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Ryuichi Mashima

Showing results (11-20 of 42) with videos related to

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International Journal of Molecular Sciences|February 26, 2022
Physiology and Pathophysiology of Heparan Sulfate in Animal Models: Its Biosynthesis and DegradationRyuichi Mashima, Torayuki Okuyama, Mari Ohira
Molecular Genetics and Metabolism Reports|September 14, 2018
Quantification of 11 enzyme activities of lysosomal storage disorders using liquid chromatography-tandem mass spectrometryMari Ohira, Torayuki Okuyama, Ryuichi Mashima
International Journal of Molecular Sciences|April 17, 2020
Biomarkers for Lysosomal Storage Disorders with an Emphasis on Mass SpectrometryRyuichi Mashima, Torayuki Okuyama, Mari Ohira
Analytical Biochemistry|February 11, 2003
Simultaneous determination of methionine sulfoxide and methionine in blood plasma using gas chromatography-mass spectrometryRyuichi Mashima, Takako Nakanishi-Ueda, Yorihiro Yamamoto
Molecular Genetics and Metabolism Reports|September 6, 2022
LC-MS/MS-based enzyme assay for lysosomal acid lipase using dried blood spotsMari Ohira, Marianne Barr, Torayuki Okuyama, et al.
Molecular Genetics and Metabolism Reports|September 15, 2016
Levels of enzyme activities in six lysosomal storage diseases in Japanese neonates determined by liquid chromatography-tandem mass spectrometryRyuichi Mashima, Eri Sakai, Motomichi Kosuga, et al.
Molecular Genetics and Metabolism Reports|January 13, 2018
Quantification of the enzyme activities of iduronate-2-sulfatase, <i>N</i>-acetylgalactosamine-6-sulfatase and <i>N</i>-acetylgalactosamine-4-sulfatase using liquid chromatography-tandem mass spectrometryRyuichi Mashima, Mari Ohira, Torayuki Okuyama, et al.
Immunological Reviews|November 14, 2009
The roles of Dok family adapters in immunoreceptor signalingRyuichi Mashima, Yukihiro Hishida, Tohru Tezuka, et al.
Scientific Reports|May 15, 2023
A novel mucopolysaccharidosis type II mouse model with an iduronate-2-sulfatase-P88L mutationRyuichi Mashima, Mari Ohira, Torayuki Okuyama, et al.
Molecular Genetics and Metabolism Reports|June 23, 2016
The levels of urinary glycosaminoglycans of patients with attenuated and severe type of mucopolysaccharidosis II determined by liquid chromatography-tandem mass spectrometryRyuichi Mashima, Eri Sakai, Misa Tanaka, et al.
Pageof 5

Showing results (11-20 of 42) with videos related to

Sort By:
Pageof 5
International Journal of Molecular Sciences|February 26, 2022
Physiology and Pathophysiology of Heparan Sulfate in Animal Models: Its Biosynthesis and DegradationRyuichi Mashima, Torayuki Okuyama, Mari Ohira
Molecular Genetics and Metabolism Reports|September 14, 2018
Quantification of 11 enzyme activities of lysosomal storage disorders using liquid chromatography-tandem mass spectrometryMari Ohira, Torayuki Okuyama, Ryuichi Mashima
International Journal of Molecular Sciences|April 17, 2020
Biomarkers for Lysosomal Storage Disorders with an Emphasis on Mass SpectrometryRyuichi Mashima, Torayuki Okuyama, Mari Ohira
Analytical Biochemistry|February 11, 2003
Simultaneous determination of methionine sulfoxide and methionine in blood plasma using gas chromatography-mass spectrometryRyuichi Mashima, Takako Nakanishi-Ueda, Yorihiro Yamamoto
Molecular Genetics and Metabolism Reports|September 6, 2022
LC-MS/MS-based enzyme assay for lysosomal acid lipase using dried blood spotsMari Ohira, Marianne Barr, Torayuki Okuyama, et al.
Molecular Genetics and Metabolism Reports|September 15, 2016
Levels of enzyme activities in six lysosomal storage diseases in Japanese neonates determined by liquid chromatography-tandem mass spectrometryRyuichi Mashima, Eri Sakai, Motomichi Kosuga, et al.
Molecular Genetics and Metabolism Reports|January 13, 2018
Quantification of the enzyme activities of iduronate-2-sulfatase, <i>N</i>-acetylgalactosamine-6-sulfatase and <i>N</i>-acetylgalactosamine-4-sulfatase using liquid chromatography-tandem mass spectrometryRyuichi Mashima, Mari Ohira, Torayuki Okuyama, et al.
Immunological Reviews|November 14, 2009
The roles of Dok family adapters in immunoreceptor signalingRyuichi Mashima, Yukihiro Hishida, Tohru Tezuka, et al.
Scientific Reports|May 15, 2023
A novel mucopolysaccharidosis type II mouse model with an iduronate-2-sulfatase-P88L mutationRyuichi Mashima, Mari Ohira, Torayuki Okuyama, et al.
Molecular Genetics and Metabolism Reports|June 23, 2016
The levels of urinary glycosaminoglycans of patients with attenuated and severe type of mucopolysaccharidosis II determined by liquid chromatography-tandem mass spectrometryRyuichi Mashima, Eri Sakai, Misa Tanaka, et al.
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