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Difference between revisions of "Wanders RJA"

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{{Person}}
{{Person
|lastname=Wanders
|firstname=Ronald
|institution=Lab Genetic Metabolic Diseases, Room F0-223
Academic Medical Center
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University of Amsterdam
|address=Meibergdreef 9
|area code=1105 AZ
|city=Amsterdam
|country=The Netherlands
|mailaddress=r.j.wanders@amc.uva.nl
}}
{{Labelingperson}}

Revision as of 13:41, 18 January 2017

Name Wanders Ronald,
Institution Lab Genetic Metabolic Diseases, Room F0-223

Academic Medical Center

University of Amsterdam

Address Meibergdreef 9, 1105 AZ
City Amsterdam
State/Province
Country The Netherlands
Email r.j.wanders@amc.uva.nl
Weblink
O2k-Network Lab


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Publications

 PublishedReference
Knottnerus 2018 Rev Endocr Metab Disord2018Knottnerus SJG, Bleeker JC, Wรผst RCI, Ferdinandusse S, IJlst L, Wijburg FA, Wanders RJA, Visser G, Houtkooper RH (2018) Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle. Rev Endocr Metab Disord 19:93-106. https://doi.org/10.1007/s11154-018-9448-1
Van Zutphen 2016 J Hepatol2016van Zutphen T, Ciapaite J, Bloks VW, Ackereley C, Gerding A, Jurdzinski A, Allgayer de Moraes R, Zhang L, Wolters JC, Bischoff R, Wanders RJA, Houten SM, Bronte-Tinkew D, Shatseva T, Lewis GF, Groen AK, Reijngoud DJ, Bakker BM, Jonker JW, Kim PK, Bandsma RH (2016) Malnutrition-associated liver steatosis and ATP depletion is caused by peroxisomal and mitochondrial dysfunction. J Hepatol 65:1198-1208.
Houten 2016 Annu Rev Physiol2016Houten SM, Violante S, Ventura FV, Wanders RJ (2016) The biochemistry and physiology of mitochondrial fatty acid ฮฒ-oxidation and its genetic disorders. Annu Rev Physiol 78:23-44. doi: 10.1146/annurev-physiol-021115-105045
Wessels 2015 Am J Physiol2015Wessels B, van den Broek NM, Ciapaite J, Houten SM, Wanders RJA, Nicolay K, Prompers JJ (2015) Carnitine supplementation in high-fat diet-fed rats does not ameliorate lipid-induced skeletal muscle mitochondrial dysfunction in vivo. Am J Physiol 309(7):E670-8.
Houten 2010 J Inherit Metab Dis2010Houten SM, Wanders RJ (2010) A general introduction to the biochemistry of mitochondrial fatty acid ฮฒ-oxidation. J Inherit Metab Dis 33:469-77.
Van den Broek 2010 FASEB J2010van den Broek NM, Ciapaite J, De Feyter HM, Houten SM, Wanders RJA, Jeneson JA, Nicolay K, Prompers JJ (2010) Increased mitochondrial content rescues in vivo muscle oxidative capacity in long-term high-fat-diet-fed rats. FASEB J 24:1354-64.
Oezen 2005 Hum Mol Genet2005Oezen I, Rossmanith W, Forss-Petter S, Kemp S, Voigtlander T, Moser-Thier K, Wanders RJA, Bittner RE, Berger J (2005) Accumulation of very long-chain fatty acids does not affect mitochondrial function in adrenoleukodystrophy protein deficiency. Hum Mol Genet 14:1127-37.

Abstracts

 PublishedReference
Wuest 2018 MiP2018a2018
Wuest Rob
Reduction of acylcarnitines restores electrophysiological abnormalities in VLCAD deficient hiPSC-cardiomyocytes.