FAQ

GCM2 gene

Known as: GCMB, GCM2, GLIAL CELLS MISSING, DROSOPHILA, HOMOLOG OF, 2 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1993-2017
02419932017

Papers overview

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2016
2016
GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism.
Primary hyperparathyroidism (PHPT) is a common endocrine disease characterized by parathyroid hormone excess and hypercalcemia… (More)
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2009
2009
Glial cells missing-2 (GCM2) transactivates the calcium-sensing receptor gene: effect of a dominant-negative GCM2 mutant associated with autosomal dominant hypoparathyroidism.
Glial cells missing-2 (GCM2) is a transcription factor expressed in the parathyroid hormone (PTH)-secreting cells of the… (More)
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2008
2008
Dominant-negative GCMB mutations cause an autosomal dominant form of hypoparathyroidism.
CONTEXT Hypoparathyroidism (HP) is characterized by low PTH levels, hypocalcemia, and hyperphosphatemia. Heterozygous mutations… (More)
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2005
2005
Resolving embryonic blood cell fate choice in Drosophila: interplay of GCM and RUNX factors.
The differentiation of Drosophila embryonic blood cell progenitors (prohemocytes) into plasmatocytes or crystal cells is… (More)
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2005
2005
Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism.
H ypoparathyroidism is a heterogeneous group of disorders with both acquired and inherited causes, each presenting clinically… (More)
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2005
2005
GCMB mutation in familial isolated hypoparathyroidism with residual secretion of parathyroid hormone.
Isolated hypoparathyroidism is an uncommon metabolic disorder characterized by hypocalcemia and hyperphosphatemia, with absent or… (More)
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2004
2004
Expression of GCMB by intrathymic parathyroid hormone-secreting adenomas indicates their parathyroid cell origin.
GCMA and GCMB are related transcription factors that are critically important for embryological development of the placenta and… (More)
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1999
1999
Isolation and expression analysis of a novel human homologue of the Drosophila glial cells missing (gcm) gene.
A novel human homologue (GCMB) of the Drosophila glial cells missing gene (dGCM) was isolated using RACE. GCMB contained a gcm… (More)
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1999
1999
GCMB, a second human homolog of the fly glide/gcm gene.
Glial cells play fundamental roles in neurogenesis. In addition, defective or abnormal gliogenesis is associated with severe… (More)
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1995
1995
Binding characteristics of glucocorticoid receptor in synaptic plasma membrane from rat brain.
The study was carried out to identify the specific glucocorticoid membrane binding site (GCMB) on synaptic plasma membrane (SPM… (More)
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