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Research | 12 September 2020
Loss-of-function variants in NEK1 are associated with an increased risk of sporadic ALS in the Japanese population
- Hiroya Naruse
- , Hiroyuki Ishiura
- , Jun Mitsui
- , Yuji Takahashi
- , Takashi Matsukawa
- , Jun Yoshimura
- , Koichiro Doi
- , Shinichi Morishita
- , Jun Goto
- , Tatsushi Toda
- & Shoji Tsuji
Journal of Human Genetics , 1–5

Rights & permissionsfor article Loss-of-function variants in <i>NEK1</i> are associated with an increased risk of sporadic ALS in the Japanese population . Opens in a new window.
Research | 25 May 2020
Bardet–Biedl syndrome and related disorders in Japan
- Makito Hirano
- , Wataru Satake
- , Nobuko Moriyama
- , Ken Saida
- , Nobuhiko Okamoto
- , Pei-Chieng Cha
- , Yutaka Suzuki
- , Susumu Kusunoki
- & Tatsushi Toda
Journal of Human Genetics 65 , 847–853

Rights & permissionsfor article Bardet–Biedl syndrome and related disorders in Japan . Opens in a new window.
Amendments and Corrections | 25 August 2017
Correction: Corrigendum: Novel missense mutation in DLL4 in a Japanese sporadic case of Adams–Oliver syndrome
- Miwako Nagasaka
- , Mariko Taniguchi-Ikeda
- , Hidehito Inagaki
- , Yuya Ouchi
- , Daisuke Kurokawa
- , Keiji Yamana
- , Risa Harada
- , Kandai Nozu
- , Yoshitada Sakai
- , Sushil K Mishra
- , Yoshiki Yamaguchi
- , Ichiro Morioka
- , Tatsushi Toda
- , Hiroki Kurahashi
- & Kazumoto Iijima
Journal of Human Genetics 62 , 869–869

Rights & permissionsfor article Correction: Corrigendum: Novel missense mutation in <i>DLL4</i> in a Japanese sporadic case of Adams–Oliver syndrome . Opens in a new window.
Research | 28 February 2020 | Open
Neuron-specific analysis of histone modifications with post-mortem brains
- Kagari Koshi-Mano
- , Tatsuo Mano
- , Maho Morishima
- , Shigeo Murayama
- , Akira Tamaoka
- , Shoji Tsuji
- , Tatsushi Toda
- & Atsushi Iwata
Scientific Reports 10 , 1–11

Rights & permissionsfor article Neuron-specific analysis of histone modifications with post-mortem brains . Opens in a new window.
Research | 2 September 2019 | Open
Genome-wide association studies identify polygenic effects for completed suicide in the Japanese population
- Ikuo Otsuka
- , Masato Akiyama
- , Osamu Shirakawa
- , Satoshi Okazaki
- , Yukihide Momozawa
- , Yoichiro Kamatani
- , Takeshi Izumi
- , Shusuke Numata
- , Motonori Takahashi
- , Shuken Boku
- , Ichiro Sora
- , Ken Yamamoto
- , Yasuhiro Ueno
- , Tatsushi Toda
- , Michiaki Kubo
- & Akitoyo Hishimoto
Neuropsychopharmacology 44 , 2119–2124

Rights & permissionsfor article Genome-wide association studies identify polygenic effects for completed suicide in the Japanese population . Opens in a new window.
Research | 1 May 2020 | Open
Genome-wide association study identifies zonisamide responsive gene in Parkinson’s disease patients
- Pei-Chieng Cha
- , Wataru Satake
- , Yuko Ando-Kanagawa
- , Ken Yamamoto
- , Miho Murata
- & Tatsushi Toda
Journal of Human Genetics 65 , 693–704

