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Efficacy and safety of oral propranolol for infantile hemangioma in Japan

Pediatrics international, 2017-08, Vol.59 (8), p.869-877

2017

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Rapid and comprehensive diagnostic method for repeat expansion diseases using nanopore sequencing

Npj genomic medicine, 2022-10, Vol.7 (1), p.62-62, Article 62

2022

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Cerebellar ataxia-dominant phenotype in patients with ERCC4 mutations

Journal of human genetics, 2018-04, Vol.63 (4), p.417-423

2018

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Orthogonal Glycosylation Reactions on Solid Phase and Synthesis of a Library Consisting of a Complete Set of Fucosyl Galactose Isomers

Angewandte Chemie (International ed.), 2006-06, Vol.45 (23), p.3851-3854

2006

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Discrimination of 16 Structural Isomers of Fucosyl Galactoside Based on Energy-Resolved Mass Spectrometry

Journal of the American Society for Mass Spectrometry, 2007-10, Vol.18 (10), p.1873-1879

2007

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A Method of Orthogonal Oligosaccharide Synthesis Leading to a Combinatorial Library Based on Stationary Solid-Phase Reaction

Chemistry, an Asian journal, 2006-12, Vol.1 (6), p.798-813

2006

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Synthesis of a library of fucopyranosyl-galactopyranosides consisting of a complete set of anomeric configurations and linkage positions

Carbohydrate research, 2006-07, Vol.341 (10), p.1476-1487

2006

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Population Pharmacokinetics and Pharmacodynamics of Oral Propranolol in Pediatric Patients With Infantile Hemangioma

Journal of clinical pharmacology, 2018-10, Vol.58 (10), p.1361-1370

2018

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Ion-trap mass spectrometry unveils the presence of isomeric oligosaccharides in an analyte: stage-discriminated correlation of energy-resolved mass spectrometry

Carbohydrate research, 2009-02, Vol.344 (3), p.384-394

2009

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Development of highly potent D-glucosamine-based chiral fluorescent labeling reagents and a microwave-assisted beta-selective glycosidation of a methyl glycoside reagent

Bioscience, biotechnology, and biochemistry, 2005-05, Vol.69 (5), p.1054-1057

2005

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Exome Sequencing Reveals a Homozygous SYT14 Mutation in Adult-Onset, Autosomal-Recessive Spinocerebellar Ataxia with Psychomotor Retardation

American journal of human genetics, 2011-08, Vol.89 (2), p.320-327

2011

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Cover Picture: A Method of Orthogonal Oligosaccharide Synthesis Leading to a Combinatorial Library Based on Stationary Solid-Phase Reaction (Chem. Asian J. 6/2006)

Chemistry, an Asian journal, 2006-12, Vol.1 (6), p.757-757

2006

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A rapid diagnostic method for a retrotransposal insertional mutation into the FCMD gene in Japanese patients with Fukuyama congenital muscular dystrophy

American journal of medical genetics, 2004-05, Vol.127A (1), p.54-57

2004

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Development of Highly Potent D-Glucosamine-Based Chiral Fluorescent Labeling Reagents and a Microwave-Assisted [beta]-Selective Glycosidation of a Methyl Glycoside Reagent

Bioscience, biotechnology, and biochemistry, 2005-05, Vol.69 (5), p.1054

2005

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Abstracts for the 6th Congress of Asian Sleep Research Society

Sleep and biological rhythms, 2009-10, Vol.7 (4), p.A1-A49

2009

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Orthogonal Glycosylation Reactions on Solid Phase and Synthesis of a Library Consisting of a Complete Set of Fucosyl Galactose Isomers

Angewandte Chemie, 2006-06, Vol.118 (23), p.3935-3938

2006

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Prevention of gastroesophageal reflux in the severely disabled patients using pectin gel

No to hattatsu, 2002-09, Vol.34 (5), p.437

2002

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Assignment of the human GLI2 gene to 2q14 by fluorescence in situ hybridization

Genomics (San Diego, Calif.), 1996-08, Vol.36 (1), p.220-221

1996

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Assignment of the HumanGLI2Gene to 2q14 by Fluorescencein SituHybridization

