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Tatsushi Toda
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21
Kobayashi, Kazuhiro
18
Nagai, Yoshitaka
13
Fujikake, Nobuhiro
11
Nakahori, Yutaka
10
Popiel, Akiko
9
Nakamura, Yusuke
8
Kurahashi, Hiroki
8
Tachikawa, Masaji
7
Takeda, Satoshi
7
Tokunaga, Katsushi
7
Sasaki, Junko
7
Kanazawa, Ichiro
6
Kano, Hiroki
6
Chiyonobu, Tomohiro
6
Nakagome, Y
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All Publications
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2009: Mitsui Jun; Mizuta Ikuko; Toyoda Atsushi; Ashida Ryo; Takahashi Yuji; Goto Jun; Fukuda Yoko; Date Hidetoshi; Iwata Atsushi; Yamamoto Mitsutoshi; Hattori Nobutaka; Murata Miho; Toda Tatsushi; Tsuji Shoji
Mutations for Gaucher disease confer high susceptibility to Parkinson disease.
Archives of neurology 2009;66(5):571-6.
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2009: Tomita Kenji; Popiel H Akiko; Nagai Yoshitaka; Toda Tatsushi; Yoshimitsu Yuji; Ohno Hiroaki; Oishi Shinya; Fujii Nobutaka
Structure-activity relationship study on polyglutamine binding peptide QBP1.
Bioorganic & medicinal chemistry 2009;17(3):1259-63.
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2009: Kanagawa Motoi; Nishimoto Akemi; Chiyonobu Tomohiro; Takeda Satoshi; Miyagoe-Suzuki Yuko; Wang Fan; Fujikake Nobuhiro; Taniguchi Mariko; Lu Zhongpeng; Tachikawa Masaji; Nagai Yoshitaka; Tashiro Fumi; Miyazaki Jun-Ichi; Tajima Youichi; Takeda Shin'ichi; Endo Tamao; Kobayashi Kazuhiro; Campbell Kevin P; Toda Tatsushi
Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy.
Human molecular genetics 2009;18(4):621-31.
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2009: Popiel H Akiko; Nagai Yoshitaka; Fujikake Nobuhiro; Toda Tatsushi
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.
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2008: Fujikake Nobuhiro; Nagai Yoshitaka; Popiel H Akiko; Okamoto Yuma; Yamaguchi Masamitsu; Toda Tatsushi
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.
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2008: Mizuta Ikuko; Tsunoda Tatsuhiko; Satake Wataru; Nakabayashi Yuko; Watanabe Masahiko; Takeda Atsushi; Hasegawa Kazuko; Nakashima Kenji; Yamamoto Mitsutoshi; Hattori Nobutaka; Murata Miho; Toda Tatsushi
Calbindin 1, fibroblast growth factor 20, and alpha-synuclein in sporadic Parkinson's disease.
Human genetics 2008;124(1):89-94.
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2007: Toda Tatsushi
[Hint and luck for identification of a gene for Fukuyama muscular dystrophy, fukutin]
Rinsho shinkeigaku = Clinical neurology 2007;47(11):743-8.
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2007: Kano Hiroki; Kurahashi Hiroki; Toda Tatsushi
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.
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2007: Toda Tatsushi
[Molecular genetics of Parkinson's disease]
Brain and nerve = Shinkei kenkyu no shinpo 2007;59(8):815-23.
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2007: Takahashi Yasuo; Okamoto Yuma; Popiel H Akiko; Fujikake Nobuhiro; Toda Tatsushi; Kinjo Masataka; Nagai Yoshitaka
Detection of polyglutamine protein oligomers in cells by fluorescence correlation spectroscopy.
The Journal of biological chemistry 2007;282(33):24039-48.
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2007: Chiyonobu Tomohiro; Hayashi Shin; Kobayashi Kazuhiro; Morimoto Masafumi; Miyanomae Yuri; Nishimura Akira; Nishimoto Akemi; Ito Chiyomi; Imoto Issei; Sugimoto Tohru; Jia Zhengping; Inazawa Johji; Toda Tatsushi
Partial tandem duplication of GRIA3 in a male with mental retardation.
American journal of medical genetics. Part A 2007;143A(13):1448-55.
