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Masaki Iwanami

Showing results (1-10 of 6) with videos related to

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Genes to Cells : Devoted to Molecular & Cellular Mechanisms|June 22, 2005
Cell-type specific utilization of multiple negative feedback loops generates developmental constancyMasaki Iwanami, Yasushi Hiromi, Masataka Okabe
Investigative Ophthalmology & Visual Science|February 4, 2012
High prevalence of mutations in the EYS gene in Japanese patients with autosomal recessive retinitis pigmentosaMasaki Iwanami, Mio Oshikawa, Tomomi Nishida, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 24, 2013
Comparison of LogMAR Eye charts with angular vision for visually impaired: the Berkeley rudimentary vision test vs LogMAR One target Landolt ring Eye chartMarie Miwa, Masaki Iwanami, Mari S Oba, et al.
Stem Cell Research & Therapy|April 12, 2022
Evaluation of photoreceptor-directed fibroblasts derived from retinitis pigmentosa patients with defects in the EYS gene: a possible cost-effective cellular model for mechanism-oriented drugDilip Rai, Masaki Iwanami, Yoriko Takahashi, et al.
Stem Cell Research & Therapy|October 26, 2018
The manner of decay of genetically defective EYS gene transcripts in photoreceptor-directed fibroblasts derived from retinitis pigmentosa patients depends on the type of mutationYuko Seko, Masaki Iwanami, Kiyoko Miyamoto-Matsui, et al.
Molecular Vision|December 10, 2019
Five major sequence variants and copy number variants in the <i>EYS</i> gene account for one-third of Japanese patients with autosomal recessive and simplex retinitis pigmentosaMasaki Iwanami, Akio Oishi, Ken Ogino, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|June 22, 2005
Cell-type specific utilization of multiple negative feedback loops generates developmental constancyMasaki Iwanami, Yasushi Hiromi, Masataka Okabe
Investigative Ophthalmology & Visual Science|February 4, 2012
High prevalence of mutations in the EYS gene in Japanese patients with autosomal recessive retinitis pigmentosaMasaki Iwanami, Mio Oshikawa, Tomomi Nishida, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 24, 2013
Comparison of LogMAR Eye charts with angular vision for visually impaired: the Berkeley rudimentary vision test vs LogMAR One target Landolt ring Eye chartMarie Miwa, Masaki Iwanami, Mari S Oba, et al.
Stem Cell Research & Therapy|April 12, 2022
Evaluation of photoreceptor-directed fibroblasts derived from retinitis pigmentosa patients with defects in the EYS gene: a possible cost-effective cellular model for mechanism-oriented drugDilip Rai, Masaki Iwanami, Yoriko Takahashi, et al.
Stem Cell Research & Therapy|October 26, 2018
The manner of decay of genetically defective EYS gene transcripts in photoreceptor-directed fibroblasts derived from retinitis pigmentosa patients depends on the type of mutationYuko Seko, Masaki Iwanami, Kiyoko Miyamoto-Matsui, et al.
Molecular Vision|December 10, 2019
Five major sequence variants and copy number variants in the <i>EYS</i> gene account for one-third of Japanese patients with autosomal recessive and simplex retinitis pigmentosaMasaki Iwanami, Akio Oishi, Ken Ogino, et al.
Pageof 1