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Yasuyuki Suzuki

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TOP 3
Suzuki Y; Aoyama A; Kato T; Shimozawa N; Orii T
Retinitis pigmentosa and mucopolysaccharidosis type II: an extremely attenuated phenotype.
Kuratsubo Izumi; Suzuki Yasuyuki; Orii Koji O; Kato Tomomi; Orii Tadao; Kondo Naomi
Psychological status of patients with mucopolysaccharidosis type II and their parents.
Suzuki Yasuyuki; Yamamoto Tetsuya; Araie Makoto; Iwase Aiko; Tomidokoro Atsuo; Abe Haruki; Shirato Shiroaki; Kuwayama Yasuaki; Mishima Hiromu K; Shimizu Hiroyuki; Tomita Goji; Inoue Yoichi; Kitazawa Yoshiaki
[Tajimi Study review]

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All Publications

2009: Suzuki Y; Aoyama A; Kato T; Shimozawa N; Orii T
Retinitis pigmentosa and mucopolysaccharidosis type II: an extremely attenuated phenotype.
Journal of inherited metabolic disease 2009;32(4):582-3.
2009: Kuratsubo Izumi; Suzuki Yasuyuki; Orii Koji O; Kato Tomomi; Orii Tadao; Kondo Naomi
Psychological status of patients with mucopolysaccharidosis type II and their parents.
Pediatrics international : official journal of the Japan Pediatric Society 2009;51(1):41-7.
2008: Suzuki Yasuyuki; Yamamoto Tetsuya; Araie Makoto; Iwase Aiko; Tomidokoro Atsuo; Abe Haruki; Shirato Shiroaki; Kuwayama Yasuaki; Mishima Hiromu K; Shimizu Hiroyuki; Tomita Goji; Inoue Yoichi; Kitazawa Yoshiaki
[Tajimi Study review]
Nippon Ganka Gakkai zasshi 2008;112(12):1039-58.
2008: Matsumoto Naoya; Sato Yuichi; Suzuki Yasuyuki; Kasama Shu; Nakano Yoshimochi; Kato Masahiko; Yoda Shunichi; Miki Takaaki; Iida Jun; Kunimasa Taeko; Tadehara Futoshi; Nagao Ken; Hirayama Atsushi
Incremental prognostic value of cardiac function assessed by ECG-gated myocardial perfusion SPECT for the prediction of future acute coronary syndrome.
Circulation journal : official journal of the Japanese Circulation Society 2008;72(12):2035-9.
2008: Takahashi Yuji; Seki Naomi; Ishiura Hiroyuki; Mitsui Jun; Matsukawa Takashi; Kishino Atsushi; Onodera Osamu; Aoki Masashi; Shimozawa Nobuyuki; Murayama Shigeo; Itoyama Yasuto; Suzuki Yasuyuki; Sobue Gen; Nishizawa Masatoyo; Goto Jun; Tsuji Shoji
Development of a high-throughput microarray-based resequencing system for neurological disorders and its application to molecular genetics of amyotrophic lateral sclerosis.
Archives of neurology 2008;65(10):1326-32.
2008: Kawamoto Yasuhiro; Kobayashi Yoshito; Suzuki Yasuyuki; Inoue Haruhisa; Tomimoto Hidekazu; Akiguchi Ichiro; Budka Herbert; Martins L Miguel; Downward Julian; Takahashi Ryosuke
Accumulation of HtrA2/Omi in neuronal and glial inclusions in brains with alpha-synucleinopathies.
Journal of neuropathology and experimental neurology 2008;67(10):984-93.
2008: Kuratsubo Izumi; Suzuki Yasuyuki; Shimozawa Nobuyuki; Kondo Naomi
Parents of childhood X-linked adrenoleukodystrophy: high risk for depression and neurosis.
Brain & development 2008;30(7):477-82.
2008: Suzuki Yasuyuki; Gibbs Trevor; Fujisaki Kazuhiko
Medical education in Japan: a challenge to the healthcare system.
Medical teacher 2008;30(9-10):846-50.
2007: Matsumoto Naoya; Sato Yuichi; Suzuki Yasuyuki; Kunimasa Taeko; Yoda Shunichi; Iida Jun; Nakano Yoshimochi; Yoshimura Akihiro; Miki Takaaki; Kato Masahiko; Matsuo Shinro; Saito Satoshi; Hirayama Atsushi
Prognostic value of myocardial perfusion single-photon emission computed tomography for the prediction of future cardiac events in a Japanese population: a middle-term follow-up study.
Circulation journal : official journal of the Japanese Circulation Society 2007;71(10):1580-5.
2007: Kato Tomomi; Kato Zenichiro; Kuratsubo Izumi; Ota Tetsuo; Orii Tadao; Kondo Naomi; Suzuki Yasuyuki
Evaluation of ADL in patients with Hunter disease using FIM score.
Brain & development 2007;29(5):298-305.
2006: Matsumoto Naoya; Sato Yuichi; Suzuki Yasuyuki; Yoda Shunichi; Kunimasa Taeko; Kato Masahiko; Tadehara Futoshi; Lewin Howard C; Hyun Mark C; Saito Satoshi
Usefulness of rapid low-dose/high-dose 1-day 99mTc-sestamibi ECG-gated myocardial perfusion single-photon emission computed tomography.
Circulation journal : official journal of the Japanese Circulation Society 2006;70(12):1585-9.
2006: Matsumoto Naoya; Sato Yuichi; Kunimasa Taeko; Matsuo Shinro; Kato Masahiko; Yoda Shunichi; Suzuki Yasuyuki; Tani Shigemasa; Takahashi Motoichiro; Saito Satoshi
Noncompaction of the ventricular myocardium mimicking ischemic cardiomyopathy.
Annals of nuclear medicine 2006;20(9):639-41.
2006: Kato Tomomi; Isogai Koji; Orii Koji; Kuratsubo Izumi; Kondo Naomi; Orii Tadao; Suzuki Yasuyuki
Portal hypertension in a patient with Hunter disease.
Journal of inherited metabolic disease 2006;29(5):686.
2006: Sato Ayumi; Arimura Yukiko; Manago Yoshimasa; Nishikawa Kaori; Aoki Kumiko; Wada Etsuko; Suzuki Yasuyuki; Osaka Hitoshi; Setsuie Rieko; Sakurai Mikako; Amano Taiju; Aoki Shunsuke; Wada Keiji; Noda Mami
Parkin potentiates ATP-induced currents due to activation of P2X receptors in PC12 cells.
Journal of cellular physiology 2006;209(1):172-82.
2006: Suzuki Yasuyuki; Iwase Aiko; Araie Makoto; Yamamoto Tetsuya; Abe Haruki; Shirato Shiroaki; Kuwayama Yasuaki; Mishima Hiromu K; Shimizu Hiroyuki; Tomita Goji; Inoue Yoichi; Kitazawa Yoshiaki;
Risk factors for open-angle glaucoma in a Japanese population: the Tajimi Study.
Ophthalmology 2006;113(9):1613-7.
2006: Funato Michinori; Shimozawa Nobuyuki; Nagase Tomoko; Takemoto Yasuhiko; Suzuki Yasuyuki; Imamura Yoshihiko; Matsumoto Tadashi; Tsukamoto Toshiro; Kojidani Tomoko; Osumi Takashi; Fukao Toshiyuki; Kondo Naomi
Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies.
Brain & development 2006;28(5):287-92.
2005: Yamamoto Tetsuya; Iwase Aiko; Araie Makoto; Suzuki Yasuyuki; Abe Haruki; Shirato Shiroaki; Kuwayama Yasuaki; Mishima Hiromu K; Shimizu Hiroyuki; Tomita Goji; Inoue Yoichi; Kitazawa Yoshiaki;
The Tajimi Study report 2: prevalence of primary angle closure and secondary glaucoma in a Japanese population.
Ophthalmology 2005;112(10):1661-9.
2005: Suzuki Yasuyuki; Takemoto Yasuhiko; Shimozawa Nobuyuki; Imanaka Tsuneo; Kato Shunichi; Furuya Hirokazu; Kaga Makiko; Kato Koji; Hashimoto Naohiro; Onodera Osamu; Tsuji Shoji
Natural history of X-linked adrenoleukodystrophy in Japan.
Brain & development 2005;27(5):353-7.
2005: Hashimoto Kazuyuki; Kato Zenichiro; Nagase Tomoko; Shimozawa Nobuyuki; Kuwata Kazuo; Omoya Kentaro; Li Ailian; Matsukuma Eiji; Yamamoto Yutaka; Ohnishi Hidenori; Tochio Hidehito; Shirakawa Masahiro; Suzuki Yasuyuki; Wanders Ronald J A; Kondo Naomi
Molecular mechanism of a temperature-sensitive phenotype in peroxisomal biogenesis disorder.
Pediatric research 2005;58(2):263-9.
2005: Kunimatsu Shiho; Tomita Goji; Araie Makoto; Aihara Makoto; Suzuki Yasuyuki; Iwase Aiko; Koseki Nobuyuki; Matsumoto Shun; Yamazaki Yoshio; Yoshikawa Keiji
Frequency doubling technology and scanning laser tomography in eyes with generalized enlargement of optic disc cupping.
Journal of glaucoma 2005;14(4):280-7.
2005: Suda T; Suzuki Y; Matsui T; Inoue T; Niide O; Yoshimaru T; Suzuki H; Ra C; Ochiai T
Dapsone suppresses human neutrophil superoxide production and elastase release in a calcium-dependent manner.
The British journal of dermatology 2005;152(5):887-95.
