Inhibition of Growth Hormone (GH) Secretion by a Mutant GH-I Gene Product in Neuroendocrine Cells Containing Secretory Granules: An Implication for Isolated GH Deficiency Inherited in an Autosomal Dominant Manner
Author:
Publisher
The Endocrine Society
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Cited by 54 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Common and Uncommon Mouse Models of Growth Hormone Deficiency;Endocrine Reviews;2024-06-10
2. IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency;European Journal of Endocrinology;2022-11-03
3. Isolated Growth Hormone Deficiency Type 2 due to a novel GH1 Mutation: A Case Report;Journal of Clinical Research in Pediatric Endocrinology;2019-12-01
4. Decreased Activity of the Ghrhr and Gh Promoters Causes Dominantly Inherited GH Deficiency in Humanized GH1 Mouse Models;Endocrinology;2019-08-22
5. Decreased Activity of the Ghrhr and Gh Promoters Causes Dominantly Inherited GH Deficiency;2019-02-08
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