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2007: Satake Wataru; Mizuta Ikuko; Suzuki Satoko; Nakabayashi Yuko; Ito Chiyomi; Watanabe Masahiko; Takeda Atsushi; Hasegawa Kazuko; Sakoda Saburo; Yamamoto Mitsutoshi; Hattori Nobutaka; Murata Miho; Toda Tatsushi
Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population.
Neuroreport 2007;18(9):937-40.
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2007: Nagai Yoshitaka; Popiel H Akiko; Fujikake Nobuhiro; Toda Tatsushi
[Therapeutic strategies for the polyglutamine diseases]
Brain and nerve = Shinkei kenkyu no shinpo 2007;59(4):393-404.
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2007: Nagai Yoshitaka; Inui Takashi; Popiel H Akiko; Fujikake Nobuhiro; Hasegawa Kazuhiro; Urade Yoshihiro; Goto Yuji; Naiki Hironobu; Toda Tatsushi
A toxic monomeric conformer of the polyglutamine protein.
Nature structural & molecular biology 2007;14(4):332-40.
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2007: Popiel H Akiko; Nagai Yoshitaka; Fujikake Nobuhiro; Toda Tatsushi
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.
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2006: Xiong Hui; Kobayashi Kazuhiro; Tachikawa Masaji; Manya Hiroshi; Takeda Satoshi; Chiyonobu Tomohiro; Fujikake Nobuhiro; Wang Fan; Nishimoto Akemi; Morris Glenn E; Nagai Yoshitaka; Kanagawa Motoi; Endo Tamao; Toda Tatsushi
Molecular interaction between fukutin and POMGnT1 in the glycosylation pathway of alpha-dystroglycan.
Biochemical and biophysical research communications 2006;350(4):935-41.
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2006: Taniguchi Mariko; Kurahashi Hiroki; Noguchi Satoru; Fukudome Takayasu; Okinaga Takeshi; Tsukahara Toshifumi; Tajima Youichi; Ozono Keiichi; Nishino Ichizo; Nonaka Ikuya; Toda Tatsushi
Aberrant neuromuscular junctions and delayed terminal muscle fiber maturation in alpha-dystroglycanopathies.
Human molecular genetics 2006;15(8):1279-89.
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2006: Mizuta Ikuko; Satake Wataru; Nakabayashi Yuko; Ito Chiyomi; Suzuki Satoko; Momose Yoshio; Nagai Yoshitaka; Oka Akira; Inoko Hidetoshi; Fukae Jiro; Saito Yuko; Sawabe Motoji; Murayama Shigeo; Yamamoto Mitsutoshi; Hattori Nobutaka; Murata Miho; Toda Tatsushi
Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease.
Human molecular genetics 2006;15(7):1151-8.
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2006: Taniguchi Mariko; Kurahashi Hiroki; Noguchi Satoru; Sese Jun; Okinaga Takeshi; Tsukahara Toshifumi; Guicheney Pascale; Ozono Keiichi; Nishino Ichizo; Morishita Shinichi; Toda Tatsushi
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.
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2006: Kariya Shingo; Hirano Makito; Uesato Shinichi; Nagai Yoshitaka; Nagaoka Yasuo; Furiya Yoshiko; Asai Hirohide; Fujikake Nobuhiro; Toda Tatsushi; Ueno Satoshi
Cytoprotective effect of novel histone deacetylase inhibitors against polyglutamine toxicity.
Neuroscience letters 2006;392(3):213-5.
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2006: Kanagawa Motoi; Toda Tatsushi
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.
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2005: Kano Hiroki; Kurosawa Kenji; Horii Emiko; Ikegawa Shiro; Yoshikawa Hideki; Kurahashi Hiroki; Toda Tatsushi
Genomic rearrangement at 10q24 in non-syndromic split-hand/split-foot malformation.
Human genetics 2005;118(3-4):477-83.
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2005: Toda Tatsushi
[Alpha-dystroglycanopathy (FCMD, MEB, etc): abnormal glycosylation and muscular dystrophy]
Rinsho shinkeigaku = Clinical neurology 2005;45(11):932-4.
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2005: Toda T; Chiyonobu T; Xiong H; Tachikawa M; Kobayashi K; Manya H; Takeda S; Taniguchi M; Kurahashi H; Endo T
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.
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2005: Fujikake Nobuhiro; Nagai Yoshitaka; Popiel H Akiko; Kano Hiroki; Yamaguchi Masamitsu; Toda Tatsushi
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.