Rights & permissionsfor article Genome-wide association study identifies zonisamide responsive gene in Parkinson’s disease patients . Opens in a new window.
Research | 6 July 2017
Deep-intronic variant of fukutin is the most prevalent point mutation of Fukuyama congenital muscular dystrophy in Japan
- Kazuhiro Kobayashi
- , Reiko Kato
- , Eri Kondo-Iida
- , Mariko Taniguchi-Ikeda
- , Makiko Osawa
- , Kayoko Saito
- & Tatsushi Toda
Journal of Human Genetics 62 , 945–948

Rights & permissionsfor article Deep-intronic variant of <i>fukutin</i> is the most prevalent point mutation of Fukuyama congenital muscular dystrophy in Japan . Opens in a new window.
Research | 27 April 2017
Novel missense mutation in DLL4 in a Japanese sporadic case of Adams–Oliver syndrome
- Miwako Nagasaka
- , Mariko Taniguchi-Ikeda
- , Hidehito Inagaki
- , Yuya Ouchi
- , Daisuke Kurokawa
- , Keiji Yamana
- , Risa Harada
- , Kandai Nozu
- , Yoshitada Sakai
- , Sushil K Mishra
- , Yoshiki Yamaguchi
- , Ichiro Morioka
- , Tatsushi Toda
- , Hiroki Kurahashi
- & Kazumoto Iijima
Journal of Human Genetics 62 , 851–855

Rights & permissionsfor article Novel missense mutation in <i>DLL4</i> in a Japanese sporadic case of Adams–Oliver syndrome . Opens in a new window.
Comments and Opinion | 13 October 2016
Ichiro Kanazawa, MD, PhD, 1941–2016
- Tatsushi Toda
Journal of Human Genetics 62 , 133–134

Rights & permissionsfor article Ichiro Kanazawa, MD, PhD, 1941–2016 . Opens in a new window.
Research | 19 May 2016
Analysis of phenotype, enzyme activity and genotype of Chinese patients with POMT1 mutation
- Haipo Yang
- , Hiroshi Manya
- , Kazuhiro Kobayashi
- , Hui Jiao
- , Xiaona Fu
- , Jiangxi Xiao
- , Xiaoqing Li
- , Jingmin Wang
- , Yuwu Jiang
- , Tatsushi Toda
- , Tamao Endo
- , Xiru Wu
- & Hui Xiong
Journal of Human Genetics 61 , 753–759

Rights & permissionsfor article Analysis of phenotype, enzyme activity and genotype of Chinese patients with <i>POMT1</i> mutation . Opens in a new window.
Research | 7 January 2016
Next-generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother
- Mariko Taniguchi-Ikeda
- , Yasuhiro Takeshima
- , Tomoko Lee
- , Masahiro Nishiyama
- , Hiroyuki Awano
- , Mariko Yagi
- , Ai Unzaki
- , Kandai Nozu
- , Hisahide Nishio
- , Masafumi Matsuo
- , Hiroki Kurahashi
- , Tatsushi Toda
- , Ichiro Morioka
- & Kazumoto Iijima
Journal of Human Genetics 61 , 351–355

Rights & permissionsfor article Next-generation sequencing discloses a nonsense mutation in the <i>dystrophin</i> gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother . Opens in a new window.
Research | 16 July 2015 | Open
A de novo mutation of the MYH7 gene in a large Chinese family with autosomal dominant myopathy
- ...) ever reported in China. Tatsushi Toda at the Kobe University Graduate...
- Tetsuya Oda
- , Hui Xiong
- , Kazuhiro Kobayashi
- , Shuo Wang
- , Wataru Satake
- , Hui Jiao
- , Yanling Yang
- , Pei-Chieng Cha
- , Yukiko K Hayashi
- , Ichizo Nishino
- , Yutaka Suzuki
- , Sumio Sugano
- , Xiru Wu
- & Tatsushi Toda
Human Genome Variation 2 , 1–7

