161 results on '"Betzi S"'
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2. SYNJ2BP complex with a synthetic Vangl2 peptide (3mer).
3. Crystal structure of dCK C4S-S74E mutant in complex with UDP and the OR0274 inhibitor
4. Crystal structure of dCK C4S-S74E mutant in complex with UDP and the OR0642 inhibitor
5. Crystal structure of dCK C4S-S74E mutant in complex with UDP and the dCKi1 inhibitor
6. Le projet parental à l’épreuve du médical : parcours de soins en AMP et expériences vécues de l’infertilité en France en 2020
7. Bromodomain-containing 2 BD2 in complex with the inhibitor CRCM5484
8. Inhibiting Type VI Secretion System Activity with a Biomimetic Peptide Designed To Target the Baseplate Wedge Complex
9. P–509 Patients’ Uses and Experiences of Medically-Assisted Reproduction in France in 2020
10. Pharmacological inhibition of syntenin PDZ2 domain impairs breast cancer cell activities and exosome loading with syndecan and EpCAM cargo
11. FIRST DOMAIN OF HUMAN BROMODOMAIN BRD4 IN COMPLEX WITH INHIBITOR F1
12. FIRST DOMAIN OF HUMAN BROMODOMAIN BRD4 IN COMPLEX WITH INHIBITOR #17
13. Crystal structure of dCK mutant C3S
14. Crystal structure of dCK mutant C3S in complex with masitinib and UDP
15. Crystal structure of dCK mutant C3S in complex with imatinib and UDP
16. Crystal Structure of GRASP Domain of GRASP55 with N terminal extra residues
17. Crystal Structure of GRASP55 GRASP domain in complex with JAM-C C-terminus
18. Crystal Structure of GRASP55 GRASP domain in complex with JAM-B C-terminus
19. Accelerating small compounds discovery targeting protein-protein interaction
20. FIRST DOMAIN OF HUMAN BROMODOMAIN BRD4 IN COMPLEX WITH INHIBITOR N-{3-[4-(3-chlorophenyl)piperazin-1-yl]propyl}-1-{3-methyl-[1,2,4]triazolo[4,3-b]pyridazin-6-yl}piperidine-4-carboxamide
21. FIRST DOMAIN OF HUMAN BROMODOMAIN BRD4 IN COMPLEX WITH INHIBITOR 4-[(1-methyl-2-oxo-1,2-dihydroquinolin-4-yl)oxy]-N-({1-[(3-methylphe methyl]piperidin-4-yl}methyl)butanamide
22. FIRST DOMAIN OF HUMAN BROMODOMAIN BRD4 IN COMPLEX WITH INHIBITOR 3-Butyl-8-(6-butyl-5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-ylsulfanylmethyl)-7-ethyl-3,7-dihydropurine-2,6-dione
23. FIRST DOMAIN OF HUMAN BROMODOMAIN BRD4 IN COMPLEX WITH INHIBITOR 3-(4-Chlorobenzyl)-7-ethyl-3,7-dihydropurine-2,6-dione
24. First domain of human bromodomain BRD4 in complex with inhibitor 8-(5-Amino-1H-[1,2,4]triazol-3-ylsulfanylmethyl)-3-(4-chlorobenzyl)-7-ethyl-3,7-dihydropurine-2,6-dione
25. E. cloacae C115D MurA in complex with UDP
26. CDK2 in complex with inhibitor RC-3-89
27. CDK2 in complex with inhibitor L4-14
28. CDK2 in complex with inhibitor RC-2-88
29. CDK2 in complex with inhibitor RC-2-38
30. CDK2 in complex with inhibitor RC-2-40
31. CDK2 in complex with inhibitor RC-2-23
32. CDK2 in complex with inhibitor RC-1-136
33. CDK2 in complex with inhibitor RC-2-12
34. CDK2 in complex with inhibitor RC-2-72
35. CDK2 in complex with inhibitor RC-3-96
36. CDK2 in complex with inhibitor L4
37. CDK2 in complex with inhibitor KVR-1-84
38. CDK2 in complex with inhibitor JWS-6-260
39. CDK2 in complex with inhibitor KVR-1-150
40. CDK2 in complex with inhibitor JWS-6-76
41. CDK2 in complex with inhibitor KVR-1-9
42. CDK2 in complex with inhibitor KVR-2-88
43. CDK2 in complex with inhibitor NSK-MC2-55
44. CDK2 in complex with inhibitor KVR-1-67
45. CDK2 in complex with inhibitor L3-3
46. CDK2 in complex with inhibitor KVR-1-74
47. CDK2 in complex with inhibitor KVR-2-92
48. CDK2 in complex with inhibitor JWS-6-52
49. CDK2 in complex with inhibitor NSK-MC1-12
50. CDK2 in complex with inhibitor L2-2
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