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Journal Abstract Search

154 related items for PubMed ID: 22051042

  • 1. 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.
    Vet Ophthalmol; 2012 Jan; 15(1):18-22. PubMed ID: 22051042
    [Abstract] [Full Text] [Related]

  • 2. 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.
    Vet Ophthalmol; 2007 Jan; 10(6):368-75. PubMed ID: 17970998
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  • 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.
    Brief Funct Genomics; 2010 May; 9(3):193-207. PubMed ID: 20353955
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  • 4. 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.
    Genetics; 2008 Aug; 179(4):1861-70. PubMed ID: 18660533
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  • 5. 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.
    Philos Trans R Soc Lond B Biol Sci; 2015 Jan 19; 370(1660):20130386. PubMed ID: 25487337
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  • 6. 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.
    PLoS One; 2013 Jan 19; 8(10):e78280. PubMed ID: 24167615
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  • 8. Additional evidence supports GRM6 p.Thr178Met as a cause of congenital stationary night blindness in three horse breeds.
    Esdaile E, Knickelbein KE, Donnelly CG, Ferneding M, Motta MJ, Story BD, Avila F, Finno CJ, Gilger BC, Sandmeyer L, Thomasy S, Bellone RR.
    Vet Ophthalmol; 2024 May 19; 27(3):248-255. PubMed ID: 37815029
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  • 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.
    Equine Vet J; 2021 Mar 19; 53(2):316-323. PubMed ID: 32654228
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  • 10. Congenital stationary night blindness in a Thoroughbred and a Paso Fino.
    Nunnery C, Pickett JP, Zimmerman KL.
    Vet Ophthalmol; 2005 Mar 19; 8(6):415-9. PubMed ID: 16359365
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  • 11. Congenital stationary night blindness: an animal model.
    Witzel DA, Smith EL, Wilson RD, Aguirre GD.
    Invest Ophthalmol Vis Sci; 1978 Aug 19; 17(8):788-95. PubMed ID: 308060
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  • 13. 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.
    Anim Genet; 2020 Feb 19; 51(1):111-116. PubMed ID: 31793009
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  • 16. Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness.
    Nakamura M, Ito S, Terasaki H, Miyake Y.
    Invest Ophthalmol Vis Sci; 2001 Jun 19; 42(7):1610-6. PubMed ID: 11381068
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  • 17. Behavioral phenotypic properties of a natural occurring rat model of congenital stationary night blindness with Cacna1f mutation.
    An J, Wang L, Guo Q, Li L, Xia F, Zhang Z.
    J Neurogenet; 2012 Sep 19; 26(3-4):363-73. PubMed ID: 22800190
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  • 18. An equine chromosome 3 inversion is associated with the tobiano spotting pattern in German horse breeds.
    Haase B, Jude R, Brooks SA, Leeb T.
    Anim Genet; 2008 Jun 19; 39(3):306-9. PubMed ID: 18410476
    [Abstract] [Full Text] [Related]

  • 19. Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanisms.
    Zeitz C, Robson AG, Audo I.
    Prog Retin Eye Res; 2015 Mar 19; 45():58-110. PubMed ID: 25307992
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  • 20. Mutations in NYX of individuals with high myopia, but without night blindness.
    Zhang Q, Xiao X, Li S, Jia X, Yang Z, Huang S, Caruso RC, Guan T, Sergeev Y, Guo X, Hejtmancik JF.
    Mol Vis; 2007 Mar 01; 13():330-6. PubMed ID: 17392683
    [Abstract] [Full Text] [Related]

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