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...

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Bibliografiset tiedot
Julkaisussa:Endocrinology
Päätekijät: Kapali, Jyoti, Kabat, Brock E., Schmidt, Kelly L., Stallings, Caitlin E., Tippy, Mason, Jung, Deborah O., Edwards, Brian S., Nantie, Leah B., Raeztman, Lori T., Navratil, Amy M., Ellsworth, Buffy S.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Endocrine Society 2016
Aiheet:
Original Research
Linkit: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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