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The FEBS journal, 2011-01, Vol.278 (2), p.182-194
2011
Link zum Volltext
European journal of clinical nutrition, 2013-05, Vol.67 (5), p.541-547
2013
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Frontiers in cell and developmental biology, 2016-01, Vol.3, p.83-83
2016
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Obesity reviews, 2011-09, Vol.12 (9), p.724-739
2011
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Nature communications, 2018-05, Vol.9 (1), p.1761-13, Article 1761
2018
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Reviews in endocrine & metabolic disorders, 2018-03, Vol.19 (1), p.93-106
2018
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PloS one, 2016-04, Vol.11 (4), p.e0154597-e0154597
2016
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Orphanet journal of rare diseases, 2012-10, Vol.7 (1), p.83-83
2012
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Orphanet journal of rare diseases, 2012-08, Vol.7 (1), p.51-51
2012
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Journal of inherited metabolic disease, 2010-10, Vol.33 (5), p.479-494
2010
Link zum Volltext
Proceedings of the National Academy of Sciences - PNAS, 2013-01, Vol.110 (4), p.1279-1284
2013
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Orphanet journal of rare diseases, 2023-11, Vol.18 (1), p.1-358, Article 358
2023
Link zum Volltext
Journal of inherited metabolic disease, 2014-09, Vol.37 (5), p.709-714
2014
Link zum Volltext
Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia
- Vaz, Frédéric M
- McDermott, John H
- Alders, Mariëlle
- Wortmann, Saskia B
- Kölker, Stefan
- Pras-Raves, Mia L
- Vervaart, Martin A T
- van Lenthe, Henk
- Luyf, Angela C M
- Elfrink, Hyung L
- Metcalfe, Kay
- Cuvertino, Sara
- Clayton, Peter E
- Yarwood, Rebecca
- Lowe, Martin P
- Lovell, Simon
- Rogers, Richard C
- van Kampen, Antoine H C
- Ruiter, Jos P N
- Wanders, Ronald J A
- Ferdinandusse, Sacha
- van Weeghel, Michel
- Engelen, Marc
- Banka, Siddharth
2019
Link zum Volltext
British journal of pharmacology, 2011-12, Vol.164 (7), p.1753-1766
2011
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PloS one, 2016-05, Vol.11 (5), p.e0155143-e0155143
2016
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Journal of inherited metabolic disease, 2008-04, Vol.31 (2), p.205-216
2008
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PloS one, 2011-12, Vol.6 (12), p.e28539-e28539
2011
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The important role of biochemical and functional studies in the diagnostics of peroxisomal disorders
2016
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Annual review of physiology, 2016-01, Vol.78 (1), p.23-44
2016
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The human peroxisomal ABC half transporter ALDP functions as a homodimer and accepts acyl–CoA esters
2008
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Journal of inherited metabolic disease, 2012-01, Vol.35 (1), p.5-12
2012
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Scientific reports, 2022-02, Vol.12 (1), p.2512-2512, Article 2512
2022
Link zum Volltext
International Journal of Obesity, 2014-06, Vol.38 (6), p.794-800
2014
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Brain (London, England : 1878), 2009-02, Vol.132 (2), p.482-492
2009
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