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1 eaching applications in drug development and molecular pharmacology.
2 nflicting data from available structures and molecular pharmacology.
3 3 therapies, but little is known about their 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 major goal in the field of neuroscience and molecular pharmacology.
7 ted quinoline drugs may have quite different molecular pharmacology.
8 grate large databases on gene expression and molecular pharmacology.
9 he article by Cassel et al. in this issue of Molecular Pharmacology, address this question and demons
11 tribution by Micheva et al. in this issue of Molecular Pharmacology adds to our understanding of the
12 erential binding to a given target, detailed molecular pharmacology analysis accurately predicts util
16 pose that precise determinations of GHSR(1a) molecular pharmacology and pathway-specific physiologica
17 detection will facilitate exploration of the molecular pharmacology and plasticity of exocytosis at m
18 aging will facilitate the exploration of the molecular pharmacology and plasticity of exocytosis at M
19 techniques to foster understanding of A(1)AR molecular pharmacology and signaling in living cells.
20 optogenetics, whole-cell electrophysiology, molecular pharmacology and single cell RT-PCR in mice.
23 coma research, including molecular genetics, molecular pharmacology, and the search for novel antigla
30 -atomic resolution and have great promise in molecular pharmacology, especially in the context of map
31 cular switches all contribute to the complex molecular pharmacology exhibited by mGlu receptor allost
35 effectors through heterotrimeric G-proteins, molecular pharmacology has probed the basic organization
49 s has provided new insights into the complex molecular pharmacology of 17AAG and suggested new genes
50 that underscores the need to understand the molecular pharmacology of a compound's activity, includi
51 and adds significant new knowledge about the molecular pharmacology of a diverse range of clinically
53 tool for unraveling the cellular biology and molecular pharmacology of both naturally occurring and s
56 Our results improve understanding of the molecular pharmacology of CCR5 and help further elucidat
57 dition to providing useful insights into the molecular pharmacology of CYC202 in human cancer cells,
59 re we describe the discovery, synthesis, and molecular pharmacology of delta-opioid receptor-selectiv
60 will highlight how our understanding of the molecular pharmacology of ER ligands has been utilized i
61 ng could provide valuable information on the molecular pharmacology of established and novel drugs.
63 tform (SyncroPatch 768PE) to investigate the molecular pharmacology of GS-967 and eleclazine on peak
69 ur work provides important insights into the molecular pharmacology of NCC and a blueprint for develo
70 yrosine residues differentially affected the molecular pharmacology of orthosteric and allosteric lig
73 re useful pharmacological tools to probe the molecular pharmacology of the delta receptor and to expl
74 10 years, and consider our knowledge of the molecular pharmacology of the drug in the context of cli
76 t the most extensive characterization of the molecular pharmacology of the most widely used CB2R liga
77 marizing the common and unique chemistry and molecular pharmacology of the six FDA-approved siRNA the
81 information necessary for understanding the molecular pharmacology of this receptor, thus underlinin
93 d synthetic neuroactive steroid analogs with molecular pharmacology similar to allopregnanolone (SGE-
96 on two articles in the October 2015 issue of Molecular Pharmacology that investigate the role of mu-o
98 rmacology and Experimental Therapeutics, and Molecular Pharmacology These revisions relate to data an
99 true to the original goals for the journal, Molecular Pharmacology today remains an outstanding venu
100 s Perspective, former and current editors of Molecular Pharmacology, together with the guest editors
103 Collectively, the newly characterized FPR2 molecular pharmacology will facilitate the design of mor
105 to hTA1 structure and function, contrast its molecular pharmacology with that of related receptors, a