Search

Your search keyword '"Mitschler, Andre"' showing total 136 results

Search Constraints

Start Over You searched for: Author "Mitschler, Andre" Remove constraint Author: "Mitschler, Andre"
136 results on '"Mitschler, Andre"'

Search Results

4. X-rays-Induced Cooperative Atomic Movement in a Protein Crystal

5. Structure of the E6/E6AP/p53 complex required for HPV-mediated degradation of p53

8. X-rays-Induced Cooperative Atomic Movement in a Protein Crystal

9. Structural adaptability in the ligand-binding pocket of the ecdysone hormone receptor

10. Transmembrane signaling across the ligand-gated FhuA receptor: crystal structures of free and ferrichrome-bound states reveal allosteric changes

12. Discovery of N-Substituted 3-Amino-4-(3-boronopropyl)pyrrolidine-3-carboxylic Acids as Highly Potent Third-Generation Inhibitors of Human Arginase I and II

13. Targeting Acidic Mammalian chitinase Is Effective in Animal Model of Asthma

14. Probing The Roles Of Two Tryptophans Surrounding The Unique Zinc Coordination Site In Lipase Family I.5

15. Targeting Acidic Mammalian chitinase Is Effective in Animal Model of Asthma

16. Discovery of N-Substituted 3-Amino-4-(3-boronopropyl)pyrrolidine-3-carboxylic Acids as Highly Potent Third-Generation Inhibitors of Human Arginase I and II

20. High resolution neutron and X-ray diffraction RT studies of an H-FABP – Oleic acid complex: study of the internal water cluster and the ligand binding by a transferred multipolar electron density distribution

23. Perdeuteration: Vital to visualising solvent in neutron crystallography?

24. Radiation-induced disorder of a protein crystal

25. Discovery of (R)-2-Amino-6-borono-2-(2-(piperidin-1-yl)ethyl)hexanoic Acid and Congeners As Highly Potent Inhibitors of Human Arginases I and II for Treatment of Myocardial Reperfusion Injury

26. Neutron structure of type-III antifreeze protein allows the reconstruction of AFP-ice interface

27. Neutron macromolecular crystallography with LADI-III

28. X-ray-induced deterioration of disulfide bridges at atomic resolution

32. Unusual Binding Mode of the 2S4R Stereoisomer of the Potent Aldose Reductase Cyclic Imide Inhibitor Fidarestat (2S4S) in the 15 K Crystal Structure of the Ternary Complex Refined at 0.78 Å Resolution: Implications for the Inhibition Mechanism

34. Factorizing Selectivity Determinants of Inhibitor Binding toward Aldose and Aldehyde Reductases: Structural and Thermodynamic Properties of the Aldose Reductase Mutant Leu300Pro−Fidarestat Complex

36. Discovery of 3-[(4,5,7-Trifluorobenzothiazol-2-yl)methyl]indole-N-acetic Acid (Lidorestat) and Congeners as Highly Potent and Selective Inhibitors of Aldose Reductase for Treatment of Chronic Diabetic Complications

37. High-Resolution Structures of Human Aldose Reductase Holoenzyme in Complex with Stereoisomers of the Potent Inhibitor Fidarestat: Stereospecific Interaction between the Enzyme and a Cyclic Imide Type Inhibitor

40. Ultrahigh resolution drug design. II. Atomic resolution structures of human aldose reductase holoenzyme complexed with fidarestat and minalrestat: Implications for the binding of cyclic imide inhibitors

41. X-ray crystallography at subatomic resolution

45. Discoveryof (R)-2-Amino-6-borono-2-(2-(piperidin-1-yl)ethyl)hexanoicAcid and Congeners As Highly Potent Inhibitors of Human ArginasesI and II for Treatment of Myocardial Reperfusion Injury.

Catalog

Books, media, physical & digital resources