Works by Takaaki Hayashi

Results: 122

High-Resolution Adaptive Optics Retinal Image Analysis at Early Stage Central Areolar Choroidal Dystrophy With PRPH2 Mutation.

Published in:

2016

By:

Kiyoko Gocho;
Keiichiro Akeo;
Naoko Itoh;
Shuhei Kameya;
Takaaki Hayashi;
Satoshi Katagiri;
Tamaki Gekka;
Yasuhiro Ohkuma;
Hiroshi Tsuneoka;
Hiroshi Takahashi;
Gocho, Kiyoko;
Akeo, Keiichiro;
Itoh, Naoko;
Kameya, Shuhei;
Hayashi, Takaaki;
Katagiri, Satoshi;
Gekka, Tamaki;
Ohkuma, Yasuhiro;
Tsuneoka, Hiroshi;
Takahashi, Hiroshi

Publication type:

journal article

Spontaneous Resolution of Large Macular Retinoschisis in Enhanced S-Cone Syndrome.

Published in:

2016

By:

Takaaki Hayashi;
Tamaki Gekka;
Hiroshi Tsuneoka;
Hayashi, Takaaki;
Gekka, Tamaki;
Tsuneoka, Hiroshi

Publication type:

journal article

Diphenylprolinol Silyl Ethers as Efficient Organocatalysts for the Asymmetric Michael Reaction of Aldehydes and NitroalkenesWe thank Prof. K. Saigo and Dr. Y. Ishida (The University of Tokyo) for the use of a high-pressure mercury lamp. This work was partially supported by a Grand-in-Aid for Scientific Research on Priority Area (A): “Creation of Biologically Functional Molecules”, from the Ministry of Education, Culture, Sports, Science, and Technology of Japan.

Published in:

Angewandte Chemie, 2005, v. 117, n. 27, p. 4284, doi. 10.1002/ange.200500599

By:

Yujiro Hayashi;
Hiroaki Gotoh;
Takaaki Hayashi;
Mitsuru Shoji

Publication type:

Article

Genotype-Phenotype Correlations in RP1 -Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN.

Published in:

Journal of Clinical Medicine, 2021, v. 10, n. 11, p. 2265, doi. 10.3390/jcm10112265

By:

Mizobuchi, Kei;
Hayashi, Takaaki;
Oishi, Noriko;
Kubota, Daiki;
Kameya, Shuhei;
Higasa, Koichiro;
Futami, Takuma;
Kondo, Hiroyuki;
Hosono, Katsuhiro;
Kurata, Kentaro;
Hotta, Yoshihiro;
Yoshitake, Kazutoshi;
Iwata, Takeshi;
Matsuura, Tomokazu;
Nakano, Tadashi

Publication type:

Article

Autosomal dominant optic atrophy with OPA1 gene mutations accompanied by auditory neuropathy and other systemic complications in a Japanese cohort.

Published in:

Molecular Vision, 2019, v. 25, p. 559

By:

Akiko Maeda-Katahira;
Natsuko Nakamura;
Takaaki Hayashi;
Satoshi Katagiri;
Satoko Shimizu;
Hisao Ohde;
Tatsuo Matsunaga;
Kimitaka Kaga;
Tadashi Nakano;
Shuhei Kameya;
Tomokazu Matsuura;
Kaoru Fujinami;
Takeshi Iwata;
Kazushige Tsunoda

Publication type:

Article

Early onset flecked retinal dystrophy associated with new compound heterozygous RPE65 variants.

Published in:

Molecular Vision, 2018, v. 24, p. 286

By:

Satoshi Katagiri;
Katsuhiro Hosono;
Takaaki Hayashi;
Kentaro Kurata;
Kei Mizobuchi;
Tomokazu Matsuura;
Kazutoshi Yoshitake;
Takeshi Iwata;
Tadashi Nakano;
Yoshihiro Hotta

Publication type:

Article

Unique, Fast, and All-or-none Click Reaction on Cyclodextrin and Amylose.

Published in:

Chemistry Letters, 2013, v. 42, n. 6, p. 643, doi. 10.1246/cl.130095

By:

Hatsuo Yamamura;
Kyohei Shimohara;
Ryuji Kurata;
Yusuke Fujita;
Kensuke Murata;
Takaaki Hayashi;
Atsushi Miyagawa

Publication type:

Article

Carboxylated phytosterol derivative-introduced liposomes for skin environment-responsive transdermal drug delivery system.

