Ikeda S - Search Results

1

Modulation of Tmem135 Leads to Retinal Pigmented Epithelium Pathologies in Mice.

Landowski M, Grindel S, Shahi PK, Johnson A, Western D, Race A, Shi F, Benson J, Gao M, Santoirre E, Lee WH, Ikeda S, Pattnaik BR, Ikeda A. Landowski M, et al. Among authors: ikeda s, ikeda a. Invest Ophthalmol Vis Sci. 2020 Oct 1;61(12):16. doi: 10.1167/iovs.61.12.16. Invest Ophthalmol Vis Sci. 2020. PMID: 33064130 Free PMC article.

2

Cell-specific expression of tubby gene family members (tub, Tulp1,2, and 3) in the retina.

Ikeda S, He W, Ikeda A, Naggert JK, North MA, Nishina PM. Ikeda S, et al. Among authors: ikeda a. Invest Ophthalmol Vis Sci. 1999 Oct;40(11):2706-12. Invest Ophthalmol Vis Sci. 1999. PMID: 10509669

3

Towards understanding the function of the tubby gene family in the retina.

Ikeda S, Ikeda A, Naggert JK, Nishina PM. Ikeda S, et al. Among authors: ikeda a. Adv Exp Med Biol. 2003;533:309-14. doi: 10.1007/978-1-4615-0067-4_38. Adv Exp Med Biol. 2003. PMID: 15180278 Review. No abstract available.

4

Reduced synaptic vesicle density and aberrant synaptic localization caused by a splice site mutation in the Rs1h gene.

Johnson BA, Ikeda S, Pinto LH, Ikeda A. Johnson BA, et al. Among authors: ikeda s, ikeda a. Vis Neurosci. 2006 Nov-Dec;23(6):887-98. doi: 10.1017/S0952523806230244. Vis Neurosci. 2006. PMID: 17266781

5

Genetic modification of the schisis phenotype in a mouse model of X-linked retinoschisis.

Johnson BA, Aoyama N, Friedell NH, Ikeda S, Ikeda A. Johnson BA, et al. Among authors: ikeda s, ikeda a. Genetics. 2008 Mar;178(3):1785-94. doi: 10.1534/genetics.107.084905. Epub 2008 Feb 3. Genetics. 2008. PMID: 18245825 Free PMC article.

6

Effect of destrin mutations on the gene expression profile in vivo.

Verdoni AM, Aoyama N, Ikeda A, Ikeda S. Verdoni AM, et al. Among authors: ikeda s, ikeda a. Physiol Genomics. 2008 Jun 12;34(1):9-21. doi: 10.1152/physiolgenomics.00285.2007. Epub 2008 Apr 1. Physiol Genomics. 2008. PMID: 18381839 Free PMC article.

7

Defects in actin dynamics lead to an autoinflammatory condition through the upregulation of CXCL5.

Verdoni AM, Smith RS, Ikeda A, Ikeda S. Verdoni AM, et al. Among authors: ikeda s, ikeda a. PLoS One. 2008 Jul 16;3(7):e2701. doi: 10.1371/journal.pone.0002701. PLoS One. 2008. PMID: 18628996 Free PMC article.

8

Serum response factor is essential for the proper development of skin epithelium.

Verdoni AM, Ikeda S, Ikeda A. Verdoni AM, et al. Among authors: ikeda s, ikeda a. Mamm Genome. 2010 Feb;21(1-2):64-76. doi: 10.1007/s00335-009-9245-y. Epub 2010 Jan 3. Mamm Genome. 2010. PMID: 20047077 Free PMC article.

9

Mutation in archain 1, a subunit of COPI coatomer complex, causes diluted coat color and Purkinje cell degeneration.

Xu X, Kedlaya R, Higuchi H, Ikeda S, Justice MJ, Setaluri V, Ikeda A. Xu X, et al. Among authors: ikeda s, ikeda a. PLoS Genet. 2010 May 20;6(5):e1000956. doi: 10.1371/journal.pgen.1000956. PLoS Genet. 2010. PMID: 20502676 Free PMC article.

10

A pathogenic relationship between a regulator of the actin cytoskeleton and serum response factor.

Verdoni AM, Schuster KJ, Cole BS, Ikeda A, Kao WW, Ikeda S. Verdoni AM, et al. Among authors: ikeda s, ikeda a. Genetics. 2010 Sep;186(1):147-57. doi: 10.1534/genetics.110.117309. Epub 2010 Jul 6. Genetics. 2010. PMID: 20610412 Free PMC article.

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