Works by Iwata, Takeshi

Results: 86

Establishment of the Indian Chapter for Asian Eye Genetics Consortium.

Published in:

2016

By:

Takeshi Iwata;
Iwata, Takeshi

Publication type:

Editorial

Novel homozygous CLN3 missense variant in isolated retinal dystrophy: A case report and electron microscopic findings.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1308

By:

Mizobuchi, Kei;
Hayashi, Takaaki;
Yoshitake, Kazutoshi;
Fujinami, Kaoru;
Tachibana, Toshiaki;
Tsunoda, Kazushige;
Iwata, Takeshi;
Nakano, Tadashi

Publication type:

Article

Publication of nuclear magnetic resonance experimental data with semantic web technology and the application thereof to biomedical research of proteins.

Published in:

Journal of Biomedical Semantics, 2016, v. 7, p. 1, doi. 10.1186/s13326-016-0057-1

By:

Masashi Yokochi;
Naohiro Kobayashi;
Ulrich, Eldon L.;
Akira R. Kinjo;
Takeshi Iwata;
Yannis E. Ioannidis;
Livny, Miron;
Markley, John L.;
Haruki Nakamura;
Chojiro Kojima;
Toshimichi Fujiwara

Publication type:

Article

Elevated Plasma Levels of Drebrin in Glaucoma Patients With Neurodegeneration.

Published in:

Frontiers in Neuroscience, 2019, p. N.PAG, doi. 10.3389/fnins.2019.00326

By:

Gan, Yi-Jing;
Fang, Ai-Wu;
Liu, Chang;
Liu, Bai-Jing;
Yang, Feng-Mei;
Guan, Ji-Tian;
Lan, Chun-Lin;
Dai, Xiao-Dan;
Li, Tong;
Cao, Ying;
Ran, Yun;
Gong, Xian-Hui;
Jin, Zi-Bing;
Cui, Ren-Zhe;
Iwata, Takeshi;
Qu, Jia;
Lu, Fan;
Chi, Zai-Long

Publication type:

Article

Protein Data Bank Japan: Celebrating our 20th anniversary during a global pandemic as the Asian hub of three dimensional macromolecular structural data.

Published in:

Protein Science: A Publication of the Protein Society, 2022, v. 31, n. 1, p. 173, doi. 10.1002/pro.4211

By:

Bekker, Gert‐Jan;
Yokochi, Masashi;
Suzuki, Hirofumi;
Ikegawa, Yasuyo;
Iwata, Takeshi;
Kudou, Takahiro;
Yura, Kei;
Fujiwara, Toshimichi;
Kawabata, Takeshi;
Kurisu, Genji

Publication type:

Article

New tools and functions in data-out activities at Protein Data Bank Japan (PDBj).

Published in:

Protein Science: A Publication of the Protein Society, 2018, v. 27, n. 1, p. 95, doi. 10.1002/pro.3273

By:

Kinjo, Akira R.;
Bekker, Gert‐Jan;
Wako, Hiroshi;
Endo, Shigeru;
Tsuchiya, Yuko;
Sato, Hiromu;
Nishi, Hafumi;
Kinoshita, Kengo;
Suzuki, Hirofumi;
Kawabata, Takeshi;
Yokochi, Masashi;
Iwata, Takeshi;
Kobayashi, Naohiro;
Fujiwara, Toshimichi;
Kurisu, Genji;
Nakamura, Haruki

Publication type:

Article

A Japanese boy with double diagnoses of 2p15p16.1 microdeletion syndrome and RP2-associated retinal disorder.

Published in:

Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00178-2

By:

Yamazawa, Kazuki;
Shimizu, Kenji;
Ohashi, Hirofumi;
Haruna, Hidenori;
Inoue, Satomi;
Murakami, Haruka;
Matsunaga, Tatsuo;
Iwata, Takeshi;
Tsunoda, Kazushige;
Fujinami, Kaoru

Publication type:

Article

Genetic defects of CHM and visual acuity outcome in 24 choroideremia patients from 16 Japanese families.

Published in:

Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-72623-1

By:

Hayashi, Takaaki;
Kameya, Shuhei;
Mizobuchi, Kei;
Kubota, Daiki;
Kikuchi, Sachiko;
Yoshitake, Kazutoshi;
Mizota, Atsushi;
Murakami, Akira;
Iwata, Takeshi;
Nakano, Tadashi

Publication type:

Article

Retinal pigment epithelium-specific ablation of GPx4 in adult mice recapitulates key features of geographic atrophy in age-related macular degeneration.

