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The Journal of Clinical Investigation|September 7, 2018
Targeted hypoxia reduction restores T cell infiltration and sensitizes prostate cancer to immunotherapyPriyamvada Jayaprakash, Midan Ai, Arthur Liu, et al.Journal of Medical Genetics|December 17, 2021
Ribosomal protein S6 kinase beta-1 gene variants cause hypertrophic cardiomyopathyPratul Kumar Jain, Shashank Jayappa, Thiagarajan Sairam, et al.European Journal of Medicinal Chemistry|March 15, 2025
A new potent and selective peroxisome proliferator-activated receptor alpha partial agonist displays anti-steatotic effects In vitro and behaves as a safe hypolipidemic and hypoglycemic agent in a diabetic mouse modelAntonio Laghezza, Emanuele Falbo, Federica Gilardi, et al.Nature Communications|June 27, 2023
Interspecies exciton interactions lead to enhanced nonlinearity of dipolar excitons and polaritons in MoS2 homobilayersCharalambos Louca, Armando Genco, Salvatore Chiavazzo, et al.Chest|March 16, 2026
Timely antibiotics and fluid resuscitation are associated with increased discharge to home after sepsisHallie C Prescott, Julien Weinstein, Sarah Seelye, et al.Environmental Technology & Innovation|June 28, 2022
Application of human RNase P normalization for the realistic estimation of SARS-CoV-2 viral load in wastewater: A perspective from Qatar wastewater surveillanceShimaa S El-Malah, Jayaprakash Saththasivam, Khadeeja Abdul Jabbar, et al.Journal of Medicinal Chemistry|June 28, 2021
Structure-Activity Relationship of para-Carborane Selective Estrogen Receptor β AgonistsDavid Sedlák, Tyler A Wilson, Werner Tjarks, et al.The New England Journal of Medicine|July 29, 2011
Protective effect of natural rotavirus infection in an Indian birth cohortBeryl P Gladstone, Sasirekha Ramani, Indrani Mukhopadhya, et al.Oral Oncology|December 12, 2017
Cancer stem cell and its niche in malignant progression of oral potentially malignant disordersSubin Surendran, Gangotri Siddappa, Amrutha Mohan, et al.Molecular Genetics and Metabolism|June 26, 2009
Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephalyErich Roessler, Wuhong Pei, Maia V Ouspenskaia, et al.Pageof 177