Stenbroen V - Search Results

1

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: stenbroen v. Proteome Sci. 2009 May 28;7:20. doi: 10.1186/1477-5956-7-20. Proteome Sci. 2009. PMID: 19476632 Free PMC article.

2

Proteomics reveals that redox regulation is disrupted in patients with ethylmalonic encephalopathy.

Palmfeldt J, Vang S, Stenbroen V, Pavlou E, Baycheva M, Buchal G, Monavari AA, Augoustides-Savvopoulou P, Mandel H, Gregersen N. Palmfeldt J, et al. Among authors: stenbroen v. J Proteome Res. 2011 May 6;10(5):2389-96. doi: 10.1021/pr101218d. Epub 2011 Mar 28. J Proteome Res. 2011. PMID: 21410200

3

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. Among authors: stenbroen v. Hum Genet. 2008 Aug;124(1):43-56. doi: 10.1007/s00439-008-0521-9. Epub 2008 Jun 4. Hum Genet. 2008. PMID: 18523805

4

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. Among authors: stenbroen v. 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

5

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: stenbroen v. 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.

6

Proteomic investigation of cultivated fibroblasts from patients with mitochondrial short-chain acyl-CoA dehydrogenase deficiency.

Edhager AV, Stenbroen V, Nielsen NS, Bross P, Olsen RKJ, Gregersen N, Palmfeldt J. Edhager AV, et al. Among authors: stenbroen v. Mol Genet Metab. 2014 Mar;111(3):360-368. doi: 10.1016/j.ymgme.2014.01.007. Epub 2014 Jan 24. Mol Genet Metab. 2014. PMID: 24485985

7

Quantitative proteomics suggests metabolic reprogramming during ETHE1 deficiency.

Sahebekhtiari N, Thomsen MM, Sloth JJ, Stenbroen V, Zeviani M, Gregersen N, Viscomi C, Palmfeldt J. Sahebekhtiari N, et al. Among authors: stenbroen v. Proteomics. 2016 Apr;16(7):1166-76. doi: 10.1002/pmic.201500336. Epub 2016 Mar 16. Proteomics. 2016. PMID: 26867521 Free article.

8

The ETFDH c.158A>G variation disrupts the balanced interplay of ESE- and ESS-binding proteins thereby causing missplicing and multiple Acyl-CoA dehydrogenation deficiency.

Olsen RK, Brøner S, Sabaratnam R, Doktor TK, Andersen HS, Bruun GH, Gahrn B, Stenbroen V, Olpin SE, Dobbie A, Gregersen N, Andresen BS. Olsen RK, et al. Among authors: stenbroen v. Hum Mutat. 2014 Jan;35(1):86-95. doi: 10.1002/humu.22455. Epub 2013 Oct 28. Hum Mutat. 2014. PMID: 24123825

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