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Journal Abstract Search

241 related items for PubMed ID: 28334377

  • 1. LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells.
    Neuillé M, Cao Y, Caplette R, Guerrero-Given D, Thomas C, Kamasawa N, Sahel JA, Hamel CP, Audo I, Picaud S, Martemyanov KA, Zeitz C.
    Invest Ophthalmol Vis Sci; 2017 Mar 01; 58(3):1768-1778. PubMed ID: 28334377
    [Abstract] [Full Text] [Related]

  • 2. LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation.
    Neuillé M, Morgans CW, Cao Y, Orhan E, Michiels C, Sahel JA, Audo I, Duvoisin RM, Martemyanov KA, Zeitz C.
    Eur J Neurosci; 2015 Aug 01; 42(3):1966-75. PubMed ID: 25997951
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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 Jun 08; 10(9):e0137072. PubMed ID: 26368928
    [Abstract] [Full Text] [Related]

  • 5. A missense mutation in Grm6 reduces but does not eliminate mGluR6 expression or rod depolarizing bipolar cell function.
    Peachey NS, Hasan N, FitzMaurice B, Burrill S, Pangeni G, Karst SY, Reinholdt L, Berry ML, Strobel M, Gregg RG, McCall MA, Chang B.
    J Neurophysiol; 2017 Aug 01; 118(2):845-854. PubMed ID: 28490646
    [Abstract] [Full Text] [Related]

  • 6. Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB).
    Neuillé M, El Shamieh S, Orhan E, Michiels C, Antonio A, Lancelot ME, Condroyer C, Bujakowska K, Poch O, Sahel JA, Audo I, Zeitz C.
    PLoS One; 2014 Aug 01; 9(3):e90342. PubMed ID: 24598786
    [Abstract] [Full Text] [Related]

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  • 8. Keeping the balance.
    Tom Dieck S.
    Channels (Austin); 2013 Aug 01; 7(6):418-9. PubMed ID: 24722264
    [Abstract] [Full Text] [Related]

  • 9. Extended functional rescue following AAV gene therapy in a canine model of LRIT3-congenital stationary night blindness.
    Takahashi K, Kwok JC, Sato Y, Aguirre GD, Miyadera K.
    Vision Res; 2023 Aug 01; 209():108260. PubMed ID: 37220680
    [Abstract] [Full Text] [Related]

  • 10. Different Activity Patterns in Retinal Ganglion Cells of TRPM1 and mGluR6 Knockout Mice.
    Takeuchi H, Horie S, Moritoh S, Matsushima H, Hori T, Kimori Y, Kitano K, Tsubo Y, Tachibana M, Koike C.
    Biomed Res Int; 2018 Aug 01; 2018():2963232. PubMed ID: 29854741
    [Abstract] [Full Text] [Related]

  • 11. Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness.
    Scalabrino ML, Boye SL, Fransen KM, Noel JM, Dyka FM, Min SH, Ruan Q, De Leeuw CN, Simpson EM, Gregg RG, McCall MA, Peachey NS, Boye SE.
    Hum Mol Genet; 2015 Nov 01; 24(21):6229-39. PubMed ID: 26310623
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Clinical characterisation of the CABP4-related retinal phenotype.
    Khan AO, Alrashed M, Alkuraya FS.
    Br J Ophthalmol; 2013 Mar 01; 97(3):262-5. PubMed ID: 23099293
    [Abstract] [Full Text] [Related]

  • 14. A New Mouse Model for Complete Congenital Stationary Night Blindness Due to Gpr179 Deficiency.
    Orhan E, Neuillé M, de Sousa Dias M, Pugliese T, Michiels C, Condroyer C, Antonio A, Sahel JA, Audo I, Zeitz C.
    Int J Mol Sci; 2021 Apr 23; 22(9):. PubMed ID: 33922602
    [Abstract] [Full Text] [Related]

  • 15. Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.
    Zeitz C, Jacobson SG, Hamel CP, Bujakowska K, Neuillé M, Orhan E, Zanlonghi X, Lancelot ME, Michiels C, Schwartz SB, Bocquet B, Congenital Stationary Night Blindness Consortium, Antonio A, Audier C, Letexier M, Saraiva JP, Luu TD, Sennlaub F, Nguyen H, Poch O, Dollfus H, Lecompte O, Kohl S, Sahel JA, Bhattacharya SS, Audo I.
    Am J Hum Genet; 2013 Jan 10; 92(1):67-75. PubMed ID: 23246293
    [Abstract] [Full Text] [Related]

  • 16. Restoration of mGluR6 Localization Following AAV-Mediated Delivery in a Mouse Model of Congenital Stationary Night Blindness.
    Varin J, Bouzidi N, Dias MMS, Pugliese T, Michiels C, Robert C, Desrosiers M, Sahel JA, Audo I, Dalkara D, Zeitz C.
    Invest Ophthalmol Vis Sci; 2021 Mar 01; 62(3):24. PubMed ID: 33729473
    [Abstract] [Full Text] [Related]

  • 17. Mutation screening of the LRIT3, CABP4, and GPR179 genes in Chinese patients with Schubert-Bornschein congenital stationary night blindness.
    Dan H, Song X, Li J, Xing Y, Li T.
    Ophthalmic Genet; 2017 Mar 01; 38(3):206-210. PubMed ID: 27428514
    [Abstract] [Full Text] [Related]

  • 18. Properties and functions of TRPM1 channels in the dendritic tips of retinal ON-bipolar cells.
    Schneider FM, Mohr F, Behrendt M, Oberwinkler J.
    Eur J Cell Biol; 2015 Mar 01; 94(7-9):420-7. PubMed ID: 26111660
    [Abstract] [Full Text] [Related]

  • 19. Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children.
    Miraldi Utz V, Pfeifer W, Longmuir SQ, Olson RJ, Wang K, Drack AV.
    JAMA Ophthalmol; 2018 Apr 01; 136(4):389-398. PubMed ID: 29522070
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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