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A smartphone based method for mouse fundus imaging.
Peng M, Park B, Harikrishnan H, Jahan SN, Dai J, Rayana NP, Sugali CK, Sharma TP, Imanishi S, Imanishi Y, Corson TW, Mao W. Peng M, et al. Among authors: imanishi y, imanishi s. Exp Eye Res. 2021 May;206:108530. doi: 10.1016/j.exer.2021.108530. Epub 2021 Mar 3. Exp Eye Res. 2021. PMID: 33675778 Free PMC article. Review.
Müller glia phagocytose dead photoreceptor cells in a mouse model of retinal degenerative disease.
Sakami S, Imanishi Y, Palczewski K. Sakami S, et al. Among authors: imanishi y. FASEB J. 2019 Mar;33(3):3680-3692. doi: 10.1096/fj.201801662R. Epub 2018 Nov 21. FASEB J. 2019. PMID: 30462532 Free PMC article.
Taken together, the phagocytic function of Muller glia is responsible for retinal homeostasis and reorganization under normal and pathologic conditions.-Sakami, S., Imanishi, Y., Palczewski, K. Muller glia phagocytose dead photoreceptor cells in a mouse model of ret …
Taken together, the phagocytic function of Muller glia is responsible for retinal homeostasis and reorganization under normal and pathologic …
Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton.
Tian G, Zhou Y, Hajkova D, Miyagi M, Dinculescu A, Hauswirth WW, Palczewski K, Geng R, Alagramam KN, Isosomppi J, Sankila EM, Flannery JG, Imanishi Y. Tian G, et al. Among authors: imanishi y. J Biol Chem. 2009 Jul 10;284(28):18980-93. doi: 10.1074/jbc.M109.003160. Epub 2009 May 7. J Biol Chem. 2009. PMID: 19423712 Free PMC article.
A small molecule mitigates hearing loss in a mouse model of Usher syndrome III.
Alagramam KN, Gopal SR, Geng R, Chen DH, Nemet I, Lee R, Tian G, Miyagi M, Malagu KF, Lock CJ, Esmieu WR, Owens AP, Lindsay NA, Ouwehand K, Albertus F, Fischer DF, Bürli RW, MacLeod AM, Harte WE, Palczewski K, Imanishi Y. Alagramam KN, et al. Among authors: imanishi y. Nat Chem Biol. 2016 Jun;12(6):444-51. doi: 10.1038/nchembio.2069. Epub 2016 Apr 25. Nat Chem Biol. 2016. PMID: 27110679 Free PMC article.
Autosomal recessive retinitis pigmentosa and E150K mutation in the opsin gene.
Zhu L, Imanishi Y, Filipek S, Alekseev A, Jastrzebska B, Sun W, Saperstein DA, Palczewski K. Zhu L, et al. Among authors: imanishi y. J Biol Chem. 2006 Aug 4;281(31):22289-22298. doi: 10.1074/jbc.M602664200. Epub 2006 May 31. J Biol Chem. 2006. PMID: 16737970 Free PMC article.
632 results