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SAT-416 IGSF1 Does Not Regulate FSH Synthesis or Secretion

Loss of function mutations in the human X-linked immunoglobulin superfamily, member 1 (IGSF1) gene result in central hypothyroidism, often associated with macroorchidism. Igsf1-deficient mice are also centrally hypothyroid due to impaired TRH action in the pituitary. The mechanisms underlying macroo...

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Detalles Bibliográficos
Autores principales: Brûlé, Emilie, Li, Yining, Schang, Gauthier, Wang, Ying, Zhou, Xiang, Bernard, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552201/
http://dx.doi.org/10.1210/js.2019-SAT-416

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