Published in:

Cell Death & Disease, 2024, v. 15, n. 10, p. 1, doi. 10.1038/s41419-024-07150-2

By:

Azuma, Kunihiro;
Suzuki, Takafumi;
Kobayashi, Kenta;
Nagahara, Masako;
Imai, Hirotaka;
Suga, Akiko;
Iwata, Takeshi;
Shiraya, Tomoyasu;
Aihara, Makoto;
Ueta, Takashi

Publication type:

Article

Molecular composition of drusen and possible involvement of anti-retinal autoimmunity in two different forms of macular degeneration in cynomolgus monkey (Macaca fascicularis).

Published in:

FASEB Journal, 2005, v. 19, n. 12, p. 1683, doi. 10.1096/fj.04-3525fje

By:

Umeda, Shinsuke;
Suzuki, Michihiro T.;
Okamoto, Haru;
Ono, Fumiko;
Mizota, Atsushi;
Terao, Keiji;
Yoshikawa, Yasuhiro;
Tanaka, Yasuhiko;
Iwata, Takeshi

Publication type:

Article

Compound heterozygous mutations in a mouse model of Leber congenital amaurosis reveal the role of CCT2 in photoreceptor maintenance.

Published in:

Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-06384-2

By:

Suga, Akiko;
Minegishi, Yuriko;
Yamamoto, Megumi;
Ueda, Koji;
Iwata, Takeshi

Publication type:

Article

Three cases of acute-onset bilateral photophobia.

Published in:

Japanese Journal of Ophthalmology, 2019, v. 63, n. 2, p. 172, doi. 10.1007/s10384-018-00649-0

By:

Ueno, Shinji;
Inooka, Daiki;
Meinert, Monika;
Ito, Yasuki;
Tsunoda, Kazushige;
Fujinami, Kaoru;
Iwata, Takeshi;
Ohde, Hisao;
Terasaki, Hiroko

Publication type:

Article

Heterozygous deletion of the OPA1 gene in patients with dominant optic atrophy.

Published in:

Japanese Journal of Ophthalmology, 2017, v. 61, n. 5, p. 395, doi. 10.1007/s10384-017-0522-0

By:

Hayashi, Takaaki;
Sasano, Hiroyuki;
Katagiri, Satoshi;
Tsunoda, Kazushige;
Kameya, Shuhei;
Nakazawa, Mitsuru;
Iwata, Takeshi;
Tsuneoka, Hiroshi

Publication type:

Article

In vivo imaging of a cone mosaic in a patient with achromatopsia associated with a GNAT2 variant.

Published in:

Japanese Journal of Ophthalmology, 2017, v. 61, n. 1, p. 92, doi. 10.1007/s10384-016-0484-7

By:

Ueno, Shinji;
Nakanishi, Ayami;
Kominami, Taro;
Ito, Yasuki;
Hayashi, Takaaki;
Yoshitake, Kazutoshi;
Kawamura, Yuichi;
Tsunoda, Kazushige;
Iwata, Takeshi;
Terasaki, Hiroko

Publication type:

Article

New truncation mutation of the NR2E3 gene in a Japanese patient with enhanced S-cone syndrome.

Published in:

Japanese Journal of Ophthalmology, 2016, v. 60, n. 6, p. 476, doi. 10.1007/s10384-016-0470-0

By:

Kuniyoshi, Kazuki;
Hayashi, Takaaki;
Sakuramoto, Hiroyuki;
Mishima, Hiroshi;
Tsuneoka, Hiroshi;
Tsunoda, Kazushige;
Iwata, Takeshi;
Shimomura, Yoshikazu

Publication type:

Article

Novel mutations in the gene for α-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsia.

Published in:

Japanese Journal of Ophthalmology, 2016, v. 60, n. 3, p. 187, doi. 10.1007/s10384-016-0424-6

By:

Kuniyoshi, Kazuki;
Muraki-Oda, Sanae;
Ueyama, Hisao;
Toyoda, Futoshi;
Sakuramoto, Hiroyuki;
Ogita, Hisakazu;
Irifune, Motohiro;
Yamamoto, Shuji;
Nakao, Akira;
Tsunoda, Kazushige;
Iwata, Takeshi;
Ohji, Masahito;
Shimomura, Yoshikazu

Publication type:

Article

Novel mutations in malonyl-CoA-acyl carrier protein transacylase provoke autosomal recessive optic neuropathy.