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2005: Chiyonobu Tomohiro; Sasaki Junko; Nagai Yoshitaka; Takeda Satoshi; Funakoshi Hiroshi; Nakamura Toshikazu; Sugimoto Tohru; Toda Tatsushi
Effects of fukutin deficiency in the developing mouse brain.
Neuromuscular disorders : NMD 2005;15(6):416-26.
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2005: Kurahashi Hiroki; Taniguchi Mariko; Meno Chikara; Taniguchi Yoshihiro; Takeda Satoshi; Horie Masato; Otani Hiroki; Toda Tatsushi
Basement membrane fragility underlies embryonic lethality in fukutin-null mice.
Neurobiology of disease 2005;19(1-2):208-17.
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2005: Kariya Shingo; Hirano Makito; Nagai Yoshitaka; Furiya Yoshiko; Fujikake Nobuhiro; Toda Tatsushi; Ueno Satoshi
Humanin attenuates apoptosis induced by DRPLA proteins with expanded polyglutamine stretches.
Journal of molecular neuroscience : MN 2005;25(2):165-9.
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2004: Mizuta Ikuko; Toda Tatsushi
[Searching genetic risk factors for sporadic Parkinson's disease]
Nippon rinsho. Japanese journal of clinical medicine 2004;62(9):1635-40.
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2004: Popiel Helena A; Nagai Yoshitaka; Onodera Osamu; Inui Takashi; Fujikake Nobuhiro; Urade Yoshihiro; Strittmatter Warren J; Burke James R; Ichikawa Atsushi; Toda Tatsushi
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.
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2003: Toda Tatsushi; Momose Yoshio; Murata Miho; Tamiya Gen; Yamamoto Mitsutoshi; Hattori Nobutaka; Inoko Hidetoshi
Toward identification of susceptibility genes for sporadic Parkinson's disease.
Journal of neurology 2003;250 Suppl 3():III40-3.
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2003: Zhang Wenli; Vajsar Jiri; Cao Pinjiang; Breningstall Galen; Diesen Charlotta; Dobyns William; Herrmann Ralph; Lehesjoki Anna-Elina; Steinbrecher Alice; Talim Beril; Toda Tatsushi; Topaloglu Haluk; Voit Thomas; Schachter Harry
Enzymatic diagnostic test for Muscle-Eye-Brain type congenital muscular dystrophy using commercially available reagents.
Clinical biochemistry 2003;36(5):339-44.
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2003: Toda Tatsushi; Kobayashi Kazuhiro; Takeda Satoshi; Sasaki Junko; Kurahashi Hiroki; Kano Hiroki; Tachikawa Masaji; Wang Fan; Nagai Yoshitaka; Taniguchi Kiyomi; Taniguchi Mariko; Sunada Yoshihide; Terashima Toshio; Endo Tamao; Matsumura Kiichiro
Fukuyama-type congenital muscular dystrophy (FCMD) and alpha-dystroglycanopathy.
Congenital anomalies 2003;43(2):97-104.
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2003: Takeda Satoshi; Kondo Mari; Sasaki Junko; Kurahashi Hiroki; Kano Hiroki; Arai Ken; Misaki Kazuyo; Fukui Takehiko; Kobayashi Kazuhiro; Tachikawa Masaji; Imamura Michihiro; Nakamura Yusuke; Shimizu Teruo; Murakami Tatsufumi; Sunada Yoshihide; Fujikado Takashi; Matsumura Kiichiro; Terashima Toshio; Toda Tatsushi
Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development.
Human molecular genetics 2003;12(12):1449-59.
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2003: Nagai Yoshitaka; Fujikake Nobuhiro; Ohno Katsuhito; Higashiyama Hiroyuki; Popiel Helena A; Rahadian Julia; Yamaguchi Masamitsu; Strittmatter Warren J; Burke James R; Toda Tatsushi
Prevention of polyglutamine oligomerization and neurodegeneration by the peptide inhibitor QBP1 in Drosophila.
Human molecular genetics 2003;12(11):1253-9.
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2003: Taniguchi Kiyomi; Kobayashi Kazuhiro; Saito Kayoko; Yamanouchi Hideo; Ohnuma Akira; Hayashi Yukiko K; Manya Hiroshi; Jin Dong Kyu; Lee Munhyang; Parano Enrico; Falsaperla Raffaele; Pavone Piero; Van Coster Rudy; Talim Beril; Steinbrecher Alice; Straub Volker; Nishino Ichizo; Topaloglu Haluk; Voit Thomas; Endo Tamao; Toda Tatsushi
Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease.
