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S1PR1 serves as a viable drug target against pulmonary fibrosis by increasing the integrity of the endothelial barrier of the lung Journal article
Hao, Mengyao, Fu, Rong, Tai, Jun, Tian, Zhenhuan, Yuan, Xia, Chen, Yang, Wang, Mingjin, Jiang, Huimin, Ji, Ming, Lai, Fangfang, Xue, Nina, Bai, Liping, Zhu, Yizhun, Lv, Xiaoxi, Chen, Xiaoguang, Jin, Jing. S1PR1 serves as a viable drug target against pulmonary fibrosis by increasing the integrity of the endothelial barrier of the lung[J]. Acta Pharmaceutica Sinica B, 2022, 13(3), 1110-1127.
Authors:  Hao, Mengyao;  Fu, Rong;  Tai, Jun;  Tian, Zhenhuan;  Yuan, Xia; et al.
Favorite | TC[WOS]:3 TC[Scopus]:3  IF:14.7/14.1 | Submit date：2023/01/30
Endothelial Barrier  Fty720  Idiopathic Pulmonary Fibrosis  Immh002  Protein Stability  Sphingosine-1-phosphate Receptor 1  Sphingosine-1-phosphate Receptor 1 Agonist  Tight Junction  
Self-Trapped Excitons in 2D SnP2S6 Crystal with Intrinsic Structural Distortion Journal article
Yue Zhang, Fakun Wang, Xin Feng, Zheng Zhang, Kailang Liu, Fangfang Xia, Wenxi Liang, Xiaozong Hu, Ying Ma, Huiqiao Li, Guichuan Xing, Tianyou Zhai. Self-Trapped Excitons in 2D SnP2S6 Crystal with Intrinsic Structural Distortion[J]. ADVANCED FUNCTIONAL MATERIALS, 2022.
Authors:  Yue Zhang;  Fakun Wang;  Xin Feng;  Zheng Zhang;  Kailang Liu; et al.
Favorite | TC[WOS]:33 TC[Scopus]:29  IF:18.5/19.6 | Submit date：2022/08/05
2d Snp 2s 6 Crystals  Distroted Octahedrons  Electron-phonon Coupling  Optoelectronics  Self-trapped Excitons  
Dstyk mutation leads to congenital scoliosis-like vertebral malformations in zebrafish via dysregulated mTORC1/TFEB pathway Journal article
Sun,Xianding, Zhou,Yang, Zhang,Ruobin, Wang,Zuqiang, Xu,Meng, Zhang,Dali, Huang,Junlan, Luo,Fengtao, Li,Fangfang, Ni,Zhenhong, Zhou,Siru, Chen,Hangang, Chen,Shuai, Chen,Liang, Du,Xiaolan, Chen,Bo, Huang,Haiyang, Liu,Peng, Yin,Liangjun, Qiu,Juhui, Chen,Di, Deng,Chuxia, Xie,Yangli, Luo,Lingfei, Chen,Lin. Dstyk mutation leads to congenital scoliosis-like vertebral malformations in zebrafish via dysregulated mTORC1/TFEB pathway[J]. Nature Communications, 2020, 11(1), 479.
Authors:  Sun,Xianding;  Zhou,Yang;  Zhang,Ruobin;  Wang,Zuqiang;  Xu,Meng; et al.
Favorite | TC[WOS]:35 TC[Scopus]:39  IF:14.7/16.1 | Submit date：2020/09/16
Rmrp Mutation Disrupts Chondrogenesis and Bone Ossification in Zebrafish Model of Cartilage-Hair Hypoplasia via Enhanced Wnt/β-Catenin Signaling Journal article
Sun,Xianding, Zhang,Ruobin, Liu,Mi, Chen,Hangang, Chen,Liang, Luo,Fengtao, Zhang,Dali, Huang,Junlan, Li,Fangfang, Ni,Zhenhong, Qi,Huabing, Su,Nan, Jin,Min, Yang,Jing, Tan,Qiaoyan, Du,Xiaolan, Chen,Bo, Huang,Haiyang, Chen,Shuai, Yin,Liangjun, Xu,Xiaoling, Deng,Chuxia, Luo,Lingfei, Xie,Yangli, Chen,Lin. Rmrp Mutation Disrupts Chondrogenesis and Bone Ossification in Zebrafish Model of Cartilage-Hair Hypoplasia via Enhanced Wnt/β-Catenin Signaling[J]. Journal of Bone and Mineral Research, 2019, 34(11), 2101-2116.
Authors:  Sun,Xianding;  Zhang,Ruobin;  Liu,Mi;  Chen,Hangang;  Chen,Liang; et al.
Favorite | TC[WOS]:16 TC[Scopus]:19  IF:5.1/5.8 | Submit date：2020/09/16
Cartilage-hair Hypoplasia  Rmrp  Skeletal Development  Wnt/β-catenin  Zebrafish  Beta-catenin  
Adeno-Associated Virus-Mediated RNAi against Mutant Alleles Attenuates Abnormal Calvarial Phenotypes in an Apert Syndrome Mouse Model Journal article
Luo,Fengtao, Xie,Yangli, Wang,Zuqiang, Huang,Junlan, Tan,Qiaoyan, Sun,Xianding, Li,Fangfang, Li,Can, Liu,Mi, Zhang,Dali, Xu,Meng, Su,Nan, Ni,Zhenhong, Jiang,Wanling, Chang,Jinhong, Chen,Hangang, Chen,Shuai, Xu,Xiaoling, Deng,Chuxia, Wang,Zhugang, Du,Xiaolan, Chen,Lin. Adeno-Associated Virus-Mediated RNAi against Mutant Alleles Attenuates Abnormal Calvarial Phenotypes in an Apert Syndrome Mouse Model[J]. Molecular Therapy - Nucleic Acids, 2018, 13, 291-302.
Authors:  Luo,Fengtao;  Xie,Yangli;  Wang,Zuqiang;  Huang,Junlan;  Tan,Qiaoyan; et al.
Favorite | TC[WOS]:15 TC[Scopus]:15  IF:6.5/6.7 | Submit date：2020/09/16
Adeno-associated Virus  Apert Syndrome  Craniosynostosis  Fgfr2  Molecular Therapy  Rnai  
Postnatal deletion of Alk5 gene in meniscal cartilage accelerates age-dependent meniscal degeneration in mice Journal article
Wang,Quan, Tan,Qiaoyan, Xu,Wei, Kuang,Liang, Zhang,Bin, Wang,Zuqiang, Ni,Zhenhong, Su,Nan, Jin,Min, Li,Can, Jiang,Wanling, Huang,Junlan, Li,Fangfang, Zhu,Ying, Chen,Hangang, Du,Xiaolan, Chen,Di, Deng,Chuxia, Qi,Huabing, Xie,Yangli, Chen,Lin. Postnatal deletion of Alk5 gene in meniscal cartilage accelerates age-dependent meniscal degeneration in mice[J]. Journal of Cellular Physiology, 2018, 234(1), 595-605.
Authors:  Wang,Quan;  Tan,Qiaoyan;  Xu,Wei;  Kuang,Liang;  Zhang,Bin; et al.
Favorite | TC[WOS]:6 TC[Scopus]:5  IF:4.5/5.3 | Submit date：2020/09/16
Activing Receptor-like Kinases 5 (Alk5)  Matrix Degradation  Meniscal Degeneration  Transforming Growth Factor-β (Tgf-β) Signaling