Published in:

Human Molecular Genetics, 2020, v. 29, n. 3, p. 444, doi. 10.1093/hmg/ddz311

By:

Li, Huiping;
Yuan, Shiqin;
Minegishi, Yuriko;
Suga, Akiko;
Yoshitake, Kazutoshi;
Sheng, Xunlun;
Ye, Jianping;
Smith, Stuart;
Bunkoczi, Gabor;
Yamamoto, Megumi;
Iwata, Takeshi

Publication type:

Article

Development of a Partial Discharge Inception Calculation Model of a Nonuniform Air Gap Considering the Effect of Humidity.

Published in:

Electrical Engineering in Japan, 2014, v. 186, n. 3, p. 1, doi. 10.1002/eej.22351

By:

Yanagita, Norihito;
Kato, Tatsuro;
Rokunohe, Toshiaki;
Iwata, Takeshi;
Kojima, Hiroki;
Hayakawa, Naoki;
Okubo, Hitoshi

Publication type:

Article

Prediction of Causative Genes in Inherited Retinal Disorders from Spectral-Domain Optical Coherence Tomography Utilizing Deep Learning Techniques.

Published in:

Journal of Ophthalmology, 2019, p. 1, doi. 10.1155/2019/1691064

By:

Fujinami-Yokokawa, Yu;
Pontikos, Nikolas;
Yang, Lizhu;
Tsunoda, Kazushige;
Yoshitake, Kazutoshi;
Iwata, Takeshi;
Miyata, Hiroaki;
Fujinami, Kaoru;
Japan Eye Genetics Consortium, on behalf of

Publication type:

Article

Preparation and Electroluminescent Characteristics of a Series of Cyclometalated Ir(III) Complexes Based on Phenylpyridines with a Diphenylamino Group.

Published in:

Chemistry Letters, 2005, v. 34, n. 10, p. 1378, doi. 10.1246/cl.2005.1378

By:

Nishida, Jun-ichi;
Echizen, Hidenori;
Iwata, Takeshi;
Yamashita, Yoshiro

Publication type:

Article

Preparation, Characterization, and Electroluminescence Characteristics of α-Diimine-type Platinum(II) Complexes with Perfluorinated Phenyl Groups as Ligands.

Published in:

Chemistry Letters, 2005, v. 34, n. 4, p. 592, doi. 10.1246/cl.2005.592

By:

Nishida, Jun-ichi;
Maruyama, Akihiro;
Iwata, Takeshi;
Yamashita, Yoshiro

Publication type:

Article

Photochemical mer → fac One-way Isomerization of Phosphorescent Material. Studies by Time-resolved Spectroscopy for Tris[2-(4',6'-difluorophenyl) pyridine]iridium(III) in Solution.

Published in:

Chemistry Letters, 2003, v. 32, n. 10, p. 886, doi. 10.1246/cl.2003.886

By:

Karatsu, Takashi;
Nakamura, Takeshi;
Yagai, Shiki;
Kitamura, Akihide;
Yamaguchi, Kentaro;
Matsushima, Yoshimasa;
Iwata, Takeshi;
Hori, Yoji;
Hagiwara, Toshimitsu

Publication type:

Article

Role of alpha-1 antitrypsin in Bruch's membrane integrity.

Published in:

Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-96570-x

By:

Cheng, Shun-Yun;
Giguere, Delaney;
Silverstein, Ilana;
Conza, Adrienne;
Seddon, Johanna M.;
Kim, San;
Iwata, Takeshi;
Mueller, Christian;
Punzo, Claudio

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

Missense variants in the X-linked gene PRPS1 cause retinal degeneration in females.

Published in:

Human Mutation, 2018, v. 39, n. 1, p. 80, doi. 10.1002/humu.23349

By:

Fiorentino, Alessia;
Fujinami, Kaoru;
Arno, Gavin;
Robson, Anthony G.;
Pontikos, Nikolas;
Arasanz Armengol, Monica;
Plagnol, Vincent;
Hayashi, Takaaki;
Iwata, Takeshi;
Parker, Matthew;
Fowler, Tom;
Rendon, Augusto;
Gardner, Jessica C.;
Henderson, Robert H.;
Cheetham, Michael E.;
Webster, Andrew R.;
Michaelides, Michel;
Hardcastle, Alison J.;
for the 100,000 Genomes Project, the Japan Eye Genetic Consortium and the UK Inherited Retinal Dystrophy Consortium

Publication type:

Article

Identification of four novel mutations of the XLRS1 gene in Japanese patients with X-linked juvenile retinoschisis.

