Dunø M - Search Results

1

Genetic dissection of intersubunit contacts within human protein kinase CK2.

Kusk M, Bendixen C, Dunø M, Westergaard O, Thomsen B. Kusk M, et al. Among authors: duno m. J Mol Biol. 1995 Nov 10;253(5):703-11. doi: 10.1006/jmbi.1995.0584. J Mol Biol. 1995. PMID: 7473745

2

Targeted deletions created in yeast vectors by recombinational excision.

Dunø M, Bendixen C, Krejci L, Thomsen B. Dunø M, et al. Nucleic Acids Res. 1999 Apr 15;27(8):e1. Nucleic Acids Res. 1999. PMID: 10189379 Free PMC article.

3

Homomeric interaction of the mouse Rad52 protein.

Krejci L, Thomsen B, Duno M, Westergaard O, Bendixen C. Krejci L, et al. Among authors: duno m. Mol Biol Rep. 2000 Mar;27(1):55-9. doi: 10.1023/a:1007115032543. Mol Biol Rep. 2000. PMID: 10939527

4

Genetic analysis of the Saccharomyces cerevisiae Sgs1 helicase defines an essential function for the Sgs1-Top3 complex in the absence of SRS2 or TOP1.

Dunø M, Thomsen B, Westergaard O, Krejci L, Bendixen C. Dunø M, et al. Mol Gen Genet. 2000 Sep;264(1-2):89-97. doi: 10.1007/s004380000286. Mol Gen Genet. 2000. PMID: 11016837

5

Molecular dissection of interactions between Rad51 and members of the recombination-repair group.

Krejci L, Damborsky J, Thomsen B, Duno M, Bendixen C. Krejci L, et al. Among authors: duno m. Mol Cell Biol. 2001 Feb;21(3):966-76. doi: 10.1128/MCB.21.3.966-976.2001. Mol Cell Biol. 2001. Retraction in: Mol Cell Biol. 2024;44(6):259. doi: 10.1080/10985549.2024.2358694 PMID: 11154282 Free PMC article. Retracted.

6

Chromosome location, genomic organization of the porcine COL10A1 gene and model structure of the NC1 domain.

Madsen LB, Petersen AH, Nielsen VH, Nissen PH, Dunø M, Krejci L, Bendixen C, Thomsen B. Madsen LB, et al. Among authors: duno m. Cytogenet Genome Res. 2003;102(1-4):173-8. doi: 10.1159/000075744. Cytogenet Genome Res. 2003. PMID: 14970698

7

A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases.

Ostergaard E, Duno M, Batbayli M, Vilhelmsen K, Rosenberg T. Ostergaard E, et al. Among authors: duno m. Mol Vis. 2011;17:1485-92. Epub 2011 Jun 4. Mol Vis. 2011. PMID: 21677792 Free PMC article.

8

Incidence of Aicardi-Goutières syndrome and KCNT1-related epilepsy in Denmark.

Møller RS, Zhao L, Shoaff JR, Duno M, Andersen BN, Nguyen V, Fang TC, Kupelian V, Thorén R. Møller RS, et al. Among authors: duno m. Mol Genet Metab Rep. 2022 Oct 13;33:100924. doi: 10.1016/j.ymgmr.2022.100924. eCollection 2022 Dec. Mol Genet Metab Rep. 2022. PMID: 36262748 Free PMC article.

9

Clinician's guide to genes associated with Rett-like phenotypes-Investigation of a Danish cohort and review of the literature.

Schönewolf-Greulich B, Bisgaard AM, Møller RS, Dunø M, Brøndum-Nielsen K, Kaur S, Van Bergen NJ, Lunke S, Eggers S, Jespersgaard C, Christodoulou J, Tümer Z. Schönewolf-Greulich B, et al. Among authors: duno m. Clin Genet. 2019 Feb;95(2):221-230. doi: 10.1111/cge.13153. Epub 2018 Jan 25. Clin Genet. 2019. PMID: 29023665 Review.

10

Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletion.

Dunø M, Hove H, Kirchhoff M, Devriendt K, Schwartz M. Dunø M, et al. Hum Genet. 2004 Nov;115(6):459-67. doi: 10.1007/s00439-004-1174-y. Epub 2004 Sep 18. Hum Genet. 2004. PMID: 15378350

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