Reactome | Sugahara, K

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Sugahara, K Show undefined attributes

created	[InstanceEdit:3621807] Jassal, B, 2013-05-24
dbId	3621793
displayName	Sugahara, K
firstname	Kazuyuki
initial	K
publications	[LiteratureReference:3769476] Human genetic disorders caused by mutations in genes encoding biosynthetic enzymes for sulfated glycosaminoglycans [LiteratureReference:9941269] Identification of human hyaluronidase-4 as a novel chondroitin sulfate hydrolase that preferentially cleaves the galactosaminidic linkage in the trisulfated tetrasaccharide sequence [LiteratureReference:3636854] Loss of chondroitin 6-O-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvement [LiteratureReference:9774579] Structural recognition by recombinant human heparanase that plays critical roles in tumor metastasis. Hierarchical sulfate groups with different effects and the essential target disulfated trisaccharide sequence [LiteratureReference:3636839] Spondyloepiphyseal dysplasia, Omani type: further definition of the phenotype [LiteratureReference:9941167] Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural Ehlers-Danlos syndrome [LiteratureReference:5652108] De novo mutations in SLC35A2 encoding a UDP-galactose transporter cause early-onset epileptic encephalopathy [LiteratureReference:9941057] Chondroitin Sulfate N-acetylgalactosaminyltransferase-1 (CSGalNAcT-1) Deficiency Results in a Mild Skeletal Dysplasia and Joint Laxity [LiteratureReference:3621752] Faulty initiation of proteoglycan synthesis causes cardiac and joint defects [LiteratureReference:3636906] Loss-of-function mutations of CHST14 in a new type of Ehlers-Danlos syndrome [LiteratureReference:4420321] Mutations in B3GALT6, which Encodes a Glycosaminoglycan Linker Region Enzyme, Cause a Spectrum of Skeletal and Connective Tissue Disorders
schemaClass	Person
surname	Sugahara

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