Pedersen CB - Search Results

1

Mitochondrial fatty acid oxidation defects--remaining challenges.

Gregersen N, Andresen BS, Pedersen CB, Olsen RK, Corydon TJ, Bross P. Gregersen N, et al. Among authors: pedersen cb. J Inherit Metab Dis. 2008 Oct;31(5):643-57. doi: 10.1007/s10545-008-0990-y. Epub 2008 Oct 7. J Inherit Metab Dis. 2008. PMID: 18836889

2

The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level.

Pedersen CB, Kølvraa S, Kølvraa A, Stenbroen V, Kjeldsen M, Ensenauer R, Tein I, Matern D, Rinaldo P, Vianey-Saban C, Ribes A, Lehnert W, Christensen E, Corydon TJ, Andresen BS, Vang S, Bolund L, Vockley J, Bross P, Gregersen N. Pedersen CB, et al. Hum Genet. 2008 Aug;124(1):43-56. doi: 10.1007/s00439-008-0521-9. Epub 2008 Jun 4. Hum Genet. 2008. PMID: 18523805

3

Antioxidant dysfunction: potential risk for neurotoxicity in ethylmalonic aciduria.

Pedersen CB, Zolkipli Z, Vang S, Palmfeldt J, Kjeldsen M, Stenbroen V, Schmidt SP, Wanders RJ, Ruiter JP, Wibrand F, Tein I, Gregersen N. Pedersen CB, et al. J Inherit Metab Dis. 2010 Jun;33(3):211-22. doi: 10.1007/s10545-010-9086-6. Epub 2010 May 5. J Inherit Metab Dis. 2010. PMID: 20443061

4

Toxic response caused by a misfolding variant of the mitochondrial protein short-chain acyl-CoA dehydrogenase.

Schmidt SP, Corydon TJ, Pedersen CB, Vang S, Palmfeldt J, Stenbroen V, Wanders RJ, Ruiter JP, Gregersen N. Schmidt SP, et al. Among authors: pedersen cb. J Inherit Metab Dis. 2011 Apr;34(2):465-75. doi: 10.1007/s10545-010-9255-7. Epub 2010 Dec 18. J Inherit Metab Dis. 2011. PMID: 21170680 Free PMC article.

5

Misfolding, degradation, and aggregation of variant proteins. The molecular pathogenesis of short chain acyl-CoA dehydrogenase (SCAD) deficiency.

Pedersen CB, Bross P, Winter VS, Corydon TJ, Bolund L, Bartlett K, Vockley J, Gregersen N. Pedersen CB, et al. J Biol Chem. 2003 Nov 28;278(48):47449-58. doi: 10.1074/jbc.M309514200. Epub 2003 Sep 23. J Biol Chem. 2003. PMID: 14506246 Free article.

6

The role of chaperone-assisted folding and quality control in inborn errors of metabolism: protein folding disorders.

Gregersen N, Bross P, Andrese BS, Pedersen CB, Corydon TJ, Bolund L. Gregersen N, et al. Among authors: pedersen cb. J Inherit Metab Dis. 2001 Apr;24(2):189-212. doi: 10.1023/a:1010319001722. J Inherit Metab Dis. 2001. PMID: 11405340 Review.

7

Misfolding of short-chain acyl-CoA dehydrogenase leads to mitochondrial fission and oxidative stress.

Schmidt SP, Corydon TJ, Pedersen CB, Bross P, Gregersen N. Schmidt SP, et al. Among authors: pedersen cb. Mol Genet Metab. 2010 Jun;100(2):155-62. doi: 10.1016/j.ymgme.2010.03.009. Epub 2010 Mar 19. Mol Genet Metab. 2010. PMID: 20371198

8

Variations in IBD (ACAD8) in children with elevated C4-carnitine detected by tandem mass spectrometry newborn screening.

Pedersen CB, Bischoff C, Christensen E, Simonsen H, Lund AM, Young SP, Koeberl DD, Millington DS, Roe CR, Roe DS, Wanders RJ, Ruiter JP, Keppen LD, Stein Q, Knudsen I, Gregersen N, Andresen BS. Pedersen CB, et al. Pediatr Res. 2006 Sep;60(3):315-20. doi: 10.1203/01.pdr.0000233085.72522.04. Epub 2006 Jul 20. Pediatr Res. 2006. PMID: 16857760

9

Handling of human short-chain acyl-CoA dehydrogenase (SCAD) variant proteins in transgenic mice.

Kragh PM, Pedersen CB, Schmidt SP, Winter VS, Vajta G, Gregersen N, Bolund L, Corydon TJ. Kragh PM, et al. Among authors: pedersen cb. Mol Genet Metab. 2007 Jun;91(2):128-37. doi: 10.1016/j.ymgme.2007.03.005. Epub 2007 Apr 25. Mol Genet Metab. 2007. PMID: 17462936

10

Mitochondrial proteomics on human fibroblasts for identification of metabolic imbalance and cellular stress.

Palmfeldt J, Vang S, Stenbroen V, Pedersen CB, Christensen JH, Bross P, Gregersen N. Palmfeldt J, et al. Among authors: pedersen cb. Proteome Sci. 2009 May 28;7:20. doi: 10.1186/1477-5956-7-20. Proteome Sci. 2009. PMID: 19476632 Free PMC article.

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