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Clinical & Experimental Optometry|May 29, 2024
16S rRNA sequencing in chronic dacryocystitisYongxin Zhang, Beian Liu, Meina Yang, et al.
Intractable & Rare Diseases Research|March 24, 2020
Health assessment of patients with achondroplasia, pseudoachondroplasia, and rickets based on 3D non-linear diagnosticsJian Zhang, Yanqin Lu, Yanzhou Wang, et al.
Journal of Colloid and Interface Science|January 8, 2022
Enzymatically functionalized RGD-gelatin scaffolds that recruit host mesenchymal stem cells in vivo and promote bone regenerationJunling Li, Yan Zhang, Xing Zhou, et al.
Intractable & Rare Diseases Research|March 20, 2018
Complex heterozygous WNT1 mutation in severe recessive osteogenesis imperfecta of a Chinese patientYanqin Lu, Yunzhang Dai, Yanzhou Wang, et al.
Intractable & Rare Diseases Research|March 24, 2020
Comprehensive bioinformatic analysis of Wnt1 and Wnt1-associated diseasesChuanming Peng, Yanqin Lu, Xiuzhi Ren, et al.
Intractable & Rare Diseases Research|September 1, 2021
Integrative overview of IFITMs family based on Bioinformatics analysisPengchao Liu, Yongtao Zhang, Shanshan Zhang, et al.
Advanced Healthcare Materials|January 24, 2025
TPMS-Gyroid Scaffold-Mediated Up-Regulation of ITGB1 for Enhanced Cell Adhesion and Immune-Modulatory OsteogenesisJing Wang, Zenan Huang, Zhenzhong Han, et al.
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