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EOGT gene

Known as: CHROMOSOME 3 OPEN READING FRAME 64, EGF domain specific O-linked N-acetylglucosamine transferase, AER61 
 
National Institutes of Health

Papers overview

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2019
2019
Adams-Oliver syndrome (AOS) is a rare congenital disease characterized by aplasia cutis congenita (ACC) and terminal transverse… Expand
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2018
2018
In pregnancy, resistance of endometrial decidual cells to stress signals is critical for the integrity of the fetomaternal… Expand
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Review
2017
Review
2017
Here, we describe a recently discovered O-GlcNAc transferase termed EOGT for EGF domain-specific O-GlcNAc transferase. EOGT… Expand
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2017
2017
The glycosyltransferase EOGT transfers O-GlcNAc to a consensus site in epidermal growth factor-like (EGF) repeats of a limited… Expand
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2016
2016
Purpose: To investigate the antinociceptive effect of the essential oil from the aerial parts of Gundelia. tournefortii (EOGT) in… Expand
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2015
2015
Adams-Oliver syndrome (AOS) is a rare developmental disorder characterized by the presence of aplasia cutis congenita (ACC) of… Expand
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2014
2014
Autosomal recessive Adams–Oliver syndrome was diagnosed in three remotely related Bedouin consanguineous families. Genome-wide… Expand
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2014
2014
Background: EOGT (epidermal growth factor (EGF) domain-specific O-linked N-acetylglucosamine) mutations have been identified in… Expand
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2012
2012
O-linked-β-N-acetylglucosamine (O-GlcNAc) modification is a unique cytoplasmic and nuclear protein modification that is common in… Expand
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Highly Cited
2011
Highly Cited
2011
The O-linked-N-acetylglucosamine (O-GlcNAc) modification of cytoplasmic and nuclear proteins regulates basic cellular functions… Expand
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