Pääkkönen K - Search Results

Year	Number of Results
1998	2
1999	2
2000	4
2001	3
2002	1
2003	1
2004	1
2006	1
2007	1
2008	1
2009	2
2023	1
2024	0

1

Locus for severity implicates CNS resilience in progression of multiple sclerosis.

International Multiple Sclerosis Genetics Consortium; MultipleMS Consortium. International Multiple Sclerosis Genetics Consortium, et al. Nature. 2023 Jul;619(7969):323-331. doi: 10.1038/s41586-023-06250-x. Epub 2023 Jun 28. Nature. 2023. PMID: 37380766 Free PMC article.

2

NMR resonance assignment of DnaE intein from Nostoc punctiforme.

Heinämäki K, Oeemig JS, Pääkkönen K, Djupsjöbacka J, Iwaï H. Heinämäki K, et al. Among authors: paakkonen k. Biomol NMR Assign. 2009 Jun;3(1):41-3. doi: 10.1007/s12104-008-9137-1. Epub 2009 Jan 13. Biomol NMR Assign. 2009. PMID: 19636943

3

Structural basis of PxxDY motif recognition in SH3 binding.

Aitio O, Hellman M, Kesti T, Kleino I, Samuilova O, Pääkkönen K, Tossavainen H, Saksela K, Permi P. Aitio O, et al. Among authors: paakkonen k. J Mol Biol. 2008 Sep 26;382(1):167-78. doi: 10.1016/j.jmb.2008.07.008. Epub 2008 Jul 11. J Mol Biol. 2008. PMID: 18644376

4

The mutation spectrum of the EDA gene in X-linked anhidrotic ectodermal dysplasia.

Pääkkönen K, Cambiaghi S, Novelli G, Ouzts LV, Penttinen M, Kere J, Srivastava AK. Pääkkönen K, et al. Hum Mutat. 2001 Apr;17(4):349. doi: 10.1002/humu.33. Hum Mutat. 2001. PMID: 11295832

5

Stromelysin-2 is upregulated during normal wound repair and is induced by cytokines.

Rechardt O, Elomaa O, Vaalamo M, Pääkkönen K, Jahkola T, Höök-Nikanne J, Hembry RM, Häkkinen L, Kere J, Saarialho-Kere U. Rechardt O, et al. Among authors: paakkonen k. J Invest Dermatol. 2000 Nov;115(5):778-87. doi: 10.1046/j.1523-1747.2000.00135.x. J Invest Dermatol. 2000. PMID: 11069614 Free article.

6

Clinical findings in mosaic carriers of hypohidrotic ectodermal dysplasia.

Cambiaghi S, Restano L, Pääkkönen K, Caputo R, Kere J. Cambiaghi S, et al. Among authors: paakkonen k. Arch Dermatol. 2000 Feb;136(2):217-24. doi: 10.1001/archderm.136.2.217. Arch Dermatol. 2000. PMID: 10677098

7

Solution structures of the first and fourth TSR domains of F-spondin.

Pääkkönen K, Tossavainen H, Permi P, Rakkolainen H, Rauvala H, Raulo E, Kilpeläinen I, Güntert P. Pääkkönen K, et al. Proteins. 2006 Aug 15;64(3):665-72. doi: 10.1002/prot.21030. Proteins. 2006. PMID: 16736493

8

Structural insight into dimeric interaction of the SARAH domains from Mst1 and RASSF family proteins in the apoptosis pathway.

Hwang E, Ryu KS, Pääkkönen K, Güntert P, Cheong HK, Lim DS, Lee JO, Jeon YH, Cheong C. Hwang E, et al. Among authors: paakkonen k. Proc Natl Acad Sci U S A. 2007 May 29;104(22):9236-41. doi: 10.1073/pnas.0610716104. Epub 2007 May 21. Proc Natl Acad Sci U S A. 2007. PMID: 17517604 Free PMC article.

9

Germ-line TP53 mutations in Finnish cancer families exhibiting features of the Li-Fraumeni syndrome and negative for BRCA1 and BRCA2.

Huusko P, Castrén K, Launonen V, Soini Y, Pääkkönen K, Leisti J, Vähäkangas K, Winqvist R. Huusko P, et al. Among authors: paakkonen k. Cancer Genet Cytogenet. 1999 Jul 1;112(1):9-14. doi: 10.1016/s0165-4608(98)00258-1. Cancer Genet Cytogenet. 1999. PMID: 10432928

10

Solution structure of the GUCT domain from human RNA helicase II/Gu beta reveals the RRM fold, but implausible RNA interactions.

Ohnishi S, Pääkkönen K, Koshiba S, Tochio N, Sato M, Kobayashi N, Harada T, Watanabe S, Muto Y, Güntert P, Tanaka A, Kigawa T, Yokoyama S. Ohnishi S, et al. Among authors: paakkonen k. Proteins. 2009 Jan;74(1):133-44. doi: 10.1002/prot.22138. Proteins. 2009. PMID: 18615715

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