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Tatsushi Toda

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Takeshi Uenaka; Fumio Kanda; Hisatomo Kowa; Kakuya Nagata; Yoshihisa Ohtsuka; Kenji Sekiguchi; Tatsushi Toda
Myositis with antimitochondrial antibodies diagnosed by rectus abdominis muscle biopsy.
Tatsushi Toda
[Personal genome research and neurological diseases: overview].
Takeshi Uenaka; Hirotoshi Hamaguchi; Fumio Kanda; Hisatomo Kowa; Kenji Sekiguchi; Tatsushi Toda
Reversible cerebral vasoconstriction syndrome in a stroke patient with systemic lupus erythematosus and antiphospholipid antibody.

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2013: Takeshi Uenaka; Fumio Kanda; Hisatomo Kowa; Kakuya Nagata; Yoshihisa Ohtsuka; Kenji Sekiguchi; Tatsushi Toda
Myositis with antimitochondrial antibodies diagnosed by rectus abdominis muscle biopsy.
Muscle & nerve 2013;47(5):766-8.
2013: Tatsushi Toda
[Personal genome research and neurological diseases: overview].
Brain and nerve = Shinkei kenkyū no shinpo 2013;65(3):227-34.
2013: Takeshi Uenaka; Hirotoshi Hamaguchi; Fumio Kanda; Hisatomo Kowa; Kenji Sekiguchi; Tatsushi Toda
Reversible cerebral vasoconstriction syndrome in a stroke patient with systemic lupus erythematosus and antiphospholipid antibody.
Rinshō shinkeigaku = Clinical neurology 2013;53(4):283-6.
2013: Toko Miyawaki; Kenji Sekiguchi; Takehiro Ueda; Naoko Yasui; Fumio Kanda; Tatsushi Toda
A case of juvenile parkinsonism with expanded SCA8 CTA/CTG repeats.
Rinshō shinkeigaku = Clinical neurology 2013;53(4):278-82.
2012: Naoki Nakagawa; Tamao Endo; Hiroshi Manya; Tatsushi Toda; Shogo Oka
Human natural killer-1 sulfotransferase (HNK-1ST)-induced sulfate transfer regulates laminin-binding glycans on α-dystroglycan.
The Journal of biological chemistry 2012;287(36):30823-32.
2012: Atsushi Kuga; Qi L Lu; Hiroshi Manya; Motoyoshi Nomizu; Atsushi Sudo; Michiko Tajiri; Yiumo Michael Chan; Tamao Endo; Motoi Kanagawa; Yamato Kikkawa; Kazuhiro Kobayashi; Yoshinao Wada; Tatsushi Toda
Absence of post-phosphoryl modification in dystroglycanopathy mouse models and wild-type tissues expressing non-laminin binding form of α-dystroglycan.
The Journal of biological chemistry 2012;287(12):9560-7.
2012: Masaji Tachikawa; Motoi Kanagawa; Kazuhiro Kobayashi; Chih-Chieh Yu; Tatsushi Toda
Mislocalization of fukutin protein by disease-causing missense mutations can be rescued with treatments directed at folding amelioration.
The Journal of biological chemistry 2012;287(11):8398-406.
2012: H Akiko Popiel; Toshihide Takeuchi; Tatsushi Toda; Keiji Wada; Kazuhiro Yamamoto; Hiroshi Yamane; Hiromi Fujita; Chiyomi Ito; Shin-ichi Muramatsu; Yoshitaka Nagai
Hsp40 gene therapy exerts therapeutic effects on polyglutamine disease mice via a non-cell autonomous mechanism.
PloS one 2012;7(11):e51069.
2012: Tatsushi Toda; Mariko Taniguchi-Ikeda; Kazuhiro Kobayashi
[Molecular targeting therapy for Fukuyama muscular dystrophy].
Rinshō shinkeigaku = Clinical neurology 2012;52(11):1158.
2012: Tatsushi Toda
[Subspeciality training for neurologists--neurogenetics].
Rinshō shinkeigaku = Clinical neurology 2012;52(11):933.
