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日期

2025
2
2024
11
2023
7
2022
2
2021
3
2020
5
2019
1

结果 (31)

NGS
Sialoblastomas With Solid Pattern Have FGFR2 Mutations and an Unfavorable Prognosis

Jia Xiaoli; Leng NanNan; Wang Min; Zhan Xiaohong; Li Jiang

2025 .01 阅读摘要
基因合成
Preliminary study on the correlation between enzyme activity assays and substrate preferences of microbial transglutaminase

Xinyue Zheng, Wenjie Luo, Mingfeng Wang, Xing Chen, Jing Liu, Lei Wang, Wei Zhang, Weiyao Hu, Gaofeng Dong, Hongyang Pan, Zhaojun Wang, Qiuming Chen

2025 .01 阅读摘要
NGS
Promoter capture Hi-C identifies promoter-related loops and fountain structures in Arabidopsis

Dingyue Wang, Suxin Xiao, Jiayue Shu, Lingxiao Luo, Minqi Yang, Myriam Calonje, Hang He, Baoxing Song & Yue Zhou

2024 .12 阅读摘要
寡核苷酸池
Functional RNA mining using random high-throughput screening

Li-Hua Liu, Jinde Chen, Shijing Lai, Xuemei Zhao, Min Yang, Yi-Rui Wu, Zhiqian Zhang, Ao Jiang

2024 .11 阅读摘要
寡核苷酸池
DP-ID: Interleaving and Denoising to Improve the Quality of DNA Storage Image

Qi Xu, Yitong Ma, Zuhong Lu, Kun Bi

2024 .11 阅读摘要
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
NGS
Genomic study substantiates the intensive care unit as a reservoir for carbapenem-resistant Klebsiella pneumoniae in a teaching hospital in China

Shuo Jiang, Zheng Ma, Huiluo Cao, Li Mo, Jinlan Jin, Bohai Yu, Kankan Chu, Jihua Hu

2024 .09 阅读摘要
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
NGS
Pharmacogenomic Polygenic Model of Clopidogrel Predicts Recurrent Ischemic Events in Chinese Patients With Coronary Artery Disease

Xinyi Zhang, Yuchun Cai, Pei Zhou, Wenchang Nie, Haoning Sun, Yutong Sun, Yuxuan Zhao, Congxiao Han, Chengfu Cao, Jian Liu, Xiaoyan Nie

2024 .08 阅读摘要
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
寡核苷酸池
Massively parallel CRISPR-assisted homologous recombination enables saturation editing of full-length endogenous genes in yeast

Lei Deng, Yi-Lian Zhou, Zhenkun Cai, Jie Zhu, Zenan Li, Zehua Bao

2024 .05 阅读摘要
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
NGS
Proteomic and metabolomic features in patients with HCC responding to lenvatinib and anti-PD1 therapy

Zhong-Chen Li, Jie Wang, He-Bin Liu, Yi-Min Zheng, Jian-Hang Huang, Jia-Bin Cai, Lei Zhang, Xin Liu, Ling Du, Xue-Ting Yang, Xiao-Qiang Chai, Ying-Hua Jiang, Zheng-Gang Ren, Jian Zhou, Jia Fan, De-Cai Yu, Hui-Chuan Sun, Cheng Huang, Feng Liu

2024 .02 阅读摘要
NGS
An Inflammatory Checkpoint Generated by IL1RN Splicing Offers Therapeutic Opportunity for KRAS-Mutant Intrahepatic Cholangiocarcinoma

Mao Zhang, Yingying Huang, Jiaomeng Pan, Chen Sang, Youpei Lin, Liangqing Dong, Xia Shen, Yingcheng Wu, Guohe Song, Shuyi Ji, Fen Liu, Mengcheng Wang, Yuyan Zheng, Sirui Zhang, Zefeng Wang, Jianke Ren, Daming Gao, Jian Zhou, Jia Fan, Wu Wei, Jian Lin, and

2023 .10 阅读摘要
RNA合成
Hyperhomocysteinemia lowers serum testosterone concentration via impairing testosterone production in Leydig cells

Zhiyuan Su, Zhuoliang Liu, Wenjing Lei, Kai Xia, An Xiao, Zheng Hu, Miaomiao Zhou, Fengxin Zhu, Jianwei Tian, Manqiu Yang, Dong Wang, Andy Peng Xiang, Jing Nie

2023 .07 阅读摘要
NGS
Whole-Exome Sequencing Reveals Distinct Genetic Profiles of Palindromic Rheumatism

