Identification of ST3GAL5 as a prognostic biomarker correlating with CD8+ T cell exhaustion in clear cell renal cell carcinoma
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Published in Frontiers in immunology (12.09.2022)
Published in Frontiers in immunology (12.09.2022)
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Clinical characteristics and prognosis of pediatric myelin oligodendrocyte glycoprotein antibody-associated diseases in China
Sun, Xiaoang, Liu, Meiyan, Luo, Xiaona, Yuan, Fang, Wang, Chunmei, Wang, Simei, Xu, Quanmei, Zhang, Yuanfeng, Chen, Yucai
Published in BMC pediatrics (18.11.2022)
Published in BMC pediatrics (18.11.2022)
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Proteomics analysis of digestive juice from silkworm during Bombyx mori nucleopolyhedrovirus infection
Hu, Xiaolong, Zhu, Min, Wang, Simei, Zhu, Liyuan, Xue, Renyu, Cao, Guangli, Gong, Chengliang
Published in Proteomics (Weinheim) (01.08.2015)
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Segawa syndrome caused by TH gene mutation and its mechanism
Wang, Yilin, Wang, Chunmei, Liu, Meiyan, Xu, Wuhen, Wang, Simei, Yuan, Fang, Luo, Xiaona, Xu, Quanmei, Yin, Rongrong, Wang, Anqi, Guo, Miao, Lin, Longlong, Wang, Chao, Cheng, Hongyi, Liu, Zhiping, Zhang, Yuanfeng, Zeng, Fanyi, Yan, Jingbin, Chen, Yucai
Published in Frontiers in genetics (08.12.2022)
Published in Frontiers in genetics (08.12.2022)
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Novel Mutations of the ALMS1 Gene in Patients with Alström Syndrome
Wang, Chunmei, Luo, Xiaona, Wang, Yilin, Liu, Zhao, Wu, Shengnan, Wang, Simei, Lan, Xiaoping, Xu, Quanmei, Xu, Wuhen, Yuan, Fang, Wang, Anqi, Zeng, Fanyi, Jia, Jia, Chen, Yucai
Published in Internal Medicine (01.12.2021)
Published in Internal Medicine (01.12.2021)
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Clinical characteristics and identification of novel CNOT1 variants in three unrelated Chinese families with Vissers-Bodmer Syndrome
Tang, Xiaojun, Lan, Xiaoping, Song, Xiaozhen, Xu, Wuhen, Zhang, Yuanfeng, Wang, Simei, Xiao, Man, Yang, Yongchen, Zhang, Hong, Wu, Shengnan
Published in Heliyon (29.02.2024)
Published in Heliyon (29.02.2024)
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Comprehensive landscape of the ST3GAL family reveals the significance of ST3GAL6-AS1/ST3GAL6 axis on EGFR signaling in lung adenocarcinoma cell invasion
Li, Jiaxuan, Long, Yiming, Sun, Jingya, Wu, Jiajun, He, Xiao, Wang, Simei, Wang, Xiongbiao, Miao, Xiayi, Huang, Ruimin, Yan, Jun
Published in Frontiers in cell and developmental biology (26.08.2022)
Published in Frontiers in cell and developmental biology (26.08.2022)
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Clinical features and underlying mechanisms of KAT6B disease in a Chinese boy
Sun, Xiaoang, Luo, Xiaona, Lin, Longlong, Wang, Simei, Wang, Chunmei, Yuan, Fang, Lan, Xiaoping, Yan, Jingbin, Chen, Yucai
Published in Molecular genetics & genomic medicine (01.09.2023)
Published in Molecular genetics & genomic medicine (01.09.2023)
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Generation of an induced pluripotent stem cell line from an Ohtahara syndrome patient with the hemizygous mutation p.Q503Afs28 (c.1507_1508del) in the ARX gene
Wang, Chunmei, Wang, Yilin, Xu, Wuhen, Lin, Xuefeng, Xi, Jiaming, Wang, Simei, Lin, Longlong, Yuan, Fang, Wang, Anqi, Wang, Chao, Luo, Xiaona, Xu, Quanmei, Yin, Rongrong, Zhang, Yuanfeng, Huang, Xiaoyi, Chen, Yucai
Published in Stem cell research (01.03.2022)
Published in Stem cell research (01.03.2022)
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Induced pluripotent stem cells (SHCDNi006-A cells) isolated from the peripheral blood mononuclear cells of a five-month-old Chinese girl with the heterozygous missense mutation (c.2800 G>A) in the KCNT1 gene
Luo, Xiaona, Wang, Yilin, Yuan, Fang, Lin, Longlong, Wang, Anqi, Wang, Chao, Guo, Miao, Wang, Simei, Wang, Chunmei, Xu, Quanmei, Yin, Rongrong, Cheng, Hongyi, Zhang, Yuanfeng, Liu, Zhiping, Xu, Wuhen, Yan, Jingbin, Zeng, Fanyi, Chen, Yucai
Published in Stem cell research (01.07.2022)
Published in Stem cell research (01.07.2022)