2012: Yoshihisa Ohtsuka; Kenji Sekiguchi; Fumio Kanda; Hisatomo Kowa; Ichizo Nishino; Naoko Yasui; Tatsushi Toda
[A case of amyloidosis with amyloid deposition detected only in skeletal muscles].
Rinshō shinkeigaku = Clinical neurology 2012;52(10):739-43.
2012: Toshihiko Shirafuji; Hitoshi Takahashi; Keiko Tanaka; Masatsugu Higuchi; Fumio Kanda; Kenji Sekiguchi; Hiroshi Yokozaki; Tatsushi Toda
Anti-Hu-associated paraneoplastic encephalomyelitis with esophageal small cell carcinoma.
Internal medicine (Tokyo, Japan) 2012;51(17):2423-7.
2011: Tatsushi Toda; Shoji Tsuji
[Overview for personal genome analysis].
Rinshō shinkeigaku = Clinical neurology 2011;51(11):968.
2011: Tatsushi Toda
[Novel pathomechanism and therapeutic approach for Fukuyama muscular dystrophy].
Rinshō shinkeigaku = Clinical neurology 2011;51(11):917.
2011: Atsushi Kuga; Motoi Kanagawa; Tatsushi Toda
[Recent Advances in α-dystroglycanopathy].
Brain and nerve = Shinkei kenkyū no shinpo 2011;63(11):1189-95.
2011: Mariko Taniguchi-Ikeda; Toshifumi Yokota; Chih-chieh Yu; Hasan O Akman; Salvatore DiMauro; Ryuji Kaji; Motoi Kanagawa; Kazuhiro Kobayashi; Atsushi Kuga; Hiroki Kurahashi; Kouhei Mori; Tetsuya Oda; Shin'ichi Takeda; Tatsushi Toda
Pathogenic exon-trapping by SVA retrotransposon and rescue in Fukuyama muscular dystrophy.
Nature 2011;478(7367):127-31.
2011: H Akiko Popiel; Warren J Strittmatter; Toshihide Takeuchi; Tatsushi Toda; Keiji Wada; James R Burke; Nobutaka Fujii; Shinya Oishi; Yoshitaka Nagai
The Aggregation Inhibitor Peptide QBP1 as a Therapeutic Molecule for the Polyglutamine Neurodegenerative Diseases.
Journal of amino acids 2011;2011():265084.
2010: Tatsushi Toda; Hidenao Sasaki
[Frontline of genomics research on neurological diseases].
Rinshō shinkeigaku = Clinical neurology 2010;50(11):951.
2010: Tatsushi Toda; Wataru Satake
[Gene for sporadic Parkinson's disease: common disease-common variants].
Rinshō shinkeigaku = Clinical neurology 2010;50(11):864.
2010: Motoi Kanagawa; Yoshihiro Omori; S Sato; Kazuhiro Kobayashi; Yuko Miyagoe-Suzuki; Shin'ichi Takeda; Tamao Endo; Takahisa Furukawa; Tatsushi Toda
Post-translational maturation of dystroglycan is necessary for pikachurin binding and ribbon synaptic localization.
The Journal of biological chemistry 2010;285(41):31208-16.
2009: 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
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.
Nature genetics 2009;41(12):1303-7.
2009: Tatsushi Toda
[Pathomechanism and therapeutic strategy of Fukuyama congenital muscular dystrophy and related disorders].
Rinshō shinkeigaku = Clinical neurology 2009;49(11):859-62.
2009: Jun Mitsui; Ikuko Mizuta; Atsushi Toyoda; Ryo Ashida; Yuji K Takahashi; Jun Goto; Yoko Fukuda; Hidetoshi Date; Atsushi Iwata; Mitsutoshi Yamamoto; Nobutaka Hattori; Miho Murata; Tatsushi Toda; Shoji Tsuji
Mutations for Gaucher disease confer high susceptibility to Parkinson disease.
Archives of neurology 2009;66(5):571-6.
