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Analytical Chemistry
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September 4, 2020
Lactone-Driven Ester-to-Amide Derivatization for Sialic Acid Linkage-Specific Alkylamidation
Jun-Ichi Furukawa, Hisatoshi Hanamatsu, Takashi Nishikaze, et al.
Mechanisms of Development
|
December 31, 2008
Reduced proliferative activity of primary POMGnT1-null myoblasts in vitro
Yuko Miyagoe-Suzuki, Nami Masubuchi, Kaori Miyamoto, et al.
Biological & Pharmaceutical Bulletin
|
September 3, 2015
POMGNT1 Is Glycosylated by Mucin-Type O-Glycans
Xin Xin, Keiko Akasaka-Manya, Hiroshi Manya, et al.
Journal of Human Genetics
|
May 20, 2016
Analysis of phenotype, enzyme activity and genotype of Chinese patients with POMT1 mutation
Haipo Yang, Hiroshi Manya, Kazuhiro Kobayashi, et al.
Glycobiology
|
December 20, 2013
Structural and biochemical characterization of O-mannose-linked human natural killer-1 glycan expressed on phosphacan in developing mouse brains
Jyoji Morise, Yasuhiko Kizuka, Keiko Yabuno, et al.
Nature Communications
|
April 15, 2022
CDP-ribitol prodrug treatment ameliorates ISPD-deficient muscular dystrophy mouse model
Hideki Tokuoka, Rieko Imae, Hitomi Nakashima, et al.
Biochemical and Biophysical Research Communications
|
March 9, 2002
Deficiency of alpha-dystroglycan in muscle-eye-brain disease
Hiroki Kano, Kazuhiro Kobayashi, Ralf Herrmann, et al.
Journal of Biochemistry
|
January 6, 2017
Excess APP O-glycosylation by GalNAc-T6 decreases Aβ production
Keiko Akasaka-Manya, Masaki Kawamura, Hiroki Tsumoto, et al.
The Journal of Biological Chemistry
|
June 11, 2023
O-GalNAc glycosylation determines intracellular trafficking of APP and Aβ production
Yuriko Tachida, Junko Iijima, Kazuto Takahashi, et al.
The Journal of Biological Chemistry
|
January 25, 2012
Absence of post-phosphoryl modification in dystroglycanopathy mouse models and wild-type tissues expressing non-laminin binding form of α-dystroglycan
Atsushi Kuga, Motoi Kanagawa, Atsushi Sudo, et al.
Page
of 8
Search research articles
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Showing results (51-60 of 71) with videos related to
Sort By:
Page
of 8
Analytical Chemistry
|
September 4, 2020
Lactone-Driven Ester-to-Amide Derivatization for Sialic Acid Linkage-Specific Alkylamidation
Jun-Ichi Furukawa, Hisatoshi Hanamatsu, Takashi Nishikaze, et al.
Mechanisms of Development
|
December 31, 2008
Reduced proliferative activity of primary POMGnT1-null myoblasts in vitro
Yuko Miyagoe-Suzuki, Nami Masubuchi, Kaori Miyamoto, et al.
Biological & Pharmaceutical Bulletin
|
September 3, 2015
POMGNT1 Is Glycosylated by Mucin-Type O-Glycans
Xin Xin, Keiko Akasaka-Manya, Hiroshi Manya, et al.
Journal of Human Genetics
|
May 20, 2016
Analysis of phenotype, enzyme activity and genotype of Chinese patients with POMT1 mutation
Haipo Yang, Hiroshi Manya, Kazuhiro Kobayashi, et al.
Glycobiology
|
December 20, 2013
Structural and biochemical characterization of O-mannose-linked human natural killer-1 glycan expressed on phosphacan in developing mouse brains
Jyoji Morise, Yasuhiko Kizuka, Keiko Yabuno, et al.
Nature Communications
|
April 15, 2022
CDP-ribitol prodrug treatment ameliorates ISPD-deficient muscular dystrophy mouse model
Hideki Tokuoka, Rieko Imae, Hitomi Nakashima, et al.
Biochemical and Biophysical Research Communications
|
March 9, 2002
Deficiency of alpha-dystroglycan in muscle-eye-brain disease
Hiroki Kano, Kazuhiro Kobayashi, Ralf Herrmann, et al.
Journal of Biochemistry
|
January 6, 2017
Excess APP O-glycosylation by GalNAc-T6 decreases Aβ production
Keiko Akasaka-Manya, Masaki Kawamura, Hiroki Tsumoto, et al.
The Journal of Biological Chemistry
|
June 11, 2023
O-GalNAc glycosylation determines intracellular trafficking of APP and Aβ production
Yuriko Tachida, Junko Iijima, Kazuto Takahashi, et al.
The Journal of Biological Chemistry
|
January 25, 2012
Absence of post-phosphoryl modification in dystroglycanopathy mouse models and wild-type tissues expressing non-laminin binding form of α-dystroglycan
Atsushi Kuga, Motoi Kanagawa, Atsushi Sudo, et al.
Page
of 8