Gregersen N - Search Results

1

Functional testing of keratin 14 mutant proteins associated with the three major subtypes of epidermolysis bullosa simplex.

Sørensen CB, Andresen BS, Jensen UB, Jensen TG, Jensen PK, Gregersen N, Bolund L. Sørensen CB, et al. Among authors: gregersen n. Exp Dermatol. 2003 Aug;12(4):472-9. doi: 10.1034/j.1600-0625.2002.120416.x. Exp Dermatol. 2003. PMID: 12930305

2

Identification of novel and known mutations in the genes for keratin 5 and 14 in Danish patients with epidermolysis bullosa simplex: correlation between genotype and phenotype.

Sørensen CB, Ladekjaer-Mikkelsen AS, Andresen BS, Brandrup F, Veien NK, Buus SK, Anton-Lamprecht I, Kruse TA, Jensen PK, Eiberg H, Bolund L, Gregersen N. Sørensen CB, et al. Among authors: gregersen n. J Invest Dermatol. 1999 Feb;112(2):184-90. doi: 10.1046/j.1523-1747.1999.00495.x. J Invest Dermatol. 1999. PMID: 9989794 Free article.

3

Expression of short-chain acyl-CoA dehydrogenase (SCAD) proteins in the liver of SCAD deficient mice after hydrodynamic gene transfer.

Holm DA, Dagnaes-Hansen F, Simonsen H, Gregersen N, Bolund L, Jensen TG, Corydon TJ. Holm DA, et al. Among authors: gregersen n. Mol Genet Metab. 2003 Apr;78(4):250-8. doi: 10.1016/s1096-7192(03)00038-6. Mol Genet Metab. 2003. PMID: 12706376

4

Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency.

Olsen RK, Andresen BS, Christensen E, Bross P, Skovby F, Gregersen N. Olsen RK, et al. Among authors: gregersen n. Hum Mutat. 2003 Jul;22(1):12-23. doi: 10.1002/humu.10226. Hum Mutat. 2003. PMID: 12815589

5

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.

6

Comparison between medium-chain acyl-CoA dehydrogenase mutant proteins overexpressed in bacterial and mammalian cells.

Jensen TG, Bross P, Andresen BS, Lund TB, Kristensen TJ, Jensen UB, Winther V, Kølvraa S, Gregersen N, Bolund L. Jensen TG, et al. Among authors: gregersen n. Hum Mutat. 1995;6(3):226-31. doi: 10.1002/humu.1380060305. Hum Mutat. 1995. PMID: 8535441

7

Rapid characterization of disease-causing mutations in the low density lipoprotein receptor (LDL-R) gene by overexpression in COS cells.

Jensen TG, Andresen BS, Jensen HK, Jensen LG, Heath F, Pedersen S, Nielsen V, Jensen UB, Lund TB, Gregersen N, Kølvraa S, Bolund L. Jensen TG, et al. Among authors: gregersen n. Z Gastroenterol. 1996 Jun;34 Suppl 3:9-11. Z Gastroenterol. 1996. PMID: 8767445

8

Rapid degradation of short-chain acyl-CoA dehydrogenase variants with temperature-sensitive folding defects occurs after import into mitochondria.

Corydon TJ, Bross P, Jensen TG, Corydon MJ, Lund TB, Jensen UB, Kim JJ, Gregersen N, Bolund L. Corydon TJ, et al. Among authors: gregersen n. J Biol Chem. 1998 May 22;273(21):13065-71. doi: 10.1074/jbc.273.21.13065. J Biol Chem. 1998. PMID: 9582344 Free article.

9

Clinical and molecular evidence of abnormal processing and trafficking of the vasopressin preprohormone in a large kindred with familial neurohypophyseal diabetes insipidus due to a signal peptide mutation.

Siggaard C, Rittig S, Corydon TJ, Andreasen PH, Jensen TG, Andresen BS, Robertson GL, Gregersen N, Bolund L, Pedersen EB. Siggaard C, et al. Among authors: gregersen n. J Clin Endocrinol Metab. 1999 Aug;84(8):2933-41. doi: 10.1210/jcem.84.8.5869. J Clin Endocrinol Metab. 1999. PMID: 10443701

10

Characterization of mouse Clpp protease cDNA, gene, and protein.

Andresen BS, Corydon TJ, Wilsbech M, Bross P, Schroeder LD, Hindkjaer TF, Bolund L, Gregersen N. Andresen BS, et al. Among authors: gregersen n. Mamm Genome. 2000 Apr;11(4):275-80. doi: 10.1007/s003350010052. Mamm Genome. 2000. PMID: 10754102

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