. 2013 May;27(5):2039-44. doi: 10.1096/fj.12-216689. Epub 2013 Jan 15. FASEB J. 2013. PMID: 23322164

6

Genetic basis of hyperlysinemia.

Houten SM, Te Brinke H, Denis S, Ruiter JP, Knegt AC, de Klerk JB, Augoustides-Savvopoulou P, Häberle J, Baumgartner MR, Coşkun T, Zschocke J, Sass JO, Poll-The BT, Wanders RJ, Duran M. Houten SM, et al. Among authors: te brinke h. Orphanet J Rare Dis. 2013 Apr 9;8:57. doi: 10.1186/1750-1172-8-57. Orphanet J Rare Dis. 2013. PMID: 23570448 Free PMC article.

7

Impaired amino acid metabolism contributes to fasting-induced hypoglycemia in fatty acid oxidation defects.

Houten SM, Herrema H, Te Brinke H, Denis S, Ruiter JP, van Dijk TH, Argmann CA, Ottenhoff R, Müller M, Groen AK, Kuipers F, Reijngoud DJ, Wanders RJ. Houten SM, et al. Among authors: te brinke h. Hum Mol Genet. 2013 Dec 20;22(25):5249-61. doi: 10.1093/hmg/ddt382. Epub 2013 Aug 9. Hum Mol Genet. 2013. PMID: 23933733

8

Mitochondrial protein acetylation is driven by acetyl-CoA from fatty acid oxidation.

Pougovkina O, te Brinke H, Ofman R, van Cruchten AG, Kulik W, Wanders RJ, Houten SM, de Boer VC. Pougovkina O, et al. Among authors: te brinke h. Hum Mol Genet. 2014 Jul 1;23(13):3513-22. doi: 10.1093/hmg/ddu059. Epub 2014 Feb 10. Hum Mol Genet. 2014. PMID: 24516071

9

Aberrant protein acylation is a common observation in inborn errors of acyl-CoA metabolism.

Pougovkina O, Te Brinke H, Wanders RJ, Houten SM, de Boer VC. Pougovkina O, et al. Among authors: te brinke h. J Inherit Metab Dis. 2014 Sep;37(5):709-14. doi: 10.1007/s10545-014-9684-9. Epub 2014 Feb 15. J Inherit Metab Dis. 2014. PMID: 24531926

10

Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia.

Houten SM, Denis S, Te Brinke H, Jongejan A, van Kampen AH, Bradley EJ, Baas F, Hennekam RC, Millington DS, Young SP, Frazier DM, Gucsavas-Calikoglu M, Wanders RJ. Houten SM, et al. Among authors: te brinke h. Hum Mol Genet. 2014 Sep 15;23(18):5009-16. doi: 10.1093/hmg/ddu218. Epub 2014 May 8. Hum Mol Genet. 2014. PMID: 24847004

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