产品分类
清除
日期
2024
4
2023
2
2022
1
2021
0
2020
5
2019
1
热门文章
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NGS
Empirical assessment of the enrichment-based metagenomic methods in identifying diverse respiratory pathogens
Xiaofang Jia, Wei Wang, Min Wu, Linlin Pang, Chunyi Yang, Yun Ling, Zhigang Yi, Xiaonan Zhang
2024 .10
阅读摘要
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NGS
Multi-omics analyses reveal aberrant differentiation trajectory with WNT1 loss-of-function in type XV osteogenesis imperfecta
Zhijia Tan, Peikai Chen, Jianan Zhang, Hiu Tung Shek, Zeluan Li, Xinlin Zhou, Yapeng Zhou, Shijie Yin, Lina Dong, Lin Feng, Janus Siu Him Wong, Bo Gao, Michael Kai Tsun To
2024 .08
阅读摘要
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NGS
Identification of the body fluid donor in mixtures through target mRNA cSNP sequencing
Zidong Liu, Jiaqi Wang, Lishan Li, Hailing Yang, Huan Yu, Jiajia Fan, Mingming Zhang, Yuxin Zhang, Jinding Liu, Zeqin Li, Gengqian Zhang
2024 .07
阅读摘要
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NGS
Keap1/Nrf2 signaling pathway participating in the progression of epilepsy via regulation of oxidative stress and ferroptosis in neurons
DandanWang, YunmeiCui, FanGao, WeiweiZheng, JinziLi, ZheminXian
2024 .04
阅读摘要
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NGS
Identification of VIPR2 rare and common variants in the Chinese Han population with schizophrenia
Jiajun Yin, Juan Zhou, Fang Fang, Shui Yu, Jun Wang, Jianmin Yuan, Zhenhe Zhou
2023 .04
阅读摘要
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NGS
Clinical features and molecular characterization of Chinese patients with FKBP10 variants
Zhijia Tan, Hiu Tung Shek, Peikai Chen, Zhongxin Dong, Yapeng Zhou, Shijie Yin, Anmei Qiu, Lina Dong, Bo Gao, Michael Kai Tsun To
2023 .01
阅读摘要
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NGS
Patient-reported outcomes in a Chinese cohort of osteogenesis imperfecta unveil psycho-physical stratifications associated with clinical manifestations
Peikai Chen, Zhijia Tan, Anmei Qiu, Shijie Yin, Yapeng Zhou, Zhongxin Dong, Yan Qiu, Jichun Xu, Kangsen Li, Lina Dong, Hiu Tung Shek, Jingwen Liu, Eric H. K. Yeung, Bo Gao, Kenneth Man Chee Cheung & Michael Kai-Tsun To
2022 .06
阅读摘要
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NGS
Identification of SHANK2 Pathogenic Variants in a Chinese Uygur Population with Schizophrenia
Han Zhang, Dong Wang, Jianhua Chen, Xiuli Li, Qizhong Yi, Yongyong Shi
2020 .09
阅读摘要
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NGS
A novel genetic variant associated with benign paroxysmal positional vertigo within the LOXL1
Mingzhu Deng, Chen Liu, Weiqing Jiang, Fei Wang, Juan Zhou, Dong Wang, Yonggang Wang
2020 .08
阅读摘要
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NGS
Polymorphisms and rare variants identified by next-generation sequencing confer risk for lung cancer in han Chinese population
Li Xiaoqi, Liu Jinsheng, Wang Ke, Zhou Juan, Zhang Hang, Zhang Mancang, Shi Yongyong
2020 .04
阅读摘要
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NGS
Rare and common variants analysis of the EMB gene in patients with schizophrenia
Juan Zhou, Chuanchuan Ma, Ke Wang, Xiuli Li, Han Zhang, Jianhua Chen, Zhiqiang Li & Yongyong Shi
2020 .03
阅读摘要
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NGS
Fine-mapping of ZDHHC2 identifies risk variants for schizophrenia in the Han Chinese population
Han Zhang, Xiuli Li, Chuanchuan Ma, Ke Wang, Juan Zhou, Jianhua Chen, Yonggang Wang, Yongyong Shi
2020 .03
阅读摘要
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NGS
Amplicon targeted resequencing for SLC2A9 and SLC22A12 identified novel mutations in hypouricemia subjects
Zhaowei Zhou, Ke Wang, Juan Zhou, Can Wang, Xinde Li, Lingling Cui, Lin Han, Zhen Liu, Wei Ren, Xuefeng Wang, Keke Zhang, Zhiqiang Li, Dun Pan, Changgui Li, Yongyong Shi
2019 .05
阅读摘要