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Human Molecular Genetics|July 28, 2025
Long-read sequencing for NF1 gene analysis: enhancing diagnostic accuracy for Neurofibromatosis type 1Yu Zheng, Miaomiao Chen, Shuju Zhang, et al.
Oral Diseases|September 4, 2024
Parameters to assess the necessity of adjuvant therapy for early-stage oral squamous cell carcinomaHsueh-Ju Lu, Yu-Wei Chiu, Chih-Yu Peng, et al.
Epigenomics|July 17, 2023
The role of EZH2 in ocular diseases: a narrative reviewYu Peng, Christine Ht Bui, Xiu J Zhang, et al.
Organic Letters|June 18, 2026
A Photoacid-Assisted Ag(I)-Catalyzed Glycosylation Based on <i>ortho</i>-Methoxycarbonylethynylphenyl ThioglycosidesJing-Dong Zhang, Yu-Peng Yuan, Jiang-Cheng Wu, et al.
Parkinsonism & Related Disorders|December 8, 2022
Free water imaging as a novel biomarker in Wilson's disease: A cross-sectional studyXiao-Zhong Jing, Gai-Ying Li, Yu-Peng Wu, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|January 20, 2016
[Psychomotor retardation and intermitent convulsions for 8 months in an infant]Yuan Ding, Xi-Yuan Li, Yu-Peng Liu, et al.
Journal of Medical Genetics|March 19, 2016
AKAP2 identified as a novel gene mutated in a Chinese family with adolescent idiopathic scoliosisWei Li, YaWei Li, Lusi Zhang, et al.
International Immunopharmacology|December 13, 2024
Efficacy and safety of anti-CD19 CAR-T in a mouse model of IgG4-related diseaseYeting Sun, Sicheng Huang, Bo Zhang, et al.
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