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5. TRPM1 mutations are associated with the complete form of congenital stationary night blindness. Nakamura M; Sanuki R; Yasuma TR; Onishi A; Nishiguchi KM; Koike C; Kadowaki M; Kondo M; Miyake Y; Furukawa T Mol Vis; 2010 Mar; 16():425-37. PubMed ID: 20300565 [TBL] [Abstract][Full Text] [Related]
6. TRPM1 is a component of the retinal ON bipolar cell transduction channel in the mGluR6 cascade. Koike C; Obara T; Uriu Y; Numata T; Sanuki R; Miyata K; Koyasu T; Ueno S; Funabiki K; Tani A; Ueda H; Kondo M; Mori Y; Tachibana M; Furukawa T Proc Natl Acad Sci U S A; 2010 Jan; 107(1):332-7. PubMed ID: 19966281 [TBL] [Abstract][Full Text] [Related]
7. TRPM1: the endpoint of the mGluR6 signal transduction cascade in retinal ON-bipolar cells. Morgans CW; Brown RL; Duvoisin RM Bioessays; 2010 Jul; 32(7):609-14. PubMed ID: 20544736 [TBL] [Abstract][Full Text] [Related]
8. TRPM1: new trends for an old TRP. Oancea E; Wicks NL Adv Exp Med Biol; 2011; 704():135-45. PubMed ID: 21290293 [TBL] [Abstract][Full Text] [Related]
9. 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; 94(7-9):420-7. PubMed ID: 26111660 [TBL] [Abstract][Full Text] [Related]
10. TRPM8. Almaraz L; Manenschijn JA; de la Peña E; Viana F Handb Exp Pharmacol; 2014; 222():547-79. PubMed ID: 24756721 [TBL] [Abstract][Full Text] [Related]
11. G-protein-mediated inhibition of the Trp channel TRPM1 requires the Gβγ dimer. Shen Y; Rampino MA; Carroll RC; Nawy S Proc Natl Acad Sci U S A; 2012 May; 109(22):8752-7. PubMed ID: 22586107 [TBL] [Abstract][Full Text] [Related]
12. The TRPM1 Channel Is Required for Development of the Rod ON Bipolar Cell-AII Amacrine Cell Pathway in the Retinal Circuit. Kozuka T; Chaya T; Tamalu F; Shimada M; Fujimaki-Aoba K; Kuwahara R; Watanabe SI; Furukawa T J Neurosci; 2017 Oct; 37(41):9889-9900. PubMed ID: 28899920 [TBL] [Abstract][Full Text] [Related]
13. Redundant contribution of a Transient Receptor Potential cation channel Member 1 exon 11 single nucleotide polymorphism to equine congenital stationary night blindness. Scott ML; John EE; Bellone RR; Ching JC; Loewen ME; Sandmeyer LS; Grahn BH; Forsyth GW BMC Vet Res; 2016 Jun; 12(1):121. PubMed ID: 27329127 [TBL] [Abstract][Full Text] [Related]
14. TRPM2. Faouzi M; Penner R Handb Exp Pharmacol; 2014; 222():403-26. PubMed ID: 24756715 [TBL] [Abstract][Full Text] [Related]
15. 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; 34(18):6334-43. PubMed ID: 24790204 [TBL] [Abstract][Full Text] [Related]
16. Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses. Bellone RR; Forsyth G; Leeb T; Archer S; Sigurdsson S; Imsland F; Mauceli E; Engensteiner M; Bailey E; Sandmeyer L; Grahn B; Lindblad-Toh K; Wade CM Brief Funct Genomics; 2010 May; 9(3):193-207. PubMed ID: 20353955 [TBL] [Abstract][Full Text] [Related]
18. Identification of autoantibodies against TRPM1 in patients with paraneoplastic retinopathy associated with ON bipolar cell dysfunction. Kondo M; Sanuki R; Ueno S; Nishizawa Y; Hashimoto N; Ohguro H; Yamamoto S; Machida S; Terasaki H; Adamus G; Furukawa T PLoS One; 2011; 6(5):e19911. PubMed ID: 21611200 [TBL] [Abstract][Full Text] [Related]
19. 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; 42(3):1966-75. PubMed ID: 25997951 [TBL] [Abstract][Full Text] [Related]