Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Huifang Peng"'
Autor:
Huiqin Zhuo, Jingjing Hou, Zhijun Hong, Shuqi Yu, Huifang Peng, Lihua Zhang, Wen Xie, Xuehui Hong
Publikováno v:
Cell Death and Disease, Vol 15, Iss 8, Pp 1-15 (2024)
Abstract Recently, various cancer types have been identified to express a distinct subset of Interferon-stimulated genes (ISGs) that mediate therapy resistance. The mechanism through which cancer cells maintain prolonged Interferon stimulation effect
Externí odkaz:
https://doaj.org/article/e9eb4f3f51c4499983b8027e0cd46a1e
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 16, Iss 1, Pp 1-9 (2024)
Abstract Background The aim of this study was to investigate whether a causal relationship exists between serum uric acid (SUA) and diabetic microvascular complications using a two-sample Mendelian randomization (MR) method. Methods We used the MR ap
Externí odkaz:
https://doaj.org/article/f35c4367e303404b86d7d8560145473f
Akademický článek
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Autor:
Yuqing Jiang, Huifang Peng, Rui Zhao, Yina Chang, Jie Liu, Liujun Fu, Liping Li, Yujin Ma, Wei Li, Hongwei Jiang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 6, Pp n/a-n/a (2023)
Abstract Background X‐linked adrenal hypoplasia congenita (AHC) is a rare disorder, often manifesting as primary adrenal insufficiency (PAI) and hypogonadotropic hypogonadism (HH), and caused by variants of NR0B1, most of which are frame‐shifting
Externí odkaz:
https://doaj.org/article/776f5eb26a8d4605991c172afafc022a
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
BackgroundFinerenone and sodium-glucose cotransporter 2 inhibitors (SGLT2i) have been shown to improve cardiovascular and renal outcomes in patients with type 2 diabetes mellitus (T2DM), while the relative efficacy has not been determined.MethodsThe
Externí odkaz:
https://doaj.org/article/6922a97561454e4e979a63b94c020fb3
Autor:
Yuting Duan, Weiguang Zhang, Zhe Li, Yue Niu, Yizhi Chen, Xiaomin Liu, Zheyi Dong, Ying Zheng, Xizhao Chen, Zhe Feng, Yong Wang, Delong Zhao, Qiu Liu, Hangtian Li, Huifang Peng, Xuefeng Sun, Guangyan Cai, Hongwei Jiang, Xiangmei Chen
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Background and objectiveMetabolic syndrome (MetS) is an important risk factor for cardiovascular complications and kidney damage. Obesity- and lipid-related indices are closely related to MetS, and different indices have different predictive abilitie
Externí odkaz:
https://doaj.org/article/226d799d8a5f48069e9a29b0123f41c1
Autor:
Huifang Peng, Jie Wang, Yanyun Liu, Haiping Yang, Liping Li, Yujin Ma, Huiqin Zhuo, Hongwei Jiang
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Werner syndrome is an autosomal recessive rare disease caused by a WRN gene mutation, which is rarely reported in the Chinese population. We report the clinical and genetic data of a Chinese patient with Werner syndrome. The proband was a 40-year-old
Externí odkaz:
https://doaj.org/article/59d7bfcbbeda4f59840f60760a42c88d
Publikováno v:
Frontiers in Bioscience-Landmark, Vol 28, Iss 5, p 98 (2023)
Sodium-glucose cotransporter inhibitors (SGLT2i) play an increasingly important role in type 2 diabetes mellitus (T2DM) due to their significant cardiovascular benefits and renal protection in addition to their hypoglycemic effects. In recent years,
Externí odkaz:
https://doaj.org/article/d7361ccd87ac442db211d3b3d8572d45
Autor:
Jiayong Qiu, Yao Lou, Yingwei Zhu, Min Wang, Huifang Peng, Yingying Hao, Hongwei Jiang, Yimin Mao
Publikováno v:
Frontiers in Genetics, Vol 12 (2022)
Background: Birt-Hogg-Dubé (BHD) syndrome and congenital contractural arachnodactyly (CCA) or Beals-Hecht syndrome are clinically rare autosomal dominant genetic diseases. In this study, we describe an extremely rare family with BHD syndrome and CCA
Externí odkaz:
https://doaj.org/article/0cd9c934ed604caa9da02607540c9c1c
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
Knowledge about the precise biological role and underlying mechanism of Tagln2 in tumor progression is relatively limited, especially in angiogenesis focused on tumor derived endothelial cells (ECs) has rarely been reported. Here, the function, molec
Externí odkaz:
https://doaj.org/article/53f4a92f006846cfb4a95321ef068503