Published in:

Human Mutation, 1999, v. 13, n. 4, p. 338, doi. 10.1002/(SICI)1098-1004(1999)13:4<338::AID-HUMU16>3.0.CO;2-0

By:

Mashima, Yukihiko;
Shinoda, Kei;
Ishida, Susumu;
Ozawa, Yoko;
Kudoh, Jun;
Iwata, Takeshi;
Oguchi, Yoshihisa;
Shimizu, Nobuyoshi

Publication type:

Article

Genetic analysis of Japanese primary open-angle glaucoma patients and clinical characterization of risk alleles near CDKN2B-AS1, SIX6 and GAS7.

Published in:

PLoS ONE, 2017, v. 12, n. 12, p. 1, doi. 10.1371/journal.pone.0186678

By:

Shiga, Yukihiro;
Nishiguchi, Koji M.;
Kawai, Yosuke;
Kojima, Kaname;
Sato, Kota;
Fujita, Kosuke;
Takahashi, Mai;
Omodaka, Kazuko;
Araie, Makoto;
Kashiwagi, Kenji;
Aihara, Makoto;
Iwata, Takeshi;
Mabuchi, Fumihiko;
Takamoto, Mitsuko;
Ozaki, Mineo;
Kawase, Kazuhide;
Fuse, Nobuo;
Yamamoto, Masayuki;
Yasuda, Jun;
Nagasaki, Masao

Publication type:

Article

Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma.

Published in:

PLoS ONE, 2017, v. 12, n. 8, p. 1, doi. 10.1371/journal.pone.0183709

By:

Mabuchi, Fumihiko;
Mabuchi, Nakako;
Sakurada, Yoichi;
Yoneyama, Seigo;
Kashiwagi, Kenji;
Iijima, Hiroyuki;
Yamagata, Zentaro;
Takamoto, Mitsuko;
Aihara, Makoto;
Iwata, Takeshi;
Kawase, Kazuhide;
Shiga, Yukihiro;
Nishiguchi, Koji M.;
Nakazawa, Toru;
Ozaki, Mineo;
Araie, Makoto;
null, null

Publication type:

Article

The Serine Protease HTRA-1 Is a Biomarker for ROP and Mediates Retinal Neovascularization.

Published in:

Frontiers in Molecular Neuroscience, 2020, v. 13, p. N.PAG, doi. 10.3389/fnmol.2020.605918

By:

Owen, Leah A.;
Shirer, Kinsey;
Collazo, Samuel A.;
Szczotka, Kathryn;
Baker, Shawna;
Wood, Blair;
Carroll, Lara;
Haaland, Benjamin;
Iwata, Takeshi;
Katikaneni, Lakshmi D.;
DeAngelis, Margaret M.

Publication type:

Article

The Association Between Complement Component 2/Complement Factor B Polymorphisms and Age-related Macular Degeneration: A HuGE Review and Meta-Analysis.

Published in:

American Journal of Epidemiology, 2012, v. 176, n. 5, p. 361, doi. 10.1093/aje/kws031

By:

Thakkinstian, Ammarin;
Mcevoy, Mark;
Chakravarthy, Usha;
Chakrabarti, Subhabrata;
Mckay, Gareth J.;
Ryu, Euijung;
Silvestri, Giuliana;
Kaur, Inderjeet;
Francis, Peter;
Iwata, Takeshi;
Akahori, Masakazu;
Arning, Astrid;
Edwards, Albert O.;
Seddon, Johanna M.;
Attia, John

Publication type:

Article

A controlled ovarian stimulation procedure suitable for cynomolgus macaques.

Published in:

Experimental Animals, 2022, v. 71, n. 4, p. 426, doi. 10.1538/expanim.21-0198

By:

Nobuhiro SHIMOZAWA;
Takeshi IWATA;
Yasuhiro YASUTOMI

Publication type:

Article

Molecular genetics of inherited normal tension glaucoma.

Published in:

Indian Journal of Ophthalmology, 2024, v. 72, p. S335, doi. 10.4103/IJO.IJO_3204_23

By:

Yang Pan;
Takeshi Iwata

Publication type:

Article

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

Progress of macular atrophy during 30 months' follow-up in a patient with spinocerebellar ataxia type1 (SCA1).