2009: Motoi Kanagawa; Akemi Nishimoto; Tomohiro Chiyonobu; Shin'ichi Takeda; Yuko Miyagoe-Suzuki; Fan Wang; Nobuhiro Fujikake; Mariko Taniguchi; Zhongpeng Lu; Masaji Tachikawa; Yoshitaka Nagai; Fumi Tashiro; Jun-Ichi Miyazaki; Youichi Tajima; Satoshi Takeda; Tamao Endo; Kazuhiro Kobayashi; Kevin P Campbell; Tatsushi Toda
Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy.
Human molecular genetics 2009;18(4):621-31.
2009: Kenji Tomita; H Akiko Popiel; Yoshitaka Nagai; Tatsushi Toda; Yuji Yoshimitsu; Hiroaki Ohno; Shinya Oishi; Nobutaka Fujii
Structure-activity relationship study on polyglutamine binding peptide QBP1.
Bioorganic & medicinal chemistry 2009;17(3):1259-63.
2009: H Akiko Popiel; Yoshitaka Nagai; Nobuhiro Fujikake; Tatsushi Toda
Delivery of the aggregate inhibitor peptide QBP1 into the mouse brain using PTDs and its therapeutic effect on polyglutamine disease mice.
Neuroscience letters 2009;449(2):87-92.
2008: Nobuhiro Fujikake; Yoshitaka Nagai; H Akiko Popiel; Yuma Okamoto; Masamitsu Yamaguchi; Tatsushi Toda
Heat shock transcription factor 1-activating compounds suppress polyglutamine-induced neurodegeneration through induction of multiple molecular chaperones.
The Journal of biological chemistry 2008;283(38):26188-97.
2008: Ikuko Mizuta; Tatsuhiko Tsunoda; Wataru Satake; Yuko Nakabayashi; Masahiko Watanabe; Atsushi Takeda; Kazuko Hasegawa; Kenji Nakashima; Mitsutoshi Yamamoto; Nobutaka Hattori; Miho Murata; Tatsushi Toda
Calbindin 1, fibroblast growth factor 20, and alpha-synuclein in sporadic Parkinson's disease.
Human genetics 2008;124(1):89-94.
2007: Hiroki Kano; Hiroki Kurahashi; Tatsushi Toda
Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(48):19034-9.
2007: Tatsushi Toda
[Hint and luck for identification of a gene for Fukuyama muscular dystrophy, fukutin].
Rinshō shinkeigaku = Clinical neurology 2007;47(11):743-8.
2007: Yasuo Takahashi; Yuma Okamoto; H Akiko Popiel; Nobuhiro Fujikake; Tatsushi Toda; Masataka Kinjo; Yoshitaka Nagai
Detection of polyglutamine protein oligomers in cells by fluorescence correlation spectroscopy.
The Journal of biological chemistry 2007;282(33):24039-48.
2007: Tatsushi Toda
[Molecular genetics of Parkinson's disease].
Brain and nerve = Shinkei kenkyū no shinpo 2007;59(8):815-23.
2007: Tomohiro Chiyonobu; Shin Hayashi; Kazuhiro Kobayashi; Masafumi Morimoto; Yuri Miyanomae; Akira Nishimura; Akemi Nishimoto; Chiyomi Ito; Issei Imoto; Tohru Sugimoto; Zhengping Jia; Johji Inazawa; Tatsushi Toda
Partial tandem duplication of GRIA3 in a male with mental retardation.
American journal of medical genetics. Part A 2007;143A(13):1448-55.
2007: Wataru Satake; Ikuko Mizuta; Satoko Suzuki; Yuko Nakabayashi; Chiyomi Ito; Masahiko Watanabe; Atsushi Takeda; Kazuko Hasegawa; Saburo Sakoda; Mitsutoshi Yamamoto; Nobutaka Hattori; Miho Murata; Tatsushi Toda
Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population.
Neuroreport 2007;18(9):937-40.
2007: Yoshitaka Nagai; H Akiko Popiel; Nobuhiro Fujikake; Tatsushi Toda
[Therapeutic strategies for the polyglutamine diseases].
Brain and nerve = Shinkei kenkyū no shinpo 2007;59(4):393-404.