Chenxiang Zheng, Fan Wang, Yue Sun, Zhuochao Zhou, Yijun You, Dongyi He, Xiaoxia Zhu, Lindi Jiang, Cui Lu, Lijun Wu, Hongzhi Wang, Hanying Mei, Ting Zeng, Hui Zheng, Jialing Teng, Honglei Liu, Xiaobing Cheng, Yutong Su, Hui Shi, Qiongyi Hu, Xueming Jian,

2023 .05 阅读摘要
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
NGS
Molecular fingerprints of nuclear genome and mitochondrial genome for early diagnosis of lung adenocarcinoma

Yichun Xu, Yong Yang, Yichao Wang, Jun Su, Tianlong Chan, Jiajing Zhou, Yi Gong, Ke Wang, Yifeng Gu, Congmeng Zhang, Guanjin Wu, Ling Bi, Xiong Qin, and Junsong Han

2023 .04 阅读摘要
NGS
Clinical and molecular heterogeneity associated with tumor sidedness in colorectal liver metastasis: a multicenter propensity cohort study

Yibin Wu, Jiamin Zhou, Huipeng Wang, Guojiu Fang, Weiping Zhu, Sanjun Cai, Lu Wang

2023 .03 阅读摘要
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
NGS
A method of large DNA fragment enrichment for nanopore sequencing in region 22q11.2

Yu-Qing Lei，Liang-Pu Xu，Hua Cao，Xin-Rui Wang

2022 .10 阅读摘要
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
寡核苷酸池
Profiling CD8+ T cell epitopes of COVID-19 convalescents reveals reduced cellular immune responses to SARS-CoV-2 variants

Hang Zhang, Shasha Deng, Liting Ren, Peiyi Zheng, Xiaowen Hu, Tengchuan Jin, and Xu Tan

2021 .08 阅读摘要
NGS
Performance comparison of four types oftarget enrichment baits for exome DNA sequencing

Juan Zhou, Mancang Zhang, Xiaoqi Li, Zhuo Wang, Dun Pan and Yongyong Shi

2021 .02 阅读摘要
NGS
Artificial intelligence based identification of the functional role of hirudin in diabetic erectile dysfunction treatment

Ruocong Yang , Chao Liu , Qianqian Li , Weilu Wang , Bingbing Wu , Aiping Chen , Bin Wang , Wei Li , Jianxin Che

2021 .01 阅读摘要
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
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
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
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
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
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

NGS

引物与探针

RNA合成

基因合成

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NGS

引物与探针

RNA合成

基因合成

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生物医药工具

DNA数据存储

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发表文献

产品分类

日期

热门文章

Functional RNA mining using random high-throughput screening

Massively parallel CRISPR-assisted homologous recombination enables saturation editing of full-length endogenous genes in yeast

An Inflammatory Checkpoint Generated by IL1RN Splicing Offers Therapeutic Opportunity for KRAS-Mutant Intrahepatic Cholangiocarcinoma

Whole-Exome Sequencing Reveals Distinct Genetic Profiles of Palindromic Rheumatism

结果 (31)

Sialoblastomas With Solid Pattern Have FGFR2 Mutations and an Unfavorable Prognosis

Jia Xiaoli; Leng NanNan; Wang Min; Zhan Xiaohong; Li Jiang

Preliminary study on the correlation between enzyme activity assays and substrate preferences of microbial transglutaminase

Xinyue Zheng, Wenjie Luo, Mingfeng Wang, Xing Chen, Jing Liu, Lei Wang, Wei Zhang, Weiyao Hu, Gaofeng Dong, Hongyang Pan, Zhaojun Wang, Qiuming Chen

Promoter capture Hi-C identifies promoter-related loops and fountain structures in Arabidopsis

Dingyue Wang, Suxin Xiao, Jiayue Shu, Lingxiao Luo, Minqi Yang, Myriam Calonje, Hang He, Baoxing Song & Yue Zhou

Functional RNA mining using random high-throughput screening

Li-Hua Liu, Jinde Chen, Shijing Lai, Xuemei Zhao, Min Yang, Yi-Rui Wu, Zhiqian Zhang, Ao Jiang

DP-ID: Interleaving and Denoising to Improve the Quality of DNA Storage Image

Qi Xu, Yitong Ma, Zuhong Lu, Kun Bi

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

Genomic study substantiates the intensive care unit as a reservoir for carbapenem-resistant Klebsiella pneumoniae in a teaching hospital in China

Shuo Jiang, Zheng Ma, Huiluo Cao, Li Mo, Jinlan Jin, Bohai Yu, Kankan Chu, Jihua Hu

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

Pharmacogenomic Polygenic Model of Clopidogrel Predicts Recurrent Ischemic Events in Chinese Patients With Coronary Artery Disease

