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2. Structures of active-state orexin receptor 2 rationalize peptide and small-molecule agonist recognition and receptor activation

5. Integration of Affinity Selection–Mass Spectrometry and Functional Cell-Based Assays to Rapidly Triage Druggable Target Space within the NF-κB Pathway

6. Structural characterization of nonactive site, TrkA-selective kinase inhibitors

11. Characterization of non-active site TrkA selective kinase inhibitors and implications on obtaining kinase selectivity

12. Structural basis for selectivity and diversity in angiotensin II receptors

13. Insights into activity and inhibition from the crystal structure of human O-GlcNAcase

14. Structural characterization of nonactive site, TrkA-selective kinase inhibitors

15. Structural characterization of nonactive site, TrkA-selective kinase inhibitors.

16. Expression, purification and crystallization of human prolylcarboxypeptidase

17. Structural definition and substrate specificity of the S28 protease family: the crystal structure of human prolylcarboxypeptidase

18. Potent 2-[(pyrimidin-4-yl)amine}-1,3-thiazole-5-carbonitrile-based inhibitors of VEGFR-2 (KDR) kinase

19. Potent N-(1,3-Thiazol-2-yl)pyridin-2-amine Vascular Endothelial Growth Factor Receptor Tyrosine Kinase Inhibitors with Excellent Pharmacokinetics and Low Affinity for the hERG Ion Channel

21. Structural definition and substrate specificity of theS28 protease family: the crystal structure of humanprolylcarboxypeptidase.

22. Structural characterization of M8C10, a neutralizing antibody targeting a highly conserved prefusion-specific epitope on the metapneumovirus fusion trimerization interface.

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