Rights & permissionsfor article A <i>de novo</i> mutation of the <i>MYH7</i> gene in a large Chinese family with autosomal dominant myopathy . Opens in a new window.
Research | 13 June 2013
Molecular pathology of Sandhoff disease with p.Arg505Gln in HEXB: application of simulation analysis
- Naoko Yasui
- , Yutaka Takaoka
- , Hisahide Nishio
- , Dian K Nurputra
- , Kenji Sekiguchi
- , Hirotoshi Hamaguchi
- , Hisatomo Kowa
- , Eiichi Maeda
- , Aki Sugano
- , Kenji Miura
- , Toshiyuki Sakaeda
- , Fumio Kanda
- & Tatsushi Toda
Journal of Human Genetics 58 , 611–617

Rights & permissionsfor article Molecular pathology of Sandhoff disease with p.Arg505Gln in <i>HEXB</i>: application of simulation analysis . Opens in a new window.
Research | 25 June 2015 | Open
Prenatal genetic testing for familial severe congenital protein C deficiency
- Shinya Tairaku
- , Mariko Taniguchi-Ikeda
- , Yoko Okazaki
- , Yoriko Noguchi
- , Yuji Nakamachi
- , Takeshi Mori
- , Ikuko Kubokawa
- , Akira Hayakawa
- , Akio Shibata
- , Tomomi Emoto
- , Hiroki Kurahashi
- , Tatsushi Toda
- , Seiji Kawano
- , Hideto Yamada
- , Ichiro Morioka
- & Kazumoto Iijima
Human Genome Variation 2 , 1–3

Rights & permissionsfor article Prenatal genetic testing for familial severe congenital protein C deficiency . Opens in a new window.
Research | 21 November 2013 | Open
AGO61-dependent GlcNAc modification primes the formation of functional glycans on α-dystroglycan
- Hirokazu Yagi
- , Naoki Nakagawa
- , Takuya Saito
- , Hiroshi Kiyonari
- , Takaya Abe
- , Tatsushi Toda
- , Sz-Wei Wu
- , Kay-Hooi Khoo
- , Shogo Oka
- & Koichi Kato
Scientific Reports 3 , 1–9

Rights & permissionsfor article AGO61-dependent GlcNAc modification primes the formation of functional glycans on α-dystroglycan . Opens in a new window.
Research | 9 February 2015 | Open
Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression
- Yoshihisa Ohtsuka
- , Motoi Kanagawa
- , Chih-Chieh Yu
- , Chiyomi Ito
- , Tomoko Chiyo
- , Kazuhiro Kobayashi
- , Takashi Okada
- , Shin'ichi Takeda
- & Tatsushi Toda
Scientific Reports 5 , 1–6

Rights & permissionsfor article Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression . Opens in a new window.
Research | 16 January 2020 | Open
Crystal structures of fukutin-related protein (FKRP), a ribitol-phosphate transferase related to muscular dystrophy
- Naoyuki Kuwabara
- , Rieko Imae
- , Hiroshi Manya
- , Tomohiro Tanaka
- , Mamoru Mizuno
- , Hiroki Tsumoto
- , Motoi Kanagawa
- , Kazuhiro Kobayashi
- , Tatsushi Toda
- , Toshiya Senda
- , Tamao Endo
- & Ryuichi Kato
Nature Communications 11 , 1–11

Rights & permissionsfor article Crystal structures of fukutin-related protein (FKRP), a ribitol-phosphate transferase related to muscular dystrophy . Opens in a new window.
Research | 1 June 1993
A linkage study with DNA markers (D4S95, D4S115, and D4S111) in Japanese Huntington disease families
- Masahiko Watanabe
- , Ikuko Kondo
- , Sumiko Nissato
- , Akemi Wakisaka
- , Tatsushi Toda
- , Joh-e Ikeda
- , John J. Wasmuth
- , James F. Gusella
- & Ichiro Kanazawa
Journal of Human Genetics 38 , 193–201

