Gregersen N - Search Results

1

[Psychological, neurological and cell-mediated mechanisms by mindfulness-based therapy].

Boutrup RJ, Jørgensen MM, Gregersen N, Frost L, Aagaard H, Djernis D, van der Velden AM, Dahlgaard J. Boutrup RJ, et al. Among authors: gregersen n. Ugeskr Laeger. 2019 Jul 22;181(30):V11180784. Ugeskr Laeger. 2019. PMID: 31364970 Free article. Review. Danish.

2

Protein quality control in the endoplasmic reticulum.

Jørgensen MM, Bross P, Gregersen N. Jørgensen MM, et al. Among authors: gregersen n. APMIS Suppl. 2003;(109):86-91. APMIS Suppl. 2003. PMID: 12874956 Review.

3

Protein misfolding and degradation in genetic diseases.

Bross P, Corydon TJ, Andresen BS, Jørgensen MM, Bolund L, Gregersen N. Bross P, et al. Among authors: gregersen n. Hum Mutat. 1999;14(3):186-98. doi: 10.1002/(SICI)1098-1004(1999)14:3<186::AID-HUMU2>3.0.CO;2-J. Hum Mutat. 1999. PMID: 10477427 Review.

4

Grp78 is involved in retention of mutant low density lipoprotein receptor protein in the endoplasmic reticulum.

Jørgensen MM, Jensen ON, Holst HU, Hansen JJ, Corydon TJ, Bross P, Bolund L, Gregersen N. Jørgensen MM, et al. Among authors: gregersen n. J Biol Chem. 2000 Oct 27;275(43):33861-8. doi: 10.1074/jbc.M004663200. J Biol Chem. 2000. PMID: 10906332 Free article.

5

[Myalgic encephalomyelitis or chronic fatigue syndrome].

Brinth L, Nielsen H, Varming K, Boonen SE, Ebsen ACG, Fernández-Guerra P, Schou AS, Mehlsen J, Gregersen N, Brandslund I, Olsen RKJ. Brinth L, et al. Among authors: gregersen n. Ugeskr Laeger. 2019 Jun 10;181(24):V08180570. Ugeskr Laeger. 2019. PMID: 31267953 Free article. Review. Danish.

6

A common W556S mutation in the LDL receptor gene of Danish patients with familial hypercholesterolemia encodes a transport-defective protein.

Jensen HK, Holst H, Jensen LG, Jørgensen MM, Andreasen PH, Jensen TG, Andresen BS, Heath F, Hansen PS, Neve S, Kristiansen K, Faergeman O, Kølvraa S, Bolund L, Gregersen N. Jensen HK, et al. Among authors: gregersen n. Atherosclerosis. 1997 May;131(1):67-72. doi: 10.1016/s0021-9150(96)06059-5. Atherosclerosis. 1997. PMID: 9180246

7

Defective folding and rapid degradation of mutant proteins is a common disease mechanism in genetic disorders.

Gregersen N, Bross P, Jørgensen MM, Corydon TJ, Andresen BS. Gregersen N, et al. J Inherit Metab Dis. 2000 Jul;23(5):441-7. doi: 10.1023/a:1005663728291. J Inherit Metab Dis. 2000. PMID: 10947197 Review.

8

Repetitive sequences involved in the recombination leading to deletion of exon 5 of the low-density-lipoprotein receptor gene in a patient with familial hypercholesterolemia.

Rüdiger NS, Hansen PS, Jørgensen M, Faergeman O, Bolund L, Gregersen N. Rüdiger NS, et al. Among authors: gregersen n. Eur J Biochem. 1991 May 23;198(1):107-11. doi: 10.1111/j.1432-1033.1991.tb15992.x. Eur J Biochem. 1991. PMID: 2040272 Free article.

9

Redox signalling and mitochondrial stress responses; lessons from inborn errors of metabolism.

Olsen RK, Cornelius N, Gregersen N. Olsen RK, et al. Among authors: gregersen n. J Inherit Metab Dis. 2015 Jul;38(4):703-19. doi: 10.1007/s10545-015-9861-5. Epub 2015 May 30. J Inherit Metab Dis. 2015. PMID: 26025548 Free PMC article. Review.

10

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.

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