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Published in 2025 at "Endocrinology"
DOI: 10.1210/endocr/bqaf047
Abstract: Mutations in the pituitary-specific transcription factor PROP1 are the most common, known cause of hypopituitarism in humans. Prop1 is the first pituitary-specific gene in the hierarchy of transcription factors that regulate pituitary development. It is…
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Keywords:
prop1;
role;
stem cells;
postnatal pituitary ... See more keywords