Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Zeming Fu"'
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background: Mutations in the STRC (MIM 606440) gene, inducing DFNB16, are considered a major cause of mild–moderate autosomal recessive non-syndromic hearing loss (ARNSHL). We conducted a systematic review and meta-analysis to determine the global
Externí odkaz:
https://doaj.org/article/74566873859a46068093f85d7f68a820
Autor:
Zeming FU1, Huagen WU1 hgwu@mail.xjtu.edu.cn, Mengtao LIANG1, Zhendong GUO1, Guanghua WU1, Shuo SHANG2, Liang HOU1, Xin ZHANG3
Publikováno v:
Thermal Science. 2024, Vol. 28 Issue 3B, p2595-2604. 10p.
Autor:
Zeming FU1, Huagen WU1 hgwu@mail.xjtu.edu.cn, Baohua GAO2, Mengtao LIANG1, Guanghua WU1, Shuo SHANG3, Xin ZHANG4, Hongye HUANG1, Siwei CHEN1
Publikováno v:
Thermal Science. 2024, Vol. 28 Issue 2C, p1741-1752. 12p.
Autor:
Xin ZHANG1,2, Zeming FU3, Tianyu ZHOU1, Jinjiang LIU1, Min YANG1, Xingxin NIE1 niexingxin@xauat.edu.cn, Huagen WU3 hgwu@mail.xjtu.edu.cn, Ping CHENG1 chengp_314@163.com, Tong GUO4, Xiaoxin LUO5
Publikováno v:
Thermal Science. 2024, Vol. 28 Issue 1A, p65-75. 11p.
Publikováno v:
Advanced Engineering Materials; 11/15/2023, Vol. 25 Issue 22, p1-9, 9p
Publikováno v:
ORL. 84:425-428
A primary intracochlear schwannoma (ICS) is a unique type of vestibular schwannoma (VS); the tumor originates from the terminal branches of the cochlear nerve and is confined to the cochlea. An ICS is the most common subtype of schwannoma in the inne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::560ce3e079124385060cb317aa25c5c0
https://doi.org/10.1159/000522473
https://doi.org/10.1159/000522473
Publikováno v:
Advanced Engineering Materials. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b13fd26bf9a3be74cb8b692b46f7669
https://doi.org/10.1002/adem.202201577
https://doi.org/10.1002/adem.202201577
Autor:
Guofang Guan, Yingyuan Guo, Jingmao Lv, Hongen Xu, Zeming Fu, Shuang Han, Yanru Hao, Fang Guo, Jie Bai, Duo-Jiao Yu, Dejun Zhang
Publikováno v:
Translational Pediatrics. 10:378-387
Background X-linked deafness-4 (DFNX4) caused by the functional loss of the SMPX gene is one form of nonsyndromic hearing loss with postlingual onset. This study aimed to investigate the cause of X-linked inherited sensorineural nonsyndromic hearing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::032e18d3ab1c24f0055f6c271c8176eb
https://doi.org/10.21037/tp-20-435
https://doi.org/10.21037/tp-20-435
Publikováno v:
Tropical Journal of Pharmaceutical Research. 19:299-304
Purpose: To determine the protective effect of ethosuximide on the hearing of NOD/LtJ mice, and the underlying mechanism of action. Methods: The mice were randomly assigned to control and treatment groups (20 mice per group). Mice in the treatment gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe31784d5634776bf44e05e314a319f3
https://doi.org/10.4314/tjpr.v19i2.12
https://doi.org/10.4314/tjpr.v19i2.12
Publikováno v:
Journal of Cancer
TROP2 (trophoblast cell surface antigen 2) overexpression has been reported in many human cancers. The correlation between TROP2 and tumor aggressiveness has implied it could be a prognostic indicator. However, the roles of TROP2 and their underlying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ccaef67355a8f17b91d967938f8f147
https://doi.org/10.7150/jca.40339
https://doi.org/10.7150/jca.40339