2007: Yoshitaka Nagai; Takashi Inui; H Akiko Popiel; Nobuhiro Fujikake; Kazuhiro Hasegawa; Yoshihiro Urade; Yuji Goto; Hironobu Naiki; Tatsushi Toda
A toxic monomeric conformer of the polyglutamine protein.
Nature structural & molecular biology 2007;14(4):332-40.
2007: H Akiko Popiel; Yoshitaka Nagai; Nobuhiro Fujikake; Tatsushi Toda
Protein transduction domain-mediated delivery of QBP1 suppresses polyglutamine-induced neurodegeneration in vivo.
Molecular therapy : the journal of the American Society of Gene Therapy 2007;15(2):303-9.
2006: Hui Xiong; Kazuhiro Kobayashi; Masaji Tachikawa; Hiroshi Manya; Satoshi Takeda; Tomohiro Chiyonobu; Nobuhiro Fujikake; Fan Wang; Akemi Nishimoto; Glenn E Morris; Yoshitaka Nagai; Motoi Kanagawa; Tamao Endo; Tatsushi Toda
Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan.
Biochemical and biophysical research communications 2006;350(4):935-41.
2006: Mariko Taniguchi; Hiroki Kurahashi; Satoru Noguchi; Takayasu Fukudome; Takeshi Okinaga; Toshifumi Tsukahara; Youichi Tajima; Keiichi Ozono; Ichizo Nishino; Ikuya Nonaka; Tatsushi Toda
Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in alpha-dystroglycanopathies.
Human molecular genetics 2006;15(8):1279-89.
2006: Mariko Taniguchi; Hiroki Kurahashi; Satoru Noguchi; Jun Sese; Takeshi Okinaga; Toshifumi Tsukahara; Pascale Guicheney; Keiichi Ozono; Ichizo Nishino; Shinichi Morishita; Tatsushi Toda
Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?
Biochemical and biophysical research communications 2006;342(2):489-502.
2006: Ikuko Mizuta; Wataru Satake; Yuko Nakabayashi; Chiyomi Ito; Satoko Suzuki; Yoshio Momose; Yoshitaka Nagai; Akira Oka; Hidetoshi Inoko; Jiro Fukae; Yuko Saito; Motoji Sawabe; Shigeo Murayama; Mitsutoshi Yamamoto; Nobutaka Hattori; Miho Murata; Tatsushi Toda
Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease.
Human molecular genetics 2006;15(7):1151-8.
2006: Shingo Kariya; Makito Hirano; Shinichi Uesato; Yoshitaka Nagai; Yasuo Nagaoka; Yoshiko Furiya; Hirohide Asai; Nobuhiro Fujikake; Tatsushi Toda; Satoshi Ueno
Cytoprotective effect of novel histone deacetylase inhibitors against polyglutamine toxicity.
Neuroscience letters 2006;392(3):213-5.
2006: Motoi Kanagawa; Tatsushi Toda
The genetic and molecular basis of muscular dystrophy: roles of cell-matrix linkage in the pathogenesis.
Journal of human genetics 2006;51(11):915-26.
2005: Hiroki Kano; Kenji Kurosawa; Emiko Horii; Shiro Ikegawa; Hideki Yoshikawa; Hiroki Kurahashi; Tatsushi Toda
Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation.
Human genetics 2005;118(3-4):477-83.
2005: Tatsushi Toda
[Alpha-dystroglycanopathy (FCMD, MEB, etc): abnormal glycosylation and muscular dystrophy].
Rinshō shinkeigaku = Clinical neurology 2005;45(11):932-4.
2005: Tatsushi Toda; Tomohiro Chiyonobu; H Xiong; Masaji Tachikawa; Kazuhiro Kobayashi; Hiroshi Manya; Shin'ichi Takeda; Mariko Taniguchi; Hiroki Kurahashi; Takeshi Endo
Fukutin and alpha-dystroglycanopathies.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2005;24(2):60-3.
2005: Nobuhiro Fujikake; Yoshitaka Nagai; H Akiko Popiel; Hiroki Kano; Masamitsu Yamaguchi; Tatsushi Toda
Alternative splicing regulates the transcriptional activity of Drosophila heat shock transcription factor in response to heat/cold stress.