Published in:

Journal of Liposome Research, 2018, v. 28, n. 4, p. 275, doi. 10.1080/08982104.2017.1369995

By:

Yamazaki, Naoko;
Yamakawa, Satoshi;
Sugimoto, Takumi;
Yoshizaki, Yuta;
Teranishi, Ryoma;
Hayashi, Takaaki;
Kotaka, Aki;
Shinde, Chiharu;
Kumei, Takayuki;
Sumida, Yasushi;
Shimizu, Toru;
Ohashi, Yukihiro;
Yuba, Eiji;
Harada, Atsushi;
Kono, Kenji

Publication type:

Article

Clinical heterogeneity between two Japanese siblings with congenital achromatopsia.

Published in:

Visual Neuroscience, 2004, v. 21, n. 3, p. 413, doi. 10.1017/s0952523804213396

By:

TAKAAKI HAYASHI;
KENICHI KOZAKI;
KENJI KITAHARA;
AKIKO KUBO;
YOSHITERU NISHIO;
SATOSHI OMOTO;
YOSUKE NAKAMURA;
AKIRA WATANABE;
KAZUSHIGE TODA;
YASUO UEOKA

Publication type:

Article

Reconstruction of Photoreceptor Outer Layers after Steroid Therapy in Solar Retinopathy.

Published in:

2018

By:

Nakamura, Masaki;
Komatsu, Koji;
Katagiri, Satoshi;
Hayashi, Takaaki;
Nakano, Tadashi

Publication type:

Case Study

Efficacy of reduced-fluence photodynamic therapy for serous retinal pigment epithelial detachment with choroidal hyperpermeability.

Published in:

2013

By:

Asako Shibata;
Yasuhiro Ohkuma;
Takaaki Hayashi;
Hiroshi Tsuneoka

Publication type:

Case Study

Choroidal neovascularization after blunt ocular trauma in angioid streaks.

Published in:

Clinical Ophthalmology, 2013, v. 7, p. 1347, doi. 10.2147/OPTH.S45818

By:

Kubota, Masaomi;
Hayashi, Takaaki;
Arai, Kota;
Tsuneoka, Hiroshi

Publication type:

Article

Paraquat- and Diquat-Induced Oxygen Radical Generation and Lipid Peroxidation in Rat Brain Microsomes.

Published in:

Journal of Biochemistry, 2002, v. 131, n. 4, p. 565, doi. 10.1093/oxfordjournals.jbchem.a003135

By:

Yumino, Kunio;
Kawakami, Ikuo;
Tamura, Mamoru;
Hayashi, Takaaki;
Nakamura, Masao

Publication type:

Article

Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 90, doi. 10.1038/8798

By:

Hayashi, Takaaki;
Motulsky, Arno G.;
Deeb, Samir S.

Publication type:

Article

The importance of gene order in expression of the red and green visual pigment genes and in color vision.

Published in:

Color Research & Application, 2001, v. 26, n. S1, p. S79, doi. 10.1002/1520-6378(2001)26:1+<::AID-COL18>3.0.CO;2-4

By:

Hayashi, Takaaki;
Yamaguchi, Tomohiko;
Kitahara, Kenji;
Sharpe, Lindsay T.;
Jägle, Herbert;
Yamade, Shinichi;
Ueyama, Hisao;
Motulsky, Arno G.;
Deeb, Samir S.

Publication type:

Article

Number and arrangement of the red and green visual pigment genes in color-normal Japanese males.

Published in:

Color Research & Application, 2001, v. 26, n. S1, p. S84, doi. 10.1002/1520-6378(2001)26:1+<::AID-COL19>3.0.CO;2-1

By:

Ueyama, Hisao;
Hayashi, Sachiko;
Tanabe, Shoko;
Tanaka, Yuki;
Hayashi, Takaaki;
Deeb, Samir S.;
Yamade, Shinichi;
Ohkubo, Iwao

Publication type:

Article

Genetic Analyses of Elys Mutations in Drosophila Show Maternal-Effect Lethality and Interactions with Nucleoporin Genes.

