Wanders RJ - Search Results

1

Peripheral nervous system plasmalogens regulate Schwann cell differentiation and myelination.

da Silva TF, Eira J, Lopes AT, Malheiro AR, Sousa V, Luoma A, Avila RL, Wanders RJ, Just WW, Kirschner DA, Sousa MM, Brites P. da Silva TF, et al. Among authors: wanders rj. J Clin Invest. 2014 Jun;124(6):2560-70. doi: 10.1172/JCI72063. Epub 2014 Apr 24. J Clin Invest. 2014. PMID: 24762439 Free PMC article.

2

Alkyl-glycerol rescues plasmalogen levels and pathology of ether-phospholipid deficient mice.

Brites P, Ferreira AS, da Silva TF, Sousa VF, Malheiro AR, Duran M, Waterham HR, Baes M, Wanders RJ. Brites P, et al. Among authors: wanders rj. PLoS One. 2011;6(12):e28539. doi: 10.1371/journal.pone.0028539. Epub 2011 Dec 6. PLoS One. 2011. PMID: 22163031 Free PMC article.

3

Functions and biosynthesis of plasmalogens in health and disease.

Brites P, Waterham HR, Wanders RJ. Brites P, et al. Among authors: wanders rj. Biochim Biophys Acta. 2004 Mar 22;1636(2-3):219-31. doi: 10.1016/j.bbalip.2003.12.010. Biochim Biophys Acta. 2004. PMID: 15164770 Review.

4

Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme.

Heikoop JC, van Roermund CW, Just WW, Ofman R, Schutgens RB, Heymans HS, Wanders RJ, Tager JM. Heikoop JC, et al. Among authors: wanders rj. J Clin Invest. 1990 Jul;86(1):126-30. doi: 10.1172/JCI114674. J Clin Invest. 1990. PMID: 2365812 Free PMC article.

5

Plasmalogens participate in very-long-chain fatty acid-induced pathology.

Brites P, Mooyer PA, El Mrabet L, Waterham HR, Wanders RJ. Brites P, et al. Among authors: wanders rj. Brain. 2009 Feb;132(Pt 2):482-92. doi: 10.1093/brain/awn295. Epub 2008 Nov 20. Brain. 2009. PMID: 19022859

6

Mutational spectrum in the PEX7 gene and functional analysis of mutant alleles in 78 patients with rhizomelic chondrodysplasia punctata type 1.

Motley AM, Brites P, Gerez L, Hogenhout E, Haasjes J, Benne R, Tabak HF, Wanders RJ, Waterham HR. Motley AM, et al. Among authors: wanders rj. Am J Hum Genet. 2002 Mar;70(3):612-24. doi: 10.1086/338998. Epub 2002 Jan 7. Am J Hum Genet. 2002. PMID: 11781871 Free PMC article.

7

Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata.

Brites P, Motley AM, Gressens P, Mooyer PA, Ploegaert I, Everts V, Evrard P, Carmeliet P, Dewerchin M, Schoonjans L, Duran M, Waterham HR, Wanders RJ, Baes M. Brites P, et al. Among authors: wanders rj. Hum Mol Genet. 2003 Sep 15;12(18):2255-67. doi: 10.1093/hmg/ddg236. Epub 2003 Jul 15. Hum Mol Genet. 2003. PMID: 12915479

8

Identification of PEX7 as the second gene involved in Refsum disease.

van den Brink DM, Brites P, Haasjes J, Wierzbicki AS, Mitchell J, Lambert-Hamill M, de Belleroche J, Jansen GA, Waterham HR, Wanders RJ. van den Brink DM, et al. Among authors: wanders rj. Am J Hum Genet. 2003 Feb;72(2):471-7. doi: 10.1086/346093. Epub 2003 Jan 9. Am J Hum Genet. 2003. PMID: 12522768 Free PMC article.

9

Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblasts.

Heikoop JC, Van den Berg M, Strijland A, Weijers PJ, Schutgens RB, Just WW, Wanders RJ, Tager JM. Heikoop JC, et al. Among authors: wanders rj. Biochim Biophys Acta. 1991 Jul 26;1097(1):62-70. doi: 10.1016/0925-4439(91)90025-5. Biochim Biophys Acta. 1991. PMID: 1677591

10

Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor.

Motley AM, Hettema EH, Hogenhout EM, Brites P, ten Asbroek AL, Wijburg FA, Baas F, Heijmans HS, Tabak HF, Wanders RJ, Distel B. Motley AM, et al. Among authors: wanders rj. Nat Genet. 1997 Apr;15(4):377-80. doi: 10.1038/ng0497-377. Nat Genet. 1997. PMID: 9090382

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