Search | IOVS | ARVO Journals

iovs

Issues
Topics
For Authors
About
- Editorial Board

Journals Home

MANAGE ALERTS

Access Provided By:
MIT Libraries

Forgot password?

Create an Account

To View More...

Purchase this article with an account.

or

Subscribe Now

Issues
Topics
For Authors
About
- Editorial Board

Narrow View

NARROW

Content Type

Meeting Abstract (6)
Journal Articles (3)

Journal

Investigative Ophthalmology & Visual Science (9)

Article Type

ARVO Annual Meeting Abstract (6)
Glaucoma (2)
Biochemistry and Molecular Biology (1)

Topics

Eye Anatomy and Disorders (3)
Genetics (3)
Glaucoma (2)
Biochemistry and Molecular Biology (1)
Retina (1)

Tags

genes (3)
glaucoma (2)
japanese (2)
open-angle glaucoma (2)
polymorphism (2)
angiotensin receptor antagonists (1)
animals, transgenic (1)
electroretinography (1)
genotype (1)
genotype determination (1)

Specify Date Range

From: To: Apply

Showing 1 – 9 of 9

SORT: Best Match Most Recent Oldest

VIEW: Basic | Expanded

ARVO Annual Meeting Abstract April 2014

A novel exon 17 deletion mutation of RPGRIP1 gene in two siblings with Leber congenital amaurosis.

Takuro Fujimaki; Takahide Suzuki; Ai Yanagawa; Eisuke Arai; Keiko Fujiki; Yuko Wada; Akira Murakami

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3284.

ARVO Annual Meeting Abstract April 2014

Partial NMNAT1 deletions cause Leber Congenital Amaurosis

Frauke Coppieters; Takuro Fujimaki; Marieke De Bruyne; Annelot Baert; Mineo Kondo; Akira Murakami; Elfride De Baere

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):3285.

ARVO Annual Meeting Abstract June 2013

NMNAT1 p.Arg237Cys mutation in Japanese patients with Leber congenital amaurosis

Tomoka Kambe; Takuro Fujimaki; Shuri Kawamorita; Eisuke Arai; Ai Miyazaki; Keiko Fujiki; Fumino Iwata; Chieko Tamura; Akira Murakami

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1312.

ARVO Annual Meeting Abstract June 2013

Genetic and clinical features of FEVR and Norrie disease

Eisuke Arai; Takuro Fujimaki; Ai Miyazaki; Keiko Fujiki; Fumino Iwata; Takenori Inomata; Hiroyuki Kawano; Toshiyuki Yokoyama; Akihisa Okumura; Akira Murakami

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):1331.

ARVO Annual Meeting Abstract April 2011

Developmental Abnormality Of Schlemm's Canal In Primary Open Angle Glaucoma

Teruhiko Hamanaka; Akira Matsuda; Nobuo Ishida; Takuro Fujimaki; Akira Murakami

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):4668.

ARVO Annual Meeting Abstract April 2011

Genetic Analysis of Indonesian Patients with Retinitis Pigmentosa (RP)

Takuro Fujimaki; Arief S. Kartasasmita; Keiko Fujiki; Erwin Iskandar; Iwan Sovani; Akira Murakami

Invest. Ophthalmol. Vis. Sci.. 2011; 52(14):5393.

Glaucoma June 2005

Genetic Polymorphisms in the Angiotensin II Receptor Gene and Their Association with Open-Angle Glaucoma in a Japanese Population

PDF

Kouhei Hashizume; Yukihiko Mashima; Tomoyo Fumayama; Yuichiro Ohtake; Itaru Kimura; Kazuhide Yoshida; Karin Ishikawa; Noriko Yasuda; Takuro Fujimaki; Ryo Asaoka; Takahisa Koga; Takashi Kanamoto; Takeo Fukuchi; Koichi Miyaki
TAGS: genes, genotype, glaucoma, intraocular pressure, japanese, open-angle glaucoma, polymorphism, receptor, angiotensin ii, angiotensin receptor antagonists
Invest. Ophthalmol. Vis. Sci.. 2005; 46(6):1993-2001. https://doi.org/10.1167/iovs.04-1100

Glaucoma December 2004

Variants in Optineurin Gene and Their Association with Tumor Necrosis Factor-α Polymorphisms in Japanese Patients with Glaucoma

PDF

Tomoyo Funayama; Karin Ishikawa; Yuichiro Ohtake; Tomihiko Tanino; Daijiro Kurosaka; Itaru Kimura; Kotaro Suzuki; Hidenao Ideta; Kenji Nakamoto; Noriko Yasuda; Takuro Fujimaki; Akira Murakami; Ryo Asaoka; Yoshihiro Hotta; Hidenobu Tanihara; Takashi Kanamoto; Hiromu Mishima; Takeo Fukuchi; Haruki Abe; Takeshi Iwata; Naoki Shimada; Jun Kudoh; Nobuyoshi Shimizu; Yukihiko Mashima
TAGS: genes, genotype determination, glaucoma, japanese, open-angle glaucoma, optn gene, polymorphism, tumor necrosis factors, tumor necrosis
Invest. Ophthalmol. Vis. Sci.. 2004; 45(12):4359-4367. https://doi.org/10.1167/iovs.03-1403

Biochemistry and Molecular Biology October 2000

HRG4 (UNC119) Mutation Found in Cone–Rod Dystrophy Causes Retinal Degeneration in a Transgenic Model

PDF

Akira Kobayashi; Tomomi Higashide; Duco Hamasaki; Shinya Kubota; Hitoshi Sakuma; Weijun An; Takuro Fujimaki; Margaret J. McLaren; Richard G. Weleber; George Inana
TAGS: animals, transgenic, electroretinography, mice, transgenic, mutation, retinal degeneration, retinitis pigmentosa, transgenes, mice, genes, photoreceptors
Invest. Ophthalmol. Vis. Sci.. 2000; 41(11):3268-3277.

« Previous

Advertisement

Follow @ARVOiovs

IOVS Home
Issues
Topics
For Authors
About
- Editorial Board

Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

JOURNALS HOME
TOPICS
ABOUT ARVO JOURNALS

Copyright © 2025 Association for Research in Vision and Ophthalmology.

Access Provided By:
MIT Libraries

Forgot password?

To View More...

Purchase this article with an account.

Create an Account

or

Subscribe Now

×

×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×

This site uses cookies. By continuing to use our website, you are agreeing to our privacy policy.Accept