Published in:

G3: Genes | Genomes | Genetics, 2018, v. 8, n. 7, p. 2421, doi. 10.1534/g3.118.200361

By:

Kazuyuki Hirai;
Zhuo Wang;
Kohei Miura;
Takaaki Hayashi;
Takeshi Awasaki;
Moe Wada;
Yoko Keira;
Hiroyuki O. Ishikawa;
Kyoichi Sawamura

Publication type:

Article

Functional Characteristics of Diverse PAX6 Mutations Associated with Isolated Foveal Hypoplasia.

Published in:

Genes, 2023, v. 14, n. 7, p. 1483, doi. 10.3390/genes14071483

By:

Matsushita, Itsuka;
Izumi, Hiroto;
Ueno, Shinji;
Hayashi, Takaaki;
Fujinami, Kaoru;
Tsunoda, Kazushige;
Iwata, Takeshi;
Kiuchi, Yoshiaki;
Kondo, Hiroyuki

Publication type:

Article

Genetic and Phenotypic Landscape of PRPH2 -Associated Retinal Dystrophy in Japan.

Published in:

Genes, 2021, v. 12, n. 11, p. 1817, doi. 10.3390/genes12111817

By:

Oishi, Akio;
Fujinami, Kaoru;
Mawatari, Go;
Naoi, Nobuhisa;
Ikeda, Yasuhiro;
Ueno, Shinji;
Kuniyoshi, Kazuki;
Hayashi, Takaaki;
Kondo, Hiroyuki;
Mizota, Atsushi;
Shinoda, Kei;
Kusuhara, Sentaro;
Nakamura, Makoto;
Iwata, Takeshi;
Tsujikawa, Akitaka;
Tsunoda, Kazushige

Publication type:

Article

Configuration of the neoaortic root after chimney reconstruction in the Norwood procedure.

Published in:

European Journal of Cardio-Thoracic Surgery, 2024, v. 65, n. 4, p. 1, doi. 10.1093/ejcts/ezae103

By:

Asada, Satoshi;
Oda, Shinichiro;
Maeda, Yoshinobu;
Fujita, Shuhei;
Hongu, Hisayuki;
Yamashita, Eijiro;
Nakatsuji, Hiroki;
Nagase, Takashi;
Nakai, Rie;
Hayashi, Takaaki;
Ikarashi, Jin;
Goto, Yasutaka;
Yamagishi, Masaaki

Publication type:

Article

The Structural Abnormalities Are Deeply Involved in the Cause of RPGRIP1 -Related Retinal Dystrophy in Japanese Patients.

Published in:

International Journal of Molecular Sciences, 2023, v. 24, n. 18, p. 13678, doi. 10.3390/ijms241813678

By:

Torii, Kaoruko;
Nishina, Sachiko;
Morikawa, Hazuki;
Mizobuchi, Kei;
Takayama, Masakazu;
Tachibana, Nobutaka;
Kurata, Kentaro;
Hikoya, Akiko;
Sato, Miho;
Nakano, Tadashi;
Fukami, Maki;
Azuma, Noriyuki;
Hayashi, Takaaki;
Saitsu, Hirotomo;
Hotta, Yoshihiro

Publication type:

Article

Clinical Course and Electron Microscopic Findings in Lymphocytes of Patients with DRAM2-Associated Retinopathy.

Published in:

International Journal of Molecular Sciences, 2020, v. 21, n. 4, p. 1331, doi. 10.3390/ijms21041331

By:

Kuniyoshi, Kazuki;
Hayashi, Takaaki;
Kameya, Shuhei;
Katagiri, Satoshi;
Mizobuchi, Kei;
Tachibana, Toshiaki;
Kubota, Daiki;
Sakuramoto, Hiroyuki;
Tsunoda, Kazushige;
Fujinami, Kaoru;
Yoshitake, Kazutoshi;
Iwata, Takeshi;
Nakano, Tadashi;
Kusaka, Shunji

Publication type:

Article

X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers.

