Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Da Yong Wang"'
Autor:
Xiao‐Nan Wu, Hong‐Yang Wang, Xiao‐Long Zhang, Guo‐Hui Chen, Jing Guan, Yun Gao, Da‐Yong Wang, Qiu‐Ju Wang
Publikováno v:
World Journal of Otorhinolaryngology-Head and Neck Surgery, Vol 10, Iss 3, Pp 165-172 (2024)
Abstract Objective The objective of this study was to explore the clinical characteristics and management of sudden hearing loss (HL) during pregnancy, thus better guiding the clinical practice. Methods The clinical and follow‐up data of 17 patient
Externí odkaz:
https://doaj.org/article/e17fa0582c06453d97f51504ccf7d52b
Autor:
Xian-Ling Li, Qin-Ming Zhang, Shou-Yan Lu, Ting-Ting Liu, Shuan-Ling Li, Long Chen, Fang-Nan Xie, Li Wang, Chuang-Hui Zhang, Da-Yong Wang, Liu-Ming Huang
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Objective In this study, we aimed to enhance the treatment protocols and help understand the harm caused by the accidental ingestion of magnetic beads by children. Methods Data were collected from 72 children with multiple gastrointestinal p
Externí odkaz:
https://doaj.org/article/4a97e838b2b046dfa3483ff0e2c8ba88
Publikováno v:
European Physical Journal C: Particles and Fields, Vol 83, Iss 10, Pp 1-8 (2023)
Abstract A sensitivity study for the search for the charged lepton flavor violating process $$\tau \rightarrow \gamma \mu $$ τ → γ μ at the Super $$\tau $$ τ -Charm Facility is performed with a fast simulation. With the expected performance of
Externí odkaz:
https://doaj.org/article/e0c6474860f940a9a7fc02d09b837da0
Autor:
Zhu-Ping Cao, Qi-Feng Li, Shi-Qi Liu, Jian-Hua Niu, Jing-Ru Zhao, Ya-Jun Chen, Da-Yong Wang, Xiao-Song Li, Xin Chen
Publikováno v:
Chinese Medical Journal, Vol 132, Iss 6, Pp 726-730 (2019)
Externí odkaz:
https://doaj.org/article/19bf7f2aea3a4bffbd6fe79c4db6d64d
Autor:
Da‐Yong Wang, Jing Zhang, Hai‐Xia Li, Yan‐Xia Zhang, Mi‐Rong Jing, Chun‐Bo Cai, Di Wang, Hui‐Wen Qi, Yi‐Zhen Wang, Hao‐Jie Chen, Tao Li, Yuan‐Kun Zhai, Xin‐Ying Ji, Dong‐Dong Wu
Publikováno v:
Molecular Carcinogenesis. 62:652-664
Publikováno v:
Chinese Journal of Chemical Physics. 36:66-74
Crystallographic group is an important character to describe the crystal structure, but it is difficult to identify the crystallographic group of crystal when only chemical composition is given. Here, we present a machine-learning method to predict t
Autor:
Dong-Dong Wu, Ying-Ran Gao, Tao Li, Da-Yong Wang, Dan Lu, Shi-Yu Liu, Ya Hong, Hui-Bin Ning, Jun-Ping Liu, Jia Shang, Jun-Feng Shi, Jian-She Wei, Xin-Ying Ji
Publikováno v:
BMC Cancer, Vol 18, Iss 1, Pp 1-15 (2018)
Abstract Background PEST-containing nuclear protein (PCNP), a novel nuclear protein, is involved in cell proliferation and tumorigenesis. However, the precise mechanism of action of PCNP in the process of tumor growth has not yet been fully elucidate
Externí odkaz:
https://doaj.org/article/dcd2b6903c4f4f28aa2c15e07c748282
Autor:
Dan Bing, Da-Yong Wang, Lan Lan, Li-Dong Zhao, Zi-Fang Yin, Lan Yu, Guo-Hui Chen, Jing Guan, Qiu-Ju Wang
Publikováno v:
Chinese Medical Journal, Vol 131, Iss 3, Pp 307-315 (2018)
Background: Bilateral sudden sensorineural hearing loss (BSSHL) is rare and assumed to be a different clinical entity compared to unilateral SSHL (USSHL). This study examined the differences between the idiopathic BSSHL and USSHL. Methods: Forty-six
Externí odkaz:
https://doaj.org/article/9dd62b43860c43f0a33dc70e0e225f96
Autor:
Wan Du, Ming-Kun Han, Da-Yong Wang, Bing Han, Liang Zong, Lan Lan, Ju Yang, Qi Shen, Lin-Yi Xie, Lan Yu, Jing Guan, Qiu-Ju Wang
Publikováno v:
Chinese Medical Journal, Vol 130, Iss 1, Pp 88-92 (2017)
Background: The molecular genetic research showed the association between X-linked hearing loss and mutations in POU3F4. This research aimed to identify a POU3F4 mutation in a nonsyndromic X-linked recessive hearing loss family. Methods: A series of
Externí odkaz:
https://doaj.org/article/4b05e8b75cba437f9ab42aa3b42811a2
Autor:
Li Wang, Qiong-Fen Lin, Hong-Yang Wang, Jing Guan, Lan Lan, Lin-Yi Xie, Lan Yu, Ju Yang, Cui Zhao, Jin-Long Liang, Han-Lin Zhou, Huan-Ming Yang, Wen-Ping Xiong, Qiu-Jing Zhang, Da-Yong Wang, Qiu-Ju Wang
Publikováno v:
Chinese Medical Journal, Vol 130, Iss 6, Pp 703-709 (2017)
Background: Hypoparathyroidism-deafness-renal dysplasia (HDR) syndrome is an autosomal dominant disorder primarily caused by haploinsufficiency of GATA binding protein 3 (GATA3) gene mutations, and hearing loss is the most frequent phenotypic feature
Externí odkaz:
https://doaj.org/article/48e28e7b2a1e4d7a982d4b8f3a59883c