2005: Shimozawa Nobuyuki; Nagase Tomoko; Takemoto Yasuhiko; Funato Michinori; Kondo Naomi; Suzuki Yasuyuki
Molecular and neurologic findings of peroxisome biogenesis disorders.
Journal of child neurology 2005;20(4):326-9.
2005: Tomatsu S; Gutierrez M A; Ishimaru T; Peña O M; Montaño A M; Maeda H; Velez-Castrillon S; Nishioka T; Fachel A A; Cooper A; Thornley M; Wraith E; Barrera L A; Laybauer L S; Giugliani R; Schwartz I V; Frenking G Schulze; Beck M; Kircher S G; Paschke E; Yamaguchi S; Ullrich K; Isogai K; Suzuki Y; Orii T; Noguchi A
Heparan sulfate levels in mucopolysaccharidoses and mucolipidoses.
Journal of inherited metabolic disease 2005;28(5):743-57.
2005: Kato Tomomi; Kato Zenichiro; Kuratsubo Izumi; Tanaka Noboru; Ishigami Tabito; Kajihara Jun-Ichi; Sukegawa-Hayasaka Kazuko; Orii Koji; Isogai Koji; Fukao Toshiyuki; Shimozawa Nobuyuki; Orii Tadao; Kondo Naomi; Suzuki Yasuyuki
Mutational and structural analysis of Japanese patients with mucopolysaccharidosis type II.
Journal of human genetics 2005;50(8):395-402.
2004: Wakida Kenji; Matsuyama Zenjiro; Suzuki Yasuyuki; Sawada Michio; Tsurumi Hisashi; Kimura Akio; Hayashi Yuichi; Hashizume Tatsuma; Hozumi Isao; Inuzuka Takashi
[Diagnosis of adult type of Niemann-Pick disease (type C) in two brothers by filipin staining of bone marrow smears]
No to shinkei = Brain and nerve 2004;56(12):1047-53.
2004: Mayama Chihiro; Araie Makoto; Suzuki Yasuyuki; Ishida Kyoko; Yamamoto Tetsuya; Kitazawa Yoshiaki; Shirakashi Motohiro; Abe Haruki; Tsukamoto Hidetoshi; Mishima Hiromu K; Yoshimura Kenichi; Ohashi Yasuo
Statistical evaluation of the diagnostic accuracy of methods used to determine the progression of visual field defects in glaucoma.
Ophthalmology 2004;111(11):2117-25.
2004: Iwase Aiko; Suzuki Yasuyuki; Araie Makoto; Yamamoto Tetsuya; Abe Haruki; Shirato Shiroaki; Kuwayama Yasuaki; Mishima Hiromu K; Shimizu Hiroyuki; Tomita Goji; Inoue Yoichi; Kitazawa Yoshiaki;
The prevalence of primary open-angle glaucoma in Japanese: the Tajimi Study.
Ophthalmology 2004;111(9):1641-8.
2004: Shimozawa Nobuyuki; Tsukamoto Toshiro; Nagase Tomoko; Takemoto Yasuhiko; Koyama Naoki; Suzuki Yasuyuki; Komori Masayuki; Osumi Takashi; Jeannette Gootjes; Wanders Ronald J A; Kondo Naomi
Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene.
Human mutation 2004;23(6):552-8.
2004: Tomatsu Shunji; Okamura Kazuo; Taketani Takeshi; Orii Koji O; Nishioka Tatsuo; Gutierrez Monica A; Velez-Castrillon Susana; Fachel Abgela A; Grubb Jeffrey H; Cooper Alan; Thornley Margaret; Wraith Ed; Barrera Luis A; Giugliani Roberto; Schwartz Ida V; Frenking Gudrun Schulze; Beck Michael; Kircher Susanne G; Paschke Eduard; Yamaguchi Seiji; Ullrich Kurt; Isogai Koji; Suzuki Yasuyuki; Orii Tadao; Kondo Naomi; Creer Michael; Noguchi Akihiko
Development and testing of new screening method for keratan sulfate in mucopolysaccharidosis IVA.
Pediatric research 2004;55(4):592-7.
2004: Nagase Tomoko; Shimozawa Nobuyuki; Takemoto Yasuhiko; Suzuki Yasuyuki; Komori Masayuki; Kondo Naomi
Peroxisomal localization in the developing mouse cerebellum: implications for neuronal abnormalities related to deficiencies in peroxisomes.
Biochimica et biophysica acta 2004;1671(1-3):26-33.
2003: Takemoto Yasuhiko; Suzuki Yasuyuki; Horibe Ryoko; Shimozawa Nobuyuki; Wanders Ronald J A; Kondo Naomi
Gas chromatography/mass spectrometry analysis of very long chain fatty acids, docosahexaenoic acid, phytanic acid and plasmalogen for the screening of peroxisomal disorders.
Brain & development 2003;25(7):481-7.
2003: Matsumoto Naomi; Tamura Shigehiko; Furuki Satomi; Miyata Non; Moser Ann; Shimozawa Nobuyuki; Moser Hugo W; Suzuki Yasuyuki; Kondo Naomi; Fujiki Yukio
Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.
American journal of human genetics 2003;73(2):233-46.
2003: Aoki Minako; Matsui Eiko; Kaneko Hideo; Inoue Ryosuke; Fukao Toshiyuki; Watanabe Mizuho; Teramoto Takahide; Kato Zenichiro; Suzuki Kiyotaka; Suzuki Yasuyuki; Kasahara Kimiko; Kondo Naomi
A novel single-nucleotide substitution, Leu 467 Pro, in the interferon-gamma receptor 1 gene associated with allergic diseases.
International journal of molecular medicine 2003;12(2):185-91.
2003: Suzuki Yasuyuki; Kano Tsuneo; Katayama Yoichi; Tejima Emiri; Harada Tadashi
Reduction of infarction volume by bolus injection of pamiteplase, a modified tissue plasminogen activator with a longer half-life.
Neurological research 2003;25(5):477-80.
2003: Shimozawa Nobuyuki; Nagase Tomoko; Takemoto Yasuhiko; Ohura Toshihiro; Suzuki Yasuyuki; Kondo Naomi
Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: evidence for a founder haplotype for the most common PEX10 gene mutation.
American journal of medical genetics. Part A 2003;120A(1):40-3.
2003: Usui T; Nakajima F; Ideta R; Kaji Y; Suzuki Y; Araie M; Miyauchi S; Heldin P; Yamashita H
Hyaluronan synthase in trabecular meshwork cells.
The British journal of ophthalmology 2003;87(3):357-60.
2003: Hu Chao-Yu; Matsuo Hiroshi; Tomita Goji; Suzuki Yasuyuki; Araie Makoto; Shirato Shiroaki; Tanaka Sumiyoshi
Clinical characteristics and leakage of functioning blebs after trabeculectomy with mitomycin-C in primary glaucoma patients.
Ophthalmology 2003;110(2):345-52.
2003: Iwata M; Fushimi N; Suzuki Y; Suzuki M; Sakimoto T; Sawa M
Intercellular adhesion molecule-1 expression on human corneal epithelial outgrowth from limbal explant in culture.
The British journal of ophthalmology 2003;87(2):203-7.
2003: Shimozawa Nobuyuki; Nagase Tomoko; Takemoto Yasuhiko; Suzuki Yasuyuki; Kondo Naomi
Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene.
Advances in experimental medicine and biology 2003;544():71.
2002: Matsuo Hiroshi; Tomita Goji; Suzuki Yasuyuki; Araie Makoto
Learning effect and measurement variability in frequency-doubling technology perimetry in chronic open-angle glaucoma.
Journal of glaucoma 2002;11(6):467-73.
2002: Mayama Chihiro; Suzuki Yasuyuki; Araie Makoto; Ishida Kyoko; Akira Tsuji; Yamamoto Tetsuya; Kitazawa Yoshiaki; Funaki Shigeo; Shirakashi Motohiro; Abe Haruki; Tsukamoto Hidetoshi; Okada Koji; Mishima Hiromu K
Myopia and advanced-stage open-angle glaucoma.
Ophthalmology 2002;109(11):2072-7.
2002: Yoshimaru T; Suzuki Y; Matsui T; Yamashita K; Ochiai T; Yamaki M; Shimizu K
Blockade of superoxide generation prevents high-affinity immunoglobulin E receptor-mediated release of allergic mediators by rat mast cell line and human basophils.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2002;32(4):612-8.
2002: Matsuo Hiroshi; Tomidokoro Atsuo; Suzuki Yasuyuki; Shirato Shiroaki; Araie Makoto
Late-onset transconjunctival oozing and point leak of aqueous humor from filtering bleb after trabeculectomy.
American journal of ophthalmology 2002;133(4):456-62.
2002: Shimozawa Nobuyuki; Nagase Tomoko; Takemoto Yasuhiko; Suzuki Yasuyuki; Fujiki Yukio; Wanders Ronald J A; Kondo Naomi
A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome.
Biochemical and biophysical research communications 2002;292(1):109-12.
2002: Tomatsu Shunji; Orii Koji O; Islam M Rafiqul; Shah Gul N; Grubb Jeffrey H; Sukegawa Kazuko; Suzuki Yasuyuki; Orii Tadao; Kondo Naomi; Sly William S
Methylation patterns of the human beta-glucuronidase gene locus: boundaries of methylation and general implications for frequent point mutations at CpG dinucleotides.
Genomics 2002;79(3):363-75.
2002: Suzuki Yasuyuki; Iai Mizue; Kamei Atsushi; Tanabe Yuzo; Chida Shoichi; Yamaguchi Seiji; Zhang Zhongyi; Takemoto Yasuhiko; Shimozawa Nobuyuki; Kondo Naomi
Peroxisomal acyl CoA oxidase deficiency.
