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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

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Adams–Oliver syndrome caused by mutations of the EOGT gene
Adams–Oliver syndrome (AOS) is a rare congenital disease characterized by aplasia cutis congenita (ACC) and terminal transverse… Expand
2018
2018
The Glycosyltransferase EOGT Regulates Adropin Expression in Decidualizing Human Endometrium
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
EOGT and O-GlcNAc on secreted and membrane proteins.
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
O-GlcNAc on NOTCH1 EGF repeats regulates ligand-induced Notch signaling and vascular development in mammals
The glycosyltransferase EOGT transfers O-GlcNAc to a consensus site in epidermal growth factor-like (EGF) repeats of a limited… Expand
2016
2016
Chemical composition and antinociceptive effects of essential oil from aerial parts of Gundelia tournefortii L Asteraceae (Compositae) in rats
Purpose: To investigate the antinociceptive effect of the essential oil from the aerial parts of Gundelia. tournefortii (EOGT) in… Expand
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Highly Cited
2015
Highly Cited
2015
Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome.
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
Impaired O-Linked N-Acetylglucosaminylation in the Endoplasmic Reticulum by Mutated Epidermal Growth Factor (EGF) Domain-specific O-Linked N-Acetylglucosamine Transferase Found in Adams-Oliver…
Background: EOGT (epidermal growth factor (EGF) domain-specific O-linked N-acetylglucosamine) mutations have been identified in… Expand
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2014
2014
Autosomal recessive Adams–Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase
Autosomal recessive Adams–Oliver syndrome was diagnosed in three remotely related Bedouin consanguineous families. Genome-wide… Expand
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Highly Cited
2012
Highly Cited
2012
O-linked-N-acetylglucosamine modification of mammalian Notch receptors by an atypical O-GlcNAc transferase Eogt1.
O-linked-β-N-acetylglucosamine (O-GlcNAc) modification is a unique cytoplasmic and nuclear protein modification that is common in… Expand
Highly Cited
2011
Highly Cited
2011
O-linked-N-acetylglucosamine on extracellular protein domains mediates epithelial cell-matrix interactions.
The O-linked-N-acetylglucosamine (O-GlcNAc) modification of cytoplasmic and nuclear proteins regulates basic cellular functions… Expand
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