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ST3GAL3 gene

Known as: ST3GALII, ST3Gal III, SIALYLTRANSFERASE 6 
National Institutes of Health

Papers overview

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2020
2020
Three missense variants of ST3GAL3 are known to be responsible for a congenital disorder of glycosylation determining a… 
2020
2020
The number of reported genes causing non‐syndromic autosomal recessive intellectual disability (NS‐ARID) is increasing. For… 
2019
2019
The aberrant expression of sialyltransferase has a role in cell differentiation, neoplastic transformation and the progression of… 
2018
2018
The receptive uterine endometrium specifically expresses certain glycosyltransferases, and the corresponding oligosaccharides… 
2015
2015
The major regulators of melanogenesis are glycoproteins, however no role for glycosylation in the pathway has yet been described… 
2003
2003
Bisubstrate-type sialyltransferase inhibitors 1/2a-e, having CMP-NeuAc and N-acetyllactosamine (or lactose) moieties connected by… 
1997
1997
BACKGROUND Biosynthesis of sialyl Lewis(x) (sLe(x)) requires a sialyltransferase for alpha-2,3-sialylation and a… 
Highly Cited
1996
Highly Cited
1996
T cell surface sialylation changes during maturation in the thymus. We have previously demonstrated increased expression of mRNA…