نتایج جستجو برای: hcn4

تعداد نتایج: 319  

2017
Laurie L. Baggio John R. Ussher Brent A. McLean Xiemin Cao M. Golam Kabir Erin E. Mulvihill Alexandra S. Mighiu Hangjun Zhang Andreas Ludwig Randy J. Seeley Scott P. Heximer Daniel J. Drucker

OBJECTIVES Glucagon-like peptide-1 (GLP-1) is secreted from enteroendocrine cells and exerts a broad number of metabolic actions through activation of a single GLP-1 receptor (GLP-1R). The cardiovascular actions of GLP-1 have garnered increasing attention as GLP-1R agonists are used to treat human subjects with diabetes and obesity that may be at increased risk for development of heart disease....

2015
Nana Li Haitao Jia Zhen Liu Jing Tao Song Chen Xiaohong Li Ying Deng Xi Jin Jiaping Song Liangtao Zhang Yu Liang Wei Wang Jun Zhu

Phenylketonuria (PKU) is an inherited autosomal recessive disorder of phenylalanine metabolism, mainly caused by a deficiency of phenylalanine hydroxylase (PAH). The incidence of various PAH mutations differs among race and ethnicity. Here we report a spectrum of PAH mutations complied from 796 PKU patients from mainland China. The all 13 exons and adjacent intronic regions of the PAH gene were...

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