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CHST3 wt Allele

Known as: Carbohydrate (Chondroitin 6) Sulfotransferase 3 wt Allele, C6ST, C6ST1 
Human CHST3 wild-type allele is located in the vicinity of 10q22.1 and is approximately 49 kb in length. This allele, which encodes carbohydrate… 
National Institutes of Health

Related topics

Related topics

2 relations
Carbohydrate Metabolismprotein metabolism

Papers overview

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Review
2012
Review
2012
ISCSM2011 chondroitin sulfate E-type structure at tumor cell surface is involved in experimental metastasis.
Chondroitin sulfate/dermatan sulfate (CS/DS) proteoglycans at the surface of tumor cells play key roles in malignant… 
2003
2003
Hypertonic Saline Dextran Alleviates Hepatic Injury in Hypovolemic Rats Undergoing Porta Hepatis Occlusion
To monitor the ischemic and/or reperfusion injury after porta hepatis occlusion (Pringle maneuver) in livers subjected to… 
2003
2003
Epidermal growth factor increases cortisol production and type II 3 beta-hydroxysteroid dehydrogenase/Delta(5)-Delta(4)-isomerase expression in human adrenocortical carcinoma cells: evidence for a…
We tested the ability of epidermal growth factor (EGF) to regulate a key enzyme in the adrenal synthesis of glucocorticoids… 
2003
2003
Functional characterization of the human 11 beta-hydroxysteroid dehydrogenase 1B (11 beta-HSD 1B) variant.
11 beta-Hydroxysteroid dehydrogenase type 1 (11 beta-HSD 1) catalyzes the interconversion of inactive into active glucocorticoids… 
2003
2003
C6ST expression in sciatic nerve explant culture of adult rats
2001
2001
Biosynthesis of the neurosteroid 3 alpha-hydroxy-4-pregnen-20-one (3 alpha hp), a specific inhibitor of FSH release.
The gonadal steroid 3 alpha-hydroxy-4-pregnen-20-one (3 alpha HP) is a neuroactive steroid with anxiolytic and analgesic actions… 
Highly Cited
1996
Highly Cited
1996
Studies of 3 beta-hydroxysteroid dehydrogenase genes in infants and children manifesting premature pubarche and increased adrenocorticotropin-stimulated delta 5-steroid levels.
Classic 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) deficiency congenital adrenal hyperplasia (CAH) results from a mutation… 
1995
1995
The human 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene cluster on chromosome 1p13 contains a presumptive pseudogene; 3 beta-HSD and CYP17 do not segregate with dominantly inherited hirsutism…
Four hirsute females from a family exhibiting idiopathic dominant hirsutism were examined. Basal blood levels of delta 5 and… 
Highly Cited
1994
Highly Cited
1994
Detection and functional characterization of the novel missense mutation Y254D in type II 3 beta-hydroxysteroid dehydrogenase (3 beta HSD) gene of a female patient with nonsalt-losing 3 beta HSD…
Three beta-hydroxysteroid dehydrogenase/delta 5-delta 4-isomerase (3 beta HSD) deficiency is a form of congenital adrenal… 
Highly Cited
1994
Highly Cited
1994
Mutation in 3 beta-hydroxysteroid dehydrogenase type II associated with pseudohermaphroditism in males and premature pubarche or cryptic expression in females.
A mutation (A82T) is described in the coding sequence of the gene for 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) type II… 
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