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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Detalhes bibliográficos
Publicado no:Endocrinology
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: Endocrine Society 2016
Assuntos:
Original Research
Acesso em linha: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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