Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yichuan Yao"'
Autor:
Yichuan Yao, Yunru Yang, Qiqin Wu, Mengyao Liu, Wei Bao, Qiutong Wang, Meijun Cheng, Yunuo Chen, Yuan Cai, Mei Zhang, Jingxue Yao, Hongliang He, Changjiang Jin, Tian Xue, Changcheng Zheng, Tengchuan Jin, Dali Tong
The surge of SARS-CoV-2 Omicron infection in most Chinese residents at the end of 2022 provided a unique opportunity to understand how the immune system responds to the Omicron infection in a population with limited contact to prior SARS-CoV-2 varian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78a930b6faa8819c8882ffe62c18509d
https://doi.org/10.1101/2023.02.28.23286535
https://doi.org/10.1101/2023.02.28.23286535
Autor:
Zilong Qiu, Tian Xue, Yingzhou Hu, Yunqin Li, Kai Dong, Jin Bao, Mei Zhang, Min Hu, Yichuan Yao, Xintian Hu, Shouzhen Li, Wenchao Wang, Yuan Cai, Min Wei, Huan Zhao, Yun Wang, Yonghao Gu, Yuqian Ma
Publikováno v:
Science Bulletin. 66:374-385
Retinitis pigmentosa (RP) is a form of inherited retinal degenerative diseases that ultimately involves the macula, which is present in primates but not in the rodents. Therefore, creating nonhuman primate (NHP) models of RP is of critical importance
Autor:
Yayu Wang, Wenping Zeng, Bingqian Lin, Yichuan Yao, Canjun Li, Wenqi Hu, Haotian Wu, Jiamin Huang, Mei Zhang, Tian Xue, Dejian Ren, Lili Qu, Chunlei Cang
Publikováno v:
Science Advances
Description
The disease-associated protein CLN7 forms an organellar chloride channel and regulates lysosomal calcium signaling and function.
Neuronal ceroid lipofuscinoses (NCLs) are a group of autosomal recessive lysosomal storage diseases
The disease-associated protein CLN7 forms an organellar chloride channel and regulates lysosomal calcium signaling and function.
Neuronal ceroid lipofuscinoses (NCLs) are a group of autosomal recessive lysosomal storage diseases
Autor:
Dali Tong, Mei Zhang, Yunru Yang, Han Xia, Haiyang Tong, Huajun Zhang, Weihong Zeng, Muziying Liu, Yan Wu, Huan Ma, Xue Hu, Weiyong Liu, Yuan Cai, Yanfeng Yao, Yichuan Yao, Kunpeng Liu, Shifang Shan, Yajuan Li, Ge Gao, Weiwei Guo, Yun Peng, Shaohong Chen, Juhong Rao, Jiaxuan Zhao, Juan Min, Qingjun Zhu, Yanmin Zheng, Lianxin Liu, Chao Shan, Kai Zhong, Zilong Qiu, Tengchuan Jin, Sandra Chiu, Zhiming Yuan, Tian Xue
Coronavirus disease 2019 (COVID-19), which is triggered by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, continues to threaten global public health. Developing a vaccine that only requires single immunization but provides lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b86927ea53cbe41c7beee02ce680ae3e
https://doi.org/10.1101/2021.05.19.444881
https://doi.org/10.1101/2021.05.19.444881
Autor:
Huan Zhao, Yichuan Yao, Weiping Xu, Tasneem Akhtar, Haohuan Xie, Yuan Cai, Ling-Yun Li, Kai Zhong, Tian Xue, Yonghao Gu, J. Chen, Jin Bao, Mei Zhang, Kai Dong
Publikováno v:
Stem cells (Dayton, Ohio)REFERENCES. 39(7)
Retinal organoids (ROs) derived from human inducible pluripotent stem cells (hiPSCs) exhibit considerable therapeutic potential. However, current quality control of ROs during in vitro differentiation is largely limited to the detection of molecular
Autor:
Yonghao Gu, Xintian Hu, Wenchao Wang, Yuqian Ma, Yun Wang, Mei Zhang, Yunqin Li, Zilong Qiu, Kai Dong, Min Hu, Yuan Cai, Tian Xue, Yingzhou Hu, Min Wei, Shouzhen Li, Huan Zhao, Yichuan Yao, Jin Bao
Retinitis pigmentosa (RP) is a form of inherited retinal degenerative disease that ultimately involves the macula, which is present in primates but not in the rodents. Therefore, creating nonhuman primate (NHP) models of RP is of critical importance
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54c49cb9bf1433ec211a0e1ede2c8bcc
https://doi.org/10.1101/2020.07.29.226787
https://doi.org/10.1101/2020.07.29.226787
Autor:
Yichuan Yao, Huan Zhao, Zilong Qiu, Yuan Cai, Tian Xue, Mei Zhang, Ling-Yun Li, Jin Bao, Xiao Li, Tian-Lin Cheng, Yuqian Ma
Publikováno v:
Science Advances
An HDR-based Cas9/RecA system was developed to precisely correct the Pde6b mutation in rods of rd1 mice to restore their vision.
Although Cas9-mediated genome editing has been widely used to engineer alleles in animal models of human inherited d
Although Cas9-mediated genome editing has been widely used to engineer alleles in animal models of human inherited d