These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

270 related items for PubMed ID: 28490646

  • 1. 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]

  • 2. Reduced expression of the nob8 gene does not normalize the distribution or function of mGluR6 in the mouse retina.
    Kinoshita J, Hasan N, Bell BA, Peachey NS.
    Mol Vis; 2019 Aug 01; 25():890-901. PubMed ID: 32025181
    [Abstract] [Full Text] [Related]

  • 3. 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]

  • 4. Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness.
    Qian H, Ji R, Gregg RG, Peachey NS.
    Vis Neurosci; 2015 Jan 01; 32():E004. PubMed ID: 26241901
    [Abstract] [Full Text] [Related]

  • 5. GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.
    Peachey NS, Ray TA, Florijn R, Rowe LB, Sjoerdsma T, Contreras-Alcantara S, Baba K, Tosini G, Pozdeyev N, Iuvone PM, Bojang P, Pearring JN, Simonsz HJ, van Genderen M, Birch DG, Traboulsi EI, Dorfman A, Lopez I, Ren H, Goldberg AF, Nishina PM, Lachapelle P, McCall MA, Koenekoop RK, Bergen AA, Kamermans M, Gregg RG.
    Am J Hum Genet; 2012 Feb 10; 90(2):331-9. PubMed ID: 22325362
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. 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]

  • 8. 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 Mar 01; 10(9):e0137072. PubMed ID: 26368928
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.
    Peachey NS, Pearring JN, Bojang P, Hirschtritt ME, Sturgill-Short G, Ray TA, Furukawa T, Koike C, Goldberg AF, Shen Y, McCall MA, Nawy S, Nishina PM, Gregg RG.
    J Neurophysiol; 2012 Nov 23; 108(9):2442-51. PubMed ID: 22896717
    [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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindness.
    Gregg RG, Kamermans M, Klooster J, Lukasiewicz PD, Peachey NS, Vessey KA, McCall MA.
    J Neurophysiol; 2007 Nov 09; 98(5):3023-33. PubMed ID: 17881478
    [Abstract] [Full Text] [Related]

  • 15. Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindness.
    Naeem MA, Gottsch AD, Ullah I, Khan SN, Husnain T, Butt NH, Qazi ZA, Akram J, Riazuddin S, Ayyagari R, Hejtmancik JF, Riazuddin SA.
    Mol Vis; 2015 Nov 09; 21():1261-71. PubMed ID: 26628857
    [Abstract] [Full Text] [Related]

  • 16. Presence of the Gpr179(nob5) allele in a C3H-derived transgenic mouse.
    Balmer J, Ji R, Ray TA, Selber F, Gassmann M, Peachey NS, Gregg RG, Enzmann V.
    Mol Vis; 2013 Nov 09; 19():2615-25. PubMed ID: 24415894
    [Abstract] [Full Text] [Related]

  • 17. A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene.
    Sergouniotis PI, Robson AG, Li Z, Devery S, Holder GE, Moore AT, Webster AR.
    Acta Ophthalmol; 2012 May 09; 90(3):e192-7. PubMed ID: 22008250
    [Abstract] [Full Text] [Related]

  • 18. Ultrastructural localization of GPR179 and the impact of mutant forms on retinal function in CSNB1 patients and a mouse model.
    Klooster J, van Genderen MM, Yu M, Florijn RJ, Riemslag FC, Bergen AA, Gregg RG, Peachey NS, Kamermans M.
    Invest Ophthalmol Vis Sci; 2013 Oct 23; 54(10):6973-81. PubMed ID: 24084093
    [Abstract] [Full Text] [Related]

  • 19. 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 Oct 23; 94(7-9):420-7. PubMed ID: 26111660
    [Abstract] [Full Text] [Related]

  • 20. GPR179 is required for high sensitivity of the mGluR6 signaling cascade in depolarizing bipolar cells.
    Ray TA, Heath KM, Hasan N, Noel JM, Samuels IS, Martemyanov KA, Peachey NS, McCall MA, Gregg RG.
    J Neurosci; 2014 Apr 30; 34(18):6334-43. PubMed ID: 24790204
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.