Rights & permissionsfor article A linkage study with DNA markers (D4S95, D4S115, and D4S111) in Japanese Huntington disease families . Opens in a new window.
1 December 1996
A novel (CA)_n polymorphism on 6p21.1-21.2
Journal of Human Genetics 41 , 423–425

Rights & permissionsfor article A novel (CA)<sub>n</sub> polymorphism on 6p21.1-21.2 . Opens in a new window.
Research | 1 December 1995
Dinucleotide repeat polymorphism on chromosome 9q32
Journal of Human Genetics 40 , 333–334

Rights & permissionsfor article Dinucleotide repeat polymorphism on chromosome 9q32 . Opens in a new window.
Research | 1 August 1999
Spermatogenic ability is different among males in different Y chromosome lineage
- Yoko Kuroki
- , Teruaki Iwamoto
- , Juwon Lee
- , Miki Yoshiike
- , Shiari Nozawa
- , Takayasu Nishida
- , Ashraf A. Ewis
- , Hideki Nakamura
- , Tatsushi Toda
- , K. Tokunaga
- , Svetlana E. Kotliarova
- , Nobuyuki Kondoh
- , Eitetsu Koh
- , Mikio Namiki
- , Toshikatsu Shinka
- & Y. Nakahori
Journal of Human Genetics 44 , 289–292

Rights & permissionsfor article Spermatogenic ability is different among males in different Y chromosome lineage . Opens in a new window.
Research | 5 July 2007
Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia
- Takeshi Amino
- , Kinya Ishikawa
- , Shuta Toru
- , Taro Ishiguro
- , Nozomu Sato
- , Taiji Tsunemi
- , Miho Murata
- , Kazuhiro Kobayashi
- , Johji Inazawa
- , Tatsushi Toda
- & Hidehiro Mizusawa
Journal of Human Genetics 52 , 643–649

Rights & permissionsfor article Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia . Opens in a new window.
Research | 1 December 2008
LRRK2 P755L variant in sporadic Parkinson’s disease
- Hiroyuki Tomiyama
- , Ikuko Mizuta
- , Yuanzhe Li
- , Manabu Funayama
- , Hiroyo Yoshino
- , Lin Li
- , Miho Murata
- , Mitsutoshi Yamamoto
- , Shin-ichiro Kubo
- , Yoshikuni Mizuno
- , Tatsushi Toda
- & Nobutaka Hattori
Journal of Human Genetics 53 , 1012–1015

Rights & permissionsfor article <i>LRRK2</i> P755L variant in sporadic Parkinson’s disease . Opens in a new window.
Research | 23 July 1998
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
- Kazuhiro Kobayashi
- , Yutaka Nakahori
- , Masashi Miyake
- , Kiichiro Matsumura
- , Eri Kondo-Iida
- , Yoshiko Nomura
- , Masaya Segawa
- , Mieko Yoshioka
- , Kayoko Saito
- , Makiko Osawa
- , Kenzo Hamano
- , Youichi Sakakihara
- , Ikuya Nonaka
- , Yasuo Nakagome
- , Ichiro Kanazawa
- , Yusuke Nakamura
- , Katsushi Tokunaga
- & Tatsushi Toda
Nature 394 , 388–392

Rights & permissionsfor article An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy . Opens in a new window.
Research | 1 July 1999
Genetic variations on the Y chromosome in the Japanese population and implications for modern human Y chromosome lineage
- Toshikatsu Shinka
- , Keiko Tomita
- , Tatsushi Toda
- , Svetlana E. Kotliarova
- , Juwon Lee
- , Yoko Kuroki
- , Dong Kyu Jin
- , Katsushi Tokunaga
- , Hideki Nakamura
- & Y. Nakahori
Journal of Human Genetics 44 , 240–245

