Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Huijiao Zhang"'
Autor:
Yunpeng Wang, Yu Xu, Huijiao Zhang, Danyang Yin, Yiming Pan, Xiwen He, Shuaiting Li, Zhi Cheng, Gaohui Zhu, Ting Zhao, Huizhe Huang, Min Zhu
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2024)
IntroductionIndividuals with 17-beta-hydroxysteroid dehydrogenase type 3 (17β-HSD3) deficiency face a multitude of challenges, primarily concerning genital appearance, potential malignancy risks, and fertility issues. This study reports our findings
Externí odkaz:
https://doaj.org/article/acb440dc604f4c7e84ffdf379003a487
Publikováno v:
Nursing Open, Vol 10, Iss 8, Pp 5244-5251 (2023)
Abstract Aims and objectives To construct a risk assessment scale for medical adhesive‐related skin injuries (MARSI) at the peripherally inserted central catheter (PICC) insertion site in oncology patients and test its reliability and validity. Des
Externí odkaz:
https://doaj.org/article/efe07fbfac0a4908bce7a0b490cad3f6
Publikováno v:
Analytical Methods. 14:921-925
Surface enhanced Raman spectroscopy (SERS), as a molecule-specific method using plasmonic nanostructures to significantly enhance signal intensity, has been employed in various fields.
Autor:
Ting Deng, Kaijiang Liu, Liang Chen, Xiaojun Chen, Hua Wen Li, Hongyan Guo, Huijiao Zhang, Libing Xiang, Xin Feng, Xiaoyu Wang, Hextan YS Ngan, Jianguo Zhao, Dongling Zou, Qing Liu, Jihong Liu
Publikováno v:
Journal of Gynecologic Oncology. 34
Autor:
Kuan, Feng, Huijiao, Zhang, Zhenyu, Jiang, Min, Zhou, Yuan-Qin, Min, Fei, Deng, Peiqing, Li, Hualin, Wang, Yun-Jia, Ning
Publikováno v:
Journal of Medical Virology. 95
Autophagy is emerging as a critical player in host defense against diverse infections, in addition to its conserved function to maintain cellular homeostasis. Strikingly, some pathogens have evolved strategies to evade, subvert or exploit different s
Publikováno v:
Advances in Clinical and Experimental Medicine. 30:289-299
Background 3β-HSD deficiency is a rare type of congenital adrenal hyperplasia (CAH), which is caused by HSD3B2 gene mutations. Objectives In order to improve the understanding and diagnosis of the disease, we analyzed and summarized the clinical cha
Publikováno v:
Ann Transl Med
BACKGROUND: Hypophosphatasia (HPP) is a rare hereditary disorder characterized by defective bone and tooth mineralization caused by mutations in the alkaline phosphatase (ALPL) gene encoding tissue-nonspecific alkaline phosphatase (TNSALP). Here we p
Autor:
Yue Mao, Borong Yu, Huijiao Zhang, Yuanyuan Ma, Fangwei Han, Binbin Zhou, Lili Yang, Zhangang Han
Publikováno v:
SSRN Electronic Journal.
Background: Defects in conserved non-coding elements (CNEs) are associated with a large number of genetic diseases. The short-chain homeobox gene (SHOX) is regulated by different CNEs in the upstream and downstream, and these CNEs can act as enhancer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8a0d21d882fb254589a78bcd2465905
https://doi.org/10.21203/rs.3.rs-54595/v1
https://doi.org/10.21203/rs.3.rs-54595/v1
Publikováno v:
Annals of Translational Medicine. 9:888-888
Background Hypophosphatasia (HPP) is a rare hereditary disorder characterized by defective bone and tooth mineralization caused by mutations in the alkaline phosphatase (ALPL) gene encoding tissue-nonspecific alkaline phosphatase (TNSALP). Here we pe