Published in:

Documenta Ophthalmologica, 2021, v. 142, n. 1, p. 87, doi. 10.1007/s10633-020-09782-z

By:

Hirose, Ayane;
Katagiri, Satoshi;
Hayashi, Takaaki;
Matsuura, Tomokazu;
Nagai, Norihiro;
Fujinami, Kaoru;
Iwata, Takeshi;
Tsunoda, Kazushige

Publication type:

Article

Late-onset night blindness with peripheral flecks accompanied by progressive trickle-like macular degeneration.

Published in:

Documenta Ophthalmologica, 2019, v. 139, n. 3, p. 171, doi. 10.1007/s10633-019-09705-7

By:

Tsunoda, Kazushige;
Fujinami, Kaoru;
Yoshitake, Kazutoshi;
Iwata, Takeshi

Publication type:

Article

Novel biallelic loss-of-function KCNV2 variants in cone dystrophy with supernormal rod responses.

Published in:

Documenta Ophthalmologica, 2019, v. 138, n. 3, p. 229, doi. 10.1007/s10633-019-09679-6

By:

Kutsuma, Tomoko;
Katagiri, Satoshi;
Hayashi, Takaaki;
Yoshitake, Kazutoshi;
Iejima, Daisuke;
Gekka, Tamaki;
Kohzaki, Kenichi;
Mizobuchi, Kei;
Baba, Yukari;
Terauchi, Ryo;
Matsuura, Tomokazu;
Ueno, Shinji;
Iwata, Takeshi;
Nakano, Tadashi

Publication type:

Article

Differences in ocular findings in two siblings: one with complete and other with incomplete achromatopsia.

Published in:

Documenta Ophthalmologica, 2017, v. 134, n. 2, p. 141, doi. 10.1007/s10633-017-9577-y

By:

Ueno, Shinji;
Nakanishi, Ayami;
Sayo, Akira;
Kominami, Taro;
Ito, Yasuki;
Hayashi, Takaaki;
Tsunoda, Kazushige;
Iwata, Takeshi;
Terasaki, Hiroko

Publication type:

Article

Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutations.

Published in:

Documenta Ophthalmologica, 2015, v. 131, n. 1, p. 71, doi. 10.1007/s10633-015-9497-7

By:

Kuniyoshi, Kazuki;
Sakuramoto, Hiroyuki;
Yoshitake, Kazutoshi;
Ikeo, Kazuho;
Furuno, Masaaki;
Tsunoda, Kazushige;
Kusaka, Shunji;
Shimomura, Yoshikazu;
Iwata, Takeshi

Publication type:

Article

Novel nonsense and splice site mutations in CRB1 gene in two Japanese patients with early-onset retinal dystrophy.

Published in:

Documenta Ophthalmologica, 2015, v. 130, n. 1, p. 49, doi. 10.1007/s10633-014-9464-8

By:

Kuniyoshi, Kazuki;
Ikeo, Kazuho;
Sakuramoto, Hiroyuki;
Furuno, Masaaki;
Yoshitake, Kazutoshi;
Hatsukawa, Yoshikazu;
Nakao, Akira;
Tsunoda, Kazushige;
Kusaka, Shunji;
Shimomura, Yoshikazu;
Iwata, Takeshi

Publication type:

Article

Longitudinal clinical course of three Japanese patients with Leber congenital amaurosis/early-onset retinal dystrophy with RDH12 mutation.

Published in:

Documenta Ophthalmologica, 2014, v. 128, n. 3, p. 219, doi. 10.1007/s10633-014-9436-z

By:

Kuniyoshi, Kazuki;
Sakuramoto, Hiroyuki;
Yoshitake, Kazutoshi;
Abe, Kosuke;
Ikeo, Kazuho;
Furuno, Masaaki;
Tsunoda, Kazushige;
Kusaka, Shunji;
Shimomura, Yoshikazu;
Iwata, Takeshi

Publication type:

Article

Autosomal recessive cone-rod dystrophy associated with compound heterozygous mutations in the EYS gene.

Published in:

Documenta Ophthalmologica, 2014, v. 128, n. 3, p. 211, doi. 10.1007/s10633-014-9435-0

By:

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

Publication type:

Article

Two siblings with late-onset cone-rod dystrophy and no visible macular degeneration.

