Human genetic disorders and knockout mice deficient in glycosaminoglycan - sprookjes - yvandenbroek - TriplyDB

Human genetic disorders and knockout mice deficient in glycosaminoglycan

Human genetic disorders and knockout mice deficient in glycosaminoglycan

http://www.wikidata.org/entity/Q26995332

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Chondroitin / dermatan sulfate modification enzymes in zebrafish development.Inactivation of Fam20B in Joint Cartilage Leads to Chondrosarcoma and Postnatal Ossification Defects.Insights in the etiopathology of galactosyltransferase II (GalT-II) deficiency from transcriptome-wide expression profiling of skin fibroblasts of two sisters with compound heterozygosity for two novel B3GALT6 mutations.Biosynthesis of glycosaminoglycans: associated disorders and biochemical tests.TGF-β Stimulates Expression of Chondroitin Polymerizing Factor in Nucleus Pulposus Cells Through the Smad3, RhoA/ROCK1, and MAPK Signaling Pathways.Biological roles of glycans.Drug-Mediated Regulation of Glycosaminoglycan Biosynthesis.Identification of biallelic EXTL3 mutations in a novel type of spondylo-epi-metaphyseal dysplasia.Mutations in Biosynthetic Enzymes for the Protein Linker Region of Chondroitin/Dermatan/Heparan Sulfate Cause Skeletal and Skin Dysplasias Inactivation of Fam20B in the dental epithelium of mice leads to supernumerary incisors.Dynamic Expression of Genes Involved in Proteoglycan/Glycosaminoglycan Metabolism during Skin Development

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Human genetic disorders and knockout mice deficient in glycosaminoglycan

http://www.wikidata.org/entity/Q26995332

description

2014 nî lūn-bûn

@nan

2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հուլիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Human genetic disorders and knockout mice deficient in glycosaminoglycan

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Human genetic disorders and knockout mice deficient in glycosaminoglycan

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Human genetic disorders and knockout mice deficient in glycosaminoglycan

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type

label

Human genetic disorders and knockout mice deficient in glycosaminoglycan

@ast

Human genetic disorders and knockout mice deficient in glycosaminoglycan

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Human genetic disorders and knockout mice deficient in glycosaminoglycan

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prefLabel

Human genetic disorders and knockout mice deficient in glycosaminoglycan

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Human genetic disorders and knockout mice deficient in glycosaminoglycan

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Human genetic disorders and knockout mice deficient in glycosaminoglycan

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BioMed Research International

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Human genetic disorders and knockout mice deficient in glycosaminoglycan

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Kazuyuki Sugahara

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Shuhei Yamada

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Shuji Mizumoto

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Creative Commons Attribution 3.0 Unported

P2860

Secreted sulfatases Sulf1 and Sulf2 have overlapping yet essential roles in mouse neonatal survival

Expression of heparan sulfate D-glucosaminyl 3-O-sulfotransferase isoforms reveals novel substrate specificities

Multiple isoforms of heparan sulfate D-glucosaminyl 3-O-sulfotransferase. Isolation, characterization, and expression of human cdnas and identification of distinct genomic loci

Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse

Molecular cloning and characterization of a human uronyl 2-sulfotransferase that sulfates iduronyl and glucuronyl residues in dermatan/chondroitin sulfate

The tumor suppressor EXT-like gene EXTL2 encodes an alpha1, 4-N-acetylhexosaminyltransferase that transfers N-acetylgalactosamine and N-acetylglucosamine to the common glycosaminoglycan-protein linkage region. The key enzyme for the chain initiation

Human homolog of Caenorhabditis elegans sqv-3 gene is galactosyltransferase I involved in the biosynthesis of the glycosaminoglycan-protein linkage region of proteoglycans

Cloning and expression of a proteoglycan UDP-galactose:beta-xylose beta1,4-galactosyltransferase I. A seventh member of the human beta4-galactosyltransferase gene family

Molecular basis for the progeroid variant of Ehlers-Danlos syndrome. Identification and characterization of two mutations in galactosyltransferase I gene

The putative tumor suppressors EXT1 and EXT2 form a stable complex that accumulates in the Golgi apparatus and catalyzes the synthesis of heparan sulfate

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495764

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scholarly article

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108998

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10.1155/2014/495764

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2014

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Kazuyuki Sugahara

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2014-07-13T00:00:00Z

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264832667

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25126564

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Angliavandeniai

Ehlers-Danlos syndrome

multiple epiphyseal dysplasia

osteochondrodysplasia

Enchondromatosis

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4122003

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