FEBS letters 2005;579(17):3842-8.
2005: Tomohiro Chiyonobu; Junko Sasaki; Yoshitaka Nagai; Satoshi Takeda; Hiroshi Funakoshi; Toshikazu Nakamura; Tohru Sugimoto; Tatsushi Toda
Effects of fukutin deficiency in the developing mouse brain.
Neuromuscular disorders : NMD 2005;15(6):416-26.
2005: Hiroki Kurahashi; Mariko Taniguchi; Chikara Meno; Yoshihiro Taniguchi; Satoshi Takeda; Masato Horie; Hiroki Otani; Tatsushi Toda
Basement membrane fragility underlies embryonic lethality in fukutin-null mice.
Neurobiology of disease 2005;19(1-2):208-17.
2005: Shingo Kariya; Makito Hirano; Yoshitaka Nagai; Yoshiko Furiya; Nobuhiro Fujikake; Tatsushi Toda; Satoshi Ueno
Humanin attenuates apoptosis induced by DRPLA proteins with expanded polyglutamine stretches.
Journal of molecular neuroscience : MN 2005;25(2):165-9.
2004: Ikuko Mizuta; Tatsushi Toda
[Searching genetic risk factors for sporadic Parkinson's disease].
Nihon rinsho. Japanese journal of clinical medicine 2004;62(9):1635-40.
2004: H Akiko Popiel; Yoshitaka Nagai; Osamu Onodera; Takashi Inui; Nobuhiro Fujikake; Yoshihiro Urade; Warren J Strittmatter; James R Burke; Atsushi Ichikawa; Tatsushi Toda
Disruption of the toxic conformation of the expanded polyglutamine stretch leads to suppression of aggregate formation and cytotoxicity.
Biochemical and biophysical research communications 2004;317(4):1200-6.
2003: Tatsushi Toda; Yoshio Momose; Miho Murata; Gen Tamiya; Mitsutoshi Yamamoto; Nobutaka Hattori; Hidetoshi Inoko
Toward identification of susceptibility genes for sporadic Parkinson's disease.
Journal of neurology 2003;250 Suppl 3():III40-3.
2003: Wenli Zhang; Jiri Vajsar; Pinjiang Cao; Galen Breningstall; Charlotta Diesen; William B Dobyns; Ralph Herrmann; Anna-Elina Lehesjoki; Alice Steinbrecher; Beril Talim; Tatsushi Toda; Haluk Topaloglu; Thomas Voit; Harry Schachter
Enzymatic diagnostic test for Muscle-Eye-Brain type congenital muscular dystrophy using commercially available reagents.
Clinical biochemistry 2003;36(5):339-44.
2003: Satoshi Takeda; Mari Kondo; Junko Sasaki; Hiroki Kurahashi; Hiroki Kano; Ken Arai; Kazuyo Misaki; Takehiko Fukui; Kazuhiro Kobayashi; Masaji Tachikawa; Michihiro Imamura; Yusuke Nakamura; Teruo Shimizu; Tatsufumi Murakami; Yoshihide Sunada; Takashi Fujikado; Kiichiro Matsumura; Toshio Terashima; Tatsushi Toda
Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development.
Human molecular genetics 2003;12(12):1449-59.
2003: Tatsushi Toda; Kazuhiro Kobayashi; Satoshi Takeda; Junko Sasaki; Hiroki Kurahashi; Hiroki Kano; Masaji Tachikawa; Fan Wang; Yoshitaka Nagai; Kiyomi Taniguchi; Mariko Taniguchi; Yoshihide Sunada; Toshio Terashima; Tamao Endo; Kiichiro Matsumura
Fukuyama-type congenital muscular dystrophy (FCMD) and alpha-dystroglycanopathy.
Congenital anomalies 2003;43(2):97-104.
2003: Yoshitaka Nagai; Nobuhiro Fujikake; Katsuhito Ohno; Hiroyuki Higashiyama; H Akiko Popiel; Julia Rahadian; Masamitsu Yamaguchi; Warren J Strittmatter; James R Burke; Tatsushi Toda
Prevention of polyglutamine oligomerization and neurodegeneration by the peptide inhibitor QBP1 in Drosophila.
