PROKR2mutations in idiopathic hypogonadotropic hypogonadism: selective disruption of the binding to aGα‐protein leads to biased signaling-Reference-Cited by-同舟云学术

PROKR2mutations in idiopathic hypogonadotropic hypogonadism: selective disruption of the binding to aGα‐protein leads to biased signaling

Author:

Zhao Yaguang¹²³,Wu Jiayu¹²³,Jia Hong¹²³,Wang Xinying¹²³,Zheng Ruizhi⁴,Jiang Fang¹²³,Chen Dan-Na⁵,Chen Zhiheng⁶,Li Jia-Da¹²³

Affiliation:

1. School of Life SciencesCentral South University Changsha China

2. Hunan Key Laboratory of Animal Models for Human DiseasesCentral South University Changsha China

3. Hunan Key Laboratory of Medical GeneticsCentral South University Changsha China

4. Department of EndocrinologyThe People's Hospital of Henan Province Zhengzhou China

5. Department of Basic Medical SciencesChangsha Medical University Changsha China

6. Department of PediatricsThe Third Xiangya HospitalCentral South University Changsha China

Funder

National High-tech Research and Development Program

National Basic Research Program of China

National Natural Science Foundation of China

Education Department of Hunan Province

Central South University

Natural Science Foundation of Hunan Province

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Link

Reference43 articles.

3. Genetic basis and variable phenotypic expression of Kallmann syndrome: towards a unifying theory;Mitchell A. L.;Trends Endocrinol. Metab.,2011

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