Bruland O - Search Results

1

Functional characterization of all-trans retinoic acid-induced differentiation factor (ATRAID).

Mehrasa R, Cristea I, Bredrup C, Rødahl E, Bruland O. Mehrasa R, et al. Among authors: bruland o. FEBS Open Bio. 2023 Oct;13(10):1874-1886. doi: 10.1002/2211-5463.13685. Epub 2023 Sep 7. FEBS Open Bio. 2023. PMID: 37530719 Free PMC article.

2

Decorin accumulation contributes to the stromal opacities found in congenital stromal corneal dystrophy.

Bredrup C, Stang E, Bruland O, Palka BP, Young RD, Haavik J, Knappskog PM, Rødahl E. Bredrup C, et al. Among authors: bruland o. Invest Ophthalmol Vis Sci. 2010 Nov;51(11):5578-82. doi: 10.1167/iovs.09-4933. Epub 2010 May 19. Invest Ophthalmol Vis Sci. 2010. PMID: 20484579

3

Development of congenital stromal corneal dystrophy is dependent on export and extracellular deposition of truncated decorin.

Mellgren AE, Bruland O, Vedeler A, Saraste J, Schönheit J, Bredrup C, Knappskog PM, Rødahl E. Mellgren AE, et al. Among authors: bruland o. Invest Ophthalmol Vis Sci. 2015 May;56(5):2909-15. doi: 10.1167/iovs.14-16014. Invest Ophthalmol Vis Sci. 2015. PMID: 26029887

4

Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome.

Xu L, Jensen H, Johnston JJ, Di Maria E, Kloth K, Cristea I, Sapp JC, Darling TN, Huryn LA, Tranebjærg L, Cinotti E, Kubisch C, Rødahl E, Bruland O, Biesecker LG, Houge G, Bredrup C. Xu L, et al. Among authors: bruland o. Am J Hum Genet. 2018 Dec 6;103(6):976-983. doi: 10.1016/j.ajhg.2018.10.013. Epub 2018 Nov 15. Am J Hum Genet. 2018. PMID: 30449416 Free PMC article.

5

A tyrosine kinase-activating variant Asn666Ser in PDGFRB causes a progeria-like condition in the severe end of Penttinen syndrome.

Bredrup C, Stokowy T, McGaughran J, Lee S, Sapkota D, Cristea I, Xu L, Tveit KS, Høvding G, Steen VM, Rødahl E, Bruland O, Houge G. Bredrup C, et al. Among authors: bruland o. Eur J Hum Genet. 2019 Apr;27(4):574-581. doi: 10.1038/s41431-018-0323-z. Epub 2018 Dec 20. Eur J Hum Genet. 2019. PMID: 30573803 Free PMC article.

6

Clinical features and molecular genetics of patients with ABCA4-retinal dystrophies.

Holtan JP, Aukrust I, Jansson RW, Berland S, Bruland O, Gjerde BL, Stokowy T, Bojovic O, Forsaa V, Austeng D, Rødahl E, Bredrup C, Knappskog PM, Bragadóttir R. Holtan JP, et al. Among authors: bruland o. Acta Ophthalmol. 2021 Aug;99(5):e733-e746. doi: 10.1111/aos.14679. Epub 2020 Nov 30. Acta Ophthalmol. 2021. PMID: 33258285 Free article.

7

Temperature-dependent autoactivation associated with clinical variability of PDGFRB Asn666 substitutions.

Bredrup C, Cristea I, Safieh LA, Di Maria E, Gjertsen BT, Tveit KS, Thu F, Bull N, Edward DP, Hennekam RCM, Høvding G, Haugen OH, Houge G, Rødahl E, Bruland O. Bredrup C, et al. Among authors: bruland o. Hum Mol Genet. 2021 Mar 25;30(1):72-77. doi: 10.1093/hmg/ddab014. Hum Mol Genet. 2021. PMID: 33450762 Free PMC article.

8

K⁺ regulates relocation of Pellino-2 to the site of NLRP3 inflammasome activation in macrophages.

Cristea I, Bruland O, Rødahl E, Bredrup C. Cristea I, et al. Among authors: bruland o. FEBS Lett. 2021 Oct;595(19):2437-2446. doi: 10.1002/1873-3468.14176. Epub 2021 Sep 1. FEBS Lett. 2021. PMID: 34387857 Free article.

9

Pellino-2 in nonimmune cells: novel interaction partners and intracellular localization.

Cristea I, Bruland O, Aukrust I, Rødahl E, Bredrup C. Cristea I, et al. Among authors: bruland o. FEBS Lett. 2021 Dec;595(23):2909-2921. doi: 10.1002/1873-3468.14212. Epub 2021 Nov 12. FEBS Lett. 2021. PMID: 34674267 Free article.

10

A Pellino-2 variant is associated with constitutive NLRP3 inflammasome activation in a family with ocular pterygium-digital keloid dysplasia.

Cristea I, Abarca H, Christensen Mellgren AE, Trubnykova M, Mehrasa R, Peters DJM, Houge G, Hennekam RCM, Rødahl E, Bruland O, Bredrup C. Cristea I, et al. Among authors: bruland o. FEBS Lett. 2023 May;597(9):1290-1299. doi: 10.1002/1873-3468.14597. Epub 2023 Feb 24. FEBS Lett. 2023. PMID: 36776133 Free article.

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