Published in:

2013

By:

Hiroyuki Sakuramoto;
Kazuki Kuniyoshi;
Kazushige Tsunoda;
Masakazu Akahori;
Takeshi Iwata;
Yoshikazu Shimomura

Publication type:

Case Study

RP2‐associated retinal disorder in a Japanese cohort: Report of novel variants and a literature review, identifying a genotype–phenotype association.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 3, p. 675, doi. 10.1002/ajmg.c.31830

By:

Fujinami, Kaoru;
Liu, Xiao;
Ueno, Shinji;
Mizota, Atsushi;
Shinoda, Kei;
Kuniyoshi, Kazuki;
Fujinami‐Yokokawa, Yu;
Yang, Lizhu;
Arno, Gavin;
Pontikos, Nikolas;
Kameya, Shuhei;
Kominami, Taro;
Terasaki, Hiroko;
Sakuramoto, Hiroyuki;
Nakamura, Natsuko;
Kurihara, Toshihide;
Tsubota, Kazuo;
Miyake, Yozo;
Yoshiake, Kazutoshi;
Iwata, Takeshi

Publication type:

Article

Clinical and genetic characteristics of 10 Japanese patients with PROM1‐associated retinal disorder: A report of the phenotype spectrum and a literature review in the Japanese population.

Published in:

American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 3, p. 656, doi. 10.1002/ajmg.c.31826

By:

Fujinami, Kaoru;
Oishi, Akio;
Yang, Lizhu;
Arno, Gavin;
Pontikos, Nikolas;
Yoshitake, Kazutoshi;
Fujinami‐Yokokawa, Yu;
Liu, Xiao;
Hayashi, Takaaki;
Katagiri, Satoshi;
Mizobuchi, Kei;
Mizota, Atsushi;
Shinoda, Kei;
Nakamura, Natsuko;
Kurihara, Toshihide;
Tsubota, Kazuo;
Miyake, Yozo;
Iwata, Takeshi;
Tsujikawa, Akitaka;
Tsunoda, Kazushige

Publication type:

Article

HTRA1 Regulates Subclinical Inflammation and Activates Proangiogenic Response in the Retina and Choroid.

Published in:

International Journal of Molecular Sciences, 2022, v. 23, n. 18, p. N.PAG, doi. 10.3390/ijms231810206

By:

Ahamed, Waseem;
Yu, Richard Ming Chuan;
Pan, Yang;
Iwata, Takeshi;
Barathi, Veluchamy Amutha;
Wey, Yeo Sia;
Tun, Sai Bo Bo;
Qiu, Beiying;
Tan, Alison;
Wang, Xiaomeng;
Cheung, Chui Ming Gemmy;
Wong, Tien Yin;
Yanagi, Yasuo

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

Compound heterozygous splice site variants in the SCLT1 gene highlight an additional candidate locus for Senior-Løken syndrome.

Published in:

Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-35152-6

By:

Katagiri, Satoshi;
Hayashi, Takaaki;
Yoshitake, Kazutoshi;
Murai, Noriyuki;
Matsui, Zenichi;
Kubo, Hiroyuki;
Satoh, Hiroyuki;
Matsufuji, Senya;
Takamura, Tsuyoshi;
Yokoo, Takashi;
Omori, Yoshihiro;
Furukawa, Takahisa;
Iwata, Takeshi;
Nakano, Tadashi

Publication type:

Article

Role of ARMS2/HTRA1 risk alleles in the pathogenesis of neovascular age-related macular degeneration.

Published in:

Taiwan Journal of Ophthalmology, 2024, v. 14, n. 4, p. 531, doi. 10.4103/tjo.TJO-D-23-00152

By:

Pan, Yang;
Iwata, Takeshi

Publication type:

Article

Biological Magnetic Resonance Data Bank.

Published in:

Nucleic Acids Research, 2023, v. 51, n. D1, p. D368, doi. 10.1093/nar/gkac1050

By:

Hoch, Jeffrey C;
Baskaran, Kumaran;
Burr, Harrison;
Chin, John;
Eghbalnia, Hamid R;
Fujiwara, Toshimichi;
Gryk, Michael R;
Iwata, Takeshi;
Kojima, Chojiro;
Kurisu, Genji;
Maziuk, Dmitri;
Miyanoiri, Yohei;
Wedell, Jonathan R;
Wilburn, Colin;
Yao, Hongyang;
Yokochi, Masashi

Publication type:

Article