Human molecular genetics 2003;12(11):1253-9.
2003: Kiyomi Taniguchi; Kazuhiro Kobayashi; Kayoko Saito; Hideo Yamanouchi; Akira Ohnuma; Yukiko K Hayashi; Hiroshi Manya; Dong Kyu Jin; Munhyang Lee; Enrico Parano; Raffaele Falsaperla; Piero Pavone; Rudy Van Coster; Beril Talim; Alice Steinbrecher; Volker Straub; Ichizo Nishino; Haluk Topaloglu; Thomas Voit; Tamao Endo; Tatsushi Toda
Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease.
Human molecular genetics 2003;12(5):527-34.
2002: Masato Horie; Kazuhiro Kobayashi; Satoshi Takeda; Yusuke Nakamura; Gary E Lyons; Tatsushi Toda
Isolation and characterization of the mouse ortholog of the Fukuyama-type congenital muscular dystrophy gene.
Genomics 2002;80(5):482-6.
2002: Tomohiro Chiyonobu; Takao Yoshihara; Yoko Fukushima; Yasutoshi Yamamoto; Kentaro Tsunamoto; Yasutaka Nishimura; Hiroyuki Ishida; Tatsushi Toda; Yasuo Kasubuchi
Sister and brother with Vici syndrome: agenesis of the corpus callosum, albinism, and recurrent infections.
American journal of medical genetics 2002;109(1):61-6.
2002: Hiroki Kano; Kazuhiro Kobayashi; Ralf Herrmann; Masaji Tachikawa; Hiroshi Manya; Ichizo Nishino; Ikuya Nonaka; Volker Straub; Beril Talim; Thomas Voit; Haluk Topaloglu; Tamao Endo; Hideki Yoshikawa; Tatsushi Toda
Deficiency of alpha-dystroglycan in muscle-eye-brain disease.
Biochemical and biophysical research communications 2002;291(5):1283-6.
2002: Masaji Tachikawa; Yoshitaka Nagai; Koichiro Nakamura; Kazuhiro Kobayashi; Tsutomu Fujiwara; Hye-Jung Han; Yuko Nakabayashi; Yaeko Ichikawa; Jun Goto; Ichiro Kanazawa; Yusuke Nakamura; Tatsushi Toda
Identification of CAG repeat-containing genes expressed in human brain as candidate genes for autosomal dominant spinocerebellar ataxias and other neurodegenerative diseases.
Journal of human genetics 2002;47(6):275-8.
2002: Yoshio Momose; Miho Murata; Kazuhiro Kobayashi; Masaji Tachikawa; Yuko Nakabayashi; Ichiro Kanazawa; Tatsushi Toda
Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphisms.
Annals of neurology 2002;51(1):133-6.
2001: Kazuhiro Kobayashi; Junko Sasaki; E Kondo-Iida; Y Fukuda; M Kinoshita; Y Sunada; Yusuke Nakamura; Tatsushi Toda
Structural organization, complete genomic sequences and mutational analyses of the Fukuyama-type congenital muscular dystrophy gene, fukutin.
FEBS letters 2001;489(2-3):192-6.
2000: Junko Sasaki; K Ishikawa; Kazuhiro Kobayashi; E Kondo-Iida; M Fukayama; H Mizusawa; S Takashima; Yoichi Sakakihara; Yusuke Nakamura; Tatsushi Toda
Neuronal expression of the fukutin gene.
Human molecular genetics 2000;9(20):3083-90.
2000: Tatsushi Toda
[Fukuyama-type congenital muscular dystrophy].
Rinshō shinkeigaku = Clinical neurology 2000;40(12):1297-9.
2000: Tatsushi Toda; Kazuhiro Kobayashi; E Kondo-Iida; Junko Sasaki; Yusuke Nakamura
The Fukuyama congenital muscular dystrophy story.
Neuromuscular disorders : NMD 2000;10(3):153-9.
1999: Tatsushi Toda; Kazuhiro Kobayashi
Fukuyama-type congenital muscular dystrophy: the first human disease to be caused by an ancient retrotransposal integration.
