Shuji MIZUMOTO, 水本 秀二
Meijo University
H-index: 35
Asia-Japan
Top articles of Shuji MIZUMOTO, 水本 秀二
Global mapping of glycosylation pathways in human-derived cells
Developmental Cell
2021/3/16
Hyaluronan degradation and release of a hyaluronan-aggrecan complex from perineuronal nets in the aged mouse brain
Biochimica et Biophysica Acta (BBA)-General Subjects
2021/2/1
Systematic investigation of the skin in Chst14−/− mice: A model for skin fragility in musculocontractural Ehlers–Danlos syndrome caused by CHST14 variants (mcEDS-CHST14)
Glycobiology
2021/2
Myopathy Associated With Dermatan Sulfate-Deficient Decorin and Myostatin in Musculocontractural Ehlers-Danlos Syndrome: A Mouse Model Investigation
Frontiers in cell and developmental biology
2021
An Overview of in vivo Functions of Chondroitin Sulfate and Dermatan Sulfate Revealed by Their Deficient Mice
2021/1/1
Congenital Disorders of Deficiency in Glycosaminoglycan Biosynthesis
2021
A new mouse model of Ehlers-Danlos syndrome generated using CRISPR/Cas9-mediated genomic editing
Disease Models & Mechanisms
2021/12/1
Memories of Professor Kazuyuki Sugahara
2021/3/25
b3galt6 knock-out zebrafish recapitulate β3GalT6-deficiency disorders in human and reveal a trisaccharide proteoglycan linkage region
Frontiers in cell and developmental biology
2020/12/10
Congenital Disorders Caused by Defects in Catabolism of Glycosaminoglycans
Trends in Glycoscience and Glycotechnology
2020/7
Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis
Journal of Medical Genetics
2020/7/1
Delineation of musculocontractural Ehlers–Danlos Syndrome caused by dermatan sulfate epimerase deficiency
Molecular genetics & genomic medicine
2020/5
Congenital Disorders Caused by Defects in Anabolism of Glycosaminoglycans
Trends in Glycoscience and Glycotechnology
2020/3/25
CSGALNACT1‐congenital disorder of glycosylation: A mild skeletal dysplasia with advanced bone age
Human mutation
2020/3
Recent Advances in the Pathophysiology of Musculocontractural Ehlers-Danlos Syndrome
2020/1