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Generation of human induced pluripotent stem cells from oral mucosa

Journal of bioscience and bioengineering, 2010-09, Vol.110 (3), p.345-350

2010

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A metabonomic approach identifies human urinary phenylacetylglutamine as a novel marker of interstitial cystitis

Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2009-11, Vol.877 (30), p.3806-3812

2009

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Combination with a defucosylated anti-HM1.24 monoclonal antibody plus lenalidomide induces marked ADCC against myeloma cells and their progenitors

PloS one, 2013-12, Vol.8 (12), p.e83905

2013

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Proteomic alteration in gastic adenocarcinomas from Japanese patients

Molecular cancer, 2006-12, Vol.5 (1), p.75-75, Article 75

2006

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Induction of Sca-1 in the duct cells of the mouse submandibular gland by obstruction of the main excretory duct

Journal of oral pathology & medicine, 2011-09, Vol.40 (8), p.651-658

2011

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Metabolic correction in microglia derived from Sandhoff disease model mice

Journal of neurochemistry, 2005-09, Vol.94 (6), p.1631-1638

2005

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Novel missense mutations in the human lysosomal sialidase gene in sialidosis patients and prediction of structural alterations of mutant enzymes

Journal of human genetics, 2002-01, Vol.47 (1), p.29-37

2002

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Clinical, biochemical, and cytochemical studies on a Japanese Salla disease case associated with a renal disorder

Journal of human genetics, 2004-12, Vol.49 (12), p.656-663

2004

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Up-regulation of insulin-like growth factor-binding protein 3 by 5-fluorouracil (5-FU) leads to the potent anti-proliferative effect of androgen deprivation therapy combined with 5-FU in human prostate cancer cell lines

International journal of oncology, 2011-06, Vol.38 (6), p.1489-1500

2011

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Hydroxyflutamide enhances cellular sensitivity to 5-fluorouracil by suppressing thymidylate synthase expression in bicalutamide-resistant human prostate cancer cells

International journal of oncology, 2011-03, Vol.38 (3), p.665-676

2011

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Protective Protein/Cathepsin A Loss in Cultured Cells Derived from an Early-Infantile Form of Galactosialidosis Patients Homozygous for the A1184-G Transition (Y395C Mutation)

Biochemical and biophysical research communications, 1998-06, Vol.247 (1), p.12-17

1998

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Expression of protective protein in human tissue

Pediatric neurology, 1999-03, Vol.20 (3), p.210-214

1999

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Screening and detection of gene mutations in Japanese patients with Fabry disease by non-radioactive single-stranded conformation polymorphism analysis

Brain & development (Tokyo. 1979), 1997-03, Vol.19 (2), p.111-116

1997

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Left Postpneumonectomy Syndrome Successfully Treated with Endobronchial Stent

Internal Medicine, 1998, Vol.37(10), pp.880-883

1998

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Immunofluorescence imaging diagnosis of Fabry heterozygotes using confocal laser scanning microscopy

Clinical genetics, 1993-12, Vol.44 (6), p.302-306

1993

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Three-dimensional brain visualization for metachromatic leukodystrophy

Brain & development (Tokyo. 1979), 1996-09, Vol.18 (5), p.394-399

1996

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Characterization of two α-galactosidase mutants (Q279E and R301Q) found in an atypical variant of Fabry disease

Biochimica et biophysica acta, 2000-06, Vol.1501 (2), p.227-235

2000

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Endothelin-1 in the brain of patients with galactosialidosis: Its abnormal increase and distribution pattern

Annals of neurology, 2000-01, Vol.47 (1), p.122-126

2000

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Protective protein gene mutations in galactosialidosis

The Journal of clinical investigation, 1993-06, Vol.91 (6), p.2393-2398

1993

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Novel missense mutation (M72V) of α-galactosidase gene and its expression product in an atypical fabry hemizygote

Human mutation, 1998, Vol.11 (S1), p.S213-S216

1998

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Immunofluorescence analysis of trihexosylceramide accumulated in the hearts of variant hemizygotes and heterozygotes with Fabry disease

The American journal of cardiology, 1996-07, Vol.78 (1), p.116-117

1996

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Intracellular processing and maturation of mutant gene products in hereditary β-galactosidase deficiency (β-galactosidosis)

Human genetics, 1994-02, Vol.93 (2), p.109-114

1994

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Galactosialidosis: Simultaneous deficiency of esterase, carboxy-terminal deamidase and acid carboxypeptidase activities

Biochemical and biophysical research communications, 1990-11, Vol.172 (3), p.1175-1179

1990

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Urinary excretion of the vitronectin receptor (integrin α Vβ 3) in patients with Fabry disease

Clinica chimica acta, 1999, Vol.279 (1), p.55-68

1999

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Acid carboxypeptidase deficiency in galactosialidosis

Jinrui idengaku zasshi. Japanese journal of human genetics, 1991-06, Vol.36 (2), p.171-177

1991

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Generation of human induced pluripotent stem cells from oral mucosa

A metabonomic approach identifies human urinary phenylacetylglutamine as a novel marker of interstitial cystitis

Combination with a defucosylated anti-HM1.24 monoclonal antibody plus lenalidomide induces marked ADCC against myeloma cells and their progenitors

Proteomic alteration in gastic adenocarcinomas from Japanese patients

Induction of Sca-1 in the duct cells of the mouse submandibular gland by obstruction of the main excretory duct

Metabolic correction in microglia derived from Sandhoff disease model mice

Novel missense mutations in the human lysosomal sialidase gene in sialidosis patients and prediction of structural alterations of mutant enzymes

Clinical, biochemical, and cytochemical studies on a Japanese Salla disease case associated with a renal disorder

Up-regulation of insulin-like growth factor-binding protein 3 by 5-fluorouracil (5-FU) leads to the potent anti-proliferative effect of androgen deprivation therapy combined with 5-FU in human prostate cancer cell lines

Hydroxyflutamide enhances cellular sensitivity to 5-fluorouracil by suppressing thymidylate synthase expression in bicalutamide-resistant human prostate cancer cells

Protective Protein/Cathepsin A Loss in Cultured Cells Derived from an Early-Infantile Form of Galactosialidosis Patients Homozygous for the A1184-G Transition (Y395C Mutation)

Expression of protective protein in human tissue

Screening and detection of gene mutations in Japanese patients with Fabry disease by non-radioactive single-stranded conformation polymorphism analysis

Left Postpneumonectomy Syndrome Successfully Treated with Endobronchial Stent

Immunofluorescence imaging diagnosis of Fabry heterozygotes using confocal laser scanning microscopy

Three-dimensional brain visualization for metachromatic leukodystrophy

Characterization of two α-galactosidase mutants (Q279E and R301Q) found in an atypical variant of Fabry disease

Endothelin-1 in the brain of patients with galactosialidosis: Its abnormal increase and distribution pattern

Protective protein gene mutations in galactosialidosis

Novel missense mutation (M72V) of α-galactosidase gene and its expression product in an atypical fabry hemizygote

Immunofluorescence analysis of trihexosylceramide accumulated in the hearts of variant hemizygotes and heterozygotes with Fabry disease

Intracellular processing and maturation of mutant gene products in hereditary β-galactosidase deficiency (β-galactosidosis)

Galactosialidosis: Simultaneous deficiency of esterase, carboxy-terminal deamidase and acid carboxypeptidase activities

Urinary excretion of the vitronectin receptor (integrin α Vβ 3) in patients with Fabry disease

Acid carboxypeptidase deficiency in galactosialidosis

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