Kemp S - Search Results

1

Wanders RJ, Visser WF, van Roermund CW, Kemp S, Waterham HR. Wanders RJ, et al. Among authors: kemp s. Pflugers Arch. 2007 Feb;453(5):719-34. doi: 10.1007/s00424-006-0142-x. Epub 2006 Oct 13. Pflugers Arch. 2007. PMID: 17039367 Review.

2

ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy.

Kemp S, Mooyer PA, Bolhuis PA, van Geel BM, Mandel JL, Barth PG, Aubourg P, Wanders RJ. Kemp S, et al. J Inherit Metab Dis. 1996;19(5):667-74. doi: 10.1007/BF01799844. J Inherit Metab Dis. 1996. PMID: 8892025

3

ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations.

Kemp S, Pujol A, Waterham HR, van Geel BM, Boehm CD, Raymond GV, Cutting GR, Wanders RJ, Moser HW. Kemp S, et al. Hum Mutat. 2001 Dec;18(6):499-515. doi: 10.1002/humu.1227. Hum Mutat. 2001. PMID: 11748843 Review.

4

Analysis of very long-chain fatty acids using electrospray ionization mass spectrometry.

Valianpour F, Selhorst JJ, van Lint LE, van Gennip AH, Wanders RJ, Kemp S. Valianpour F, et al. Among authors: kemp s. Mol Genet Metab. 2003 Jul;79(3):189-96. doi: 10.1016/s1096-7192(03)00098-2. Mol Genet Metab. 2003. PMID: 12855224

5

Method for measurement of peroxisomal very-long-chain fatty acid beta-oxidation in human skin fibroblasts using stable-isotope-labeled tetracosanoic acid.

Kemp S, Valianpour F, Mooyer PA, Kulik W, Wanders RJ. Kemp S, et al. Clin Chem. 2004 Oct;50(10):1824-6. doi: 10.1373/clinchem.2004.038539. Clin Chem. 2004. PMID: 15388659 No abstract available.

6

Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophy.

Kemp S, Valianpour F, Denis S, Ofman R, Sanders RJ, Mooyer P, Barth PG, Wanders RJ. Kemp S, et al. Mol Genet Metab. 2005 Feb;84(2):144-51. doi: 10.1016/j.ymgme.2004.09.015. Mol Genet Metab. 2005. PMID: 15670720

7

Evidence for two enzymatic pathways for omega-oxidation of docosanoic acid in rat liver microsomes.

Sanders RJ, Ofman R, Valianpour F, Kemp S, Wanders RJ. Sanders RJ, et al. Among authors: kemp s. J Lipid Res. 2005 May;46(5):1001-8. doi: 10.1194/jlr.M400510-JLR200. Epub 2005 Feb 16. J Lipid Res. 2005. PMID: 15716582 Free article.

8

Accumulation of very long-chain fatty acids does not affect mitochondrial function in adrenoleukodystrophy protein deficiency.

Oezen I, Rossmanith W, Forss-Petter S, Kemp S, Voigtländer T, Moser-Thier K, Wanders RJ, Bittner RE, Berger J. Oezen I, et al. Among authors: kemp s. Hum Mol Genet. 2005 May 1;14(9):1127-37. doi: 10.1093/hmg/ddi125. Epub 2005 Mar 16. Hum Mol Genet. 2005. PMID: 15772093

9

Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage.

Ferrer I, Kapfhammer JP, Hindelang C, Kemp S, Troffer-Charlier N, Broccoli V, Callyzot N, Mooyer P, Selhorst J, Vreken P, Wanders RJ, Mandel JL, Pujol A. Ferrer I, et al. Among authors: kemp s. Hum Mol Genet. 2005 Dec 1;14(23):3565-77. doi: 10.1093/hmg/ddi384. Epub 2005 Oct 13. Hum Mol Genet. 2005. PMID: 16223892

10

A novel cell model to study the function of the adrenoleukodystrophy-related protein.

Gueugnon F, Volodina N, Taouil JE, Lopez TE, Gondcaille C, Grand AS, Mooijer PA, Kemp S, Wanders RJ, Savary S. Gueugnon F, et al. Among authors: kemp s. Biochem Biophys Res Commun. 2006 Mar 3;341(1):150-7. doi: 10.1016/j.bbrc.2005.12.152. Epub 2006 Jan 6. Biochem Biophys Res Commun. 2006. PMID: 16412981

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