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Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses.
Bellone RR, Forsyth G, Leeb T, Archer S, Sigurdsson S, Imsland F, Mauceli E, Engensteiner M, Bailey E, Sandmeyer L, Grahn B, Lindblad-Toh K, Wade CM. Bellone RR, et al. Among authors: archer s. Brief Funct Genomics. 2010 May;9(3):193-207. doi: 10.1093/bfgp/elq002. Epub 2010 Mar 29. Brief Funct Genomics. 2010. PMID: 20353955
Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse.
Bellone RR, Holl H, Setaluri V, Devi S, Maddodi N, Archer S, Sandmeyer L, Ludwig A, Foerster D, Pruvost M, Reissmann M, Bortfeldt R, Adelson DL, Lim SL, Nelson J, Haase B, Engensteiner M, Leeb T, Forsyth G, Mienaltowski MJ, Mahadevan P, Hofreiter M, Paijmans JL, Gonzalez-Fortes G, Grahn B, Brooks SA. Bellone RR, et al. Among authors: archer s. PLoS One. 2013 Oct 22;8(10):e78280. doi: 10.1371/journal.pone.0078280. eCollection 2013. PLoS One. 2013. PMID: 24167615 Free PMC article.
Genetic investigation of equine recurrent uveitis in Appaloosa horses.
Rockwell H, Mack M, Famula T, Sandmeyer L, Bauer B, Dwyer A, Lassaline M, Beeson S, Archer S, McCue M, Bellone RR. Rockwell H, et al. Among authors: archer s. Anim Genet. 2020 Feb;51(1):111-116. doi: 10.1111/age.12883. Epub 2019 Dec 2. Anim Genet. 2020. PMID: 31793009
1,209 results