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The Lancet. Respiratory Medicine|May 20, 2023
Safety and immunogenicity of heterologous boosting with orally aerosolised or intramuscular Ad5-nCoV vaccine and homologous boosting with inactivated vaccines (BBIBP-CorV or CoronaVac) in children and adolescents: a randomised, open-label, parallel-controlled, non-inferiority, single-centre studyTao Huang, Sheng Zhang, De-Fang Dai, et al.Genome Medicine|November 8, 2024
Exploring multi-omics and clinical characteristics linked to accelerated biological aging in Asian women of reproductive age: insights from the S-PRESTO studyLi Chen, Karen Mei-Ling Tan, Jia Xu, et al.European Urology|October 23, 2022
FGFR3 Mutational Activation Can Induce Luminal-like Papillary Bladder Tumor Formation and Favors a Male Sex BiasMing-Jun Shi, Jacqueline Fontugne, Aura Moreno-Vega, et al.Journal of Global Health|July 3, 2026
Folate and global health review series, part 4: syntheses on folate and autoimmune diseases and skeletal outcomesSamantha Yoo, Azita Montazeri, Derrick Bennett, et al.Ebiomedicine|April 11, 2025
Molecular heterogeneity of CD30+ peripheral T-cell lymphoma with prognostic significance and therapeutic implications: a retrospective multi-centre studyYu-Jia Huo, Shu Cheng, Hong-Mei Yi, et al.Journal of Global Health|January 30, 2026
Folate and global health umbrella review series, part 1: methodological framework and syntheses on anaemia and neural tube defectsSamantha Yoo, Azita Montazeri, Derrick Bennett, et al.Clinical and Translational Medicine|March 7, 2023
p16INK4A flow cytometry of exfoliated cervical cells: Its role in quantitative pathology and clinical diagnosis of squamous intraepithelial lesionsYifeng He, Jun Shi, Hui Zhao, et al.Journal of Global Health|February 20, 2026
Folate and global health umbrella review series, part 2: syntheses on cancersSamantha Yoo, Azita Montazeri, Derrick Bennett, et al.Journal of Human Genetics|July 11, 2014
No association between Y chromosomal haplogroups and severe acne in the Han Chinese populationMei-Hua Guo, Wen-Juan Wu, Long Fan, et al.Nature Genetics|July 20, 2004
Mutations in EFHC1 cause juvenile myoclonic epilepsyToshimitsu Suzuki, Antonio V Delgado-Escueta, Kripamoy Aguan, et al.Pageof 191