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Generation of an induced pluripotent stem cell line SHCDNi001-A from a one-year-old Chinese girl with mitochondrial DNA depletion syndrome 13
Yuan, Fang, Wang, Chunmei, Xi, Jiaming, Wang, Simei, Lin, Longlong, Wang, Yilin, Wang, Anqi, Wang, Chao, Luo, Xiaona, Xu, Quanmei, Yin, Rongrong, Cheng, Hongyi, Zhang, Yuanfeng, Sun, Xiaomin, Chen, Yucai
Published in Stem cell research (01.05.2020)
Published in Stem cell research (01.05.2020)
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Generation and characterization of the induced pluripotent stem cell line SHCDNi004-A from a ten-year-old Chinese boy with X-linked mental retardation in IL1RAPL1 deficiency
Yuan, Fang, Wang, Simei, Wang, Yilin, Wang, Anqi, Wang, Chao, Luo, Xiaona, Xu, Quanmei, Yin, Rongrong, Cheng, Hongyi, Wang, Chunmei, Guo, Miao, Zhang, Yuanfeng, Xi, Jiaming, Yang, Jie, Sun, Xiaomin, Yan, Jingbin, Zeng, Fanyi, Chen, Yucai
Published in Stem cell research (01.05.2021)
Published in Stem cell research (01.05.2021)
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Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseases
Liu, Meiyan, Sun, Xiaoang, Lin, Longlong, Luo, Xiaona, Wang, Simei, Wang, Chunmei, Zhang, Yuanfeng, Xu, Quanmei, Xu, Wuhen, Wu, Shengnan, Lan, Xiaoping, Chen, Yucai
Published in Frontiers in pediatrics (17.11.2022)
Published in Frontiers in pediatrics (17.11.2022)
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Induced pluripotent stem cells (SHCDNi002-A cells) isolated from the peripheral blood mononuclear cells of a 1-year-old Chinese girl with mediator complex subunit 12-related syndrome
Wang, Yilin, Yuan, Fang, Wang, Anqi, Wang, Chao, Lin, Longlong, Wang, Simei, Wang, Chunmei, Luo, Xiaona, Xu, Quanmei, Yin, Rongrong, Cheng, Hongyi, Zhang, Yuanfeng, Sun, Xiaomin, Xi, Jiaming, Yan, Jingbin, Zeng, Fanyi, Chen, Yucai
Published in Stem cell research (01.07.2020)
Published in Stem cell research (01.07.2020)
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Generation of an induced pluripotent stem cell line (SHCDNi003-A) from a one-year-old Chinese Han infant with Allan–Herndon–Dudley syndrome
Wang, Anqi, Xi, Jiaming, Yuan, Fang, Wang, Yilin, Wang, Simei, Wang, Chunmei, Wang, Chao, Lin, Longlong, Luo, Xiaona, Xu, Quanmei, Yin, Rongrong, Cheng, Hongyi, Zhang, Yuanfeng, Sun, Xiaomin, Yang, Jie, Yan, Jingbin, Zeng, Fanyi, Chen, Yucai
Published in Stem cell research (01.07.2020)
Published in Stem cell research (01.07.2020)
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Clinical Study of 8 Cases of CHD2 Gene Mutation-Related Neurological Diseases and Their Mechanisms
Luo, Xiaona, Sun, Xiaoang, Wang, Yilin, Lin, Longlong, Yuan, Fang, Wang, Simei, Zhang, Wenjing, Ji, Xiaobing, Liu, Meiyan, Wu, Shengnan, Lan, Xiaoping, Zhang, Jie, Yan, Jingbin, Zeng, Fanyi, Chen, Yucai
Published in Frontiers in cell and developmental biology (21.03.2022)
Published in Frontiers in cell and developmental biology (21.03.2022)
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Mechanisms of Congenital Myasthenia Caused by Three Mutations in the COLQ Gene
Luo, Xiaona, Wang, Chunmei, Lin, Longlong, Yuan, Fang, Wang, Simei, Wang, Yilin, Wang, Anqi, Wang, Chao, Wu, Shengnan, Lan, Xiaoping, Xu, Quanmei, Yin, Rongrong, Cheng, Hongyi, Zhang, Yuanfeng, Xi, Jiaming, Zhang, Jie, Sun, Xiaomin, Yan, Jingbin, Zeng, Fanyi, Chen, Yucai
Published in Frontiers in pediatrics (29.11.2021)
Published in Frontiers in pediatrics (29.11.2021)
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Correlation Between Tic Disorders and Serum 25-Hydroxyvitamin D Levels in Chinese Children
Wang, Simei, Xu, Quanmei, Wang, Anqi, Yuan, Fang, Luo, Xiaona, Wang, Yilin, Guo, Miao, Zhang, Yuanfeng, Zhang, Wenjing, Ji, Xiaobing, Ren, Yun, Chen, Yucai
Published in Frontiers in pediatrics (09.05.2022)
Published in Frontiers in pediatrics (09.05.2022)
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Comparative analysis of open and closed tracheal suction systems on mechanical ventilation efficiency in adults: A systematic review and meta-analysis
Liang, Zhenghua, Liao, Qian, Xu, Jinlong, Wang, Simei, Liu, Qiuyu, Liu, Zefang, Wen, Dan
Published in Australian critical care (05.09.2024)
Published in Australian critical care (05.09.2024)
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