Undlien DE - Search Results

1

A conserved eEF2 coding variant in SCA26 leads to loss of translational fidelity and increased susceptibility to proteostatic insult.

Hekman KE, Yu GY, Brown CD, Zhu H, Du X, Gervin K, Undlien DE, Peterson A, Stevanin G, Clark HB, Pulst SM, Bird TD, White KP, Gomez CM. Hekman KE, et al. Among authors: undlien de. Hum Mol Genet. 2012 Dec 15;21(26):5472-83. doi: 10.1093/hmg/dds392. Epub 2012 Sep 21. Hum Mol Genet. 2012. PMID: 23001565 Free PMC article.

2

Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease.

Skinningsrud B, Husebye ES, Gervin K, Løvås K, Blomhoff A, Wolff AB, Kemp EH, Egeland T, Undlien DE. Skinningsrud B, et al. Among authors: undlien de. Eur J Hum Genet. 2008 Aug;16(8):977-82. doi: 10.1038/ejhg.2008.33. Epub 2008 Feb 27. Eur J Hum Genet. 2008. PMID: 18301444

3

Intra-individual changes in DNA methylation not mediated by cell-type composition are correlated with aging during childhood.

Gervin K, Andreassen BK, Hjorthaug HS, Carlsen KCL, Carlsen KH, Undlien DE, Lyle R, Munthe-Kaas MC. Gervin K, et al. Among authors: undlien de. Clin Epigenetics. 2016 Oct 21;8:110. doi: 10.1186/s13148-016-0277-3. eCollection 2016. Clin Epigenetics. 2016. PMID: 27785156 Free PMC article.

4

X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene.

Skinningsrud B, Husebye ES, Gilfillan GD, Frengen E, Erichsen A, Gervin K, Ormerod E, Egeland T, Undlien DE. Skinningsrud B, et al. Among authors: undlien de. J Clin Endocrinol Metab. 2009 Oct;94(10):4086-93. doi: 10.1210/jc.2009-0923. Epub 2009 Sep 22. J Clin Endocrinol Metab. 2009. PMID: 19773398

5

DNA methylation and gene expression changes in monozygotic twins discordant for psoriasis: identification of epigenetically dysregulated genes.

Gervin K, Vigeland MD, Mattingsdal M, Hammerø M, Nygård H, Olsen AO, Brandt I, Harris JR, Undlien DE, Lyle R. Gervin K, et al. Among authors: undlien de. PLoS Genet. 2012 Jan;8(1):e1002454. doi: 10.1371/journal.pgen.1002454. Epub 2012 Jan 19. PLoS Genet. 2012. PMID: 22291603 Free PMC article.

6

Multiple loci in the HLA complex are associated with Addison's disease.

Skinningsrud B, Lie BA, Lavant E, Carlson JA, Erlich H, Akselsen HE, Gervin K, Wolff AB, Erichsen MM, Løvås K, Husebye ES, Undlien DE. Skinningsrud B, et al. Among authors: undlien de. J Clin Endocrinol Metab. 2011 Oct;96(10):E1703-8. doi: 10.1210/jc.2011-0645. Epub 2011 Aug 3. J Clin Endocrinol Metab. 2011. PMID: 21816777

7

T cell-specific T-box transcription factor haplotype is associated with allergic asthma in children.

Munthe-Kaas MC, Carlsen KH, Håland G, Devulapalli CS, Gervin K, Egeland T, Carlsen KL, Undlien D. Munthe-Kaas MC, et al. J Allergy Clin Immunol. 2008 Jan;121(1):51-6. doi: 10.1016/j.jaci.2007.07.068. Epub 2007 Oct 18. J Allergy Clin Immunol. 2008. PMID: 17949803

8

CD14 polymorphisms and serum CD14 levels through childhood: a role for gene methylation?

Munthe-Kaas MC, Torjussen TM, Gervin K, Lødrup Carlsen KC, Carlsen KH, Granum B, Hjorthaug HS, Undlien D, Lyle R. Munthe-Kaas MC, et al. J Allergy Clin Immunol. 2010 Jun;125(6):1361-8. doi: 10.1016/j.jaci.2010.02.010. Epub 2010 Apr 15. J Allergy Clin Immunol. 2010. PMID: 20398919

9

Limitations and possibilities of low cell number ChIP-seq.

Gilfillan GD, Hughes T, Sheng Y, Hjorthaug HS, Straub T, Gervin K, Harris JR, Undlien DE, Lyle R. Gilfillan GD, et al. Among authors: undlien de. BMC Genomics. 2012 Nov 21;13:645. doi: 10.1186/1471-2164-13-645. BMC Genomics. 2012. PMID: 23171294 Free PMC article.

10

Extensive variation and low heritability of DNA methylation identified in a twin study.

Gervin K, Hammerø M, Akselsen HE, Moe R, Nygård H, Brandt I, Gjessing HK, Harris JR, Undlien DE, Lyle R. Gervin K, et al. Among authors: undlien de. Genome Res. 2011 Nov;21(11):1813-21. doi: 10.1101/gr.119685.110. Epub 2011 Sep 26. Genome Res. 2011. PMID: 21948560 Free PMC article.

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