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GLUCOCORTICOID DEFICIENCY 2

Known as: FGD2, Familial Glucocorticoid Deficiency 2, GCCD2 
 
National Institutes of Health

Related topics

Related topics

5 relations

Broader (1)

Adrenal gland hypofunction
Autosomal recessive inheritanceHyperpigmentationHypoglycemiaMRAP, 7-BP DEL, NT17

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
The prognostic value of faciogenital dysplasias as biomarkers in head and neck squamous cell carcinoma.
Aim: This present study aims to investigate the prognostic value of FGD genes for predicting the overall survival in head and… Expand
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2018
2018
MRAP deficiency impairs adrenal progenitor cell differentiation and gland zonation
Melanocortin 2 receptor accessory protein (MRAP) is a single transmembrane domain accessory protein and a critical component of… Expand
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2013
2013
PI5P migrates out of the PIP shadow.
In a recent study published in EMBO reports, the group of Jorgen Wesche identified a new role for PI5P as a positive regulator of… Expand
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Review
2013
Review
2013
Involvement of melanocortin receptor accessory proteins (MRAPs) in the function of melanocortin receptors.
The melanocortin system integrates different agonists, competitive or inverse agonists, and receptors. Recent investigations have… Expand
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2008
2008
FGD2, a CDC42-specific exchange factor expressed by antigen-presenting cells, localizes to early endosomes and active membrane ruffles.
Members of the Fgd (faciogenital dysplasia) gene family encode a group of critical guanine nucleotide exchange factors (GEFs… Expand
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Review
2008
Review
2008
Frabin and other related Cdc42-specific guanine nucleotide exchange factors couple the actin cytoskeleton with the plasma membrane
Frabin, together with, at least, FGD1, FGD2, FGD3 and FGD1-related Cdc42-GEF (FRG), is a member of a family of Cdc42-specific gua… Expand
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