Tuning up the right signal: chemical and genetic approaches to study GPCR functions. - Wikidata - awgldk - TriplyDB

Tuning up the right signal: chemical and genetic approaches to study GPCR functions.

Tuning up the right signal: chemical and genetic approaches to study GPCR functions.

http://www.wikidata.org/entity/Q38200334

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Peptidomics for the discovery and characterization of neuropeptides and hormones Orphan GPR110 (ADGRF1) targeted by N-docosahexaenoylethanolamine in development of neurons and cognitive function.Gs-DREADD Knock-In Mice for Tissue-Specific, Temporal Stimulation of Cyclic AMP Signaling Novobiocin and peptide analogs of α-factor are positive allosteric modulators of the yeast G protein-coupled receptor Ste2p.The first structure-activity relationship studies for designer receptors exclusively activated by designer drugs.New paradigms in GPCR drug discovery.The delivery of therapeutic oligonucleotides Fluorescent knock-in mice to decipher the physiopathological role of G protein-coupled receptors.Transmembrane Helix Assembly by Max-Min Ant System Algorithm.What can we learn from molecular dynamics simulations for GPCR drug design?Adenosine and Sleep.State-of-the-Art Techniques to Causally Link Neural Plasticity to Functional Recovery in Experimental Stroke Research.

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Tuning up the right signal: chemical and genetic approaches to study GPCR functions.

http://www.wikidata.org/entity/Q38200334

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article científic

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Tuning up the right signal: chemical and genetic approaches to study GPCR functions.

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Tuning up the right signal: chemical and genetic approaches to study GPCR functions.

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Tuning up the right signal: chemical and genetic approaches to study GPCR functions.

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J.CEB.2013.11.006

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Current Opinion in Cell Biology

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Tuning up the right signal: chemical and genetic approaches to study GPCR functions.

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Bryan L Roth

http://www.w3.org/2001/XMLSchema#string

Patrick M Giguere

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Wesley K Kroeze

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P2860

Functional Selectivity and Classical Concepts of Quantitative Pharmacology

Structures of the CXCR4 chemokine GPCR with small-molecule and cyclic peptide antagonists

Predicting new molecular targets for known drugs

Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand

Controlling signaling with a specifically designed Gi-coupled receptor

A Specific Cholesterol Binding Site Is Established by the 2.8 Å Structure of the Human β2-Adrenergic Receptor

Structural Basis for Molecular Recognition at Serotonin Receptors

Structural Features for Functional Selectivity at Serotonin Receptors

Allele-specific activation of genetically engineered receptors

How many drug targets are there?

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51-55

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scholarly article

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10.1016/J.CEB.2013.11.006

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27

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2013-12-08T00:00:00Z

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261219819

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24680430

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G protein-coupled receptor

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3971376

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