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Foxo1 Is Required for Normal Somatotrope Differentiation
The etiology for half of congenital hypopituitarism cases is unknown. Our long-term goal is to expand the molecular diagnoses for congenital hypopituitarism by identifying genes that contribute to this condition. We have previously shown that the forkhead box transcription factor, FOXO1, is present...
שמור ב:
| הוצא לאור ב: | Endocrinology |
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| Main Authors: | , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Endocrine Society
2016
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5086538/ https://ncbi.nlm.nih.gov/pubmed/27631552 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/en.2016-1372 |
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