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Sequence interpretation. Functional annotation of mouse genome sequences.
Nadeau JH, Balling R, Barsh G, Beier D, Brown SD, Bucan M, Camper S, Carlson G, Copeland N, Eppig J, Fletcher C, Frankel WN, Ganten D, Goldowitz D, Goodnow C, Guenet JL, Hicks G, Hrabe de Angelis M, Jackson I, Jacob HJ, Jenkins N, Johnson D, Justice M, Kay S, Kingsley D, Lehrach H, Magnuson T, Meisler M, Poustka A, Rinchik EM, Rossant J, Russell LB, Schimenti J, Shiroishi T, Skarnes WC, Soriano P, Stanford W, Takahashi JS, Wurst W, Zimmer A; International Mouse Mutagenesis Consortium. Nadeau JH, et al. Among authors: meisler m. Science. 2001 Feb 16;291(5507):1251-5. doi: 10.1126/science.1058244. Science. 2001. PMID: 11233449 No abstract available.
Identification of genes within the Krd deletion on mouse chromosome 19.
Ji W, Herron B, Jones JM, Jenkins NA, Gilbert DJ, Copeland NG, Swank R, Flaherty L, Meisler MH. Ji W, et al. Among authors: meisler mh. Mamm Genome. 1999 Apr;10(4):399-401. doi: 10.1007/s003359901010. Mamm Genome. 1999. PMID: 10087301 Free article. No abstract available.
Location of the 9257 and ataxia mutations on mouse chromosome 18.
Griffith AJ, Radice GL, Burgess DL, Kohrman DC, Hansen GM, Justice MJ, Johnson KR, Davisson MT, Meisler MH. Griffith AJ, et al. Among authors: meisler mh. Mamm Genome. 1996 Jun;7(6):417-9. doi: 10.1007/s003359900124. Mamm Genome. 1996. PMID: 8662222 Free article.
A targeted deleterious allele of the splicing factor SCNM1 in the mouse.
Howell VM, de Haan G, Bergren S, Jones JM, Culiat CT, Michaud EJ, Frankel WN, Meisler MH. Howell VM, et al. Among authors: meisler mh. Genetics. 2008 Nov;180(3):1419-27. doi: 10.1534/genetics.108.094227. Epub 2008 Sep 14. Genetics. 2008. PMID: 18791226 Free PMC article.
276 results