A mammalian model for Laron syndrome produced by targeted disruption of the mouse growth hormone receptor/binding protein gene (the Laron mouse)

Laron syndrome [growth hormone (GH) insensitivity syndrome] is a hereditary dwarfism resulting from defects in the GH receptor (GHR) gene. GHR deficiency has not been reported in mammals other than humans. Many aspects of GHR dysfunction remain unknown because of ethical and practical limitations in...

Полное описание

Сохранить в:

Библиографические подробности
Опубликовано в::	Proc Natl Acad Sci U S A
Главные авторы:	Zhou, Yihua, Xu, Bixiong C., Maheshwari, Hiralal G., He, Li, Reed, Michael, Lozykowski, Maria, Okada, Shigeru, Cataldo, Lori, Coschigamo, Karen, Wagner, Thomas E., Baumann, Gerhard, Kopchick, John J.
Формат:	Artigo
Язык:	Inglês
Опубликовано:	National Academy of Sciences 1997
Предметы:	Biological Sciences
Online-ссылка:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC24289/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9371826/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.94.24.13215
Метки:	Добавить метку Нет меток, Требуется 1-ая метка записи!

A mammalian model for Laron syndrome produced by targeted disruption of the mouse growth hormone receptor/binding protein gene (the Laron mouse)

Схожие документы