Similar articles for PMID: 25487337

Year	Number of Results
1935	1
1952	2
1953	1
1973	1
1974	1
1975	1
1978	1
1979	1
1990	2
1992	1
1994	1
1995	1
1996	1
1997	1
1998	1
1999	1
2001	2
2005	1
2007	2
2008	2
2009	3
2010	4
2011	5
2012	9
2013	9
2014	4
2015	12
2016	9
2017	10
2018	7
2019	9
2020	10
2021	7
2022	7
2023	2
2024	0

1

Twenty-five thousand years of fluctuating selection on leopard complex spotting and congenital night blindness in horses.

Ludwig A, Reissmann M, Benecke N, Bellone R, Sandoval-Castellanos E, Cieslak M, Fortes GG, Morales-Muñiz A, Hofreiter M, Pruvost M. Ludwig A, et al. Philos Trans R Soc Lond B Biol Sci. 2015 Jan 19;370(1660):20130386. doi: 10.1098/rstb.2013.0386. Philos Trans R Soc Lond B Biol Sci. 2015. PMID: 25487337 Free PMC article.

2

Redundant contribution of a Transient Receptor Potential cation channel Member 1 exon 11 single nucleotide polymorphism to equine congenital stationary night blindness.

Scott ML, John EE, Bellone RR, Ching JC, Loewen ME, Sandmeyer LS, Grahn BH, Forsyth GW. Scott ML, et al. BMC Vet Res. 2016 Jun 21;12(1):121. doi: 10.1186/s12917-016-0745-1. BMC Vet Res. 2016. PMID: 27329127 Free PMC article.

3

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. Brief Funct Genomics. 2010 May;9(3):193-207. doi: 10.1093/bfgp/elq002. Epub 2010 Mar 29. Brief Funct Genomics. 2010. PMID: 20353955

4

Congenital stationary night blindness is associated with the leopard complex in the Miniature Horse.

Sandmeyer LS, Bellone RR, Archer S, Bauer BS, Nelson J, Forsyth G, Grahn BH. Sandmeyer LS, et al. Vet Ophthalmol. 2012 Jan;15(1):18-22. doi: 10.1111/j.1463-5224.2011.00903.x. Epub 2011 Apr 19. Vet Ophthalmol. 2012. PMID: 22051042

5

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. PLoS One. 2013 Oct 22;8(10):e78280. doi: 10.1371/journal.pone.0078280. eCollection 2013. PLoS One. 2013. PMID: 24167615 Free PMC article.

6

Differential gene expression of TRPM1, the potential cause of congenital stationary night blindness and coat spotting patterns (LP) in the Appaloosa horse (Equus caballus).

Bellone RR, Brooks SA, Sandmeyer L, Murphy BA, Forsyth G, Archer S, Bailey E, Grahn B. Bellone RR, et al. Genetics. 2008 Aug;179(4):1861-70. doi: 10.1534/genetics.108.088807. Epub 2008 Jul 27. Genetics. 2008. PMID: 18660533 Free PMC article.

7

Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient.

Lee YJ, Joo K, Seong MW, Park KH, Park SS, Woo SJ. Lee YJ, et al. Korean J Ophthalmol. 2020 Apr;34(2):170-172. doi: 10.3341/kjo.2019.0080. Korean J Ophthalmol. 2020. PMID: 32233153 Free PMC article. No abstract available.

8

Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children.

Miraldi Utz V, Pfeifer W, Longmuir SQ, Olson RJ, Wang K, Drack AV. Miraldi Utz V, et al. JAMA Ophthalmol. 2018 Apr 1;136(4):389-398. doi: 10.1001/jamaophthalmol.2018.0185. JAMA Ophthalmol. 2018. PMID: 29522070 Free PMC article.

9

Whole-genome sequencing identifies missense mutation in GRM6 as the likely cause of congenital stationary night blindness in a Tennessee Walking Horse.

Hack YL, Crabtree EE, Avila F, Sutton RB, Grahn R, Oh A, Gilger B, Bellone RR. Hack YL, et al. Equine Vet J. 2021 Mar;53(2):316-323. doi: 10.1111/evj.13318. Epub 2020 Aug 3. Equine Vet J. 2021. PMID: 32654228

10

Clinical and electroretinographic characteristics of congenital stationary night blindness in the Appaloosa and the association with the leopard complex.

Sandmeyer LS, Breaux CB, Archer S, Grahn BH. Sandmeyer LS, et al. Vet Ophthalmol. 2007 Nov-Dec;10(6):368-75. doi: 10.1111/j.1463-5224.2007.00572.x. Vet Ophthalmol. 2007. PMID: 17970998

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