Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Zhijie Niu"'
Autor:
Zhijie Niu, Yongjing Lai, Wenwen Zhou, Lingyuan Liu, Songhua Tan, Guangyao He, Jingyu Li, Fen Tang, Yupei Su, Yanglong Xu, Lei Liu, Lihong Xie, Qin Fang, Anzhou Tang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 9, Pp n/a-n/a (2022)
Abstract Background Osteogenesis imperfecta type I (OI‐I) is a rare genetic disorder characterized by skeletal deformity, bone fragility, blue sclerae, dentinogenesis imperfecta, and hearing loss. The current study aimed to confirm the clinical dia
Externí odkaz:
https://doaj.org/article/864a683ee94b450a9b3a11438c6565b3
Autor:
Pengcheng Zhao, Wei Xia, Jianglian Wei, Yiwei Feng, Mao Xie, Zhijie Niu, Heng Liu, Shenghui Ke, Huayu Liu, Anzhou Tang, Guangyao He
Publikováno v:
Dose-Response, Vol 20 (2022)
Background Animal models suitable for investigating mechanisms behind radiation-induced muscle injury are lacking. We developed a tree shrew model of such injury and investigated pathological changes and mechanisms. Methods Animals were divided into
Externí odkaz:
https://doaj.org/article/e922c48187464dde9ae5c79836d1fc07
Autor:
Zhijie Niu, Yong Feng, Lingyun Mei, Jie Sun, Xueping Wang, Juncheng Wang, Zhengmao Hu, Yunpeng Dong, Hongsheng Chen, Chufeng He, Yalan Liu, Xinzhang Cai, Xuezhong Liu, Lu Jiang
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0178384 (2017)
X-linked hearing impairment is the rarest form of genetic hearing loss (HL) and represents only a minor fraction of all cases. The aim of this study was to investigate the cause of X-linked inherited sensorineural HL in a four-generation Chinese fami
Externí odkaz:
https://doaj.org/article/029ac6b4b6c6470da8d46cbef595c21d
Autor:
Xueping Wang, Yalan Liu, Hongsheng Chen, Lingyun Mei, Chufeng He, Lu Jiang, Zhijie Niu, Jie Sun, Hunjin Luo, Jiada Li, Yong Feng
Publikováno v:
PLoS ONE, Vol 10, Iss 11, p e0143142 (2015)
TYR, DCT and MITF are three important genes involved in maintaining the mature phenotype and producing melanin; they therefore participate in neural crest cell development into melanocytes. Previous studies have revealed that the Wnt signaling factor
Externí odkaz:
https://doaj.org/article/3d015e21cc584554b2ea2a97041e1981
Autor:
Heng Liu, Shenghui Ke, Mao Xie, Zhijie Niu, Huayu Liu, Jingyu Li, Anzhou Tang, Wei Xia, Guangyao He
Publikováno v:
Biochemical and Biophysical Research Communications. 668:125-132
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8e3cb906ce6c7c7632c775cfdff2a87
https://doi.org/10.1016/j.bbrc.2023.05.078
https://doi.org/10.1016/j.bbrc.2023.05.078
Autor:
Jingyu Li, Xiang Yi, Guangyao He, Dongfang Yao, Xiang Bin, Yiwei Feng, Zhijie Niu, Qianying Tan, Anzhou Tang
Publikováno v:
Auris Nasus Larynx. 49:703-708
To retrospectively analyze the risk factors for death in patients with nasal or nasopharyngeal bleeding after radiotherapy for nasopharyngeal carcinoma, and to explore clinical management strategies for the disease.This was a retrospective case-contr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a07ac83c10d5d27cf4f6bc9a913d0e2f
https://doi.org/10.1016/j.anl.2022.01.006
https://doi.org/10.1016/j.anl.2022.01.006
Autor:
Guangli Wang, Gaofeng Zhang, Ningxia Zhu, Chunjiang Zhu, Mafei Kang, Guidan Zuo, Zhijie Niu, Wei Ye, Baodong Tian, Rui Cai
Publikováno v:
Biochemical Genetics.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49519368d14b66fc65ecff2061d2b870
https://doi.org/10.1007/s10528-023-10340-w
https://doi.org/10.1007/s10528-023-10340-w
Publikováno v:
Interpretation. 9:T1157-T1165
A stage of mafic magmatic activity occurred in Early Permian in the Dabasong Uplift of Junggar Basin, part of the magma intruded into the normal sedimentary and shallow buried fine sandstone to form diabase, and part of the magma erupted to form basa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0d47b579fb8379c9a53548849bbb709
https://doi.org/10.1190/int-2021-0004.1
https://doi.org/10.1190/int-2021-0004.1
Autor:
Zhijie Niu, Xueping Wang, Jian Song, Hongsheng Cheng, Jie Sun, Jia-Da Li, Yong Feng, Lingyun Mei, Fen Tang, Lu Jiang, Xinzhang Cai, Chufeng He, Yalan Liu
Publikováno v:
European Archives of Oto-Rhino-Laryngology. 278:2807-2815
Waardenburg syndrome type 1 (WS1) is a rare genetic disorder characterized by dystopia canthorum, abnormal iris pigmentation, and congenital hearing loss with variable penetrance.WS1 is caused by mutations in paired box gene 3 (PAX3). The current stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4725ed2d2560872f6114298f3cda3f81
https://doi.org/10.1007/s00405-020-06361-5
https://doi.org/10.1007/s00405-020-06361-5
Autor:
Wei Jiang, Zhuokai He, Jin-Hui Liang, Rui Cai, Rong Jun Zhang, Yu-Fei Pan, Xi Yang, Zhijie Niu, Xiaolan Ruan
Publikováno v:
CancerReferences. 127(17)
Background The authors aimed to investigate the efficacy and safety of apatinib in patients with metastatic or locoregionally recurrent nasopharyngeal carcinoma (NPC). Methods A multicenter, single-arm, prospective phase 2 study was conducted on pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28efb70156dfe085ef9a7ff777759d89
https://pubmed.ncbi.nlm.nih.gov/34043812
https://pubmed.ncbi.nlm.nih.gov/34043812