The Journal of pediatrics 2002;140(1):128-30.
2002: Funaki Shigeo; Shirakashi Motohiro; Yaoeda Kiyoshi; Abe Haruki; Kunimatsu Shiho; Suzuki Yasuyuki; Tomita Goji; Araie Makoto; Yamada Noriko; Uchida Hideya; Yamamoto Tetsuya; Kitazawa Yoshiaki
Specificity and sensitivity of glaucoma detection in the Japanese population using scanning laser polarimetry.
The British journal of ophthalmology 2002;86(1):70-4.
2002: Takemoto Yasuhiko; Suzuki Yasuyuki; Tamakoshi Akiko; Onodera Osamu; Tsuji Shoji; Hashimoto Takashi; Shimozawa Nobuyuki; Orii Tadao; Kondo Naomi
Epidemiology of X-linked adrenoleukodystrophy in Japan.
Journal of human genetics 2002;47(11):590-3.
2001: Suzuki Y; Shimozawa N; Orii T; Tsukamoto T; Osumi T; Fujiki Y; Kondo N
Genetic and molecular bases of peroxisome biogenesis disorders.
Genetics in medicine : official journal of the American College of Medical Genetics 2001;3(5):372-6.
2001: Ogawa K; Suzuki Y; Oishi M; Mizutani T; Nakayama T
[A case of Machado-Joseph disease presenting pure cerebellar ataxia]
Rinsho shinkeigaku = Clinical neurology 2001;41(8):512-4.
2001: Wu L L; Suzuki Y; Kunimatsu S; Araie M; Iwase A; Tomita G
Frequency doubling technology and confocal scanning ophthalmoscopic optic disc analysis in open-angle glaucoma with hemifield defects.
Journal of glaucoma 2001;10(4):256-60.
2001: Tamura S; Matsumoto N; Imamura A; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.
The Biochemical journal 2001;357(Pt 2):417-26.
2001: Tejima E; Katayama Y; Suzuki Y; Kano T; Lo E H
Hemorrhagic transformation after fibrinolysis with tissue plasminogen activator: evaluation of role of hypertension with rat thromboembolic stroke model.
Stroke; a journal of cerebral circulation 2001;32(6):1336-40.
2001: Suzuki Y; Yoshimaru T; Yamashita K; Matsui T; Yamaki M; Shimizu K
Exposure of RBL-2H3 mast cells to Ag(+) induces cell degranulation and mediator release.
Biochemical and biophysical research communications 2001;283(3):707-14.
2001: Suzuki Y; Shimozawa N; Imamura A; Fukuda S; Zhang Z; Orii T; Kondo N
Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.
Journal of inherited metabolic disease 2001;24(2):151-65.
2001: Suzuki Y; Kitazawa Y; Araie M; Yamagami J; Yamamoto T; Ishida K; Tsuji A; Abe H; Shirakashi M; Funaki S; Mishima H K; Tsukamoto H; Okada K; Shibata T
Mathematical and optimal clustering of test points of the central 30-degree visual field of glaucoma.
Journal of glaucoma 2001;10(2):121-8.
2001: Ichiki Y; Akiyama T; Shimozawa N; Suzuki Y; Kondo N; Kitajima Y
An extremely severe case of cutaneous calcinosis with juvenile dermatomyositis, and successful treatment with diltiazem.
The British journal of dermatology 2001;144(4):894-7.
2001: Suzuki Y
[Refsum disease]
Nippon rinsho. Japanese journal of clinical medicine 2001;59 Suppl 3():326-8.
2001: Chono M; Suzuki Y; Nemoto K; Yamane H; Murofushi N; Yamaguchi I
Expression pattern of the CsPK3 auxin-responsive protein kinase gene.
Bioscience, biotechnology, and biochemistry 2001;65(3):605-12.
2001: Yamamoto Y; Atoji Y; Hobo S; Yoshihara T; Suzuki Y
Morphology of the nerve endings in laryngeal mucosa of the horse.
Equine veterinary journal 2001;33(2):150-8.
2001: Suzuki Y; Imamura A; Shimozawa N; Kondo N
The clinical course of childhood and adolescent adrenoleukodystrophy before and after Lorenzo's oil.
Brain & development 2001;23(1):30-3.
2001: Atoji Y; Yamamoto Y; Suzuki Y
Innervation of NADPH diaphorase-containing neurons correlated with acetylcholinesterase, tyrosine hydroxylase, and neuropeptides in the pigeon cloaca.
Journal of anatomy 2001;198(Pt 2):181-8.
2001: Suzuki Y; Uemura S; Saito Y; Murofushi N; Schmitz G; Theres K; Yamaguchi I
A novel transposon tagging element for obtaining gain-of-function mutants based on a self-stabilizing Ac derivative.
Plant molecular biology 2001;45(2):123-31.
2001: Atoji Y; Yamamoto Y; Suzuki Y
Distribution of NADPH diaphorase-containing neurons in the pigeon central nervous system.
Journal of chemical neuroanatomy 2001;21(1):1-22.
2001: Iwata M; Suzuki Y; Imai Y; Ono Y; Sawa M
Differential effects of protein tyrosine kinase inhibitors on interferon-gamma-induction of major histocompatibility complex class II and intercellular adhesion molecule-1 expression in human corneal epithelial cells.
Japanese journal of ophthalmology 2001;45(1):13-21.
2001: Suzuki Y
[Zellweger syndrome]
Ryoikibetsu shokogun shirizu 2001;(34 Pt 2):841-2.
2001: Suzuki Y
[Refsum disease]
Ryoikibetsu shokogun shirizu 2001;(34 Pt 2):571-2.
2001: Suzuki Y
[Adrenoleukodystrophy]
Ryoikibetsu shokogun shirizu 2001;(33):152-3.
2001: Matsumoto N; Tamura S; Moser A; Moser H W; Braverman N; Suzuki Y; Shimozawa N; Kondo N; Fujiki Y
The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.
Journal of human genetics 2001;46(5):273-7.
2000: Ojima K; Hosaka M; Suzuki Y
Functional and positional difference and classification of the fungiform papillae on the rabbit tongue seen in microvascular cast specimens by means of scanning electron microscope.
Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft 2000;182(6):521-4.
2000: Yamamoto Y; Ootsuka T; Atoji Y; Suzuki Y
Tyrosine hydroxylase- and neuropeptides-immunoreactive nerves in canine trachea.
American journal of veterinary research 2000;61(11):1380-3.
2000: Wu L L; Suzuki Y; Ideta R; Araie M
Central corneal thickness of normal tension glaucoma patients in Japan.
Japanese journal of ophthalmology 2000;44(6):643-7.
2000: Yamamoto Y; Kusakabe T; Hayashida Y; Yoshida T; Matsuda H; Atoji Y; Suzuki Y
Laryngeal endocrine cells: topographic distribution and adaptation to chronic hypercapnic hypoxia.
Histochemistry and cell biology 2000;114(4):277-82.
2000: Atoji Y; Mizutani K; Yamamoto Y; Suzuki Y
Innervation of the pigeon oviduct: correlation of NADPH diaphorase with acetylcholinesterase, tyrosine hydroxylase, and neuropeptides.
Autonomic neuroscience : basic & clinical 2000;84(1-2):1-7.
2000: Imamura A; Shimozawa N; Suzuki Y; Zhang Z; Tsukamoto T; Fujiki Y; Orii T; Osumi T; Wanders R J; Kondo N
Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1.
Pediatric research 2000;48(4):541-5.
2000: Ghaedi K; Honsho M; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.
American journal of human genetics 2000;67(4):976-81.
2000: Ojima K; Mitsuhashi F; Nasu M; Suzuki Y
Functional angioarchitectural comparison of the fungiform papillae of rat, rabbit, cat in scanning electron microscopic specimens.
Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft 2000;182(5):451-7.
2000: Matsui T; Suzuki Y; Yamashita K; Yoshimaru T; Suzuki-Karasaki M; Hayakawa S; Yamaki M; Shimizu K
Diphenyleneiodonium prevents reactive oxygen species generation, tyrosine phosphorylation, and histamine release in RBL-2H3 mast cells.
Biochemical and biophysical research communications 2000;276(2):742-8.
2000: Shimozawa N; Suzuki Y; Zhang Z; Imamura A; Ghaedi K; Fujiki Y; Kondo N
Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures.
Human molecular genetics 2000;9(13):1995-9.
2000: Yamashita K; Suzuki Y; Matsui T; Yoshimaru T; Yamaki M; Suzuki-Karasaki M; Hayakawa S; Shimizu K
Epigallocatechin gallate inhibits histamine release from rat basophilic leukemia (RBL-2H3) cells: role of tyrosine phosphorylation pathway.
Biochemical and biophysical research communications 2000;274(3):603-8.
2000: Suzuki Y; Isogai K; Teramoto T; Tashita H; Shimozawa N; Nishimura M; Asano T; Oda M; Kamei A; Ishiguro H; Kato S; Ohashi T; Kobayashi H; Eto Y; Kondo N
Bone marrow transplantation for the treatment of X-linked adrenoleukodystrophy.
Journal of inherited metabolic disease 2000;23(5):453-8.
2000: Yamamoto Y; Atoji Y; Suzuki Y
Calbindin D28k-immunoreactive afferent nerve endings in the laryngeal mucosa.
The Anatomical record 2000;259(3):237-47.
2000: Atoji Y; Yamamoto Y; Suzuki Y
Parvalbumin in cortical epithelial cells of the pigeon thymus.
Journal of anatomy 2000;196 ( Pt 3)():305-11.
