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277 related items for PubMed ID: 23425697

  • 1. Visual signal pathway reorganization in the Cacna1f mutant rat model.
    Tao Y, Chen T, Liu B, Xue JH, Zhang L, Xia F, Pang JJ, Zhang ZM.
    Invest Ophthalmol Vis Sci; 2013 Mar 19; 54(3):1988-97. PubMed ID: 23425697
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  • 2. 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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  • 3. A Naturally Occurring Canine Model of Autosomal Recessive Congenital Stationary Night Blindness.
    Kondo M, Das G, Imai R, Santana E, Nakashita T, Imawaka M, Ueda K, Ohtsuka H, Sakai K, Aihara T, Kato K, Sugimoto M, Ueno S, Nishizawa Y, Aguirre GD, Miyadera K.
    PLoS One; 2015 Sep 19; 10(9):e0137072. PubMed ID: 26368928
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  • 4. Cacna1f gene decreased contractility of skeletal muscle in rat model with congenital stationary night blindness.
    An J, Zhang L, Jiao B, Lu F, Xia F, Yu Z, Zhang Z.
    Gene; 2015 May 15; 562(2):210-9. PubMed ID: 25748727
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  • 9. Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A).
    Waldner DM, Giraldo Sierra NC, Bonfield S, Nguyen L, Dimopoulos IS, Sauvé Y, Stell WK, Bech-Hansen NT.
    Channels (Austin); 2018 Jan 01; 12(1):17-33. PubMed ID: 29179637
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  • 10. Keeping the balance.
    Tom Dieck S.
    Channels (Austin); 2013 Jan 01; 7(6):418-9. PubMed ID: 24722264
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  • 11. Congenital stationary night blindness in mice - a tale of two Cacna1f mutants.
    Lodha N, Bonfield S, Orton NC, Doering CJ, McRory JE, Mema SC, Rehak R, Sauvé Y, Tobias R, Stell WK, Bech-Hansen NT.
    Adv Exp Med Biol; 2010 Jan 01; 664():549-58. PubMed ID: 20238058
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  • 12. 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 01; 42(7):1610-6. PubMed ID: 11381068
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  • 13. Photoreceptor degeneration in two mouse models for congenital stationary night blindness type 2.
    Regus-Leidig H, Atorf J, Feigenspan A, Kremers J, Maw MA, Brandstätter JH.
    PLoS One; 2014 Jun 01; 9(1):e86769. PubMed ID: 24466230
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  • 14. Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics.
    Dinet V, Ciccotosto GD, Delaunay K, Borras C, Ranchon-Cole I, Kostic C, Savoldelli M, El Sanharawi M, Jonet L, Pirou C, An N, Abitbol M, Arsenijevic Y, Behar-Cohen F, Cappai R, Mascarelli F.
    Mol Brain; 2016 Jun 08; 9(1):64. PubMed ID: 27267879
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  • 15. Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer.
    Al Oreany AA, Al Hadlaq A, Schatz P.
    Graefes Arch Clin Exp Ophthalmol; 2016 Oct 08; 254(10):1951-1956. PubMed ID: 27084085
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  • 17. Novel truncating mutation in CACNA1F in a young male patient diagnosed with optic atrophy.
    Pasutto F, Ekici A, Reis A, Kremers J, Huchzermeyer C.
    Ophthalmic Genet; 2018 Dec 08; 39(6):741-748. PubMed ID: 30260717
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  • 18. Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindness.
    Orhan E, Prézeau L, El Shamieh S, Bujakowska KM, Michiels C, Zagar Y, Vol C, Bhattacharya SS, Sahel JA, Sennlaub F, Audo I, Zeitz C.
    Invest Ophthalmol Vis Sci; 2013 Dec 09; 54(13):8041-50. PubMed ID: 24222301
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  • 19. A novel p.Gly603Arg mutation in CACNA1F causes Åland island eye disease and incomplete congenital stationary night blindness phenotypes in a family.
    Vincent A, Wright T, Day MA, Westall CA, Héon E.
    Mol Vis; 2011 Dec 09; 17():3262-70. PubMed ID: 22194652
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  • 20. Dysregulation of Ca(v)1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2.
    Liu X, Kerov V, Haeseleer F, Majumder A, Artemyev N, Baker SA, Lee A.
    Channels (Austin); 2013 Dec 09; 7(6):514-23. PubMed ID: 24064553
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