Published in:

International Journal of Molecular Sciences, 2019, v. 20, n. 6, p. 1518, doi. 10.3390/ijms20061518

By:

Kurata, Kentaro;
Hosono, Katsuhiro;
Miyamichi, Daisuke;
Sato, Miho;
Hotta, Yoshihiro;
Hayashi, Takaaki;
Mizobuchi, Kei;
Katagiri, Satoshi;
Nakano, Tadashi;
Nishina, Sachiko;
Azuma, Noriyuki

Publication type:

Article

Genome mining of the sordarin biosynthetic gene cluster from Sordaria araneosa Cain ATCC 36386: characterization of cycloaraneosene synthase and GDP-6-deoxyaltrose transferase.

Published in:

Journal of Antibiotics, 2016, v. 69, n. 7, p. 541, doi. 10.1038/ja.2016.40

By:

Kudo, Fumitaka;
Matsuura, Yasunori;
Hayashi, Takaaki;
Fukushima, Masayuki;
Eguchi, Tadashi

Publication type:

Article

Arsenic-containing ribofuranosides and dimethylarsinic acid in green seaweed, Codium fragile.

Published in:

Applied Organometallic Chemistry, 1988, v. 2, n. 4, p. 365, doi. 10.1002/aoc.590020414

By:

Jin, Kazuo;
Hayashi, Takaaki;
Shibata, Yasuyuki;
Morita, Masatoshi

Publication type:

Article

A novel stop-gain NF1 variant in neurofibromatosis type 1 and bilateral optic atrophy without optic gliomas.

Published in:

Ophthalmic Genetics, 2024, v. 45, n. 2, p. 186, doi. 10.1080/13816810.2023.2245464

By:

Fukunaga, Naoko;
Hayashi, Takaaki;
Yamada, Yuki;
Mizobuchi, Kei;
Ohta, Arihito;
Nakano, Tadashi

Publication type:

Article

Complete congenital stationary night blindness associated with a novel NYX variant (p.Asn216Lys) in middle-aged and older adult patients.

Published in:

2021

By:

Hayashi, Takaaki;
Murakami, Yusuke;
Mizobuchi, Kei;
Koyanagi, Yoshito;
Sonoda, Koh-Hei;
Nakano, Tadashi

Publication type:

Report

Heterozygous GGC repeat expansion of NOTCH2NLC in a patient with neuronal intranuclear inclusion disease and progressive retinal dystrophy.

Published in:

2020

By:

Hayashi, Takaaki;
Katagiri, Satoshi;
Mizobuchi, Kei;
Yoshitake, Kazutoshi;
Kameya, Shuhei;
Matsuura, Tomokazu;
Iwata, Takeshi;
Nakano, Tadashi

Publication type:

Letter

Autosomal dominant retinitis pigmentosa with macular involvement associated with a disease haplotype that included a novel <italic>PRPH2</italic> variant (p.Cys250Gly).

Published in:

Ophthalmic Genetics, 2018, v. 39, n. 3, p. 357, doi. 10.1080/13816810.2018.1459737

By:

Katagiri, Satoshi;
Hayashi, Takaaki;
Mizobuchi, Kei;
Yoshitake, Kazutoshi;
Iwata, Takeshi;
Nakano, Tadashi

Publication type:

Article

Case of cone dystrophy with normal fundus appearance associated with biallelic POC1B variants.

Published in:

2018

By:

Kominami, Azusa;
Ueno, Shinji;
Kominami, Taro;
Nakanishi, Ayami;
Ito, Yasuki;
Fujinami, Kaoru;
Tsunoda, Kazushige;
Hayashi, Takaaki;
Kikuchi, Sachiko;
Kameya, Shuhei;
Iwata, Takeshi;
Terasaki, Hiroko

Publication type:

Case Study

A novel homozygous CYP4V2 variant (p.S121Y) associated with a choroideremia-like phenotype.

Published in:

Ophthalmic Genetics, 2017, v. 38, n. 3, p. 286, doi. 10.1080/13816810.2016.1193880

By:

Katagiri, Satoshi;
Hayashi, Takaaki;
Gekka, Tamaki;
Tsuneoka, Hiroshi

Publication type:

Article

A novel heterozygous splice site OPA1 mutation causes exon 10 skipping in Japanese patients with dominant optic atrophy.