2000: Tanaka Y; Suzuki Y; Shimozawa N; Nanba E; Kondo N
Congenital myotonic dystrophy: report of paternal transmission.
Brain & development 2000;22(2):132-4.
2000: Shimozawa N; Zhang Z; Imamura A; Suzuki Y; Fujiki Y; Tsukamoto T; Osumi T; Aubourg P; Wanders R J; Kondo N
Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient.
Biochemical and biophysical research communications 2000;268(1):31-5.
2000: Imamura A; Shimozawa N; Suzuki Y; Zhang Z; Tsukamoto T; Fujiki Y; Orii T; Osumi T; Kondo N
Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans.
Brain & development 2000;22(1):8-12.
2000: Ojima K; Mitsuhashi F; Nasu M; Suzuki Y
Angioarchitectural form, functional distributive pattern and classification of the fungiform papillae on the crossbred Japanese cat tongue anterodorsal surface in scanning electron microscopic specimens.
Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft 2000;182(1):53-8.
2000: Ojima K; Mitsuhashi F; Nasu M; Suzuki Y
Angioarchitectural form, functional distributive pattern and classification of the filiform papillae on the crossbred Japanese cat tongue anterodorsal surface in scanning electron microscopic specimens.
Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft 2000;182(1):47-52.
2000: Yamamoto Y; Atoji Y; Suzuki Y
Morphology of the glomerular nerve endings in the dorsal nasal ligament of the dog.
Archives of histology and cytology 2000;63(5):467-72.
2000: Suzuki Y; Shimozawa N; Imamura A; Kondo N
[Peroxisomal disorders]
Ryoikibetsu shokogun shirizu 2000;(29 Pt 4):452-9.
2000: Takabayashi A; Ihara K; Sasaki Y; Suzuki Y; Nishima S; Izuhara K; Hamasaki N; Hara T
Childhood atopic asthma: positive association with a polymorphism of IL-4 receptor alpha gene but not with that of IL-4 promoter or Fc epsilon receptor I beta gene.
Experimental and clinical immunogenetics 2000;17(2):63-70.
1999: Kondo N; Suzuki Y; Shimozawa N; Takahashi Y; Fukao T
[Genetics of neurologic disorders in children]
Nippon rinsho. Japanese journal of clinical medicine 1999;57 Suppl():700-6.
1999: Kunimatsu S; Suzuki Y; Shirato S; Araie M
[Usefulness of gaze tracking during perimetry in glaucomatous eyes]
Nippon Ganka Gakkai zasshi 1999;103(10):748-53.
1999: Shimozawa N; Imamura A; Zhang Z; Suzuki Y; Orii T; Tsukamoto T; Osumi T; Fujiki Y; Wanders R J; Besley G; Kondo N
Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders.
Journal of medical genetics 1999;36(10):779-81.
1999: Yamazaki Y; Yoshikawa K; Kunimatsu S; Koseki N; Suzuki Y; Matsumoto S; Araie M
Influence of myopic disc shape on the diagnostic precision of the Heidelberg Retina Tomograph.
Japanese journal of ophthalmology 1999;43(5):392-7.
1999: Toyama R; Mukai S; Itagaki A; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Wanders R J; Fujiki Y
Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants.
Human molecular genetics 1999;8(9):1673-81.
1999: Shimozawa N; Zhang Z; Suzuki Y; Imamura A; Tsukamoto T; Osumi T; Fujiki Y; Orii T; Barth P G; Wanders R J; Kondo N
Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients.
Biochemical and biophysical research communications 1999;262(2):504-8.
1999: Atoji Y; Yamamoto Y; Suzuki Y
Thymic epithelial cysts in the pigeon.
Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft 1999;181(4):365-70.
1999: Suzuki Y; Shirato S; Adachi M; Hamada C
Risk factors for the progression of treated primary open-angle glaucoma: a multivariate life-table analysis.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 1999;237(6):463-7.
1999: Shimozawa N; Suzuki Y; Zhang Z; Imamura A; Toyama R; Mukai S; Fujiki Y; Tsukamoto T; Osumi T; Orii T; Wanders R J; Kondo N
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.
Human molecular genetics 1999;8(6):1077-83.
1999: Yamazaki Y; Yoshikawa K; Kunimatsu S; Koseki N; Suzuki Y; Matsumoto S; Araie M
[Influence of myopic disc shape in a classification program of the Heidelberg retina tomograph]
Nippon Ganka Gakkai zasshi 1999;103(5):392-8.
1999: Ghaedi K; Kawai A; Okumoto K; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein.
Experimental cell research 1999;248(2):489-97.
1999: Ghaedi K; Itagaki A; Toyama R; Tamura S; Matsumura T; Kawai A; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals.
Experimental cell research 1999;248(2):482-8.
1999: Suzuki Y; Shimozawa N; Imamura A; Zhang Z; Kondo N
[Newly identified peroxisomal disorders]
No to shinkei = Brain and nerve 1999;51(4):295-302.
1999: Muraoka M; Fukuzawa H; Nishida A; Okano K; Tsuchihara T; Shimoda A; Suzuki Y; Sato M; Osumi M; Sakai H
The effects of various GTP analogues on microtubule assembly.
Cell structure and function 1999;24(2):101-9.
1999: Shimada N; Suzuki Y; Nakajima M; Conrad U; Murofushi N; Yamaguchi I
Expression of a functional single-chain antibody against GA24/19 in transgenic tobacco.
Bioscience, biotechnology, and biochemistry 1999;63(4):779-83.
1999: Suzuki Y; Shimada N; Niwa R; Yokoi M; Nakajima M; Murofushi N; Yamaguchi I
Preparation and application of anti-idiotypic antibody against anti-gibberellin A4 antibody.
Bioscience, biotechnology, and biochemistry 1999;63(4):648-54.
1999: Yamamoto Y; Atoji Y; Suzuki Y
Calretinin immunoreactive nerve endings in the trachea and bronchi of the rat.
The Journal of veterinary medical science / the Japanese Society of Veterinary Science 1999;61(3):267-9.
1999: Atoji Y; Yamamoto Y; Suzuki Y; Sayed R
Ultrastructure of the thyroid gland of the one-humped camel (Camelus dromedarius).
Anatomia, histologia, embryologia 1999;28(1):23-6.
1999: Matsuzono Y; Kinoshita N; Tamura S; Shimozawa N; Hamasaki M; Ghaedi K; Wanders R J; Suzuki Y; Kondo N; Fujiki Y
Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(5):2116-21.
1999: Suzuki Y; Ono Y
Involvement of reactive oxygen species produced via NADPH oxidase in tyrosine phosphorylation in human B- and T-lineage lymphoid cells.
Biochemical and biophysical research communications 1999;255(2):262-7.
1999: Shirato S; Inoue R; Fukushima K; Suzuki Y
Clinical evaluation of SITA: a new family of perimetric testing strategies.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 1999;237(1):29-34.
1999: Zhang Z; Suzuki Y; Shimozawa N; Fukuda S; Imamura A; Tsukamoto T; Osumi T; Fujiki Y; Orii T; Wanders R J; Barth P G; Moser H W; Paton B C; Besley G T; Kondo N
Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders.
Human mutation 1999;13(6):487-96.
1999: Suzuki Y; Zhang Z; Shimozawa N; Muro M; Shono H; Toda S; Miyahara S; Hashimoto T; Usuda N; Ito M; Takashima S; Kondo N
Prenatal diagnosis of peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency.
Journal of human genetics 1999;44(3):143-7.
1999: Shimozawa N; Suzuki Y; Zhang Z; Miura K; Matsumoto A; Nagaya M; Castillo-Taucher S; Kondo N
A novel nonsense mutation of the PEX7 gene in a patient with rhizomelic chondrodysplasia punctata.
Journal of human genetics 1999;44(2):123-5.
1998: Sayed R; Atoji Y; Kamel G; Moneim M A; Yamamoto Y; Suzuki Y
Pulmonary development in the fetal one-humped camel: morphometry.
Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft 1998;180(6):573-85.
1998: Honsho M; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
American journal of human genetics 1998;63(6):1622-30.
1998: Imamura A; Tamura S; Shimozawa N; Suzuki Y; Zhang Z; Tsukamoto T; Orii T; Kondo N; Osumi T; Fujiki Y
Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders.
Human molecular genetics 1998;7(13):2089-94.
1998: Yamamoto Y; Kondo A; Atoji Y; Tsubone H; Suzuki Y
Morphology of intraepithelial corpuscular nerve endings in the nasal respiratory mucosa of the dog.
Journal of anatomy 1998;193 ( Pt 4)():581-6.
1998: Atoji Y; Yamamoto Y; Suzuki Y
Apocrine sweat glands in the circumanal glands of the dog.
The Anatomical record 1998;252(3):403-12.
1998: Sayed R; Atoji Y; Kamel G; Yamamoto Y; Suzuki Y
Surface ultrastructure of fetal bronchial epithelium in camel.
Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft 1998;180(5):439-44.
1998: Yamada Y; Inoue R; Fukao T; Kaneko H; Isogai K; Fukuda S; Shimozawa N; Suzuki Y; Kondo N; Azuma E; Sakurai M
Ataxia telangiectasia associated with B-cell lymphoma: the effect of a half-dose of the drugs administered according to the acute lymphoblastic leukemia standard risk protocol.
Pediatric hematology and oncology 1998;15(5):425-9.
1998: Kinoshita N; Ghaedi K; Shimozawa N; Wanders R J; Matsuzono Y; Imanaka T; Okumoto K; Suzuki Y; Kondo N; Fujiki Y
Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals.
