Showing results (41-50 of 23,903) with videos related to
Sort By:
Pageof 2,391
Proceedings of the National Academy of Sciences of the United States of America|January 2, 2013
Histone deacetylase inhibitors increase glucocerebrosidase activity in Gaucher disease by modulation of molecular chaperonesChunzhang Yang, Shervin Rahimpour, Jie Lu, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 11, 2020
Therapeutic Targeting of SDHB-Mutated Pheochromocytoma/Paraganglioma with Pharmacologic Ascorbic AcidYang Liu, Ying Pang, Boqun Zhu, et al.Proceedings of the National Academy of Sciences of the United States of America|December 20, 2013
Celastrol increases glucocerebrosidase activity in Gaucher disease by modulating molecular chaperonesChunzhang Yang, Cody L Swallows, Chao Zhang, et al.Brain Research|March 3, 2011
Carbon dioxide influence on nitric oxide production in endothelial cells and astrocytes: cellular mechanismsAli R Fathi, Chunzhang Yang, Kamran D Bakhtian, et al.Nature Communications|February 7, 2025
D-2-hydroxyglutarate impairs DNA repair through epigenetic reprogrammingFengchao Lang, Karambir Kaur, Haiqing Fu, et al.Cancer Research|February 17, 2017
Chemosensitivity of IDH1-Mutated Gliomas Due to an Impairment in PARP1-Mediated DNA RepairYanxin Lu, Jakub Kwintkiewicz, Yang Liu, et al.Proceedings of the National Academy of Sciences of the United States of America|December 14, 2011
Histone deacetylase inhibitors prevent the degradation and restore the activity of glucocerebrosidase in Gaucher diseaseJie Lu, Chunzhang Yang, Masako Chen, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 17, 2023
Protein Kinase B (PKB/AKT) Protects IDH-Mutated Glioma from Ferroptosis via Nrf2Yang Liu, Fu-Ju Chou, Fengchao Lang, et al.Oncotarget|March 3, 2016
Hypotaurine evokes a malignant phenotype in glioma through aberrant hypoxic signalingPeng Gao, Chunzhang Yang, Cody L Nesvick, et al.Journal of Neurosurgery|April 1, 2014
De novo VHL germline mutation detected in a patient with mild clinical phenotype of von Hippel-Lindau diseaseXinghua Ding, Chao Zhang, Jason M Frerich, et al.Pageof 2,391