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CHST14 gene

Known as: CHST14, D4ST-1, N-ACETYLGALACTOSAMINE 4-0 SULFOTRANSFERASE 
National Institutes of Health

Related topics

Related topics

1 relation
dermatan-4-sulfotransferase-1

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Impaired Cognitive Function and Altered Hippocampal Synaptic Plasticity in Mice Lacking Dermatan Sulfotransferase Chst14/D4st1
Chondroitin sulfate (CS) and dermatan sulfate (DS) proteoglycans (PGs) are major extracellular matrix (ECM) components of the… 
2018
2018
Vascular abnormalities in the placenta of Chst14−/− fetuses: implications in the pathophysiology of perinatal lethality of the murine model and vascular lesions in human CHST14/D4ST1 deficiency
Collagen is one of the most important components of the extracellular matrix that is involved in the strength of tissues, cell… 
Highly Cited
2016
Highly Cited
2016
The phenotype of the musculocontractural type of Ehlers‐Danlos syndrome due to CHST14 mutations
The musculocontractural type of Ehlers‐Danlos syndrome (MC‐EDS) has been recently recognized as a clinical entity. MC‐EDS… 
Review
2016
Review
2016
CHST14/D4ST1 deficiency: New form of Ehlers–Danlos syndrome
Carbohydrate sulfotransferase 14/dermatan 4‐O‐sulfotransferase‐1 (CHST14/D4ST1) deficiency represents a specific form of Ehlers… 
2014
2014
Analysis of autoantibody profiles in osteoarthritis using comprehensive protein array concepts.
Osteoarthritis (OA) is the most common rheumatic disease and one of the most disabling pathologies worldwide. To date, the… 
2013
2013
Dermatan 4-O-sulfotransferase1 ablation accelerates peripheral nerve regeneration
2012
2012
Myopathy in a 20‐year‐old female patient with D4ST‐1 deficient Ehlers‐Danlos syndrome due to a homozygous CHST14 mutation
We here report on a 20‐year‐old female patient with EDS due to a homozygous CHST14 single nucleotide deletion resulting in D4ST‐1… 
2011
2011
Dermatan sulfotransferase Chst14/D4st1, but not chondroitin sulfotransferase Chst11/C4st1, regulates proliferation and neurogenesis of neural progenitor cells
Chondroitin sulfates (CSs) and dermatan sulfates (DSs) are enriched in the microenvironment of neural stem cells (NSCs) during… 
Highly Cited
2010
Highly Cited
2010
Musculocontractural Ehlers‐Danlos Syndrome (former EDS type VIB) and adducted thumb clubfoot syndrome (ATCS) represent a single clinical entity caused by mutations in the dermatan‐4‐sulfotransferase…
We present clinical and molecular findings of three patients with an EDS VIB phenotype from two consanguineous families. The… 
Highly Cited
2010
Highly Cited
2010
Loss‐of‐function mutations of CHST14 in a new type of Ehlers‐Danlos syndrome
Ehlers‐Danlos syndrome (EDS) is a heterogeneous connective tissue disorder involving skin and joint laxity and tissue fragility… 
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