Knappskog PM - Search Results

1

Population prevalence and inheritance pattern of recurrent CNVs associated with neurodevelopmental disorders in 12,252 newborns and their parents.

Smajlagić D, Lavrichenko K, Berland S, Helgeland Ø, Knudsen GP, Vaudel M, Haavik J, Knappskog PM, Njølstad PR, Houge G, Johansson S. Smajlagić D, et al. Among authors: knappskog pm. Eur J Hum Genet. 2021 Jan;29(1):205-215. doi: 10.1038/s41431-020-00707-7. Epub 2020 Aug 10. Eur J Hum Genet. 2021. PMID: 32778765 Free PMC article.

2

PKU mutations R408Q and F299C in Norway: haplotype associations, geographic distributions and phenotype characteristics.

Eiken HG, Stangeland K, Skjelkvåle L, Knappskog PM, Boman H, Apold J. Eiken HG, et al. Among authors: knappskog pm. Hum Genet. 1992 Mar;88(6):608-12. doi: 10.1007/BF02265283. Hum Genet. 1992. PMID: 1312992

3

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

4

Relative frequency, heterogeneity and geographic clustering of PKU mutations in Norway.

Eiken HG, Knappskog PM, Boman H, Thune KS, Kaada G, Motzfeldt K, Apold J. Eiken HG, et al. Among authors: knappskog pm. Eur J Hum Genet. 1996;4(4):205-13. doi: 10.1159/000472200. Eur J Hum Genet. 1996. PMID: 8875186

5

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.

6

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.

7

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.

8

[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.

9

Conformation of the substrate and pterin cofactor bound to human tryptophan hydroxylase. Important role of Phe313 in substrate specificity.

McKinney J, Teigen K, Frøystein NA, Salaün C, Knappskog PM, Haavik J, Martínez A. McKinney J, et al. Among authors: knappskog pm. Biochemistry. 2001 Dec 25;40(51):15591-601. doi: 10.1021/bi015722x. Biochemistry. 2001. PMID: 11747434

10

Expression and purification of human tryptophan hydroxylase from Escherichia coli and Pichia pastoris.

McKinney J, Knappskog PM, Pereira J, Ekern T, Toska K, Kuitert BB, Levine D, Gronenborn AM, Martinez A, Haavik J. McKinney J, et al. Among authors: knappskog pm. Protein Expr Purif. 2004 Feb;33(2):185-94. doi: 10.1016/j.pep.2003.09.014. Protein Expr Purif. 2004. PMID: 14711505

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

158 results

Search Page