Human molecular genetics 2003;12(5):527-34.
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2002: Horie Masato; Kobayashi Kazuhiro; Takeda Satoshi; Nakamura Yusuke; Lyons Gary E; Toda Tatsushi
Isolation and characterization of the mouse ortholog of the Fukuyama-type congenital muscular dystrophy gene.
Genomics 2002;80(5):482-6.
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2002: Chiyonobu Tomohiro; Yoshihara Takao; Fukushima Yoko; Yamamoto Yasutoshi; Tsunamoto Kentaro; Nishimura Yasutaka; Ishida Hiroyuki; Toda Tatsushi; Kasubuchi Yasuo
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.
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2002: Kano Hiroki; Kobayashi Kazuhiro; Herrmann Ralf; Tachikawa Masaji; Manya Hiroshi; Nishino Ichizo; Nonaka Ikuya; Straub Volker; Talim Beril; Voit Thomas; Topaloglu Haluk; Endo Tamao; Yoshikawa Hideki; Toda Tatsushi
Deficiency of alpha-dystroglycan in muscle-eye-brain disease.
Biochemical and biophysical research communications 2002;291(5):1283-6.
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2002: Momose Yoshio; Murata Miho; Kobayashi Kazuhiro; Tachikawa Masaji; Nakabayashi Yuko; Kanazawa Ichiro; Toda Tatsushi
Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphisms.
Annals of neurology 2002;51(1):133-6.
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2002: Tachikawa Masaji; Nagai Yoshitaka; Nakamura Koichiro; Kobayashi Kazuhiro; Fujiwara Tsutomu; Han Hye-Jung; Nakabayashi Yuko; Ichikawa Yaeko; Goto Jun; Kanazawa Ichiro; Nakamura Yusuke; Toda Tatsushi
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.
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2001: Kobayashi K; Sasaki J; Kondo-Iida E; Fukuda Y; Kinoshita M; Sunada Y; Nakamura Y; Toda T
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.
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2000: Toda T
[Fukuyama-type congenital muscular dystrophy]
Rinsho shinkeigaku = Clinical neurology 2000;40(12):1297-9.
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2000: Sasaki J; Ishikawa K; Kobayashi K; Kondo-Iida E; Fukayama M; Mizusawa H; Takashima S; Sakakihara Y; Nakamura Y; Toda T
Neuronal expression of the fukutin gene.
Human molecular genetics 2000;9(20):3083-90.
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2000: Toda T; Kobayashi K; Kondo-Iida E; Sasaki J; Nakamura Y
The Fukuyama congenital muscular dystrophy story.
Neuromuscular disorders : NMD 2000;10(3):153-9.
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1999: Toda T; Kobayashi K
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.
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1999: Yoshida M; Horinouchi S; Toda T
[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.
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1999: Kondo-Iida E; Kobayashi K; Watanabe M; Sasaki J; Kumagai T; Koide H; Saito K; Osawa M; Nakamura Y; Toda T
Novel mutations and genotype-phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD).
Human molecular genetics 1999;8(12):2303-9.
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1999: Kudo N; Taoka H; Toda T; Yoshida M; Horinouchi S
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.
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1999: Kotliarova S E; Toda T; Takenaka O; Matsushita I; Hida A; Shinka T; Goto J; Tokunaga K; Nakagome Y; Nakahori Y
Novel (CA)n marker DXYS241 on the nonrecombinant part of the human Y chromosome.
Human biology; an international record of research 1999;71(2):261-75.
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1999: Toda T
[Fukutin, a novel protein product responsible for Fukuyama-type congenital muscular dystrophy]
Seikagaku. The Journal of Japanese Biochemical Society 1999;71(1):55-61.
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1999: Kuroki Y; Iwamoto T; Lee J; Yoshiike M; Nozawa S; Nishida T; Ewis A A; Nakamura H; Toda T; Tokunaga K; Kotliarova S E; Kondoh N; Koh E; Namiki M; Shinka T; Nakahori Y
Spermatogenic ability is different among males in different Y chromosome lineage.
Journal of human genetics 1999;44(5):289-92.
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1999: Shinka T; Tomita K; Toda T; Kotliarova S E; Lee J; Kuroki Y; Jin D K; Tokunaga K; Nakamura H; Nakahori Y
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.