Published in:

Ophthalmic Genetics, 2016, v. 37, n. 3, p. 354, doi. 10.3109/13816810.2015.1066829

By:

Iida, Kie;
Ohkuma, Yasuhiro;
Hayashi, Takaaki;
Katagiri, Satoshi;
Fujita, Takeshi;
Tsunoda, Kazushige;
Yamada, Hisashi;
Tsuneoka, Hiroshi

Publication type:

Article

RPE65 Mutations in Two Japanese Families with Leber Congenital Amaurosis.

Published in:

Ophthalmic Genetics, 2016, v. 37, n. 2, p. 161, doi. 10.3109/13816810.2014.991931

By:

Katagiri, Satoshi;
Hayashi, Takaaki;
Kondo, Mineo;
Tsukitome, Hideyuki;
Yoshitake, Kazutoshi;
Akahori, Masakazu;
Ikeo, Kazuho;
Tsuneoka, Hiroshi;
Iwata, Takeshi

Publication type:

Article

Novel C8orf37 Mutations in Patients with Early-onset Retinal Dystrophy, Macular Atrophy, Cataracts, and High Myopia.

Published in:

Ophthalmic Genetics, 2016, v. 37, n. 1, p. 68, doi. 10.3109/13816810.2014.949380

By:

Katagiri, Satoshi;
Hayashi, Takaaki;
Yoshitake, Kazutoshi;
Akahori, Masakazu;
Ikeo, Kazuho;
Gekka, Tamaki;
Tsuneoka, Hiroshi;
Iwata, Takeshi

Publication type:

Article

Congenital Achromatopsia and Macular Atrophy Caused by a Novel Recessive PDE6C Mutation (p.E591K).

Published in:

Ophthalmic Genetics, 2015, v. 36, n. 2, p. 137, doi. 10.3109/13816810.2014.991932

By:

Katagiri, Satoshi;
Hayashi, Takaaki;
Yoshitake, Kazutoshi;
Sergeev, Yuri;
Akahori, Masakazu;
Furuno, Masaaki;
Nishino, Jo;
Ikeo, Kazuho;
Tsunoda, Kazushige;
Tsuneoka, Hiroshi;
Iwata, Takeshi

Publication type:

Article

Autosomal dominant familial exudative vitreoretinopathy in two Japanese families with FZD4 mutations (H69Y and C181R).

Published in:

Ophthalmic Genetics, 2004, v. 25, n. 2, p. 81, doi. 10.1080/13816810490514270

By:

Omoto, Satoshi;
Hayashi, Takaaki;
Kitahara, Kenji;
Takeuchi, Tomokazu;
Ueoka, Yasuo

Publication type:

Article

The molecular basis of dichromatic color visionin males with multiple red and green visual pigment genes.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 1, p. 23, doi. 10.1093/hmg/11.1.23

By:

Jagla, Wolfgang M.;
Jägle, Herbert;
Hayashi, Takaaki;
Sharpe, Lindsay T.;
Deeb, Samir S.

Publication type:

Article

ABCC6 Gene Analysis in 20 Japanese Patients with Angioid Streaks Revealing Four Frequent and Two Novel Variants and Pseudodominant Inheritance.

Published in:

Journal of Ophthalmology, 2017, p. 1, doi. 10.1155/2017/1079687

By:

Katagiri, Satoshi;
Negishi, Yuya;
Mizobuchi, Kei;
Urashima, Mitsuyoshi;
Nakano, Tadashi;
Hayashi, Takaaki

Publication type:

Article

Relatively preserved retinal function in RPE65-associated retinopathy: a case report.

Published in:

Documenta Ophthalmologica, 2025, v. 150, n. 2, p. 97, doi. 10.1007/s10633-025-10007-4

By:

Mizobuchi, Kei;
Hayashi, Takaaki;
Kameya, Shuhei;
Ohta, Yuri;
Kuribayashi, Kohei;
Shinoda, Kei

Publication type:

Article

Clinical course of two siblings with potassium voltage-gated channel modifier subfamily V member 2 (KCNV2)-associated retinopathy.

Published in:

Documenta Ophthalmologica, 2024, v. 148, n. 3, p. 173, doi. 10.1007/s10633-024-09971-0

By:

Sato, Tomoko;
Kuniyoshi, Kazuki;
Hayashi, Takaaki;
Nishiwaki, Hirokazu;
Mizobuchi, Kei;
Kusaka, Shunji

Publication type:

Article

A mild form of POC1B-associated retinal dystrophy with relatively preserved cone system function.