The Journal of biological chemistry 1998;273(37):24122-30.
1998: Okumoto K; Itoh R; Shimozawa N; Suzuki Y; Tamura S; Kondo N; Fujiki Y
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.
Human molecular genetics 1998;7(9):1399-405.
1998: Suzuki Y; Ono Y
Serum factors and the cellular redox status regulate cellular responsiveness to MHC class II-triggered homotypic B cell adhesion.
Biochemical and biophysical research communications 1998;249(1):31-7.
1998: Yamamoto Y; Atoji Y; Suzuki Y
Neurochemical markers in the nervous plexus of the canine glottis.
Journal of the autonomic nervous system 1998;71(2-3):111-9.
1998: Hara T; Shirato S; Suzuki Y
[Ocular tissue concentrations and results of filtration surgery after topical use of mitomycin C in rabbits]
Nippon Ganka Gakkai zasshi 1998;102(7):425-30.
1998: Okumoto K; Shimozawa N; Kawai A; Tamura S; Tsukamoto T; Osumi T; Moser H; Wanders R J; Suzuki Y; Kondo N; Fujiki Y
PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p.
Molecular and cellular biology 1998;18(7):4324-36.
1998: Komatsu T; Yamamoto Y; Atoji Y; Tsubota T; Suzuki Y
Immunohistochemical demonstration of cytoskeletal proteins in the testis of the Japanese black bear, Ursus thibetanus japonicus.
Anatomia, histologia, embryologia 1998;27(3):209-13.
1998: Yamamoto Y; Atoji Y; Kuramoto H; Suzuki Y
Calretinin-immunoreactive laminar nerve endings in the laryngeal mucosa of the rat.
Cell and tissue research 1998;292(3):613-7.
1998: Hara T; Shirato S; Suzuki Y
Ocular tissue concentrations of mitomycin C with variable dose and duration of application time in rabbits.
Japanese journal of ophthalmology 1998;42(3):193-8.
1998: Yamamoto Y; Atoji Y; Agungpriyono S; Suzuki Y
Morphological study of the forestomach of the Japanese serow (Capricornis crispus).
Anatomia, histologia, embryologia 1998;27(2):73-81.
1998: Tamura S; Shimozawa N; Suzuki Y; Tsukamoto T; Osumi T; Fujiki Y
A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p.
Biochemical and biophysical research communications 1998;245(3):883-6.
1998: Yamamoto Y; Ootsuka T; Atoji Y; Suzuki Y
Morphological and quantitative study of the intrinsic nerve plexuses of the canine trachea as revealed by immunohistochemical staining of protein gene product 9.5.
The Anatomical record 1998;250(4):438-47.
1998: Tamura S; Okumoto K; Toyama R; Shimozawa N; Tsukamoto T; Suzuki Y; Osumi T; Kondo N; Fujiki Y
Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(8):4350-5.
1998: Atoji Y; Yamamoto Y; Komatsu T; Suzuki Y; Tsubota T
Circumanal glands of the dog: a new classification and cell degeneration.
The Anatomical record 1998;250(3):251-67.
1998: Atoji Y; Sayed R; Yamamoto Y; Suzuki Y
Poll glands of the one-humped camel (Camelus dromedarius): a histochemical and scanning electron microscopic study.
European journal of morphology 1998;36(1):29-36.
1998: Atoji Y; Yamamoto Y; Suzuki Y
Morphology of the tongue of a male Formosan serow (Capricornis crispus swinhoei).
Anatomia, histologia, embryologia 1998;27(1):17-9.
1998: Fukuda S; Suzuki Y; Shimozawa N; Zhang Z; Orii T; Aoyama T; Hashimoto T; Kondo N
Amino acid and nucleotide sequences of human peroxisomal enoyl-CoA hydratase: 3-hydroxyacyl-CoA dehydrogenase cDNA.
Journal of inherited metabolic disease 1998;21(1):23-8.
1998: Shimozawa N; Suzuki Y; Zhang Z; Imamura A; Tsukamoto T; Osumi T; Tateishi K; Okumoto K; Fujiki Y; Orii T; Barth P G; Wanders R J; Kondo N
Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13.
Biochemical and biophysical research communications 1998;243(2):368-71.
1998: Suzuki Y
[Other peroxisomal diseases]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):340-1.
1998: Suzuki Y
[Refsum disease]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):332-4.
1998: Suzuki Y
[Acatalasemia, Takahara disease]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):330-1.
1998: Suzuki Y
[Peroxisomal 3-ketoacyl-CoA thiolase deficiency]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):328-9.
1998: Suzuki Y
[Bifunctional enzyme deficiency]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):326-7.
1998: Suzuki Y
[Peroxisomal acyl-CoA oxidase deficiency]
Ryoikibetsu shokogun shirizu 1998;(19 Pt 2):322-5.
1998: Shimozawa N; Suzuki Y; Tomatsu S; Nakamura H; Kono T; Takada H; Tsukamoto T; Fujiki Y; Orii T; Kondo N
A novel mutation, R125X in peroxisome assembly factor-1 responsible for Zellweger syndrome.
Human mutation 1998;Suppl 1():S134-6.
1998: Tomatsu S; Fukuda S; Cooper A; Wraith J E; Yamagishi A; Kato Z; Yamada N; Isogai K; Sukegawa K; Suzuki Y; Shimozawa N; Kondo N; Orii T
Fifteen polymorphisms in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene: diagnostic implications in Morquio disease.
Human mutation 1998;Suppl 1():S42-6.
1997: Suzuki Y; Lee K; Shimozawa N; Orii T; Kondo N
Biochemical and immunocytochemical properties of peroxisomes and mitochondria in bovine chromaffin cells.
Cell structure and function 1997;22(6):615-9.
1997: Suzuki Y; Komatsu T; Yamamoto Y; Atoii Y
Pathology of interdigital glands in a wild Japanese serow (Capricornis crispus) infected with parapoxvirus.
The Journal of veterinary medical science / the Japanese Society of Veterinary Science 1997;59(11):1063-5.
1997: Suzuki Y; Jiang L L; Souri M; Miyazawa S; Fukuda S; Zhang Z; Une M; Shimozawa N; Kondo N; Orii T; Hashimoto T
D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder.
American journal of human genetics 1997;61(5):1153-62.
1997: Komatsu T; Yamamoto Y; Atoji Y; Tsubota T; Suzuki Y
Seasonal changes in subcellular structures of Leydig and Sertoli cells in the Japanese black bear, Ursus thibetanus japonicus.
Archives of histology and cytology 1997;60(3):225-34.
1997: Tateishi K; Okumoto K; Shimozawa N; Tsukamoto T; Osumi T; Suzuki Y; Kondo N; Okano I; Fujiki Y
Newly identified Chinese hamster ovary cell mutants defective in peroxisome biogenesis represent two novel complementation groups in mammals.
European journal of cell biology 1997;73(4):352-9.
1997: Atoji Y; Yamamoto Y; Komatsu T; Suzuki Y
Localization of neuropeptides in endocrine cells of the chicken thymus.
The Journal of veterinary medical science / the Japanese Society of Veterinary Science 1997;59(7):601-3.
1997: Komatsu T; Tsubota T; Yamamoto Y; Atoji Y; Suzuki Y
Seasonal changes in the immunolocalization of steroidogenic enzymes in the testes of the Japanese black bear (Ursus thibetanus japonicus).
The Journal of veterinary medical science / the Japanese Society of Veterinary Science 1997;59(7):521-9.
1997: Atoji Y; Yamamoto Y; Suzuki Y
Neurotensin pathway in the chicken thymus.
Kaibogaku zasshi. Journal of anatomy 1997;72(3):181-6.
1997: Yamamoto Y; Atoji Y; Suzuki Y
Innervation of taste buds in the canine larynx as revealed by immunohistochemistry for the various neurochemical markers.
Tissue & cell 1997;29(3):339-46.
1997: Imamura A; Suzuki Y; Song X Q; Fukao T; Uchiyama A; Shimozawa N; Kamijo K; Hashimoto T; Orii T; Kondo N
Two novel missense mutations in the ATP-binding domain of the adrenoleukodystrophy gene: immunoblotting and immunocytological study of two patients.
Clinical genetics 1997;51(5):322-5.
1997: Suzuki Y; Uni S; Komatsu T; Yamamoto Y; Atoji Y
Olecranon lesions caused by Onchocerca skrjabini in wild Japanese serows (Capricornis crispus).
The Journal of veterinary medical science / the Japanese Society of Veterinary Science 1997;59(5):387-90.
1997: Okumoto K; Bogaki A; Tateishi K; Tsukamoto T; Osumi T; Shimozawa N; Suzuki Y; Orii T; Fujiki Y
Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III.
Experimental cell research 1997;233(1):11-20.
1997: Fukuda S; Yamada Y; Nishimura M; Isogai K; Terada T; Iwata M; Shimozawa N; Suzuki Y; Kondo N
Marinesco-Sjögren syndrome associated with acute myeloblastic leukemia.
Clinical genetics 1997;51(4):278-80.
1997: Jiang L L; Kurosawa T; Sato M; Suzuki Y; Hashimoto T
Physiological role of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein.
Journal of biochemistry 1997;121(3):506-13.
1997: Takasu T; Sawai S; Suzuki Y
[Distribution in organs and excretion of ethanol and its metabolites]
Nippon rinsho. Japanese journal of clinical medicine 1997;55 Suppl():16-21.
1997: Yamamoto Y; Hosono I; Atoji Y; Suzuki Y
Morphological study of the vagal afferent nerve endings in the laryngeal mucosa of the dog.
Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft 1997;179(1):65-73.