Journal of molecular medicine (Berlin, Germany) 1999;77(12):816-23.
1999: Masasuke Yoshida; Sueharu Horinouchi; Tatsushi Toda
[Control of gene expression in response to stress by a transcription factor Pap1].
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme 1999;44(15 Suppl):2396-402.
1999: E Kondo-Iida; Kazuhiro Kobayashi; M Watanabe; Junko Sasaki; T Kumagai; H Koide; Kayoko Saito; Makiko Osawa; Yusuke Nakamura; Tatsushi Toda
Novel mutations and genotype-phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD).
Human molecular genetics 1999;8(12):2303-9.
1999: N Kudo; H Taoka; Tatsushi Toda; Masasuke Yoshida; Sueharu Horinouchi
A novel nuclear export signal sensitive to oxidative stress in the fission yeast transcription factor Pap1.
The Journal of biological chemistry 1999;274(21):15151-8.
1999: Svetlana Kotliarova; Tatsushi Toda; Osamu Takenaka; Ikumi Matsushita; A Hida; Toshikatsu Shinka; J Goto; Katsushi Tokunaga; Y Nakagome; Yutaka Nakahori
Novel (CA)n marker DXYS241 on the nonrecombinant part of the human Y chromosome.
Human biology 1999;71(2):261-75.
1999: Yoko Kuroki; Takuji Iwamoto; Juwon Lee; M Yoshiike; S Nozawa; T Nishida; Ashraf A Ewis; Hajime Nakamura; Tatsushi Toda; Katsushi Tokunaga; Svetlana Kotliarova; N Kondoh; Eitetsu Koh; M Namiki; Toshikatsu Shinka; Yutaka Nakahori
Spermatogenic ability is different among males in different Y chromosome lineage.
Journal of human genetics 1999;44(5):289-92.
1999: Toshikatsu Shinka; K Tomita; Tatsushi Toda; Svetlana Kotliarova; Juwon Lee; Yoko Kuroki; D K Jin; Katsushi Tokunaga; Hajime Nakamura; Yutaka Nakahori
Genetic variations on the Y chromosome in the Japanese population and implications for modern human Y chromosome lineage.
Journal of human genetics 1999;44(4):240-5.
1999: Tatsushi Toda
[Fukutin, a novel protein product responsible for Fukuyama-type congenital muscular dystrophy].
Seikagaku. The Journal of Japanese Biochemical Society 1999;71(1):55-61.
1998: Kazuhiro Kobayashi; Yutaka Nakahori; K Mizuno; M Miyake; T Kumagai; A Honma; I Nonaka; Yusuke Nakamura; Katsushi Tokunaga; Tatsushi Toda
Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD).
Human genetics 1998;103(3):323-7.
1998: Shusuke Kuge; Tatsushi Toda; N Iizuka; Akio Nomoto
Crm1 (XpoI) dependent nuclear export of the budding yeast transcription factor yAP-1 is sensitive to oxidative stress.
Genes to cells : devoted to molecular & cellular mechanisms 1998;3(8):521-32.
1998: Kazuhiro Kobayashi; Yutaka Nakahori; M Miyake; K Matsumura; E Kondo-Iida; Y Nomura; M Segawa; M Yoshioka; Kayoko Saito; Makiko Osawa; K Hamano; Yoichi Sakakihara; I Nonaka; Y Nakagome; Ichiro Kanazawa; Yusuke Nakamura; Katsushi Tokunaga; Tatsushi Toda
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy.
Nature 1998;394(6691):388-92.
1998: Yasushi Takai; Osamu Tsutsumi; I Harada; Tomoyuki Fujii; Takeshi Kashima; Kazuhiro Kobayashi; Tatsushi Toda; Yuji Taketani
Prenatal diagnosis of Fukuyama-type congenital muscular dystrophy by microsatellite analysis.
Human reproduction (Oxford, England) 1998;13(2):320-3.
1997: Tatsushi Toda
[Gene hunting for Fukuyama-type congenital muscular dystrophy by positional cloning].
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme 1997;42(17 Suppl):2779-85.
