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Journal Abstract Search


204 related items for PubMed ID: 17405131

  • 1. Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking.
    Zeitz C, Forster U, Neidhardt J, Feil S, Kälin S, Leifert D, Flor PJ, Berger W.
    Hum Mutat; 2007 Aug; 28(8):771-80. PubMed ID: 17405131
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  • 4. Structures of the extracellular regions of the group II/III metabotropic glutamate receptors.
    Muto T, Tsuchiya D, Morikawa K, Jingami H.
    Proc Natl Acad Sci U S A; 2007 Mar 06; 104(10):3759-64. PubMed ID: 17360426
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  • 5. 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 06; 90(3):e192-7. PubMed ID: 22008250
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  • 7. Natural mutations of the anti-Mullerian hormone type II receptor found in persistent Mullerian duct syndrome affect ligand binding, signal transduction and cellular transport.
    Belville C, Maréchal JD, Pennetier S, Carmillo P, Masgrau L, Messika-Zeitoun L, Galey J, Machado G, Treton D, Gonzalès J, Picard JY, Josso N, Cate RL, di Clemente N.
    Hum Mol Genet; 2009 Aug 15; 18(16):3002-13. PubMed ID: 19457927
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  • 8. Molecular determinants of metabotropic glutamate receptor 1B trafficking.
    Chan WY, Soloviev MM, Ciruela F, McIlhinney RA.
    Mol Cell Neurosci; 2001 Mar 15; 17(3):577-88. PubMed ID: 11273651
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  • 9. The G protein-coupling profile of metabotropic glutamate receptors, as determined with exogenous G proteins, is independent of their ligand recognition domain.
    Parmentier ML, Joly C, Restituito S, Bockaert J, Grau Y, Pin JP.
    Mol Pharmacol; 1998 Apr 15; 53(4):778-86. PubMed ID: 9547371
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  • 11. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
    Bech-Hansen NT, Naylor MJ, Maybaum TA, Sparkes RL, Koop B, Birch DG, Bergen AA, Prinsen CF, Polomeno RC, Gal A, Drack AV, Musarella MA, Jacobson SG, Young RS, Weleber RG.
    Nat Genet; 2000 Nov 15; 26(3):319-23. PubMed ID: 11062471
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