PubMed (RefSeq) for id: 1395442027

Year	Number of Results
1996	1
1997	1
2000	1
2001	1
2005	3
2006	1
2007	1
2008	1
2009	4
2010	2
2011	3
2012	3
2013	3
2015	2
2016	2
2017	2
2019	2
2024	0

1

Pseudodominant inheritance of autosomal recessive congenital stationary night blindness in one family with three co-segregating deleterious GRM6 variants identified by next-generation sequencing.

Liu HY, Huang J, Xiao H, Zhang MJ, Shi FF, Jiang YH, Du H, He Q, Wang ZY. Liu HY, et al. Mol Genet Genomic Med. 2019 Dec;7(12):e952. doi: 10.1002/mgg3.952. Epub 2019 Nov 2. Mol Genet Genomic Med. 2019. PMID: 31677249 Free PMC article.

2

Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness.

Tourville A, Michiels C, Condroyer C, Meunier A, Cordonnier M, Sahel JA, Audo I, Abramowicz M, Zeitz C. Tourville A, et al. Ophthalmic Genet. 2019 Apr;40(2):182-184. doi: 10.1080/13816810.2019.1605389. Ophthalmic Genet. 2019. PMID: 31063016 No abstract available.

3

Meclofenamic acid improves the signal to noise ratio for visual responses produced by ectopic expression of human rod opsin.

Eleftheriou CG, Cehajic-Kapetanovic J, Martial FP, Milosavljevic N, Bedford RA, Lucas RJ. Eleftheriou CG, et al. Mol Vis. 2017 Jun 16;23:334-345. eCollection 2017. Mol Vis. 2017. PMID: 28659709 Free PMC article.

4

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. Dan H, et al. Ophthalmic Genet. 2017 May-Jun;38(3):206-210. doi: 10.1080/13816810.2016.1193876. Epub 2016 Jul 18. Ophthalmic Genet. 2017. PMID: 27428514

5

Association of ZNF644, GRM6, and CTNND2 genes with high myopia in the Han Chinese population: Jiangsu Eye Study.

Wang H, Su S, Yang M, Hu N, Yao Y, Zhu R, Zhou J, Liang C, Guan H. Wang H, et al. Eye (Lond). 2016 Jul;30(7):1017-22. doi: 10.1038/eye.2016.8. Epub 2016 Apr 1. Eye (Lond). 2016. PMID: 27034204 Free PMC article.

6

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. Naeem MA, et al. Mol Vis. 2015 Oct 31;21:1261-71. eCollection 2015. Mol Vis. 2015. PMID: 26628857 Free PMC article.

7

SR protein kinases promote splicing of nonconsensus introns.

Lipp JJ, Marvin MC, Shokat KM, Guthrie C. Lipp JJ, et al. Nat Struct Mol Biol. 2015 Aug;22(8):611-7. doi: 10.1038/nsmb.3057. Epub 2015 Jul 13. Nat Struct Mol Biol. 2015. PMID: 26167880

8

Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.

Bijveld MM, Florijn RJ, Bergen AA, van den Born LI, Kamermans M, Prick L, Riemslag FC, van Schooneveld MJ, Kappers AM, van Genderen MM. Bijveld MM, et al. Ophthalmology. 2013 Oct;120(10):2072-81. doi: 10.1016/j.ophtha.2013.03.002. Epub 2013 May 25. Ophthalmology. 2013. PMID: 23714322

9

Metabotropic glutamate receptor 6 signaling enhances TRPM1 calcium channel function and increases melanin content in human melanocytes.

Devi S, Markandeya Y, Maddodi N, Dhingra A, Vardi N, Balijepalli RC, Setaluri V. Devi S, et al. Pigment Cell Melanoma Res. 2013 May;26(3):348-56. doi: 10.1111/pcmr.12083. Epub 2013 Mar 27. Pigment Cell Melanoma Res. 2013. PMID: 23452348 Free PMC article.

10

Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.

Cousminer DL, Berry DJ, Timpson NJ, Ang W, Thiering E, Byrne EM, Taal HR, Huikari V, Bradfield JP, Kerkhof M, Groen-Blokhuis MM, Kreiner-Møller E, Marinelli M, Holst C, Leinonen JT, Perry JR, Surakka I, Pietiläinen O, Kettunen J, Anttila V, Kaakinen M, Sovio U, Pouta A, Das S, Lagou V, Power C, Prokopenko I, Evans DM, Kemp JP, St Pourcain B, Ring S, Palotie A, Kajantie E, Osmond C, Lehtimäki T, Viikari JS, Kähönen M, Warrington NM, Lye SJ, Palmer LJ, Tiesler CM, Flexeder C, Montgomery GW, Medland SE, Hofman A, Hakonarson H, Guxens M, Bartels M, Salomaa V; ReproGen Consortium; Murabito JM, Kaprio J, Sørensen TI, Ballester F, Bisgaard H, Boomsma DI, Koppelman GH, Grant SF, Jaddoe VW, Martin NG, Heinrich J, Pennell CE, Raitakari OT, Eriksson JG, Smith GD, Hyppönen E, Järvelin MR, McCarthy MI, Ripatti S, Widén E; Early Growth Genetics (EGG) Consortium. Cousminer DL, et al. Hum Mol Genet. 2013 Jul 1;22(13):2735-47. doi: 10.1093/hmg/ddt104. Epub 2013 Feb 27. Hum Mol Genet. 2013. PMID: 23449627 Free PMC article.

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