Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Weiliang Lu"'
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101026- (2024)
Externí odkaz:
https://doaj.org/article/3dda36e47f2b4b4294154370e8a0f067
Autor:
Chenming Xu, Jianli Li, Songchang Chen, Xiaoqiang Cai, Ruilin Jing, Xiaomei Qin, Dong Pan, Xin Zhao, Dongyang Ma, Xiufeng Xu, Xiaojun Liu, Can Wang, Bingxin Yang, Lanlan Zhang, Shuyuan Li, Yiyao Chen, Nina Pan, Ping Tang, Jieping Song, Nian Liu, Chen Zhang, Zhiwei Zhang, Xiang Qiu, Weiliang Lu, Chunmei Ying, Xiaotian Li, Congjian Xu, Yanlin Wang, Yanting Wu, He-Feng Huang, Jinglan Zhang
Publikováno v:
Cell Discovery, Vol 8, Iss 1, Pp 1-22 (2022)
Abstract Current non-invasive prenatal screening (NIPS) analyzes circulating fetal cell-free DNA (cfDNA) in maternal peripheral blood for selected aneuploidies or microdeletion/duplication syndromes. Many genetic disorders are refractory to NIPS larg
Externí odkaz:
https://doaj.org/article/e4dc48cd6d3141a390533b0de953c394
Autor:
Yu He, Xixi Wang, Weiliang Lu, Dan Zhang, Lan Huang, Yang Luo, Li Xiong, Haocheng Li, Peng Zhang, Qiu Li, Shufang Liang
Publikováno v:
Cell Death and Disease, Vol 13, Iss 2, Pp 1-15 (2022)
Abstract Phosphoglycerate kinase 1 (PGK1) has complicated and multiple functions in cancer occurrence, tumor progression and drug resistance. Sorafenib is the first-line treatment targeted drug for patients with kidney renal clear cell carcinoma (KIR
Externí odkaz:
https://doaj.org/article/005863c391874fbb9ae5c0df71a36737
Autor:
Jiasun Su, Huayu Fu, Bobo Xie, Weiliang Lu, Wei Li, Yuan Wei, Qiang Zhang, Shengkai Wei, Qiuli Chen, Yingchi Lu, Tingting Jiang, Jingsi Luo, Zailong Qin
Publikováno v:
Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-6 (2019)
Abstract Background Cri-du-chat syndrome (CdCS; OMIM#123450) is a classic contiguous gene syndrome caused by chromosome 5p terminal deletion (5p-), which characterized by a high-pitched cat-like cry, developmental delay, severe psychomotor, mental re
Externí odkaz:
https://doaj.org/article/b988669035c5424b99a896023196675a
Autor:
Jiasun Su, Weiliang Lu, Mengting Li, Qiang Zhang, Fei Chen, Shang Yi, Qi Yang, Sheng Yi, Xunzhao Zhou, Limei Huang, Yiping Shen, Jingsi Luo, Zailong Qin
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 4, Pp n/a-n/a (2021)
Abstract Background Congenital hydrocephalus‐3 with brain anomalies (HYC3, MIM 617967) is a rare form of congenital hydrocephalus characterized by severe hydrocephalus and cerebellar abnormalities, the onset of the disease occurs in utero even resu
Externí odkaz:
https://doaj.org/article/c7e3d389313f4acf9cf8e2aaaf58dddd
Autor:
Zailong Qin, Jiasun Su, Mengting Li, Qi Yang, Shang Yi, Haiyang Zheng, Qiang Zhang, Fei Chen, Sheng Yi, Weiliang Lu, Wei Li, Limei Huang, Jing Xu, Yiping Shen, Jingsi Luo
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
CHARGE syndrome is a life-threatening disease caused by mutations of chromodomain helicase DNA-binding protein 7 gene (CHD7). The disease is characterized by a pattern of congenital anomalies that involve multiple organs. In this study, five patients
Externí odkaz:
https://doaj.org/article/de5232507999436a96aefeea9ccf63f5
Autor:
Weiliang Lu, Mingxing Liang, Jiasun Su, Jin Wang, Lingxiao Li, Shujie Zhang, Zailong Qin, Limei Huang, Yingchi Lu, Shang Yi, Sheng Yi, BoBo Xie, Haiyang Zheng, Jingsi Luo, Xiaoyan Gao, Yiping Shen
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 5, Pp n/a-n/a (2020)
Abstract Background A very limited spectrum of ASCC1 pathogenic variants had been reported in six (mostly consanguineous) families with spinal muscular atrophy with congenital bone fractures 2 [OMIM #616867] since 2016. Methods A proband from a non
Externí odkaz:
https://doaj.org/article/a182b4691e5f417f9e86f6c2bf61a08c
Publikováno v:
Mathematics, Vol 9, Iss 7, p 709 (2021)
This paper introduces a fuel-switching price to the Alberta market, which is designed for encouraging power plant companies to switch from coal to natural gas when they produce electricity; this has been successfully applied to the European market. M
Externí odkaz:
https://doaj.org/article/a86c4e58d90b4dd68f6a4bd5c12e7aca
Autor:
Dan Zhang, Xiangying Xia, Xixi Wang, Peng Zhang, Weiliang Lu, Yamei Yu, Shi Deng, Hanshuo Yang, Hongxia Zhu, Ningzhi Xu, Shufang Liang
Publikováno v:
PLoS ONE, Vol 12, Iss 1, p e0170453 (2017)
Progesterone receptor membrane component 1 (PGRMC1) is widely observed with an elevated level in multiple human cancers. However, the roles of PGRMC1 in renal cancer are not clear and merit further study. In this report, we made a systematic, integra
Externí odkaz:
https://doaj.org/article/2f0ff2c8adeb4f3caba903eda294ba1a
Autor:
Xuewen Jin, Yuling Liu, Jingjing Liu, Weiliang Lu, Ziwei Liang, Dan Zhang, Gang Liu, Hongxia Zhu, Ningzhi Xu, Shufang Liang
Publikováno v:
PLoS ONE, Vol 10, Iss 8, p e0133770 (2015)
The IQ-domain GTPase-activating protein 1 (IQGAP1) is a multifunctional scaffold protein, which interacts with diverse proteins to regulate cell adhesion and cell migration. The abnormal expression of IQGAP1 widely exists in many cancers, but biologi
Externí odkaz:
https://doaj.org/article/5acec7c3dea04d9297d238d2a7d99c73