232 results on '"Park, HaJeung"'
Search Results
2. High throughput screening for SARS-CoV-2 helicase inhibitors
3. CAR directs T cell adaptation to bile acids in the small intestine
4. Evaluation of novel pyrazol-4-yl pyridine derivatives possessing arylsulfonamide tethers as c-Jun N-terminal kinase (JNK) inhibitors in leukemia cells
5. A more efficient CRISPR-Cas12a variant derived from Lachnospiraceae bacterium MA2020
6. Functional implication of the homotrimeric multidomain vacuolar sorting receptor 1 (VSR1) fromArabidopsis thaliana
7. Site-Selective Antibody Functionalization via Orthogonally Reactive Arginine and Lysine Residues
8. Potent and selective antitumor activity of a T cell-engaging bispecific antibody targeting a membrane-proximal epitope of ROR1
9. Crystal Structure of a DNA Decamer Containing a Cis-Syn Thymine Dimer
10. Evaluation of Novel Pyrazol-4yl Pyridine Derivatives Possessing Arylsulfonamide Tethers as C-Jun N-Terminal Kinase (Jnk) Inhibitors in Leukemia Cells
11. Tumor-derived OBP2A promotes prostate cancer castration resistance
12. Crystal structure of the inactive state of the receiver domain of Spo0A from Paenisporosarcina sp. TG-14, a psychrophilic bacterium isolated from an Antarctic glacier
13. Crystal structure of dihydrodipicolinate reductase (PaDHDPR) from Paenisporosarcina sp. TG-14: structural basis for NADPH preference as a cofactor
14. Crystal structure and modeling of the tetrahedral intermediate state of methylmalonate-semialdehyde dehydrogenase (MMSDH) from Oceanimonas doudoroffii
15. Sculpting a Uniquely Reactive Cysteine Residue for Site-Specific Antibody Conjugation
16. Reprogramming of the heavy-chain CDR3 regions of a human antibody repertoire
17. N-Aromatic-Substituted Indazole Derivatives as Brain-Penetrant and Orally Bioavailable JNK3 Inhibitors
18. Efficient reprogramming of the heavy-chain CDR3 regions of a human antibody repertoire
19. Discovery and Optimization of Selective Inhibitors of Meprin α (Part II)
20. Discovery and Optimization of Selective Inhibitors of Meprin α (Part II)
21. Thiophene-Pyrazolourea Derivatives as Potent, Orally Bioavailable, and Isoform-Selective JNK3 Inhibitors
22. TonB interacts with nonreceptor proteins in the outer membrane of Escherichia coli
23. Structural insights into the psychrophilic germinal protease PaGPR and its autoinhibitory loop
24. A Simple and Efficient System for Producing Recombinant Human CXCL8 in Escherichia coli
25. CAR/Nr1i3 directs T cell adaptation to bile acids in the small intestine
26. Design, Optimization, and Study of Small Molecules That Target Tau Pre-mRNA and Affect Splicing
27. Affinity maturation, humanization, and co-crystallization of a rabbit anti-human ROR2 monoclonal antibody for therapeutic applications
28. Structural characterization of a peptoid-inspired conformationally constrained oligomer (PICCO) bound to streptavidin
29. Site-Specific Lysine Arylation as an Alternative Bioconjugation Strategy for Chemically Programmed Antibodies and Antibody–Drug Conjugates
30. Shigella IpaA Binding to Talin Stimulates Filopodial Capture and Cell Adhesion
31. Structural studies of Streptococcus pneumoniae EPSP synthase in unliganded state, tetrahedral intermediate-bound state and S3P-GLP-bound state
32. Crystal structure of the cytotoxic bacterial protein colicin B at 2.5 Å resolution
33. Crystal structures of pinoresinol-lariciresinol and phenylcoumaran benzylic ether reductases and their relationship to isoflavone reductases
34. Correction: HDX-MS reveals structural determinants for RORγ hyperactivation by synthetic agonists
35. HDX-MS reveals structural determinants for RORγ hyperactivation by synthetic agonists
36. Author response: HDX-MS reveals structural determinants for RORγ hyperactivation by synthetic agonists
37. HDX-MS reveals structural determinants for RORγ hyperactivation by synthetic agonists
38. Thiophene-Pyrazolourea Derivatives as Potent, Orally Bioavailable, and Isoform-Selective JNK3 Inhibitors.
39. Cell adhesion promoted by a unique Shigella IpaA vinculin- and talin-binding site
40. Bauerenol Acetate, the Pentacyclic Triterpenoid from Tabernaemontana longipes, is an Antitrypanosomal Agent
41. Potent and Selective Antitumor Activity of a T-Cell Engaging Bispecific Antibody Targeting a Membrane-Proximal Epitope of ROR1
42. Insights into signal transduction involving PAS domain oxygen-sensingheme proteins from the X-ray crystal structure of Escherichia coli dos heme domain
43. Controlled dehydration improves the diffraction quality of two RNA crystals
44. Amino acid derived quinazolines as Rock/PKA inhibitors
45. Correction to Design and Synthesis of Highly Potent and Isoform Selective JNK3 Inhibitors: SAR Studies on Aminopyrazole Derivatives
46. Corrigendum: A Toxic RNA Catalyzes the In Cellulo Synthesis of Its Own Inhibitor
47. Berichtigung: A Toxic RNA Catalyzes the In Cellulo Synthesis of Its Own Inhibitor
48. The synthesis and characterization of potential covalent probes for chronic lymphocytic leukemic B‐cell receptors using sulfonyl fluoride
49. Crystallographic and Computational Analyses of AUUCU Repeating RNA That Causes Spinocerebellar Ataxia Type 10 (SCA10)
50. Pharmacological repression of PPARγ promotes osteogenesis
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