1997: Takahashi Y; Suzuki Y; Kumazaki K; Tanabe Y; Akaboshi S; Miura K; Shimozawa N; Kondo N; Nishiguchi T; Terada K; Orii T
Epilepsy in peroxisomal diseases.
Epilepsia 1997;38(2):182-8.
1997: Tomatsu S; Fukuda S; Cooper A; Wraith J E; Ferreira P; Di Natale P; Tortora P; Fujimoto A; Kato Z; Yamada N; Isogai K; Yamagishi A; Sukegawa K; Suzuki Y; Shimozawa N; Kondo N; Sly W S; Orii T
Fourteen novel mucopolysaccharidosis IVA producing mutations in GALNS gene.
Human mutation 1997;10(5):368-75.
1996: Suzuki Y; Shimozawa N; Takahashi Y; Imamura A; Kondo N; Orii T
Peroxisomal disorders: clinical aspects.
Annals of the New York Academy of Sciences 1996;804():442-9.
1996: Yamamoto Y; Kubota T; Atoji Y; Suzuki Y
Distribution of alpha-vascular smooth muscle actin in the smooth muscle cells of the gastrointestinal tract of the chicken.
Journal of anatomy 1996;189 ( Pt 3)():623-30.
1996: Fukuda S; Shimozawa N; Suzuki Y; Zhang Z; Tomatsu S; Tsukamoto T; Hashiguchi N; Osumi T; Masuno M; Imaizumi K; Kuroki Y; Fujiki Y; Orii T; Kondo N
Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans.
American journal of human genetics 1996;59(6):1210-20.
1996: Inoue K; Suzuki Y; Yajima S; Shimozawa N; Tomatsu S; Orii T; Kondo N
Carrier identification of X-linked adrenoleukodystrophy by measurement of very long chain fatty acids and lignoceric acid oxidation.
Clinical genetics 1996;50(5):348-52.
1996: Atoji Y; Shibata N; Yamamoto Y; Suzuki Y
Distribution of neurotensin-containing neurons in the central nervous system of the pigeon and the chicken.
The Journal of comparative neurology 1996;375(2):187-211.
1996: Suzuki Y; Shimozawa N; Imamura A; Fukuda Y; Ichihashi H; Orii T; Kondo N
Trial of docosahexaenoic acid supplementation on a Japanese patient with a peroxisome biogenesis defect.
Acta paediatrica Japonica; Overseas edition 1996;38(5):520-3.
1996: Yamamoto Y; Kubota T; Atoji Y; Suzuki Y
Structure of the perilobular sheath of the deep proventricular gland of the chicken: presence and possible role of myofibroblasts.
Cell and tissue research 1996;285(1):109-17.
1996: Atoji Y; Yamamoto Y; Suzuki Y
Neurotensin-containing endocrine cells and neurotensin receptor mRNA-expressing epithelial cells in the chicken thymus.
Archives of histology and cytology 1996;59(2):197-203.
1996: Shimozawa N; Suzuki Y; Tomatsu S; Tsukamoto T; Osumi T; Fujiki Y; Kamijo K; Hashimoto T; Kondo N; Orii T
Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.
Pediatric research 1996;39(5):812-5.
1996: Tomatsu S; Fukuda S; Yamagishi A; Cooper A; Wraith J F; Hori T; Kato Z; Yamada N; Isogai K; Sukegawa K; Kondo N; Suzuki Y; Shimozawa N; Orii T
Mucopolysaccharidosis IVA: four new exonic mutations in patients with N-acetylgalactosamine-6-sulfate sulfatase deficiency.
American journal of human genetics 1996;58(5):950-62.
1996: Komatsu T; Yamamoto Y; Tsubota T; Atoji Y; Suzuki Y
Spermatogenic cycle in the testis of the Japanese black bear (Selenarctos thibetanus japonicus).
The Journal of veterinary medical science / the Japanese Society of Veterinary Science 1996;58(4):329-35.
1996: Suzuki Y; Shimozawa N; Yajima S; Inoue K; Orii T; Kondo N
Incidence of peroxisomal disorders in Japan.
The Japanese journal of human genetics 1996;41(1):167-75.
1996: Imamura A; Suzuki Y; Song X Q; Fukao T; Shimozawa N; Orii T; Kondo N
Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysis.
Prenatal diagnosis 1996;16(3):259-61.
1996: Atoji Y; Yamamoto Y; Suzuki Y
Infraorbital glands of a male Formosan serow (Capricornis crispus swinhoei).
European journal of morphology 1996;34(2):87-94.
1996: Yajima S; Suzuki Y
[Peroxisomal disorders]
Ryoikibetsu shokogun shirizu 1996;(15):75-7.
1996: Fukuda S; Tomatsu S; Masuno M; Ogawa T; Yamagishi A; Rezvi G M; Sukegawa K; Shimozawa N; Suzuki Y; Kondo N; Imaizumi K; Kuroki Y; Okabe T; Orii T
Mucopolysaccharidosis IVA: submicroscopic deletion of 16q24.3 and a novel R386C mutation of N-acetylgalactosamine-6-sulfate sulfatase gene in a classical Morquio disease.
Human mutation 1996;7(2):123-34.
1996: Rezvi G M; Tomatsu S; Fukuda S; Yamagishi A; Cooper A; Wraith J E; Iwata H; Kato Z; Yamada N; Sukegawa K; Shimozawa N; Suzuki Y; Kondo N; Orii T
Mucopolysaccharidosis IVA: a comparative study of polymorphic DNA haplotypes in the Caucasian and Japanese populations.
Journal of inherited metabolic disease 1996;19(3):301-8.
1996: Yamagishi A; Tomatsu S; Fukuda S; Uchiyama A; Shimozawa N; Suzuki Y; Kondo N; Sukegawa K; Orii T
Mucopolysaccharidosis type I: identification of common mutations that cause Hurler and Scheie syndromes in Japanese populations.
Human mutation 1996;7(1):23-9.
1995: Tsukamoto T; Miura S; Nakai T; Yokota S; Shimozawa N; Suzuki Y; Orii T; Fujiki Y; Sakai F; Bogaki A; Yasumo H; Osumi T
Peroxisome assembly factor-2, a putative ATPase cloned by functional complementation on a peroxisome-deficient mammalian cell mutant.
Nature genetics 1995;11(4):395-401.
1995: Atoji Y; Yamamoto Y; Suzuki Y
Morphology of the interdigital glands of a Formosan serow (Capricornis crispus swinhoei).
The Journal of veterinary medical science / the Japanese Society of Veterinary Science 1995;57(5):963-4.
1995: Yanai T; Masegi T; Yoshida K; Ishikawa K; Kawada M; Iwasaki T; Yamazoe K; Suzuki Y; Goto N
Eosinophilic neuronal inclusions in the thalamus of ageing B6C3F1 mice.
Journal of comparative pathology 1995;113(3):287-90.
1995: Koseki N; Araie M; Yamagami J; Suzuki Y
Sectorization of central 10-deg visual field in open-angle glaucoma. An approach for its brief evaluation.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 1995;233(10):621-6.
1995: Yamamoto Y; Atoji Y; Suzuki Y
Nerve endings in bronchi of the dog that react with antibodies against neurofilament protein.
Journal of anatomy 1995;187 ( Pt 1)():59-65.
1995: Atoji Y; Yamamoto Y; Suzuki Y
Myoepithelial cells and innervation in the infraorbital gland of the Japanese serow (Capricornis crispus).
European journal of morphology 1995;33(3):237-46.
1995: Yamamoto Y; Atoji Y; Suzuki Y
Morphological study of the submucosal and mucosal plexuses of the sheep forestomach.
Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft 1995;177(5):405-12.
1995: Song X Q; Fukao T; Suzuki Y; Imamura A; Uchiyama A; Shimozawa N; Kondo N; Orii T
Identification of a novel frameshift mutation in a Japanese adrenoleukodystrophy patient.
Human molecular genetics 1995;4(6):1093-4.
1995: Atoji Y; Hirasawa Y; Yamamoto Y; Suzuki Y
Distribution of neurotensin-immunoreactive neurons in the digestive tract of the chicken.
Journal of the autonomic nervous system 1995;53(2-3):185-94.
1995: Shinnoh N; Yamada T; Yoshimura T; Furuya H; Yoshida Y; Suzuki Y; Shimozawa N; Orii T; Kobayashi T
Adrenoleukodystrophy: the restoration of peroxisomal beta-oxidation by transfection of normal cDNA.
Biochemical and biophysical research communications 1995;210(3):830-6.
1995: Suzuki Y
Direct measurement of retinal vessel diameter: comparison with microdensitometric methods based on fundus photographs.
Survey of ophthalmology 1995;39 Suppl 1():S57-65.
1995: Imamura A; Kamei A; Suzuki Y; Kondo N; Orii T; Takashima S
Immunohistochemistry for a bifunctional protein in patients with peroxisomal disorders.
Pediatric neurology 1995;12(4):341-5.
1995: Hori T; Tomatsu S; Nakashima Y; Uchiyama A; Fukuda S; Sukegawa K; Shimozawa N; Suzuki Y; Kondo N; Horiuchi T
Mucopolysaccharidosis type IVA: common double deletion in the N-acetylgalactosamine-6-sulfatase gene (GALNS).
Genomics 1995;26(3):535-42.
1995: Atoji Y; Yamamoto Y; Suzuki Y
The presence of chondroitin sulfate A and C within axon terminals in the superior olivary nuclei of the adult dog.
Neuroscience letters 1995;189(1):39-42.
1995: Atoji Y; Yamamoto Y; Suzuki Y
Neurotensin-immunoreactive ganglion cells in the pigeon retina.
