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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
BACKGROUND The number of reported genes causing non-syndromic autosomal recessive intellectual disability (NS-ARID) is increasing… Expand
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2019
2019
Three missense variants of ST3GAL3 are known to be responsible for a congenital disorder of glycosylation determining a… Expand
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2019
2019
The aberrant expression of sialyltransferase has a role in cell differentiation, neoplastic transformation and the progression of… Expand
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2018
2018
The receptive uterine endometrium specifically expresses certain glycosyltransferases, and the corresponding oligosaccharides… Expand
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2017
2017
Emerging evidence indicates that β-galactoside-α2,3-sialyltransferase III (ST3Gal3) involves in development, inflammation… Expand
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2015
2015
The major regulators of melanogenesis are glycoproteins, however no role for glycosylation in the pathway has yet been described… Expand
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2003
2003
Bisubstrate-type sialyltransferase inhibitors 1/2a-e, having CMP-NeuAc and N-acetyllactosamine (or lactose) moieties connected by… Expand
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1997
1997
BACKGROUND Biosynthesis of sialyl Lewis(x) (sLe(x)) requires a sialyltransferase for alpha-2,3-sialylation and a… Expand
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Highly Cited
1996
Highly Cited
1996
T cell surface sialylation changes during maturation in the thymus. We have previously demonstrated increased expression of mRNA… Expand
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