Pages that link to "Q43834622"
Jump to navigation
Jump to search
The following pages link to Identification of a novel chemical potentiator and inhibitors of UCH-L1 by in silico drug screening (Q43834622):
Displaying 10 items.
- The co-crystal structure of ubiquitin carboxy-terminal hydrolase L1 (UCHL1) with a tripeptide fluoromethyl ketone (Z-VAE(OMe)-FMK) (Q27679250) (← links)
- Identification of novel potential antibiotics for tuberculosis by in silico structure-based drug screening (Q31002197) (← links)
- Balancing act: deubiquitinating enzymes in the nervous system (Q35353963) (← links)
- An Effective Method to Identify Shared Pathways and Common Factors among Neurodegenerative Diseases (Q35843631) (← links)
- New targeted approaches against the ubiquitin–proteasome system in gastrointestinal malignancies (Q38002469) (← links)
- Deubiquitylating enzymes and DNA damage response pathways (Q38109871) (← links)
- Recent Advances in the Discovery of Deubiquitinating Enzyme Inhibitors (Q38725385) (← links)
- Isopeptidases in anticancer therapy: looking for inhibitors. (Q41466923) (← links)
- Inhibition of UCH-L1 Deubiquitinating Activity with Two Forms of LDN-57444 Has Anti-Invasive Effects in Metastatic Carcinoma Cells (Q92343428) (← links)
- Ubiquitin Carboxyl-Terminal Hydrolase L1 (UCHL1) Promotes Uterine Serous Cancer Cell Proliferation and Cell Cycle Progression (Q92447312) (← links)