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