187 results on '"Szewczyk, Magdalena M."'
Search Results
2. Epigenetic vulnerabilities of leukemia harboring inactivating EZH2 mutations
3. Measuring Protein–Protein Interactions in Cells using Nanoluciferase Bioluminescence Resonance Energy Transfer (NanoBRET) Assay
4. PRMT inhibition induces a viral mimicry response in triple-negative breast cancer
5. Enzymatic nucleosome acetylation selectively affects activity of histone methyltransferases in vitro
6. PRMT5 regulates ATF4 transcript splicing and oxidative stress response
7. A chemical probe targeting the PWWP domain alters NSD2 nucleolar localization
8. Probing CRL4DCAF12 interactions with MAGEA3 and CCT5 di-Glu C-terminal degrons
9. Huntingtin structure is orchestrated by HAP40 and shows a polyglutamine expansion-specific interaction with exon 1
10. A new method for the purification of bioviable NEU1 sialidase for enzyme replacement therapy for sialidosis
11. Chemical tools for the Gid4 subunit of the human E3 ligase C-terminal to LisH (CTLH) degradation complex
12. Characterization of inv(3) cell line OCI-AML-20 with stroma-dependent CD34 expression
13. Epigenetic vulnerabilities of leukemia harboring inactivating EZH2 mutations
14. Sialidase down-regulation reduces non-HDL cholesterol, inhibits leukocyte transmigration, and attenuates atherosclerosis in ApoE knockout mice
15. Fragment-based discovery of a chemical probe for the PWWP1 domain of NSD3
16. Epigenetic vulnerabilities of leukemia harboring inactivating EZH2 mutations
17. Author Correction: Pharmacological inhibition of PRMT7 links arginine monomethylation to the cellular stress response
18. Pharmacological inhibition of PRMT7 links arginine monomethylation to the cellular stress response
19. Discovery and Characterization of a Chemical Probe Targeting the Zinc-Finger Ubiquitin-Binding Domain of HDAC6
20. Discovery of a chemical probe for PRDM9
21. Development of HC-258, a Covalent Acrylamide TEAD Inhibitor That Reduces Gene Expression and Cell Migration.
22. Discovery of Nanomolar DCAF1 Small Molecule Ligands
23. A chemical probe to modulate human GID4 Pro/N-degron interactions
24. Chemical tools for the Gid4 subunit of the human E3 ligase C-terminal to LisH (CTLH) degradation complexElectronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3md00633f
25. Validating Small Molecule Chemical Probes for Biological Discovery
26. Discovery of a Potent and Selective Targeted NSD2 Degrader for the Reduction of H3K36me2.
27. Caloxin 1b3: A novel plasma membrane Ca 2+-pump isoform 1 selective inhibitor that increases cytosolic Ca 2+ in endothelial cells
28. PRMT5 regulates ATF4 transcript splicing and oxidative stress response
29. A chemical probe targeting the PWWP domain alters NSD2 nucleolar localization
30. Quantitative Methods to Study Protein Arginine Methyltransferase 1-9 Activity in Cells
31. Development of LM98, a Small‐Molecule TEAD Inhibitor Derived from Flufenamic Acid
32. Caloxins: a novel class of selective plasma membrane Ca2+ pump inhibitors obtained using biotechnology
33. Huntingtin structure is orchestrated by HAP40 and shows a polyglutamine expansion-specific interaction with exon 1
34. Huntingtin structure is orchestrated by HAP40 and shows a polyglutamine expansion-specific interaction with exon 1
35. Aortic smooth muscle and endothelial plasma membrane [Ca.sup.2+] pump isoforms are inhibited differently by the extracellular inhibitor caloxin 1b1
36. Design, Synthesis, and Evaluation of WD-Repeat-Containing Protein 5 (WDR5) Degraders
37. HAP40 orchestrates huntingtin structure for differential interaction with polyglutamine expanded exon 1
38. Pharmacological targeting of a PWWP domain demonstrates cooperative control of NSD2 localization
39. A First-in-Class, Highly Selective and Cell-Active Allosteric Inhibitor of Protein Arginine Methyltransferase 6
40. Discovery of Small-Molecule Antagonists of the PWWP Domain of NSD2
41. A First-in-class, Highly Selective and Cell-active Allosteric Inhibitor of Protein Arginine Methyltransferase 6 (PRMT6)
42. Discovery of Small-Molecule Antagonists of the PWWP Domain of NSD2
43. Discovery of a First-in-Class Protein Arginine Methyltransferase 6 (PRMT6) Covalent Inhibitor
44. Functional effects of caloxin 1c2, a novel engineered selective inhibitor of plasma membrane Ca2+-pump isoform 4, on coronary artery
45. Ca2+-pumps and Na+–Ca2+-exchangers in coronary artery endothelium versus smooth muscle
46. Therapeutic Targeting of RNA Splicing Catalysis through Inhibition of Protein Arginine Methylation
47. Pharmacological inhibition of PRMT7 links arginine monomethylation to the cellular stress responses
48. Abstract 1646: Discovery and characterization of BAY-6035, a novel benzodiazepine-based SMYD3 inhibitor
49. LLY-283, a Potent and Selective Inhibitor of Arginine Methyltransferase 5, PRMT5, with Antitumor Activity
50. TP-064, a potent and selective small molecule inhibitor of PRMT4 for multiple myeloma
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.