Rights & permissionsfor article Genetic variations on the Y chromosome in the Japanese population and implications for modern human Y chromosome lineage . Opens in a new window.
Research | 10 February 2011
Genetic and clinical analysis in a Chinese parkinsonism-predominant spinocerebellar ataxia type 2 family
- Hao Sun
- , Wataru Satake
- , Changjun Zhang
- , Yoshitaka Nagai
- , Youyong Tian
- , Shouzhi Fu
- , Jiankun Yu
- , Yaping Qian
- , Yuan Qian
- , Jiayou Chu
- & Tatsushi Toda
Journal of Human Genetics 56 , 330–334

Rights & permissionsfor article Genetic and clinical analysis in a Chinese parkinsonism-predominant spinocerebellar ataxia type 2 family . Opens in a new window.
Research | 31 May 2012
Screening of genes involved in chromosome segregation during meiosis I: in vitro gene transfer to mouse fetal oocytes
- Makiko Tsutsumi
- , Hiroe Kowa-Sugiyama
- , Hasbaira Bolor
- , Hiroshi Kogo
- , Hidehito Inagaki
- , Tamae Ohye
- , Kouji Yamada
- , Mariko Taniguchi-Ikeda
- , Tatsushi Toda
- & Hiroki Kurahashi
Journal of Human Genetics 57 , 515–522

Rights & permissionsfor article Screening of genes involved in chromosome segregation during meiosis I: <i>in vitro</i> gene transfer to mouse fetal oocytes . Opens in a new window.
Research | 15 November 2009
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
- Tatsushi Toda and colleagues report results of...
- Wataru Satake
- , Yuko Nakabayashi
- , Ikuko Mizuta
- , Yushi Hirota
- , Chiyomi Ito
- , Michiaki Kubo
- , Takahisa Kawaguchi
- , Tatsuhiko Tsunoda
- , Masahiko Watanabe
- , Atsushi Takeda
- , Hiroyuki Tomiyama
- , Kenji Nakashima
- , Kazuko Hasegawa
- , Fumiya Obata
- , Takeo Yoshikawa
- , Hideshi Kawakami
- , Saburo Sakoda
- , Mitsutoshi Yamamoto
- , Nobutaka Hattori
- , Miho Murata
- , Yusuke Nakamura
- & Tatsushi Toda
Nature Genetics 41 , 1303–1307

Rights & permissionsfor article Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease . Opens in a new window.
Research | 26 March 2010
Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humans
- Hiroshi Kogo
- , Hiroe Kowa-Sugiyama
- , Kouji Yamada
- , Hasbaira Bolor
- , Makiko Tsutsumi
- , Tamae Ohye
- , Hidehito Inagaki
- , Mariko Taniguchi
- , Tatsushi Toda
- & Hiroki Kurahashi
Journal of Human Genetics 55 , 293–299

Rights & permissionsfor article Screening of genes involved in chromosome segregation during meiosis I: toward the identification of genes responsible for infertility in humans . Opens in a new window.
Research | 17 December 2019 | Open
Elimination of fukutin reveals cellular and molecular pathomechanisms in muscular dystrophy-associated heart failure
- Yoshihiro Ujihara
- , Motoi Kanagawa
- , Satoshi Mohri
- , Satomi Takatsu
- , Kazuhiro Kobayashi
- , Tatsushi Toda
- , Keiji Naruse
- & Yuki Katanosaka
Nature Communications 10 , 1–17

Rights & permissionsfor article Elimination of fukutin reveals cellular and molecular pathomechanisms in muscular dystrophy-associated heart failure . Opens in a new window.
Research | 10 September 2019 | Open
Characterization of dystroglycan binding in adhesion of human induced pluripotent stem cells to laminin-511 E8 fragment
- Yumika Sugawara
- , Keisuke Hamada
- , Yuji Yamada
- , Jun Kumai
- , Motoi Kanagawa
- , Kazuhiro Kobayashi
- , Tatsushi Toda
- , Yoichi Negishi
- , Fumihiko Katagiri
- , Kentaro Hozumi
- , Motoyoshi Nomizu
- & Yamato Kikkawa
Scientific Reports 9 , 1–12

