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GLUCOCORTICOID DEFICIENCY 3 (disorder)

Known as: GLUCOCORTICOID DEFICIENCY 2, FORMERLY, GCCD3, GLUCOCORTICOID DEFICIENCY 3 
 
National Institutes of Health

Related topics

Related topics

5 relations

Broader (1)

Adrenal gland hypofunction
Autosomal recessive inheritanceHyperpigmentationHypoglycaemic episodeHypoglycemia

Papers overview

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2020
2020
Comprehensive Analysis of Aberrantly Expressed Profiles of lncRNAs and miRNAs with Associated ceRNA Network in Lung Adenocarcinoma and Lung Squamous Cell Carcinoma
Lung cancer (LC) continues to be the leading cause of cancer-related deaths worldwide and the prognosis remains poor worldwide… Expand
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2019
2019
Expression of FGD3 gene as prognostic factor in young breast cancer patients
The FGD3 gene works as a cell migration inhibitor and seems to be a promising indicator of outcome in some human cancers… Expand
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2019
2019
Tswana traditional health practitioners’ perspectives on the management of diabetes and hypertension: a qualitative study using focus group discussions
Introduction The literature suggests the involvement of Traditional Health Practitioners (THPs) perspectives in treating diabetes… Expand
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2017
2017
The preterm cervix reveals a transcriptomic signature in the presence of premature prelabor rupture of membranes
BACKGROUND: Premature prelabor rupture of fetal membranes accounts for 30% of all premature births and is associated with… Expand
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2015
2015
Non-synonymous FGD3 Variant as Positional Candidate for Disproportional Tall Stature Accounting for a Carcass Weight QTL (CW-3) and Skeletal Dysplasia in Japanese Black Cattle
Recessive skeletal dysplasia, characterized by joint- and/or hip bone-enlargement, was mapped within the critical region for a… Expand
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2011
2011
Role of FGD1, a Cdc42 guanine nucleotide exchange factor, in epidermal growth factor-stimulated c-Jun NH2-terminal kinase activation and cell migration.
FGD1 encodes a guanine nucleotide exchange factor for Cdc42. Mutations in the FGD1 gene are responsible for an X-linked disorder… Expand
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2010
2010
Proline-rich domain plays a crucial role in extracellular stimuli-responsive translocation of a Cdc42 guanine nucleotide exchange factor, FGD1.
We previously demonstrated that FGD1, the Cdc42 guanine nucleotide exchange factor (GEF) responsible for faciogenital dysplasia… Expand
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2008
2008
Novel insights into FGD3, a putative GEF for Cdc42, that undergoes SCFFWD1/β‐TrCP‐mediated proteasomal degradation analogous to that of its homologue FGD1 but regulates cell morphology and motility…
We previously demonstrated that FGD1, the Cdc42 guanine nucleotide exchange factor (GEF) responsible for faciogenital dysplasia… 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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Highly Cited
2005
Highly Cited
2005
Follicular thyroid tumors with the PAX8-PPARgamma1 rearrangement display characteristic genetic alterations.
Follicular thyroid carcinomas (FTC) arise through oncogenic pathways distinct from those involved in the papillary histotype… Expand
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