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Zhonghua Xin Xue Guan Bing Za Zhi|October 18, 2017
[CD137 induces vascular muscle cells phenotype transformation through activating nuclear factor of activated T-cells 1 signaling]W Zhong, B Li, J Liu, et al.Journal of Dental Research|February 4, 2022
BMSC-Derived ApoEVs Promote Craniofacial Bone Repair via ROS/JNK SignalingM Li, X Xing, H Huang, et al.International Journal of Cancer|June 17, 1999
Expression of mucin 1 (MUC1) in esophageal squamous-cell carcinoma: its relationship with prognosisM Sagara, S Yonezawa, K Nagata, et al.Molecular Genetics and Metabolism|February 13, 2001
Glycoconjugate metabolism in a cystic fibrosis knockout mouse modelC Mailleau, A Paul, M Colin, et al.Cell Death & Disease|September 14, 2013
Overexpression of 4EBP1, p70S6K, Akt1 or Akt2 differentially promotes Coxsackievirus B3-induced apoptosis in HeLa cellsX Li, Z Li, W Zhou, et al.Brazilian Journal of Biology = Revista Brasleira De Biologia|March 23, 2022
A comprehensive review on the documented characteristics of four Reticulitermes termites (Rhinotermitidae, Blattodea) of ChinaZ Khan, M S Khan, S Bawazeer, et al.Journal of Applied Microbiology|November 12, 2019
Diversity of sugarcane root-associated endophytic Bacillus and their activities in enhancing plant growthZ Wang, Z-X Yu, M K Solanki, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 23, 2019
Predicting the intervention threshold for initiating osteoporosis treatment among postmenopausal women in China: a cost-effectiveness analysis based on real-world dataL Cui, T He, Y Jiang, et al.Veterinary Immunology and Immunopathology|July 10, 1998
Oxidised mannan antigen conjugates preferentially stimulate T1 type immune responsesI F McKenzie, V Apostolopoulos, C Lees, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 10, 2018
Novel compound heterozygous mutations in SERPINH1 cause rare autosomal recessive osteogenesis imperfecta type XY Song, D Zhao, X Xu, et al.Pageof 1,235