Rights & permissionsfor article Characterization of dystroglycan binding in adhesion of human induced pluripotent stem cells to laminin-511 E8 fragment . Opens in a new window.
Research | 22 July 2019
Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease
- Hiroyuki Ishiura
- , Shota Shibata
- , Jun Yoshimura
- , Yuta Suzuki
- , Wei Qu
- , Koichiro Doi
- , M. Asem Almansour
- , Junko Kanda Kikuchi
- , Makiko Taira
- , Jun Mitsui
- , Yuji Takahashi
- , Yaeko Ichikawa
- , Tatsuo Mano
- , Atsushi Iwata
- , Yasuo Harigaya
- , Miho Kawabe Matsukawa
- , Takashi Matsukawa
- , Masaki Tanaka
- , Yuichiro Shirota
- , Ryo Ohtomo
- , Hisatomo Kowa
- , Hidetoshi Date
- , Aki Mitsue
- , Hiroyuki Hatsuta
- , Satoru Morimoto
- , Shigeo Murayama
- , Yasushi Shiio
- , Yuko Saito
- , Akihiko Mitsutake
- , Mizuho Kawai
- , Takuya Sasaki
- , Yusuke Sugiyama
- , Masashi Hamada
- , Gaku Ohtomo
- , Yasuo Terao
- , Yoshihiko Nakazato
- , Akitoshi Takeda
- , Yoshio Sakiyama
- , Yumi Umeda-Kameyama
- , Jun Shinmi
- , Katsuhisa Ogata
- , Yutaka Kohno
- , Shen-Yang Lim
- , Ai Huey Tan
- , Jun Shimizu
- , Jun Goto
- , Ichizo Nishino
- , Tatsushi Toda
- , Shinichi Morishita
- & Shoji Tsuji
Nature Genetics 51 , 1222–1232

Rights & permissionsfor article Noncoding CGG repeat expansions in neuronal intranuclear inclusion disease, oculopharyngodistal myopathy and an overlapping disease . Opens in a new window.
Research | 26 February 2019 | Open
Chronic cerebral hypoperfusion shifts the equilibrium of amyloid β oligomers to aggregation-prone species with higher molecular weight
- Taro Bannai
- , Tatsuo Mano
- , Xigui Chen
- , Gaku Ohtomo
- , Ryo Ohtomo
- , Takeyuki Tsuchida
- , Kagari Koshi-Mano
- , Tadafumi Hashimoto
- , Hitoshi Okazawa
- , Takeshi Iwatsubo
- , Shoji Tsuji
- , Tatsushi Toda
- & Atsushi Iwata
Scientific Reports 9 , 1–11

Rights & permissionsfor article Chronic cerebral hypoperfusion shifts the equilibrium of amyloid β oligomers to aggregation-prone species with higher molecular weight . Opens in a new window.
Research | 24 May 2018 | Open
Cell surface flip-flop of phosphatidylserine is critical for PIEZO1-mediated myotube formation
- Masaki Tsuchiya
- , Yuji Hara
- , Masaki Okuda
- , Karin Itoh
- , Ryotaro Nishioka
- , Akifumi Shiomi
- , Kohjiro Nagao
- , Masayuki Mori
- , Yasuo Mori
- , Junichi Ikenouchi
- , Ryo Suzuki
- , Motomu Tanaka
- , Tomohiko Ohwada
- , Junken Aoki
- , Motoi Kanagawa
- , Tatsushi Toda
- , Yosuke Nagata
- , Ryoichi Matsuda
- , Yasunori Takayama
- , Makoto Tominaga
- & Masato Umeda
Nature Communications 9 , 1–15

