Knappskog PM - Search Results

1

Dominant Mutations in the Autoimmune Regulator AIRE Are Associated with Common Organ-Specific Autoimmune Diseases.

Oftedal BE, Hellesen A, Erichsen MM, Bratland E, Vardi A, Perheentupa J, Kemp EH, Fiskerstrand T, Viken MK, Weetman AP, Fleishman SJ, Banka S, Newman WG, Sewell WA, Sozaeva LS, Zayats T, Haugarvoll K, Orlova EM, Haavik J, Johansson S, Knappskog PM, Løvås K, Wolff AS, Abramson J, Husebye ES. Oftedal BE, et al. Among authors: knappskog pm. Immunity. 2015 Jun 16;42(6):1185-96. doi: 10.1016/j.immuni.2015.04.021. Immunity. 2015. PMID: 26084028 Free article.

2

Tryptophan fluorescence of human phenylalanine hydroxylase produced in Escherichia coli.

Knappskog PM, Haavik J. Knappskog PM, et al. Biochemistry. 1995 Sep 19;34(37):11790-9. doi: 10.1021/bi00037a017. Biochemistry. 1995. PMID: 7547912

3

Structure/function relationships in human phenylalanine hydroxylase. Effect of terminal deletions on the oligomerization, activation and cooperativity of substrate binding to the enzyme.

Knappskog PM, Flatmark T, Aarden JM, Haavik J, Martínez A. Knappskog PM, et al. Eur J Biochem. 1996 Dec 15;242(3):813-21. doi: 10.1111/j.1432-1033.1996.0813r.x. Eur J Biochem. 1996. PMID: 9022714 Free article.

4

Urea-induced denaturation of human phenylalanine hydroxylase.

Kleppe R, Uhlemann K, Knappskog PM, Haavik J. Kleppe R, et al. Among authors: knappskog pm. J Biol Chem. 1999 Nov 19;274(47):33251-8. doi: 10.1074/jbc.274.47.33251. J Biol Chem. 1999. PMID: 10559199 Free article.

5

A structural approach into human tryptophan hydroxylase and its implications for the regulation of serotonin biosynthesis.

Martínez A, Knappskog PM, Haavik J. Martínez A, et al. Among authors: knappskog pm. Curr Med Chem. 2001 Jul;8(9):1077-91. doi: 10.2174/0929867013372616. Curr Med Chem. 2001. PMID: 11472242 Review.

6

[Why do mutations cause disease--a protein chemical perspective].

Kleppe R, Knappskog PM, Haavik J. Kleppe R, et al. Among authors: knappskog pm. Tidsskr Nor Laegeforen. 2001 Sep 30;121(23):2717-20. Tidsskr Nor Laegeforen. 2001. PMID: 11699380 Review. Norwegian.

7

Mutational analysis of the autoimmune regulator (AIRE) gene in sporadic autoimmune Addison's disease can reveal patients with unidentified autoimmune polyendocrine syndrome type I.

Bøe AS, Knappskog PM, Myhre AG, Sørheim JI, Husebye ES. Bøe AS, et al. Among authors: knappskog pm. Eur J Endocrinol. 2002 Apr;146(4):519-22. doi: 10.1530/eje.0.1460519. Eur J Endocrinol. 2002. PMID: 11916620

8

Autoantibodies against 21-hydroxylase and side-chain cleavage enzyme in autoimmune Addison's disease are mainly immunoglobulin G1.

Bøe AS, Bredholt G, Knappskog PM, Hjelmervik TO, Mellgren G, Winqvist O, Kämpe O, Husebye ES. Bøe AS, et al. Among authors: knappskog pm. Eur J Endocrinol. 2004 Jan;150(1):49-56. doi: 10.1530/eje.0.1500049. Eur J Endocrinol. 2004. PMID: 14713279

9

Chronic mucocutaneous candidiasis and primary hypothyroidism in two families.

Myhre AG, Stray-Pedersen A, Spangen S, Eide E, Veimo D, Knappskog PM, Abrahamsen TG, Husebye ES. Myhre AG, et al. Among authors: knappskog pm. Eur J Pediatr. 2004 Oct;163(10):604-11. doi: 10.1007/s00431-004-1516-8. Eur J Pediatr. 2004. PMID: 15290270

10

Pyridoxal phosphatase is a novel cancer autoantigen in the central nervous system.

Bøe AS, Bredholt G, Knappskog PM, Storstein A, Vedeler CA, Husebye ES. Bøe AS, et al. Among authors: knappskog pm. Br J Cancer. 2004 Oct 18;91(8):1508-14. doi: 10.1038/sj.bjc.6602142. Br J Cancer. 2004. PMID: 15452547 Free PMC article.

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