Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor - Wikidata - awgldk - TriplyDB

Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

http://www.wikidata.org/entity/Q28472395

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Minireview: complexity of hematopoietic stem cell regulation in the bone marrow microenvironment Optogenetic and Chemogenetic Approaches for Studying Astrocytes and Gliotransmitters Engineering GPCR signaling pathways with RASSLs Regulation of amyloid precursor protein processing by serotonin signaling An siRNA screen in pancreatic beta cells reveals a role for Gpr27 in insulin production Astrocytic adenosine receptor A2A and Gs-coupled signaling regulate memory.Ligand-mediated activation of an engineered gs g protein-coupled receptor in osteoblasts increases trabecular bone formation Remote control of neuronal signaling.Mineral composition is altered by osteoblast expression of an engineered G(s)-coupled receptor Gs G protein-coupled receptor signaling in osteoblasts elicits age-dependent effects on bone formation.Constitutive Gs activation using a single-construct tetracycline-inducible expression system in embryonic stem cells and mice.Activated Gs signaling in osteoblastic cells alters the hematopoietic stem cell niche in mice.A hybrid structural approach to analyze ligand binding by the serotonin type 4 receptor (5-HT4).Engineered GPCRs as tools to modulate signal transduction.Engineered G-protein Coupled Receptors are Powerful Tools to Investigate Biological Processes and Behaviors.Light- and drug-activated G-protein-coupled receptors to control intracellular signalling.Employing novel animal models in the design of clinically efficacious GPCR ligands.Silencing Neurons: Tools, Applications, and Experimental Constraints.Developing chemical genetic approaches to explore G protein-coupled receptor function: validation of the use of a receptor activated solely by synthetic ligand (RASSL).G protein activation by serotonin type 4 receptor dimers: evidence that turning on two protomers is more efficient.Characterization of three vasopressin receptor 2 variants: an apparent polymorphism (V266A) and two loss-of-function mutations (R181C and M311V)Loss of Gi G-Protein-Coupled Receptor Signaling in Osteoblasts Accelerates Bone Fracture Healing.

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P2860

Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

http://www.wikidata.org/entity/Q28472395

description

2007 nî lūn-bûn

@nan

2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2007年の論文

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2007年論文

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2007年論文

@zh-hant

2007年論文

@zh-hk

2007年論文

@zh-mo

2007年論文

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2007年论文

@wuu

name

Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

@ast

Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

@en

Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

@nl

type

label

Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

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Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

@en

Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

@nl

prefLabel

Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

@ast

Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

@en

Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

@nl

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Modifying ligand-induced and constitutive signaling of the human 5-HT4 receptor

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Bruce R Conklin

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

Edward C Hsiao

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Jennifer K Ng

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Lucie Pellissier

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Sylvie Claeysen

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Trieu Nguyen

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

Wei Chun Chang

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P2860

Functional Selectivity and Classical Concepts of Quantitative Pharmacology

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

Functional selectivity of dopamine D1 receptor agonists in regulating the fate of internalized receptors

Engineered G protein coupled receptors reveal independent regulation of internalization, desensitization and acute signaling

Molecular, pharmacological and functional diversity of 5-HT receptors

Characterization of serotonin(4) receptors in adrenocortical aldosterone-producing adenomas: in vivo and in vitro studies

Constitutively active mutants of 5-HT4 receptors are they in unique active states?

Classifying G-protein coupled receptors with support vector machines

The G-protein-coupled receptors in the human genome form five main families. Phylogenetic analysis, paralogon groups, and fingerprints

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