FAQ

GLUCOCORTICOID DEFICIENCY 2

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

Topic mentions per year

Topic mentions per year

1999-2013
01219992013

Related topics

Related topics

4 relations

Broader (1)

Adrenal gland hypofunction
Autosomal recessive inheritanceHyperpigmentationHypoglycemia

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
GLUCOCORTICOID DEFICIENCY 2
Hypoglycemia
Autosomal recessive inheritance
Adrenal gland hypofunction
Hyperpigmentation

Papers overview

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Review
2013
Review
2013
PI5P migrates out of the PIP shadow.
The dynamic nature of membrane phospholipid turnover was first described by Hokin and Hokin during their studies on exocrine… (More)
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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… (More)
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2011
2011
Alterations of pre-mRNA splicing in human inflammatory bowel disease.
Alternative pre-mRNA splicing is regarded as a pivotal mechanism for generating proteome diversity and complexity from a limited… (More)
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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… (More)
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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… (More)
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2007
2007
The t-complex-encoded guanine nucleotide exchange factor Fgd2 reveals that two opposing signaling pathways promote transmission ratio distortion in the mouse.
Transmission ratio distortion (TRD), the preferential inheritance of the t haplotype from t/+ males, is caused by the cooperative… (More)
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1999
1999
Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues.
FGD1 encodes a guanine nucleotide exchange factor (GEF) that specifically activates the Rho GTPase Cdc42. FGD1 gene mutations… (More)
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