The Journal of veterinary medical science / the Japanese Society of Veterinary Science 1995;57(2):341-2.
1995: Ogawa T; Tomatsu S; Fukuda S; Yamagishi A; Rezvi G M; Sukegawa K; Kondo N; Suzuki Y; Shimozawa N; Orü T
Mucopolysaccharidosis IVA: screening and identification of mutations of the N-acetylgalactosamine-6-sulfate sulfatase gene.
Human molecular genetics 1995;4(3):341-9.
1995: Tomatsu S; Fukuda S; Uchiyama A; Hori T; Nakashima Y; Sukegawa K; Kondo N; Suzuki Y; Shimozawa N; Orii T
Polymerase chain reaction detection of two novel human N-acetylgalactosamine-6-sulfate sulfatase gene polymorphisms by single-strand conformation polymorphism analysis or by StyI and StuI cleavages.
Human genetics 1995;95(2):243-4.
1995: Atoji Y; Watanabe H; Yamamoto Y; Suzuki Y
Distribution of neurotensin-containing neurons in the central nervous system of the dog.
The Journal of comparative neurology 1995;353(1):67-88.
1995: Yamamoto Y; Atoji Y; Oohira A; Suzuki Y
Immunohistochemical localization of chondroitin sulfate in the forestomach of the sheep.
European journal of histochemistry : EJH 1995;39(4):265-72.
1995: Suzuki Y
[Zellweger syndrome]
Ryoikibetsu shokogun shirizu 1995;(7):544-6.
1995: Koseki N; Araie M; Suzuki Y; Yamagami J
Visual field damage proximal to fixation in normal- and high-tension glaucoma eyes.
Japanese journal of ophthalmology 1995;39(3):274-83.
1995: Yamamoto Y; Atoji Y; Suzuki Y
Muscular architecture and VIP-like immunoreactive nerves in the gastroduodenal junction of the chicken.
Veterinary research communications 1995;19(2):85-93.
1995: Araie M; Arai M; Koseki N; Suzuki Y
Influence of myopic refraction on visual field defects in normal tension and primary open angle glaucoma.
Japanese journal of ophthalmology 1995;39(1):60-4.
1995: Tomatsu S; Fukuda S; Cooper A; Wraith J E; Yamada N; Isogai K; Kato Z; Sukegawa K; Kondo N; Suzuki Y
Two new mutations, Q473X and N487S, in a Caucasian patient with mucopolysaccharidosis IVA (Morquio disease).
Human mutation 1995;6(2):195-6.
1994: Yamamoto Y; Hayashi M; Atoji Y; Suzuki Y
Vagal afferent nerve endings in the trachealis muscle of the dog.
Archives of histology and cytology 1994;57(5):473-80.
1994: Arai M; Araie M; Suzuki Y; Koseki N
[Influence of refraction on the visual field defects in normal tension glaucoma and primary open angle glaucoma eyes]
Nippon Ganka Gakkai zasshi 1994;98(11):1121-5.
1994: Asano J; Suzuki Y; Yajima S; Inoue K; Shimozawa N; Kondo N; Murase M; Orii T
Effects of erucic acid therapy on Japanese patients with X-linked adrenoleukodystrophy.
Brain & development 1994;16(6):454-8.
1994: Hori J; Aihara M; Suzuki Y; Araie M
[Visual field defects in normal tension glaucoma and primary open angle glaucoma. Comparison in the late stage of disease]
Nippon Ganka Gakkai zasshi 1994;98(10):968-73.
1994: Tomatsu S; Fukuda S; Ogawa T; Kato Z; Isogai K; Kondo N; Suzuki Y; Shimozawa N; Sukegawa K; Orii T
A novel splice site mutation in intron 1 of the GALNS gene in a Japanese patient with mucopolysaccharidosis IVA.
Human molecular genetics 1994;3(8):1427-8.
1994: Uchiyama A; Tomatsu S; Kondo N; Suzuki Y; Shimozawa N; Fukuda S; Sukegawa K; Taki N; Inamori H; Orii T
New Gaucher disease mutations in exon 10: a novel L444R mutation produces a new NciI site the same as L444P.
Human molecular genetics 1994;3(7):1183-4.
1994: Imamura A; Komori Y; Fukutomi O; Shimozawa N; Suzuki Y; Kondo N; Orii T
Short latency somatosensory evoked potentials and 99mTc-HMPAO SPECT in a case of flunarizine-effective alternating hemiplegia in infancy.
Brain & development 1994;16(4):325-8.
1994: Adachi M; Shirato S; Kaburagi T; Suzuki Y
[Ten-year results of argon laser trabeculoplasty]
Nippon Ganka Gakkai zasshi 1994;98(4):374-8.
1994: Sekine M; Araie M; Suzuki Y; Koseki N
[Study on risk factors for progression of visual field damage in normal-tension glaucoma]
Nippon Ganka Gakkai zasshi 1994;98(4):369-73.
1994: Yamamoto Y; Kitamura N; Yamada J; Atoji Y; Suzuki Y; Yamashita T
Structure of the enteric nervous system in the sheep omasum as revealed by neurofilament protein-like immunoreactivity.
Journal of anatomy 1994;184 ( Pt 2)():399-405.
1994: Nakashima Y; Tomatsu S; Hori T; Fukuda S; Sukegawa K; Kondo N; Suzuki Y; Shimozawa N; Orii T
Mucopolysaccharidosis IV A: molecular cloning of the human N-acetylgalactosamine-6-sulfatase gene (GALNS) and analysis of the 5'-flanking region.
Genomics 1994;20(1):99-104.
1994: Masuno M; Shimozawa N; Suzuki Y; Kondo N; Orii T; Tsukamoto T; Osumi T; Fujiki Y; Imaizumi K; Kuroki Y
Assignment of the human peroxisome assembly factor-1 gene (PXMP3) responsible for Zellweger syndrome to chromosome 8q21.1 by fluorescence in situ hybridization.
Genomics 1994;20(1):141-2.
1994: Imamura A; Kamei A; Suzuki Y; Orii T; Takashima S
Developmental immunohistochemistry of bifunctional protein in human brain.
Brain research 1994;640(1-2):236-9.
1994: Yamamoto Y; Kitamura N; Yamada J; Yamashita T; Atoji Y; Suzuki Y
The nerve cell bodies found in the ovine omasal laminae.
The Journal of veterinary medical science / the Japanese Society of Veterinary Science 1994;56(1):167-8.
1994: Yamamoto Y; Atoji Y; Kita I; Suzuki Y
Maceration of fetus in the Japanese serow (Capricornis crispus).
The Journal of veterinary medical science / the Japanese Society of Veterinary Science 1994;56(1):165-6.
1994: Aoyama T; Tsushima K; Souri M; Kamijo T; Suzuki Y; Shimozawa N; Orii T; Hashimoto T
Molecular cloning and functional expression of a human peroxisomal acyl-coenzyme A oxidase.
Biochemical and biophysical research communications 1994;198(3):1113-8.
1994: Uchiyama A; Suzuki Y; Song X Q; Fukao T; Imamura A; Tomatsu S; Shimozawa N; Kondo N; Orii T
Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophy.
Biochemical and biophysical research communications 1994;198(2):632-6.
1994: Suzuki Y; Shimozawa N; Yajima S; Tomatsu S; Kondo N; Nakada Y; Akaboshi S; Lai M; Tanabe Y; Hashimoto T
Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis.
American journal of human genetics 1994;54(1):36-43.
1994: Suzuki Y; Shimozawa N; Kawabata I; Yajima S; Inoue K; Uchida Y; Izai K; Tomatsu S; Kondo N; Orii T
Prenatal diagnosis of peroxisomal disorders. Biochemical and immunocytochemical studies on peroxisomes in human amniocytes.
Brain & development 1994;16(1):27-31.
1994: Atoji Y; Nakaoka T; Yamamoto Y; Suzuki Y
Antigen stimulation alters the expression of S-100 protein in the giant macrophages and follicular dendritic cells of the guinea pig lymph nodes.
Acta anatomica 1994;149(3):203-8.
1994: Yanai T; Masegi T; Iwanaka M; Yoshida K; Ueda K; Suzuki Y; Kamiya S
Polyglucosan bodies in the brain of a cow.
Acta neuropathologica 1994;88(1):75-7.
1994: Tomatsu S; Fukuda S; Uchiyama A; Hori T; Nakashima Y; Kondo N; Suzuki Y; Shimozawa N; Sukegawa K; Orii T
Molecular analysis by Southern blot for the N-acetylgalactosamine-6-sulphate sulphatase gene causing mucopolysaccharidosis IVA in the Japanese population.
Journal of inherited metabolic disease 1994;17(5):601-5.
1994: Atoji Y; Watanabe H; Nimamoto N; Sugiyama M; Yamamoto Y; Suzuki Y
Neurotensin immunoreactive cells in the gastrointestinal epithelium of the chicken, pigeon and Japanese quail.
European journal of histochemistry : EJH 1994;38(1):65-72.
1993: Takada M; Araie M; Suzuki Y; Koseki N; Yamagami J
[The central visual field defects in low-tension glaucoma. A comparison of the central visual field defects in low-tension glaucoma with those in primary open angle glaucoma]
Nippon Ganka Gakkai zasshi 1993;97(11):1320-4.
1993: Yamada Y; Tomatsu S; Sukegawa K; Suzuki Y; Kondo N; Hopwood J J; Orii T
Mucopolysaccharidosis type II (Hunter disease): 13 gene mutations in 52 Japanese patients and carrier detection in four families.
Human genetics 1993;92(2):110-4.
