Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Wei-Qing Wu"'
Autor:
Wei-qing Wu, Jia-xun Zhang, Ying-xia Cui, Ming-chao Zhang, Xiao-hang Chen, Shan Duan, Cai-hong Zeng, Pei-ning Li, Xiao-jun Li
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Alport syndrome (AS) is an inherited glomerular basement membrane (GBM) disease leading to end-stage renal disease (ESRD). X-linked AS (XLAS) is caused by pathogenic variants in the COL4A5 gene. Many pathogenic variants causing AS have been detected,
Externí odkaz:
https://doaj.org/article/7d4874717e404963a51f6fb0b9addc75
Autor:
Qingyun Yang, Hong Ou, Xuan Xu, Xue-Ping Cai, Xiao-Ming Lin, Zhiguang Xu, Wei-Qing Wu, Pan Gao, Qiongyi Xie
Publikováno v:
Inorganic Chemistry. 60:9378-9386
To study the electronic structures and properties of [Crn(L)4Cl2] (n = 3, L = dpa: di(2-pyridyl)amido; n = 5, L = tpda: tripyridyldiamido; n = 7, L = teptra: tetrapyridyltriamine) metal string complexes, the BP86 method was used by considering the in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb22af1ecc6bcd966b2f85dfbd03ea07
https://doi.org/10.1021/acs.inorgchem.1c00206
https://doi.org/10.1021/acs.inorgchem.1c00206
Autor:
Xiao-Jun Li, Bai‐zeng Yu, Wei-Qing Wu, Ying-Xia Cui, Liu-Fei Miao, Fangfang Chen, Jia-Xun Zhang, Xing Lv, Zheng-Kun Xia, Zhi-Hong Liu
Publikováno v:
Cytogenetic and Genome Research. 160:238-244
X-linked Alport syndrome (XLAS) is a common hereditary nephropathy caused by COL4A5 gene mutations. To date, many splice site mutations have been described but few have been functionally analyzed to verify the exact splicing effects that contribute t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::819faf6554406f630c6b258772989c67
https://doi.org/10.1159/000508562
https://doi.org/10.1159/000508562
Autor:
Pan, Gao, Xue-Ping, Cai, Qiongyi, Xie, Qingyun, Yang, Hong, Ou, Wei-Qing, Wu, Xuan, Xu, Zhiguang, Xu, Xiaoming, Lin
Publikováno v:
Inorganic chemistry. 60(13)
To study the electronic structures and properties of [Cr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9ae63559b3a853c96a2f608c337e7da8
https://pubmed.ncbi.nlm.nih.gov/34137268
https://pubmed.ncbi.nlm.nih.gov/34137268
Publikováno v:
Reproductive BioMedicine Online. 35:609-615
The aim of this study was to investigate whether polymorphism and expression of CYP17, CYP1A1, COMT and SULT1A1 affected the risk of idiopathic primary ovarian insufficiency (POI) in Chinese women. DNA sequencing and real-time PCR were used to detect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b20181b8b86d6f5fdd7cfef237d327c
https://doi.org/10.1016/j.rbmo.2017.07.007
https://doi.org/10.1016/j.rbmo.2017.07.007
Autor:
Xing, Lv, Wei-Qing, Wu, Jia-Xun, Zhang, Liu-Fei, Miao, Bai-Zeng, Yu, Fang-Fang, Chen, Ying-Xia, Cui, Zheng-Kun, Xia, Zhi-Hong, Liu, Xiao-Jun, Li
Publikováno v:
Cytogenetic and genome research. 160(5)
X-linked Alport syndrome (XLAS) is a common hereditary nephropathy caused by COL4A5 gene mutations. To date, many splice site mutations have been described but few have been functionally analyzed to verify the exact splicing effects that contribute t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ec9ccc9679989f6e3932440e8fe93cc
https://pubmed.ncbi.nlm.nih.gov/32659759
https://pubmed.ncbi.nlm.nih.gov/32659759
Publikováno v:
Zhongguo Dang Dai Er Ke Za Zhi
High-throughput sequencing was performed for the peripheral blood DNA from two probands in the family with tuberous sclerosis complex (TSC) to determine the sequences of TSC-related genes TSC1 and TSC2 and their splicing regions and identify mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a624d689775f7872f778b788396df183
https://pubmed.ncbi.nlm.nih.gov/28302202
https://pubmed.ncbi.nlm.nih.gov/28302202
Publikováno v:
Reproductive BioMedicine Online. 29:311-318
The aim of this study was to investigate the role of the anti-Müllerian hormone (AMH) signalling pathway in the pathophysiology of idiopathic primary ovarian insufficiency (POI) and age at natural menopause (ANM) using a genetic approach. DNA sequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fdea735fa974811f631f6a550761c40
https://doi.org/10.1016/j.rbmo.2014.05.003
https://doi.org/10.1016/j.rbmo.2014.05.003
Autor:
Li-Li Ma, Lin-Feng Li, Bao Liu, Wei-Qing Wu, Xin-Feng Wang, Ming-Zhou Sun, Ma Re Yi, Xi-Wen Li, Hong-Xing Xiao, Lily Jiang
Publikováno v:
Tree Genetics & Genomes. 9:1321-1328
Disentangling the molecular mechanisms of adaptation in natural plant populations in response to different environmental conditions is a central topic in evolutionary biology. In the present study, we investigated a wind-pollinated woody species of C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7f6ccc86a94e398f116bceda1818094
https://doi.org/10.1007/s11295-013-0641-9
https://doi.org/10.1007/s11295-013-0641-9
Publikováno v:
Applied Mechanics and Materials. 328:128-132
The path planning relates to the safe movement and navigation of the Autonomous Underwater Vehicles (AUV). This paper discusses the way of real-time path planning for autonomous underwater vehicle based on tracking control lyapunov function. The simu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f92df980be28c158c468072e2339571
https://doi.org/10.4028/www.scientific.net/amm.328.128
https://doi.org/10.4028/www.scientific.net/amm.328.128