Rights & permissionsfor article Cell surface flip-flop of phosphatidylserine is critical for PIEZO1-mediated myotube formation . Opens in a new window.
Research | 12 September 2013
YY1 binds to α-synuclein 3′-flanking region SNP and stimulates antisense noncoding RNA expression
- Ikuko Mizuta
- , Kazuaki Takafuji
- , Yuko Ando
- , Wataru Satake
- , Motoi Kanagawa
- , Kazuhiro Kobayashi
- , Shushi Nagamori
- , Takayuki Shinohara
- , Chiyomi Ito
- , Mitsutoshi Yamamoto
- , Nobutaka Hattori
- , Miho Murata
- , Yoshikatsu Kanai
- , Shigeo Murayama
- , Masanori Nakagawa
- & Tatsushi Toda
Journal of Human Genetics 58 , 711–719

Rights & permissionsfor article YY1 binds to <i>α-synuclein</i> 3′-flanking region SNP and stimulates antisense noncoding RNA expression . Opens in a new window.
Research | 29 May 2014 | Open
TRPV2 is critical for the maintenance of cardiac structure and function in mice
- Yuki Katanosaka
- , Keiichiro Iwasaki
- , Yoshihiro Ujihara
- , Satomi Takatsu
- , Koki Nishitsuji
- , Motoi Kanagawa
- , Atsushi Sudo
- , Tatsushi Toda
- , Kimiaki Katanosaka
- , Satoshi Mohri
- & Keiji Naruse
Nature Communications 5 , 1–14

Rights & permissionsfor article TRPV2 is critical for the maintenance of cardiac structure and function in mice . Opens in a new window.
Reviews | 1 November 2006
The genetic and molecular basis of muscular dystrophy: roles of cell–matrix linkage in the pathogenesis
- Motoi Kanagawa
- & Tatsushi Toda
Journal of Human Genetics 51 , 915–926

Rights & permissionsfor article The genetic and molecular basis of muscular dystrophy: roles of cell–matrix linkage in the pathogenesis . Opens in a new window.
Research | 20 July 2008
Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation
- Shigeru Sato
- , Yoshihiro Omori
- , Kimiko Katoh
- , Mineo Kondo
- , Motoi Kanagawa
- , Kentaro Miyata
- , Kazuo Funabiki
- , Toshiyuki Koyasu
- , Naoko Kajimura
- , Tomomitsu Miyoshi
- , Hajime Sawai
- , Kazuhiro Kobayashi
- , Akiko Tani
- , Tatsushi Toda
- , Jiro Usukura
- , Yasuo Tano
- , Takashi Fujikado
- & Takahisa Furukawa
Nature Neuroscience 11 , 923–931

Rights & permissionsfor article Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation . Opens in a new window.
Research | 5 October 2011
Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy
- ...region of the fukutin gene. Tatsushi Toda and colleagues show that this...
- Mariko Taniguchi-Ikeda
- , Kazuhiro Kobayashi
- , Motoi Kanagawa
- , Chih-chieh Yu
- , Kouhei Mori
- , Tetsuya Oda
- , Atsushi Kuga
- , Hiroki Kurahashi
- , Hasan O. Akman
- , Salvatore DiMauro
- , Ryuji Kaji
- , Toshifumi Yokota
- , Shin’ichi Takeda
- & Tatsushi Toda
Nature 478 , 127–131

Rights & permissionsfor article Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy . Opens in a new window.
Research | 18 March 2007
A toxic monomeric conformer of the polyglutamine protein
- Yoshitaka Nagai
- , Takashi Inui
- , H Akiko Popiel
- , Nobuhiro Fujikake
- , Kazuhiro Hasegawa
- , Yoshihiro Urade
- , Yuji Goto
- , Hironobu Naiki
- & Tatsushi Toda
Nature Structural & Molecular Biology 14 , 332–340

Rights & permissionsfor article A toxic monomeric conformer of the polyglutamine protein . Opens in a new window.

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