TRH Action Is Impaired in Pituitaries of Male IGSF1-Deficient Mice
Loss-of-function mutations in the X-linked immunoglobulin superfamily, member 1 (IGSF1) gene cause central hypothyroidism. IGSF1 is a transmembrane glycoprotein of unknown function expressed in thyrotropin (TSH)-producing thyrotrope cells of the anterior pituitary gland. The protein is cotranslation...
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| Publicado no: | Endocrinology |
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| Principais autores: | , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Endocrine Society
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5460797/ https://ncbi.nlm.nih.gov/pubmed/28324000 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/en.2016-1788 |
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