Xinyi Zhang, Yuchun Cai, Pei Zhou, Wenchang Nie, Haoning Sun, Yutong Sun, Yuxuan Zhao, Congxiao Han, Chengfu Cao, Jian Liu, Xiaoyan Nie

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

Massively parallel CRISPR-assisted homologous recombination enables saturation editing of full-length endogenous genes in yeast

Lei Deng, Yi-Lian Zhou, Zhenkun Cai, Jie Zhu, Zenan Li, Zehua Bao

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

Proteomic and metabolomic features in patients with HCC responding to lenvatinib and anti-PD1 therapy

Zhong-Chen Li, Jie Wang, He-Bin Liu, Yi-Min Zheng, Jian-Hang Huang, Jia-Bin Cai, Lei Zhang, Xin Liu, Ling Du, Xue-Ting Yang, Xiao-Qiang Chai, Ying-Hua Jiang, Zheng-Gang Ren, Jian Zhou, Jia Fan, De-Cai Yu, Hui-Chuan Sun, Cheng Huang, Feng Liu

An Inflammatory Checkpoint Generated by IL1RN Splicing Offers Therapeutic Opportunity for KRAS-Mutant Intrahepatic Cholangiocarcinoma

Mao Zhang, Yingying Huang, Jiaomeng Pan, Chen Sang, Youpei Lin, Liangqing Dong, Xia Shen, Yingcheng Wu, Guohe Song, Shuyi Ji, Fen Liu, Mengcheng Wang, Yuyan Zheng, Sirui Zhang, Zefeng Wang, Jianke Ren, Daming Gao, Jian Zhou, Jia Fan, Wu Wei, Jian Lin, and

Hyperhomocysteinemia lowers serum testosterone concentration via impairing testosterone production in Leydig cells

Zhiyuan Su, Zhuoliang Liu, Wenjing Lei, Kai Xia, An Xiao, Zheng Hu, Miaomiao Zhou, Fengxin Zhu, Jianwei Tian, Manqiu Yang, Dong Wang, Andy Peng Xiang, Jing Nie

Whole-Exome Sequencing Reveals Distinct Genetic Profiles of Palindromic Rheumatism

Chenxiang Zheng, Fan Wang, Yue Sun, Zhuochao Zhou, Yijun You, Dongyi He, Xiaoxia Zhu, Lindi Jiang, Cui Lu, Lijun Wu, Hongzhi Wang, Hanying Mei, Ting Zeng, Hui Zheng, Jialing Teng, Honglei Liu, Xiaobing Cheng, Yutong Su, Hui Shi, Qiongyi Hu, Xueming Jian,

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

Molecular fingerprints of nuclear genome and mitochondrial genome for early diagnosis of lung adenocarcinoma

Yichun Xu, Yong Yang, Yichao Wang, Jun Su, Tianlong Chan, Jiajing Zhou, Yi Gong, Ke Wang, Yifeng Gu, Congmeng Zhang, Guanjin Wu, Ling Bi, Xiong Qin, and Junsong Han

Clinical and molecular heterogeneity associated with tumor sidedness in colorectal liver metastasis: a multicenter propensity cohort study

Yibin Wu, Jiamin Zhou, Huipeng Wang, Guojiu Fang, Weiping Zhu, Sanjun Cai, Lu Wang

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

A method of large DNA fragment enrichment for nanopore sequencing in region 22q11.2

Yu-Qing Lei，Liang-Pu Xu，Hua Cao，Xin-Rui Wang

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

Profiling CD8+ T cell epitopes of COVID-19 convalescents reveals reduced cellular immune responses to SARS-CoV-2 variants

Hang Zhang, Shasha Deng, Liting Ren, Peiyi Zheng, Xiaowen Hu, Tengchuan Jin, and Xu Tan

Performance comparison of four types oftarget enrichment baits for exome DNA sequencing

Juan Zhou, Mancang Zhang, Xiaoqi Li, Zhuo Wang, Dun Pan and Yongyong Shi

Artificial intelligence based identification of the functional role of hirudin in diabetic erectile dysfunction treatment

Ruocong Yang , Chao Liu , Qianqian Li , Weilu Wang , Bingbing Wu , Aiping Chen , Bin Wang , Wei Li , Jianxin Che

Identification of SHANK2 Pathogenic Variants in a Chinese Uygur Population with Schizophrenia

Han Zhang, Dong Wang, Jianhua Chen, Xiuli Li, Qizhong Yi, Yongyong Shi

A novel genetic variant associated with benign paroxysmal positional vertigo within the LOXL1