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1998: Kobayashi K; Nakahori Y; Mizuno K; Miyake M; Kumagai T; Honma A; Nonaka I; Nakamura Y; Tokunaga K; Toda T
Founder-haplotype analysis in Fukuyama-type congenital muscular dystrophy (FCMD).
Human genetics 1998;103(3):323-7.
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1998: Kuge S; Toda T; Iizuka N; Nomoto A
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.
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1998: Kobayashi K; Nakahori Y; Miyake M; Matsumura K; Kondo-Iida E; Nomura Y; Segawa M; Yoshioka M; Saito K; Osawa M; Hamano K; Sakakihara Y; Nonaka I; Nakagome Y; Kanazawa I; Nakamura Y; Tokunaga K; Toda T
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy.
Nature 1998;394(6691):388-92.
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1998: Takai Y; Tsutsumi O; Harada I; Fujii T; Kashima T; Kobayashi K; Toda T; Taketani Y
Prenatal diagnosis of Fukuyama-type congenital muscular dystrophy by microsatellite analysis.
Human reproduction (Oxford, England) 1998;13(2):320-3.
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1997: Toda T
[Gene hunting for Fukuyama-type congenital muscular dystrophy by positional cloning]
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme 1997;42(17 Suppl):2779-85.
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1997: Toda T; Kobayashi K
[Molecular genetics and merosin abnormality in Fukuyama-type congenital muscular dystrophy (FCMD)]
Nippon rinsho. Japanese journal of clinical medicine 1997;55(12):3169-75.
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1997: Miyake M; Nakahori Y; Matsushita I; Kobayashi K; Mizuno K; Hirai M; Kanazawa I; Nakagome Y; Tokunaga K; Toda T
YAC and cosmid contigs encompassing the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region on 9q31.
Genomics 1997;40(2):284-93.
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1996: Kotliarova S E; Toda T; Matsushita I; Nakagome Y; Nakahori Y
A novel (CA)n polymorphism on 6p21.1-21.2.
The Japanese journal of human genetics 1996;41(4):423-5.
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1996: Toda T; Miyake M; Kobayashi K; Mizuno K; Saito K; Osawa M; Nakamura Y; Kanazawa I; Nakagome Y; Tokunaga K; Nakahori Y
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.
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1996: Ikegawa S; Toda T; Okui K; Nakamura Y
Structure and chromosomal assignment of the human S1-5 gene (FBNL) that is highly homologous to fibrillin.
Genomics 1996;35(3):590-2.
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1996: Toda T
[Gene hunting for Fukuyama type congenital muscular dystrophy]
No to shinkei = Brain and nerve 1996;48(4):315-22.
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1996: Nakahori Y; Kuroki Y; Komaki R; Kondoh N; Namiki M; Iwamoto T; Toda T; Kobayashi K
The Y chromosome region essential for spermatogenesis.
Hormone research 1996;46 Suppl 1():20-3.
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1995: Toda T; Ikegawa S; Miyake M; Nakahori Y; Nakamura Y
Dinucleotide repeat polymorphism on chromosome 9q32.
The Japanese journal of human genetics 1995;40(4):333-4.
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1995: Toda T
[Recent progress, genetic diagnosis and its problem on congenital muscular dystrophies (Fukuyama and non-Fukuyama types)]
Rinsho shinkeigaku = Clinical neurology 1995;35(12):1419-21.
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1995: Toda T; Watanabe T; Matsumura K; Sunada Y; Yamada H; Nakano I; Mannen T; Kanazawa I; Shimizu T
Three-dimensional MR imaging of brain surface anomalies in Fukuyama-type congenital muscular dystrophy.
Muscle & nerve 1995;18(5):508-17.
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1995: Toda T; Yoshioka M; Nakahori Y; Kanazawa I; Nakamura Y; Nakagome Y
Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome.
Annals of neurology 1995;37(1):99-101.
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1994: Toda T; Ikegawa S; Okui K; Kondo E; Saito K; Fukuyama Y; Yoshioka M; Kumagai T; Suzumori K; Kanazawa I
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.
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1993: Miyake S; Okishio N; Samejima I; Hiraoka Y; Toda T; Saitoh I; Yanagida M
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.
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1993: Watanabe M; Kondo I; Nissato S; Wakisaka A; Toda T; Ikeda J; Wasmuth J J; Gusella J F; Kanazawa I
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.
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