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GCM2 gene

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

Papers overview

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Highly Cited
2016
Highly Cited
2016
Primary hyperparathyroidism (PHPT) is a common endocrine disease characterized by parathyroid hormone excess and hypercalcemia… Expand
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Highly Cited
2005
Highly Cited
2005
The differentiation of Drosophila embryonic blood cell progenitors (prohemocytes) into plasmatocytes or crystal cells is… Expand
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Highly Cited
2005
Highly Cited
2005
Isolated hypoparathyroidism is an uncommon metabolic disorder characterized by hypocalcemia and hyperphosphatemia, with absent or… Expand
Highly Cited
2005
Highly Cited
2005
ypoparathyroidism is a heterogeneous group of disorders with both acquired and inherited causes, each presenting clinically with… Expand
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Highly Cited
2002
Highly Cited
2002
glial cells missing (gcm) is the primary regulator of glial cell fate in Drosophila. In addition, gcm has a role in the… Expand
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Highly Cited
2001
Highly Cited
2001
The thymus and parathyroids originate from a common primordium that develops from the third pharyngeal pouch in mice and humans… Expand
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Highly Cited
2000
Highly Cited
2000
ABSTRACT The GCM family of transcription factors consists ofDrosophila melanogaster GCM, an important regulator of gliogenesis in… Expand
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1999
1999
A novel human homologue (GCMB) of the Drosophila glial cells missing gene (dGCM) was isolated using RACE. GCMB contained a gcm… Expand
1999
1999
Glial cells play fundamental roles in neurogenesis. In addition, defective or abnormal gliogenesis is associated with severe… Expand
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Highly Cited
1998
Highly Cited
1998
The glial cells missing (gcm) gene in Drosophila encodes a transcription factor that determines the choice between glial and… Expand
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