1993: Suzuki Y; Shimozawa N; Orii T
[Clinical and molecular aspects of peroxisome-deficient disorders]
Nippon rinsho. Japanese journal of clinical medicine 1993;51(9):2353-8.
1993: Suzuki T; Minamoto N; Sugiyama M; Kinjo T; Suzuki Y; Sugimura M; Atoji Y
Isolation and antibody prevalence of a parapoxvirus in wild Japanese serows (Capricornis crispus).
Journal of wildlife diseases 1993;29(3):384-9.
1993: Orii T; Suzuki Y; Shimozawa N; Yajima S; Asano J
[Peroxisomal disorders--DNA analysis]
Nippon rinsho. Japanese journal of clinical medicine 1993;51 Suppl():1068-77.
1993: Suzuki Y; Shimozawa N; Izai K; Uchida Y; Miura K; Akatsuka H; Nagaya M; Yamaguchi S; Orii T
Peroxisomal 3-ketoacyl-CoA thiolase is partially processed in fibroblasts from patients with rhizomelic chondrodysplasia punctata.
Journal of inherited metabolic disease 1993;16(5):868-71.
1993: Atoji Y; Yamamoto Y; Suzuki Y
Apocrine secretion in the infraorbital gland of the Japanese serow, Capricornis crispus: a scanning electron-microscopic study.
Acta anatomica 1993;148(1):8-13.
1992: Maeda K; Suzuki Y; Yajima S; Asano J; Yamaguchi S; Matsumoto N; Borel J; Moser H W; Orii T
Improvement of clinical and MRI findings in a boy with adrenoleukodystrophy by dietary erucic acid therapy.
Brain & development 1992;14(6):409-12.
1992: Nagasawa H; Yamaguchi S; Suzuki Y; Kobayashi M; Wada Y; Shikura K; Shimao S; Okada T; Orii T
Neuroradiological findings in glutaric aciduria type I: report of four Japanese patients.
Acta paediatrica Japonica; Overseas edition 1992;34(4):409-15.
1992: Atoji Y; Suzuki Y
Chondroitin sulfate in the extracellular matrix of the medial and lateral superior olivary nuclei in the dog.
Brain research 1992;585(1-2):287-90.
1992: Okamoto H; Sukegawa K; Tomatsu S; Suzuki Y; Orii T
Optimization of electroporation for transfection of human fibroblast cell lines with origin-defective SV40 DNA: development of human transformed fibroblast cell lines with mucopolysaccharidoses (I-VII)
Cell structure and function 1992;17(2):123-8.
1992: Suzuki Y
[Clinical biochemical and genetic aspects of peroxisome-deficient disorders]
No to hattatsu. Brain and development 1992;24(2):194-7.
1992: Yajima S; Suzuki Y; Shimozawa N; Yamaguchi S; Orii T; Fujiki Y; Osumi T; Hashimoto T; Moser H W
Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells.
Human genetics 1992;88(5):491-9.
1992: Suzuki Y; Shimozawa N; Yajima S; Orii T; Yokota S; Tashiro Y; Osumi T; Hashimoto T
Different intracellular localization of peroxisomal proteins in fibroblasts from patients with aberrant peroxisome assembly.
Cell structure and function 1992;17(1):1-8.
1992: Shimozawa N; Tsukamoto T; Suzuki Y; Orii T; Shirayoshi Y; Mori T; Fujiki Y
A human gene responsible for Zellweger syndrome that affects peroxisome assembly.
Science (New York, N.Y.) 1992;255(5048):1132-4.
1991: Yamaguchi S; Shimizu N; Orii T; Fukao T; Suzuki Y; Maeda K; Hashimoto T; Previs S F; Rinaldo P
Prenatal diagnosis and neonatal monitoring of a fetus with glutaric aciduria type II due to electron transfer flavoprotein (beta-subunit) deficiency.
Pediatric research 1991;30(5):439-43.
1991: Atoji Y; Kato A; Masegi T; Nakaoka T; Suzuki Y
S-100 immunoreactive cells in the spleen and bursa of Fabricius of broiler chickens.
Journal of comparative pathology 1991;104(3):281-8.
1991: Suzuki Y; Shimozawa N; Yajima S; Yamaguchi S; Orii T; Hashimoto T
Effects of sodium 2-[5-(4-chlorophenyl)pentyl]-oxirane-2-carboxylate (POCA) on fatty acid oxidation in fibroblasts from patients with peroxisomal diseases.
Biochemical pharmacology 1991;41(3):453-6.
1991: Yamaguchi S; Orii T; Suzuki Y; Maeda K; Oshima M; Hashimoto T
Newly identified forms of electron transfer flavoprotein deficiency in two patients with glutaric aciduria type II.
Pediatric research 1991;29(1):60-3.
1991: Atoji Y; Shirogane D; Kurono T; Suzuki Y; Sugimura M
S-100-immunoreactive giant macrophages in lymphoid tissues of the guinea pig.
Acta anatomica 1991;140(1):17-25.
1991: Suzuki Y; Araie M; Yumita A; Yamamoto T
Transscleral Nd: YAG laser cyclophotocoagulation versus cyclocryotherapy.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 1991;229(1):33-6.
1991: Suzuki Y; Masuda K; Ogino K; Sugita T; Aizu Y; Asakura T
Measurement of blood flow velocity in retinal vessels utilizing laser speckle phenomenon.
Japanese journal of ophthalmology 1991;35(1):4-15.
1990: Suzuki Y; Yamaguchi S; Orii T; Tsuneoka M; Tashiro Y
Nonspecific lipid transfer protein (sterol carrier protein-2) defective in patients with deficient peroxisomes.
Cell structure and function 1990;15(5):301-8.
1990: Suzuki Y; Yamaguchi S; Orii T
[Peroxisomes and neurological disorders]
No to shinkei = Brain and nerve 1990;42(7):611-9.
1990: Orii T; Suzuki Y; Shimozawa N; Yamaguchi S
[Clinical, pathological and biochemical abnormality in peroxisomal disorders]
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme 1990;35(8):1447-54.
1990: Atoji Y; Kitamura Y; Suzuki Y
Chondroitin sulfate proteoglycan in the extracellular matrix of the canine superior olivary nuclei.
Acta anatomica 1990;139(2):151-3.
1989: Atoji Y; Hori Y; Sugimura M; Suzuki Y
Extracellular matrix of the superior olivary nuclei in the dog.
Journal of neurocytology 1989;18(5):599-610.
1989: Suzuki Y; Shimozawa N; Orii T; Hashimoto T
Major peroxisomal membrane polypeptides are synthesized in cultured skin fibroblasts from patients with Zellweger syndrome.
Pediatric research 1989;26(2):150-3.
1989: Atoji Y; Suzuki Y; Sugimura M
The preputial gland of the Japanese serow Capricornis crispus: ultrastructure and lectin histochemistry.
Acta anatomica 1989;134(3):245-52.
1988: Atoji Y; Suzuki Y; Sugimura M
Lectin histochemistry of the interdigital gland in the Japanese serow (Capricornis crispus) in winter.
Journal of anatomy 1988;161():159-70.
1988: Shimozawa N; Suzuki Y; Orii T; Yokota S; Hashimoto T
Biochemical and morphologic aspects of peroxisomes in the human rectal mucosa: diagnosis of Zellweger syndrome simplified by rectal biopsy.
Pediatric research 1988;24(6):723-7.
1988: Suzuki Y; Shimozawa N; Orii T; Igarashi N; Kono N; Matsui A; Inoue Y; Yokota S; Hashimoto T
Zellweger-like syndrome with detectable hepatic peroxisomes: a variant form of peroxisomal disorder.
The Journal of pediatrics 1988;113(5):841-5.
1988: Shimozawa N; Suzuki Y; Orii T; Hashimoto T
Diagnosis of Zellweger syndrome by rectal biopsy: immunoblot of peroxisomal beta-oxidation enzyme and activity of dihydroxyacetone phosphate acyltransferase in rectal mucosa.
Clinica chimica acta; international journal of clinical chemistry 1988;175(3):345-7.
1988: Atoji Y; Hori Y; Suzuki Y; Sugimura M
Concanavalin A binding sites of rough endoplasmic reticulum containing intracisternal microtubules in canine neurones.
Journal of comparative pathology 1988;99(1):55-63.
1988: Minamoto N; Oki K; Tomita M; Kinjo T; Suzuki Y
Isolation and characterization of rotavirus from feral pigeon in mammalian cell cultures.
Epidemiology and infection 1988;100(3):481-92.
1988: Shimozawa N; Suzuki Y; Orii T; Hashimoto T
Immunoblot detection of enzyme proteins of peroxisomal beta-oxidation in fibroblasts, amniocytes, and chorionic villous cells. Possible marker for prenatal diagnosis of Zellweger's syndrome.
Prenatal diagnosis 1988;8(4):287-90.
1988: Suzuki Y; Shimozawa N; Orii T; Igarashi N; Kono N; Hashimoto T
Molecular analysis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: further heterogeneity of the peroxisomal disorder.
Clinica chimica acta; international journal of clinical chemistry 1988;172(1):65-76.
1987: Atoji Y; Hori Y; Sugimura M; Suzuki Y
Lectin histochemical study on the infraorbital gland of the Japanese serow (Capricornis crispus).
Acta morphologica Neerlando-Scandinavica 1987;25(4):201-13.
1987: Suzuki Y; Shimozawa N; Orii T; Aikawa J; Tada K; Kuwabara T; Hashimoto T
Biosynthesis of peroxisomal membrane polypeptides in infants with Zellweger syndrome.
Journal of inherited metabolic disease 1987;10(3):297-300.

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