Showing results (291-300 of 319) with videos related to
Sort By:
Pageof 32
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 18, 2016
A cryptic balanced translocation involving COL1A2 gene disruption cause a rare type of osteogenesis imperfectaXiao-Jie Xu, Fang Lv, Yi Liu, et al.Journal of Human Genetics|February 26, 2016
Two novel mutations in TMEM38B result in rare autosomal recessive osteogenesis imperfectaFang Lv, Xiao-Jie Xu, Jian-Yi Wang, et al.Nutrition Research and Practice|April 18, 2014
Beneficial effects of natural Jeju groundwaters on lipid metabolism in high-fat diet-induced hyperlipidemic ratsYan-Chao Wang, Jin-Miao Lu, Hui-Zi Jin, et al.Journal of Human Genetics|October 21, 2016
Novel mutations in FKBP10 in Chinese patients with osteogenesis imperfecta and their treatment with zoledronic acidXiao-Jie Xu, Fang Lv, Yi Liu, et al.Journal of Experimental & Clinical Cancer Research : CR|August 23, 2015
Intermittent high dose proton pump inhibitor enhances the antitumor effects of chemotherapy in metastatic breast cancerBi-Yun Wang, Jian Zhang, Jia-Lei Wang, et al.The Oncologist|May 31, 2024
Phase 2 study of pegylated liposomal doxorubicin plus cyclophosphamide, vincristine/vindesine, and prednisone in newly diagnosed PTCL: 8-year resultsZu-Guang Xia, Fang-Fang Lv, Qun-Ling Zhang, et al.Journal of Ethnopharmacology|December 18, 2022
Similarities and differences between Ziqin and Kuqin in anti-inflammatory, analgesic, and antioxidant activities and their core chemical composition based on the zebrafish model and spectrum-effect relationshipSiqi Sun, Axiang Yu, Ruiyang Cheng, et al.Diabetes|March 20, 2023
A Comparison of Daily Glucose Fluctuation Between GCK-MODY and Type 2 Diabetes Using Continuous Glucose Monitoring TechnologyQian Ren, Ping Zhang, Wuyan Pang, et al.Biochemical Pharmacology|June 7, 2024
ITFG2, an immune-modulatory protein, targets ATP 5b to maintain mitochondrial function in myocardial infarctionFang-Fang Bi, Miao Cao, Qing-Ming Pan, et al.Calcified Tissue International|November 1, 2016
Novel Mutations in SERPINF1 Result in Rare Osteogenesis Imperfecta Type VIJian-Yi Wang, Yi Liu, Li-Jie Song, et al.Pageof 32