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1 eaching applications in drug development and molecular pharmacology.
2 major goal in the field of neuroscience and molecular pharmacology.
3 ted quinoline drugs may have quite different molecular pharmacology.
4 m conflicting data in crystal structures and molecular pharmacology.
5 ignpost for an era spanning over 40 years in molecular pharmacology.
6 grate large databases on gene expression and molecular pharmacology.
7 he article by Cassel et al. in this issue of Molecular Pharmacology, address this question and demons
9 tribution by Micheva et al. in this issue of Molecular Pharmacology adds to our understanding of the
10 erential binding to a given target, detailed molecular pharmacology analysis accurately predicts util
13 detection will facilitate exploration of the molecular pharmacology and plasticity of exocytosis at m
14 aging will facilitate the exploration of the molecular pharmacology and plasticity of exocytosis at M
15 optogenetics, whole-cell electrophysiology, molecular pharmacology and single cell RT-PCR in mice.
17 coma research, including molecular genetics, molecular pharmacology, and the search for novel antigla
23 -atomic resolution and have great promise in molecular pharmacology, especially in the context of map
24 cular switches all contribute to the complex molecular pharmacology exhibited by mGlu receptor allost
28 effectors through heterotrimeric G-proteins, molecular pharmacology has probed the basic organization
42 s has provided new insights into the complex molecular pharmacology of 17AAG and suggested new genes
43 that underscores the need to understand the molecular pharmacology of a compound's activity, includi
45 tool for unraveling the cellular biology and molecular pharmacology of both naturally occurring and s
47 dition to providing useful insights into the molecular pharmacology of CYC202 in human cancer cells,
49 re we describe the discovery, synthesis, and molecular pharmacology of delta-opioid receptor-selectiv
50 will highlight how our understanding of the molecular pharmacology of ER ligands has been utilized i
51 ng could provide valuable information on the molecular pharmacology of established and novel drugs.
57 re useful pharmacological tools to probe the molecular pharmacology of the delta receptor and to expl
58 10 years, and consider our knowledge of the molecular pharmacology of the drug in the context of cli
59 t the most extensive characterization of the molecular pharmacology of the most widely used CB2R liga
62 information necessary for understanding the molecular pharmacology of this receptor, thus underlinin
74 on two articles in the October 2015 issue of Molecular Pharmacology that investigate the role of mu-o
76 true to the original goals for the journal, Molecular Pharmacology today remains an outstanding venu
77 s Perspective, former and current editors of Molecular Pharmacology, together with the guest editors
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