Publications

ACBD5 and VAPB mediate membrane associations between peroxisomes and the ER.

20-01-2017

ACBD5 and VAPB mediate membrane associations between peroxisomes and the ER.

Costello JL, Castro IG, Hacker C, Schrader TA, Metz J, Zeuschner D, Azadi AS, Godinho LF, Costina V, Findeisen P, Manner A, Islinger M, Schrader M.

J Cell Biol. 2017 Feb;216(2):331-342. doi: 10.1083/jcb.201607055.

ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism.

10-01-2017

ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism.

Ferdinandusse S, Falkenberg KD, Koster J, Mooyer PA, Jones R, van Roermund CW, Pizzino A, Schrader M, Wanders RJ, Vanderver A, Waterham HR.

 

J Med Genet. 2016 Oct 31. pii: jmedgenet-2016-104132. doi: 10.1136/jmedgenet-2016-104132. [Epub ahead of print]

abstract book 2nd International Conference “ Peroxisome Formation, Function and Metabolism ”

17-06-2016

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C26:0-Carnitine Is a New Biomarker for X-Linked Adrenoleukodystrophy in Mice and Man.

28-04-2016
 

C26:0-Carnitine Is a New Biomarker for X-Linked Adrenoleukodystrophy in Mice and Man.

 

van de Beek MC, Dijkstra IM,  van Lenthe H, Ofman R, Goldhaber-Pasillas D, Schauer N, Schackmann M, Engelen-Lee JY, Vaz FM, Kulik W,  Wanders RJ, Engelen M, Kemp S.

 

PLoS One. 2016 Apr 28;11(4):e0154597. doi: 10.1371/journal.pone.0154597. eCollection 2016.

Human disorders of peroxisome metabolism and biogenesis.

22-11-2015

Human disorders of peroxisome metabolism and biogenesis

Waterham HR, Ferdinandusse S, Wanders RJ.

Biochim Biophys Acta. 2015 Nov 22. pii: S0167-4889(15)00399-7. doi: 10.1016/j.bbamcr.2015.11.015. [Epub ahead of print]

Proliferation and fission of peroxisomes - An update.

26-09-2015

Proliferation and fission of peroxisomes - An update.

Schrader M, Costello JL, Godinho LF, Azadi AS, Islinger M.

Biochim Biophys Acta. 2015 Sep 26. pii: S0167-4889(15)00336-5. doi: 10.1016/j.bbamcr.2015.09.024. [Epub ahead of print] Review. No abstract available.

Heimler Syndrome Is Caused by Hypomorphic Mutations

17-09-2015

Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6.

Ratbi I, Falkenberg KD, Sommen M, Al-Sheqaih N, Guaoua S, Vandeweyer G, Urquhart JE, Chandler KE, Williams SG, Roberts NA, El Alloussi M, Black GC, Ferdinandusse S, Ramdi H, Heimler A, Fryer A, Lynch SA, Cooper N, Ong KR, Smith CE, Inglehearn CF, Mighell AJ, Elcock C, Poulter JA, Tischkowitz M, Davies SJ, Sefiani A, Mironov AA, Newman WG, Waterham HR, Van Camp G.

Am J Hum Genet. 2015 Oct 1;97(4):535-45. doi: 10.1016/j.ajhg.2015.08.011. Epub 2015 Sep 17.

The birth of yeast peroxisomes.

11-09-2015

The birth of yeast peroxisomes.

Yuan W, Veenhuis M, van der Klei IJ.

Biochim Biophys Acta. 2015 Sep 11. pii: S0167-4889(15)00301-8. doi: 10.1016/j.bbamcr.2015.09.008. [Epub ahead of print] Review.

Peroxisome-Mitochondria Interplay and Disease.

18-02-2015

Peroxisome-mitochondria interplay and disease.

Schrader M, Costello J, Godinho LF, Islinger M.

J Inherit Metab Dis. 2015 Jul;38(4):681-702. doi: 10.1007/s10545-015-9819-7. Epub 2015 Feb 17.

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Delphine Crappe and Piotr Lisik have defended their thesis

30-11-2016

Delphine Crappe and Piotr Lisik have defended their thesis...

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