Zobrazeno 1 - 10
of 48
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:
Xiao-Fan, Liu, Wei-Qing, Wu, Guo-Qing, Dong, Ting-Ting, Xiao, Yang, Liu, Yong-Zheng, Zhou, Yue-Dong, Li, Ji-Tong, Lin, Fang-Jin, Chen, Xiao-Zhong, Zhang
Publikováno v:
Zhonghua nan ke xue = National journal of andrology. 27(3)
To investigate the clinical characteristics, diagnosis, treatment and etiology of persistent Müllerian duct syndrome (PMDS).A 3-year-old boy was diagnosed with PMDS according to the clinical manifestations and the results of ultrasonography, laborat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c2f99917ca0f3869d64f04827ea5a074
https://pubmed.ncbi.nlm.nih.gov/34914305
https://pubmed.ncbi.nlm.nih.gov/34914305
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:
Shanghai kou qiang yi xue = Shanghai journal of stomatology. 27(6)
To investigate the effects of recasting on metallographic microstructure of cobalt-chromium(Co-Cr), commercially pure titanium(cpTi), palladium-copper-gallium(Pd-Cu-Ga), aurum-platinum(Au-Pt) ceramic alloys.Without adding new alloys, Co-Cr, cpTi, Pd-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e5aafd876e4fa582f48a0143efca773b
https://pubmed.ncbi.nlm.nih.gov/30899937
https://pubmed.ncbi.nlm.nih.gov/30899937
Publikováno v:
Acta Radiologica. 58:867-875
Background Magnetic resonance imaging (MRI) and functional MRI techniques have been widely used in the diagnosis of human immunodeficiency virus (HIV) infection related diseases. Purpose To explore whether magnetic resonance diffusion-weighted imagin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85f8f3a4dcf62e495645605232fef423
https://doi.org/10.1177/0284185116673123
https://doi.org/10.1177/0284185116673123
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