1997: Tatsushi Toda; Kazuhiro Kobayashi
[Molecular genetics and merosin abnormality in Fukuyama-type congenital muscular dystrophy (FCMD)].
Nihon rinsho. Japanese journal of clinical medicine 1997;55(12):3169-75.
1997: M Miyake; Yutaka Nakahori; Ikumi Matsushita; Kazuhiro Kobayashi; K Mizuno; Momoki Hirai; Ichiro Kanazawa; Y Nakagome; Katsushi Tokunaga; Tatsushi Toda
YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31.
Genomics 1997;40(2):284-93.
1996: Svetlana Kotliarova; Tatsushi Toda; Ikumi Matsushita; Y Nakagome; Yutaka Nakahori
A novel (CA)n polymorphism on 6p21.1-21.2.
The Japanese journal of human genetics 1996;41(4):423-5.
1996: Tatsushi Toda; M Miyake; Kazuhiro Kobayashi; K Mizuno; Kayoko Saito; Makiko Osawa; Y Nakamura; Ichiro Kanazawa; Y Nakagome; Katsushi Tokunaga; Yutaka Nakahori
Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kb.
American journal of human genetics 1996;59(6):1313-20.
1996: S Ikegawa; Tatsushi Toda; K Okui; Y Nakamura
Structure and chromosomal assignment of the human S1-5 gene (FBNL) that is highly homologous to fibrillin.
Genomics 1996;35(3):590-2.
1996: Tatsushi Toda
[Gene hunting for Fukuyama type congenital muscular dystrophy].
Nō to shinkei = Brain and nerve 1996;48(4):315-22.
1996: Yutaka Nakahori; Yoko Kuroki; R Komaki; N Kondoh; M Namiki; T Iwamoto; Tatsushi Toda; Kazuhiro Kobayashi
The Y chromosome region essential for spermatogenesis.
Hormone research 1996;46 Suppl 1():20-3.
1995: Tatsushi Toda; S Ikegawa; M Miyake; Yutaka Nakahori; Y Nakamura
Dinucleotide repeat polymorphism on chromosome 9q32.
The Japanese journal of human genetics 1995;40(4):333-4.
1995: Tatsushi Toda
[Recent progress, genetic diagnosis and its problem on congenital muscular dystrophies (Fukuyama and non-Fukuyama types)].
Rinshō shinkeigaku = Clinical neurology 1995;35(12):1419-21.
1995: Tatsushi Toda; T Watanabe; K Matsumura; Y Sunada; H Yamada; I Nakano; T Mannen; Ichiro Kanazawa; T Shimizu
Three-dimensional MR imaging of brain surface anomalies in Fukuyama-type congenital muscular dystrophy.
Muscle & nerve 1995;18(5):508-17.
1995: Tatsushi Toda; M Yoshioka; Yutaka Nakahori; Ichiro Kanazawa; Y Nakamura; Y Nakagome
Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome.
Annals of neurology 1995;37(1):99-101.
1994: Tatsushi Toda; Shiro Ikegawa; K Okui; E Kondo; Kayoko Saito; Yukio Fukuyama; M Yoshioka; T Kumagai; K Suzumori; Ichiro Kanazawa
Refined mapping of a gene responsible for Fukuyama-type congenital muscular dystrophy: evidence for strong linkage disequilibrium.
American journal of human genetics 1994;55(5):946-50.
1993: S Miyake; N Okishio; I Samejima; Y Hiraoka; Tatsushi Toda; I Saitoh; M Yanagida
Fission yeast genes nda1+ and nda4+, mutations of which lead to S-phase block, chromatin alteration and Ca2+ suppression, are members of the CDC46/MCM2 family.
Molecular biology of the cell 1993;4(10):1003-15.
1993: M Watanabe; Ikuko Kondo; S Nissato; A Wakisaka; Tatsushi Toda; J Ikeda; J J Wasmuth; James Gusella; Ichiro Kanazawa
A linkage study with DNA markers (D4S95, D4S115, and D4S111) in Japanese Huntington disease families.
The Japanese journal of human genetics 1993;38(2):193-201.