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keratan sulfate catabolic process

Known as: keratan sulfate catabolism, keratan sulfate degradation, keratan sulphate catabolic process 
The chemical reactions and pathways resulting in the breakdown of keratan sulfate, a glycosaminoglycan with repeat units consisting of beta-1,4… Expand
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Urinary proteomics links keratan sulfate degradation and lysosomal enzymes to early type 1 diabetes
Diabetes is the leading cause of end-stage renal disease worldwide. Our understanding of the early kidney response to chronic… Expand
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2019
2019
Identification of Pivotal Genes and Pathways in Osteoarthritic Degenerative Meniscal Lesions via Bioinformatics Analysis of the GSE52042 Dataset
Background To better understand the process of osteoarthritic degenerative meniscal lesions (DMLs) formation, this study analyzed… Expand
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2019
2019
Microenvironment of ruptured cerebral aneurysms discovered using data driven analysis of gene expression
Background It is well known that ruptured intracranial aneurysms are associated with substantial morbidity and mortality, yet our… Expand
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2017
2017
A novel method to identify hub pathways of rheumatoid arthritis based on differential pathway networks
The aim of the current study was to identify hub pathways of rheumatoid arthritis (RA) using a novel method based on differential… Expand
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2010
2010
Role of keratan sulphate (sulphated poly -N-acetyllactosamine repeats) in keratoconic cornea, histochemical, and ultrastructural analysis
AimsKeratan sulphate (KS) is the predominant glycosaminoglycan (GAG) present in the corneal stroma where it is thought to… Expand
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2004
2004
Glycosidase and sulfatase activities and their possible role in keratan sulfate degradation in metamorphosing bonefish (Albula sp.) leptocephali
During metamorphosis of leptocephalous larvae of the bonefish (Albula sp.), keratan sulfate, the principal glycosaminoglycan of… Expand
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2002
2002
Novel mutations (Asn 484 Lys, Thr 500 Ala, Gly 438 Glu) in Morquio B disease.
Primary deficiency of beta-galactosidase results in GM1 gangliosidosis and Morquio B disease. Of the more than 40 disease-causing… Expand
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