Published in:

Documenta Ophthalmologica, 2023, v. 147, n. 1, p. 59, doi. 10.1007/s10633-023-09936-9

By:

Hayashi, Takaaki;
Mizobuchi, Kei;
Kameya, Shuhei;
Ueno, Shinji;
Matsuura, Tomokazu;
Nakano, Tadashi

Publication type:

Article

Electroretinographic abnormalities in Alport syndrome with a novel COL4A5 truncated variant (p.Try20GlyfsTer19).

Published in:

Documenta Ophthalmologica, 2023, v. 146, n. 3, p. 281, doi. 10.1007/s10633-023-09935-w

By:

Mizobuchi, Kei;
Hayashi, Takaaki;
Ohira, Ryo;
Nakano, Tadashi

Publication type:

Article

Bardet–Biedl syndrome associated with novel compound heterozygous variants in BBS12 gene.

Published in:

2023

By:

Morohashi, Tamaki;
Hayashi, Takaaki;
Mizobuchi, Kei;
Nakano, Tadashi;
Morioka, Ichiro

Publication type:

Case Study

Clinical characterization of autosomal dominant retinitis pigmentosa with NRL mutation in a three-generation Japanese family.

Published in:

Documenta Ophthalmologica, 2022, v. 144, n. 3, p. 227, doi. 10.1007/s10633-022-09874-y

By:

Mizobuchi, Kei;
Hayashi, Takaaki;
Matsuura, Tomokazu;
Nakano, Tadashi

Publication type:

Article

Polypoidal choroidal vasculopathy in a patient with DMPK-associated myotonic dystrophy.

Published in:

2022

By:

Iida, Yuka;
Hayashi, Takaaki;
Tokuhisa, Teruaki;
Mizobuchi, Kei;
Omoto, Shusaku;
Nakano, Tadashi

Publication type:

Case Study

The second Japanese family with Malattia Leventinese/Doyne honeycomb retinal dystrophy.

Published in:

Documenta Ophthalmologica, 2022, v. 144, n. 1, p. 67, doi. 10.1007/s10633-021-09859-3

By:

Enomoto, Nobuko;
Hayashi, Takaaki;
Matsuura, Tomokazu;
Tanaka, Koji;
Takeuchi, Remi;
Tomita, Goji;
Mori, Ryusaburo

Publication type:

Article

Homozygous single nucleotide duplication of SLC38A8 in autosomal recessive foveal hypoplasia: The first Japanese case report.

Published in:

Documenta Ophthalmologica, 2021, v. 143, n. 3, p. 323, doi. 10.1007/s10633-021-09842-y

By:

Hayashi, Takaaki;
Kondo, Hiroyuki;
Matsushita, Itsuka;
Mizobuchi, Kei;
Baba, Akinori;
Iida, Kie;
Kubo, Hiroyuki;
Nakano, Tadashi

Publication type:

Article

Transient electroretinographic abnormalities that mimic those of KCNV2 retinopathy: a case report.

Published in:

2021

By:

Kaizuka, Chihiro;
Hayashi, Takaaki;
Mizobuchi, Kei;
Kubota, Masaomi;
Ueno, Shinji;
Nakano, Tadashi

Publication type:

Case Study

A new PDE6A missense variant p.Arg544Gln in rod–cone dystrophy.

Published in:

Documenta Ophthalmologica, 2021, v. 143, n. 1, p. 107, doi. 10.1007/s10633-021-09826-y

By:

Hayashi, Takaaki;
Mizobuchi, Kei;
Kameya, Shuhei;
Yoshitake, Kazutoshi;
Iwata, Takeshi;
Nakano, Tadashi

Publication type:

Article

Vitamin A deficiency after prolonged intake of an unbalanced diet in a Japanese hemodialysis patient.

Published in:

Documenta Ophthalmologica, 2021, v. 143, n. 1, p. 85, doi. 10.1007/s10633-021-09823-1

By:

Kishimoto, Nanami;
Hayashi, Takaaki;
Mizobuchi, Kei;
Kubota, Masaomi;
Nakano, Tadashi

Publication type:

Article