Literature DB >> 19897927

Introduction to the Japan Mouse Clinic at the RIKEN BioResource Center.

Shigeharu Wakana1, Tomohiro Suzuki, Tamio Furuse, Kimio Kobayashi, Ikuo Miura, Hideki Kaneda, Ikuko Yamada, Hiromi Motegi, Hideaki Toki, Maki Inoue, Osamu Minowa, Tetsuo Noda, Kazunori Waki, Nobuhiko Tanaka, Hiroshi Masuya, Yuichi Obata.   

Abstract

A systematic and comprehensive phenotyping platform has been developed by the RIKEN ENU-mutagenesis project between 1999 and 2007. As a result of phenotype screening on this platform, we have discovered about 400 mutants as animal models for human diseases. All information regarding these mouse mutants is now available to the public through our home page (http://www.brc.riken.jp/lab/gsc/mouse/indexJ.html). In 2008, we reconstructed the existing phenotyping platform and built a new platform. The new system has a hierarchical structure, consisting of a fundamental pipeline that utilizes the existing platform and an additional pipeline, which is optimized for more in-depth phenotyping assays. Using this system, we have started to perform more comprehensive phenotyping of mouse mutants. We have opened this system to Japanese scientists as the Japanese Mouse Clinic. It is anticipated that existing mouse mutants will be reevaluated as disease models by identifying novel phenotypes on the new platform. We will share detailed information about the standard operating procedures (SOPs) of our phenotyping analyses with other related large-scale projects, such as the European Mouse Disease Clinic (EUMODIC) and the German Mouse Clinic (GMC). Moreover, we will contribute to international efforts to standardize mouse phenotype data by sharing annotation of mutant phenotypes, which are made by internationally standardized methods, with other related projects.

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Year:  2009        PMID: 19897927     DOI: 10.1538/expanim.58.443

Source DB:  PubMed          Journal:  Exp Anim        ISSN: 0007-5124


  17 in total

Review 1.  Dissecting immunity by germline mutagenesis.

Authors:  Onjee Choi; Sophie Rutschmann
Journal:  Immunology       Date:  2012-10       Impact factor: 7.397

2.  Pheno-Pub: a total support system for the publication of mouse phenotypic data on the web.

Authors:  Tomohiro Suzuki; Tamio Furuse; Ikuko Yamada; Hiromi Motegi; Yasuyo Kozawa; Hiroshi Masuya; Shigeharu Wakana
Journal:  Mamm Genome       Date:  2013-11-13       Impact factor: 2.957

3.  Establishment of mouse line showing inducible priapism-like phenotypes.

Authors:  Daiki Hashimoto; Kota Fujimoto; Shin Morioka; Shinya Ayabe; Tomoya Kataoka; Ryutaro Fukumura; Yuko Ueda; Mizuki Kajimoto; Taiju Hyuga; Kentaro Suzuki; Isao Hara; Shinichi Asamura; Shigeharu Wakana; Atsushi Yoshiki; Yoichi Gondo; Masaru Tamura; Takehiko Sasaki; Gen Yamada
Journal:  Reprod Med Biol       Date:  2022-06-20

4.  SDOP-DB: a comparative standardized-protocol database for mouse phenotypic analyses.

Authors:  Nobuhiko Tanaka; Kazunori Waki; Hideki Kaneda; Tomohiro Suzuki; Ikuko Yamada; Tamio Furuse; Kimio Kobayashi; Hiromi Motegi; Hideaki Toki; Maki Inoue; Osamu Minowa; Tetsuo Noda; Keizo Takao; Tsuyoshi Miyakawa; Aki Takahashi; Tsuyoshi Koide; Shigeharu Wakana; Hiroshi Masuya
Journal:  Bioinformatics       Date:  2010-03-01       Impact factor: 6.937

5.  A coding variant in SR-BI (I179N) significantly increases atherosclerosis in mice.

Authors:  Antonino Picataggi; Geoffrey F Lim; Anthony P Kent; John S Millar; Daniel J Rader; Ioannis M Stylianou
Journal:  Mamm Genome       Date:  2013-05-31       Impact factor: 2.957

6.  Discoidin domain receptor 2 (DDR2) regulates body size and fat metabolism in mice.

Authors:  Ikuma Kawai; Hirokazu Matsumura; Wataru Fujii; Kunihiko Naito; Ken Kusakabe; Yasuo Kiso; Kiyoshi Kano
Journal:  Transgenic Res       Date:  2013-09-14       Impact factor: 2.788

7.  Substrains matter in phenotyping of C57BL/6 mice.

Authors:  Kazuyuki Mekada; Atsushi Yoshiki
Journal:  Exp Anim       Date:  2021-01-14

Review 8.  New insights into behaviour using mouse ENU mutagenesis.

Authors:  Peter L Oliver; Kay E Davies
Journal:  Hum Mol Genet       Date:  2012-08-13       Impact factor: 6.150

9.  Ablation of Mrds1/Ofcc1 induces hyper-γ-glutamyl transpeptidasemia without abnormal head development and schizophrenia-relevant behaviors in mice.

Authors:  Tetsuo Ohnishi; Kazuo Yamada; Akiko Watanabe; Hisako Ohba; Toru Sakaguchi; Yota Honma; Yoshimi Iwayama; Tomoko Toyota; Motoko Maekawa; Kazutada Watanabe; Sevilla D Detera-Wadleigh; Shigeharu Wakana; Takeo Yoshikawa
Journal:  PLoS One       Date:  2011-12-29       Impact factor: 3.240

10.  Tysnd1 deficiency in mice interferes with the peroxisomal localization of PTS2 enzymes, causing lipid metabolic abnormalities and male infertility.

Authors:  Yumi Mizuno; Yuichi Ninomiya; Yutaka Nakachi; Mioko Iseki; Hiroyasu Iwasa; Masumi Akita; Tohru Tsukui; Nobuyuki Shimozawa; Chizuru Ito; Kiyotaka Toshimori; Megumi Nishimukai; Hiroshi Hara; Ryouta Maeba; Tomoki Okazaki; Ali Nasser Ali Alodaib; Mohammed Al Amoudi; Minnie Jacob; Fowzan S Alkuraya; Yasushi Horai; Mitsuhiro Watanabe; Hiromi Motegi; Shigeharu Wakana; Tetsuo Noda; Igor V Kurochkin; Yosuke Mizuno; Christian Schönbach; Yasushi Okazaki
Journal:  PLoS Genet       Date:  2013-02-14       Impact factor: 5.917

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