Genomics (San Diego, Calif.), 1996-08, Vol.36 (1), p.220-221

1996

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A 1.2-Megabase BAC/PAC Contig Spanning the 14q13 Breakpoint of t(2;14) in a Mirror-Image Polydactyly Patient

Genomics (San Diego, Calif.), 1997-10, Vol.45 (1), p.11-16

1997

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Assignment of the human connexin43 gene, GJA1, to chromosome 6q22.3

Journal of human genetics, 1997-03, Vol.42 (1), p.213-216

1997

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FISH mapping of a translocation breakpoint at 6q21 (or q22) in a patient with heterotaxia

Journal of human genetics, 1997-12, Vol.42 (4), p.525-532

1997

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Molecular mapping of a translocation breakpoint at 14q13 in a patient with mirror-image polydactyly of hands and feet

Human genetics, 1997-04, Vol.99 (4), p.450-453

1997

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Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q

American journal of medical genetics, 2001-12, Vol.104 (4), p.319-322

2001

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Efficacy and safety of oral propranolol for infantile hemangioma in Japan

Rapid and comprehensive diagnostic method for repeat expansion diseases using nanopore sequencing

Cerebellar ataxia-dominant phenotype in patients with ERCC4 mutations

Orthogonal Glycosylation Reactions on Solid Phase and Synthesis of a Library Consisting of a Complete Set of Fucosyl Galactose Isomers

Discrimination of 16 Structural Isomers of Fucosyl Galactoside Based on Energy-Resolved Mass Spectrometry

A Method of Orthogonal Oligosaccharide Synthesis Leading to a Combinatorial Library Based on Stationary Solid-Phase Reaction

Synthesis of a library of fucopyranosyl-galactopyranosides consisting of a complete set of anomeric configurations and linkage positions

Population Pharmacokinetics and Pharmacodynamics of Oral Propranolol in Pediatric Patients With Infantile Hemangioma

Ion-trap mass spectrometry unveils the presence of isomeric oligosaccharides in an analyte: stage-discriminated correlation of energy-resolved mass spectrometry

Repeat conformation heterogeneity in cerebellar ataxia, neuropathy, vestibular areflexia syndrome

Development of highly potent D-glucosamine-based chiral fluorescent labeling reagents and a microwave-assisted beta-selective glycosidation of a methyl glycoside reagent

Exome Sequencing Reveals a Homozygous SYT14 Mutation in Adult-Onset, Autosomal-Recessive Spinocerebellar Ataxia with Psychomotor Retardation

Cover Picture: A Method of Orthogonal Oligosaccharide Synthesis Leading to a Combinatorial Library Based on Stationary Solid-Phase Reaction (Chem. Asian J. 6/2006)

A rapid diagnostic method for a retrotransposal insertional mutation into the FCMD gene in Japanese patients with Fukuyama congenital muscular dystrophy

Development of Highly Potent D-Glucosamine-Based Chiral Fluorescent Labeling Reagents and a Microwave-Assisted [beta]-Selective Glycosidation of a Methyl Glycoside Reagent

Abstracts for the 6th Congress of Asian Sleep Research Society

Orthogonal Glycosylation Reactions on Solid Phase and Synthesis of a Library Consisting of a Complete Set of Fucosyl Galactose Isomers

Prevention of gastroesophageal reflux in the severely disabled patients using pectin gel

Assignment of the human GLI2 gene to 2q14 by fluorescence in situ hybridization

Assignment of the HumanGLI2Gene to 2q14 by Fluorescencein SituHybridization

A 1.2-Megabase BAC/PAC Contig Spanning the 14q13 Breakpoint of t(2;14) in a Mirror-Image Polydactyly Patient

Assignment of the human connexin43 gene, GJA1, to chromosome 6q22.3

FISH mapping of a translocation breakpoint at 6q21 (or q22) in a patient with heterotaxia

Molecular mapping of a translocation breakpoint at 14q13 in a patient with mirror-image polydactyly of hands and feet

Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q

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