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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
The dynamic nature of membrane phospholipid turnover was first described by Hokin and Hokin during their studies on exocrine… (More)
  • figure 1
Is this relevant?
Review
2013
Review
2013
The melanocortin system integrates different agonists, competitive or inverse agonists, and receptors. Recent investigations have… (More)
Is this relevant?
2011
2011
Alternative pre-mRNA splicing is regarded as a pivotal mechanism for generating proteome diversity and complexity from a limited… (More)
Is this relevant?
2008
2008
Members of the Fgd (faciogenital dysplasia) gene family encode a group of critical guanine nucleotide exchange factors (GEFs… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Review
2008
Review
2008
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)
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
2007
2007
Transmission ratio distortion (TRD), the preferential inheritance of the t haplotype from t/+ males, is caused by the cooperative… (More)
  • figure 1
  • figure 2
  • figure 3
  • table 1
  • figure 4
Is this relevant?
1999
1999
FGD1 encodes a guanine nucleotide exchange factor (GEF) that specifically activates the Rho GTPase Cdc42. FGD1 gene mutations… (More)
Is this relevant?