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Page 1
The evolutionary history of the DMRT3 'Gait keeper' haplotype.
Staiger EA, Almén MS, Promerová M, Brooks S, Cothran EG, Imsland F, Jäderkvist Fegraeus K, Lindgren G, Mehrabani Yeganeh H, Mikko S, Vega-Pla JL, Tozaki T, Rubin CJ, Andersson L. Staiger EA, et al. Among authors: imsland f. Anim Genet. 2017 Oct;48(5):551-559. doi: 10.1111/age.12580. Epub 2017 Jul 25. Anim Genet. 2017. PMID: 28741731
Worldwide frequency distribution of the 'Gait keeper' mutation in the DMRT3 gene.
Promerová M, Andersson LS, Juras R, Penedo MC, Reissmann M, Tozaki T, Bellone R, Dunner S, Hořín P, Imsland F, Imsland P, Mikko S, Modrý D, Roed KH, Schwochow D, Vega-Pla JL, Mehrabani-Yeganeh H, Yousefi-Mashouf N, G Cothran E, Lindgren G, Andersson L. Promerová M, et al. Among authors: imsland f. Anim Genet. 2014 Apr;45(2):274-82. doi: 10.1111/age.12120. Epub 2014 Jan 21. Anim Genet. 2014. PMID: 24444049
Mutations in DMRT3 affect locomotion in horses and spinal circuit function in mice.
Andersson LS, Larhammar M, Memic F, Wootz H, Schwochow D, Rubin CJ, Patra K, Arnason T, Wellbring L, Hjälm G, Imsland F, Petersen JL, McCue ME, Mickelson JR, Cothran G, Ahituv N, Roepstorff L, Mikko S, Vallstedt A, Lindgren G, Andersson L, Kullander K. Andersson LS, et al. Among authors: imsland f. Nature. 2012 Aug 30;488(7413):642-6. doi: 10.1038/nature11399. Nature. 2012. PMID: 22932389 Free PMC article.
Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses.
Imsland F, McGowan K, Rubin CJ, Henegar C, Sundström E, Berglund J, Schwochow D, Gustafson U, Imsland P, Lindblad-Toh K, Lindgren G, Mikko S, Millon L, Wade C, Schubert M, Orlando L, Penedo MC, Barsh GS, Andersson L. Imsland F, et al. Nat Genet. 2016 Feb;48(2):152-8. doi: 10.1038/ng.3475. Epub 2015 Dec 21. Nat Genet. 2016. PMID: 26691985 Free PMC article.
Copy number expansion of the STX17 duplication in melanoma tissue from Grey horses.
Sundström E, Imsland F, Mikko S, Wade C, Sigurdsson S, Pielberg GR, Golovko A, Curik I, Seltenhammer MH, Sölkner J, Lindblad-Toh K, Andersson L. Sundström E, et al. Among authors: imsland f. BMC Genomics. 2012 Aug 2;13:365. doi: 10.1186/1471-2164-13-365. BMC Genomics. 2012. PMID: 22857264 Free PMC article.
Copy number variation in intron 1 of SOX5 causes the Pea-comb phenotype in chickens.
Wright D, Boije H, Meadows JR, Bed'hom B, Gourichon D, Vieaud A, Tixier-Boichard M, Rubin CJ, Imsland F, Hallböök F, Andersson L. Wright D, et al. Among authors: imsland f. PLoS Genet. 2009 Jun;5(6):e1000512. doi: 10.1371/journal.pgen.1000512. Epub 2009 Jun 12. PLoS Genet. 2009. PMID: 19521496 Free PMC article.
The Rose-comb mutation in chickens constitutes a structural rearrangement causing both altered comb morphology and defective sperm motility.
Imsland F, Feng C, Boije H, Bed'hom B, Fillon V, Dorshorst B, Rubin CJ, Liu R, Gao Y, Gu X, Wang Y, Gourichon D, Zody MC, Zecchin W, Vieaud A, Tixier-Boichard M, Hu X, Hallböök F, Li N, Andersson L. Imsland F, et al. PLoS Genet. 2012 Jun;8(6):e1002775. doi: 10.1371/journal.pgen.1002775. Epub 2012 Jun 28. PLoS Genet. 2012. PMID: 22761584 Free PMC article.
14 results