PubMed (OMIM) for id: 2911

Year	Number of Results
1994	3
1995	1
1996	1
1997	1
1998	1
2000	5
2001	1
2003	3
2005	1
2007	2
2012	1
2014	1
2015	1
2017	1
2019	1
2024	0

1

A novel truncating variant p.(Arg297*) in the GRM1 gene causing autosomal-recessive cerebellar ataxia with juvenile-onset.

Cabet S, Putoux A, Carneiro M, Labalme A, Sanlaville D, Guibaud L, Lesca G. Cabet S, et al. Eur J Med Genet. 2019 Oct;62(10):103726. doi: 10.1016/j.ejmg.2019.103726. Epub 2019 Jul 15. Eur J Med Genet. 2019. PMID: 31319223

2

Homer1a drives homeostatic scaling-down of excitatory synapses during sleep.

Diering GH, Nirujogi RS, Roth RH, Worley PF, Pandey A, Huganir RL. Diering GH, et al. Science. 2017 Feb 3;355(6324):511-515. doi: 10.1126/science.aai8355. Epub 2017 Feb 2. Science. 2017. PMID: 28154077 Free PMC article.

3

The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families.

Davarniya B, Hu H, Kahrizi K, Musante L, Fattahi Z, Hosseini M, Maqsoud F, Farajollahi R, Wienker TF, Ropers HH, Najmabadi H. Davarniya B, et al. PLoS One. 2015 Aug 26;10(8):e0129631. doi: 10.1371/journal.pone.0129631. eCollection 2015. PLoS One. 2015. PMID: 26308914 Free PMC article.

4

Structure of a class C GPCR metabotropic glutamate receptor 1 bound to an allosteric modulator.

Wu H, Wang C, Gregory KJ, Han GW, Cho HP, Xia Y, Niswender CM, Katritch V, Meiler J, Cherezov V, Conn PJ, Stevens RC. Wu H, et al. Science. 2014 Apr 4;344(6179):58-64. doi: 10.1126/science.1249489. Epub 2014 Mar 6. Science. 2014. PMID: 24603153 Free PMC article.

5

Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1.

Guergueltcheva V, Azmanov DN, Angelicheva D, Smith KR, Chamova T, Florez L, Bynevelt M, Nguyen T, Cherninkova S, Bojinova V, Kaprelyan A, Angelova L, Morar B, Chandler D, Kaneva R, Bahlo M, Tournev I, Kalaydjieva L. Guergueltcheva V, et al. Am J Hum Genet. 2012 Sep 7;91(3):553-64. doi: 10.1016/j.ajhg.2012.07.019. Epub 2012 Aug 16. Am J Hum Genet. 2012. PMID: 22901947 Free PMC article.

6

The mouse mutants recoil wobbler and nmf373 represent a series of Grm1 mutations.

Sachs AJ, Schwendinger JK, Yang AW, Haider NB, Nystuen AM. Sachs AJ, et al. Mamm Genome. 2007 Nov;18(11):749-56. doi: 10.1007/s00335-007-9064-y. Epub 2007 Oct 13. Mamm Genome. 2007. PMID: 17934773

7

Genetic analysis of the GRM1 gene in human melanoma susceptibility.

Ortiz P, Vanaclocha F, López-Bran E, Esquivias JI, López-Estebaranz JL, Martín-González M, Arrue I, García-Romero D, Ochoa C, González-Perez A, Ruiz A, Real LM. Ortiz P, et al. Eur J Hum Genet. 2007 Nov;15(11):1176-82. doi: 10.1038/sj.ejhg.5201887. Epub 2007 Jul 4. Eur J Hum Genet. 2007. PMID: 17609672

8

The gene repertoire and the common evolutionary history of glutamate, pheromone (V2R), taste(1) and other related G protein-coupled receptors.

Bjarnadóttir TK, Fredriksson R, Schiöth HB. Bjarnadóttir TK, et al. Gene. 2005 Dec 5;362:70-84. doi: 10.1016/j.gene.2005.07.029. Epub 2005 Oct 17. Gene. 2005. PMID: 16229975

9

Activation of the TRPC1 cation channel by metabotropic glutamate receptor mGluR1.

Kim SJ, Kim YS, Yuan JP, Petralia RS, Worley PF, Linden DJ. Kim SJ, et al. Nature. 2003 Nov 20;426(6964):285-91. doi: 10.1038/nature02162. Epub 2003 Nov 12. Nature. 2003. PMID: 14614461

10

PI3 kinase enhancer-Homer complex couples mGluRI to PI3 kinase, preventing neuronal apoptosis.

Rong R, Ahn JY, Huang H, Nagata E, Kalman D, Kapp JA, Tu J, Worley PF, Snyder SH, Ye K. Rong R, et al. Nat Neurosci. 2003 Nov;6(11):1153-61. doi: 10.1038/nn1134. Epub 2003 Oct 5. Nat Neurosci. 2003. PMID: 14528310

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