Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Rufei Shen"'
Autor:
Guiliang Peng, Chuanhong Guo, Yangfan Lv, Dandan Li, Ling Zhou, Rufei Shen, Yong Chen, Xin Zheng, Zheng Sun, Hongting Zheng, Min Long
Publikováno v:
BMC Endocrine Disorders, Vol 22, Iss 1, Pp 1-8 (2022)
Abstract Background Thyrotropin-secreting pituitary neuroendocrine tumors (PitNETs) are rare pituitary adenomas that are occasionally accompanied by hypersecretion of other anterior pituitary hormones, such as growth hormone (GH) and prolactin (PRL).
Externí odkaz:
https://doaj.org/article/1ecbad1b8d7641ce9b6ef23a066105df
Publikováno v:
Diabetes & Metabolism Journal, Vol 46, Iss 3, Pp 451-463 (2022)
Background The onset and progression of type 1 diabetes mellitus (T1DM) is closely related to autoimmunity. Effective monitoring of the immune system and developing targeted therapies are frontier fields in T1DM treatment. Currently, the most availab
Externí odkaz:
https://doaj.org/article/2b092515531e41838ebc4f9753f1caed
Autor:
Qian Liao, Rufei Shen, Mingyu Liao, Chenxi Ran, Ling Zhou, Yuling Zhang, Guiliang Peng, Zheng Sun, Hongting Zheng, Min Long
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundCombined 17α-hydroxylase/17,20-lyase deficiency (17-OHD) is a very rare form of congenital adrenal hyperplasia (CAH) caused by mutations in the CYP17A1 gene. Almost 100 different mutations of the CYP17A1 gene have been reported, including
Externí odkaz:
https://doaj.org/article/7505dcac347f440cafacb5aa048fd80f
Autor:
Guangmin Chen, Ling Zhou, Qimou Chen, Juan Wang, Peng Jiang, Rufei Shen, Min Long, Houdi Zhou
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Woodhouse-Sakati syndrome (WSS, MIM 241080) is a rare neuroendocrine disease characterized by hair loss, hypogonadism, diabetes, hearing loss, and extrapyramidal syndrome, and is usually caused by mutations in the DCAF17 gene as an inherited disease.
Externí odkaz:
https://doaj.org/article/b961f25fee0e4e9dad66693c08d7602c
Autor:
Xiaoyu Liao, Lingyu Song, Benhua Zeng, Bingyao Liu, Yuyang Qiu, Hua Qu, Yi Zheng, Min Long, Houdi Zhou, Yuan Wang, Yingxuan Du, Jing Xu, Rufei Shen, Qiang Tong, Leiqin Cai, Xing Li, Shaodong Guo, Gangyi Yang, Zhiming Zhu, Xiaoyun Pu, Hong Wei, Hongting Zheng
Publikováno v:
EBioMedicine, Vol 44, Iss , Pp 665-674 (2019)
Background: Increasing evidence indicates that the gut microbiota contributes to the occurrence and development of metabolic diseases. However, little is known about the effects of commonly used antidiabetic agents on the gut microbiota. In this stud
Externí odkaz:
https://doaj.org/article/6fe6f5e3be9d4bd8b6c621b8fbf66e7b
Publikováno v:
BMC Endocrine Disorders, Vol 18, Iss 1, Pp 1-5 (2018)
Abstract Background 11β-Hydroxylase deficiency (11OHD) is a common form of congenital adrenal hyperplasia that has been shown to result from inactivating CYP11B1 mutations, and pathogenic CYP11B2/CYP11B1 chimeras contribute to a minority of cases. H
Externí odkaz:
https://doaj.org/article/8d662d633cbe4dc99d782e63d663e216
Autor:
Qixian Wang, Min Long, Hua Qu, Rufei Shen, Rui Zhang, Jing Xu, Xin Xiong, Hui Wang, Hongting Zheng
Publikováno v:
Journal of Diabetes Research, Vol 2018 (2018)
Objective. Several clinical studies have reported the application of dipeptidyl peptidase-4 (DPP-4) inhibitors as treatments for type 1 diabetes mellitus (T1DM). This study aims to review the outcomes of these existing studies and to discuss the ther
Externí odkaz:
https://doaj.org/article/b9cf24f015514c578c8ddb85eb540590
Autor:
Xing Li, Mingyu Liao, Rufei Shen, Linlin Zhang, Hua Hu, Jun Wu, Xiuli Wang, Hua Qu, Shaodong Guo, Min Long, Hongting Zheng
Publikováno v:
Mediators of Inflammation, Vol 2018 (2018)
Asprosin is a white adipose tissue-derived hormone that increases abnormally in mammals with insulin resistance. However, the role of asprosin in polycystic ovary syndrome (PCOS), a disease partly characterized by insulin resistance, and its potentia
Externí odkaz:
https://doaj.org/article/92c7cdf9d869402c90ea044d1766ed1c
Autor:
Jingpeng Liu, Peng Huang, Xiaoqing Zhang, Yong Chen, Xin Zheng, Rufei Shen, Xuefeng Tang, Hui Yang, Song Li
Publikováno v:
Journal of Korean Neurosurgical Society. 66:72-81
Objective : Ischemia and hemorrhage of pituitary adenomas (PA) caused important clinical syndrome. However, the differences on clinical characteristics and surgical outcomes between these two kinds apoplexy were less reported.Methods : A retrospectiv
Autor:
Guiliang Peng, Xing Li, Yuanyuan Zhou, Jianying Bai, Pian Hong, Weixing Li, Yuling Zhang, Lei Zhang, Qian Liao, Mingyu Liao, Ling Zhou, Zheng Sun, Rufei Shen, Hongting Zheng, Min Long
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 130:714-722
Purpose To investigate the clinical characteristics and associated factors of colonic polyps in patients with acromegaly. Methods Clinical characteristics and colonoscopy findings of 86 acromegaly patients who received treatment were retrospectively