Gregersen N - Search Results

1

Riboflavin Deficiency-Implications for General Human Health and Inborn Errors of Metabolism.

Mosegaard S, Dipace G, Bross P, Carlsen J, Gregersen N, Olsen RKJ. Mosegaard S, et al. Among authors: gregersen n. Int J Mol Sci. 2020 May 28;21(11):3847. doi: 10.3390/ijms21113847. Int J Mol Sci. 2020. PMID: 32481712 Free PMC article. Review.

2

An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.

Mosegaard S, Bruun GH, Flyvbjerg KF, Bliksrud YT, Gregersen N, Dembic M, Annexstad E, Tangeraas T, Olsen RKJ, Andresen BS. Mosegaard S, et al. Among authors: gregersen n. Mol Genet Metab. 2017 Dec;122(4):182-188. doi: 10.1016/j.ymgme.2017.10.014. Epub 2017 Nov 2. Mol Genet Metab. 2017. PMID: 29122468

3

Molecular mechanisms of riboflavin responsiveness in patients with ETF-QO variations and multiple acyl-CoA dehydrogenation deficiency.

Cornelius N, Frerman FE, Corydon TJ, Palmfeldt J, Bross P, Gregersen N, Olsen RK. Cornelius N, et al. Among authors: gregersen n. Hum Mol Genet. 2012 Aug 1;21(15):3435-48. doi: 10.1093/hmg/dds175. Epub 2012 May 18. Hum Mol Genet. 2012. PMID: 22611163

4

Protein misfolding, aggregation, and degradation in disease.

Gregersen N, Bolund L, Bross P. Gregersen N, et al. Methods Mol Biol. 2003;232:3-16. doi: 10.1385/1-59259-394-1:3. Methods Mol Biol. 2003. PMID: 12840535 Review. No abstract available.

5

Basic introduction to in vivo protein folding and its defects.

Bross P, Gregersen N. Bross P, et al. Among authors: gregersen n. Methods Mol Biol. 2003;232:17-26. doi: 10.1385/1-59259-394-1:17. Methods Mol Biol. 2003. PMID: 12840536 Review. No abstract available.

6

Investigation of folding and degradation of in vitro synthesized mutant proteins in mitochondria.

Bross P, Winter V, Pedersen CB, Gregersen N. Bross P, et al. Among authors: gregersen n. Methods Mol Biol. 2003;232:285-93. doi: 10.1385/1-59259-394-1:285. Methods Mol Biol. 2003. PMID: 12840557 No abstract available.

7

Genetic defects in fatty acid beta-oxidation and acyl-CoA dehydrogenases. Molecular pathogenesis and genotype-phenotype relationships.

Gregersen N, Bross P, Andresen BS. Gregersen N, et al. Eur J Biochem. 2004 Feb;271(3):470-82. doi: 10.1046/j.1432-1033.2003.03949.x. Eur J Biochem. 2004. PMID: 14728674 Free article. Review.

8

Protein misfolding, aggregation, and degradation in disease.

Gregersen N, Bolund L, Bross P. Gregersen N, et al. Mol Biotechnol. 2005 Oct;31(2):141-50. doi: 10.1385/MB:31:2:141. Mol Biotechnol. 2005. PMID: 16170215 Review.

9

Protein misfolding and human disease.

Gregersen N, Bross P, Vang S, Christensen JH. Gregersen N, et al. Annu Rev Genomics Hum Genet. 2006;7:103-24. doi: 10.1146/annurev.genom.7.080505.115737. Annu Rev Genomics Hum Genet. 2006. PMID: 16722804 Review.

10

Mitochondrial fatty acid oxidation defects--remaining challenges.

Gregersen N, Andresen BS, Pedersen CB, Olsen RK, Corydon TJ, Bross P. Gregersen N, et al. 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

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