Pages that link to "Q27675402"
Jump to navigation
Jump to search
The following pages link to High-resolution crystal structure of human protease-activated receptor 1 (Q27675402):
Displaying 50 items.
- High-resolution structure of the human GPR40 receptor bound to allosteric agonist TAK-875 (Q24301044) (← links)
- Membrane potentials regulating GPCRs: insights from experiments and molecular dynamics simulations (Q26740438) (← links)
- G Protein-Coupled Receptors (GPCRs) in Alzheimer's Disease: A Focus on BACE1 Related GPCRs (Q26752403) (← links)
- Structural Studies of G Protein-Coupled Receptors (Q26783016) (← links)
- Post-expression strategies for structural investigations of membrane proteins (Q26849743) (← links)
- Unlocking the secrets of the gatekeeper: methods for stabilizing and crystallizing GPCRs (Q26852233) (← links)
- G-protein-coupled receptors signaling pathways in new antiplatelet drug development (Q26864951) (← links)
- Large-scale production and protein engineering of G protein-coupled receptors for structural studies (Q26866010) (← links)
- Structural biology of glycoprotein hormones and their receptors: insights to signaling (Q26991926) (← links)
- Fluorescent approaches for understanding interactions of ligands with G protein coupled receptors (Q27004213) (← links)
- Endogenous allosteric modulators of G protein-coupled receptors (Q27022831) (← links)
- Molecular modeling of the human P2Y14 receptor: A template for structure-based design of selective agonist ligands. (Q27325455) (← links)
- Precise Manipulation and Patterning of Protein Crystals for Macromolecular Crystallography Using Surface Acoustic Waves (Q27330322) (← links)
- Biophysical Fragment Screening of the β 1 -Adrenergic Receptor: Identification of High Affinity Arylpiperazine Leads Using Structure-Based Drug Design (Q27676919) (← links)
- Structure of the human smoothened receptor bound to an antitumour agent (Q27677951) (← links)
- Structure of signaling-competent neurotensin receptor 1 obtained by directed evolution in Escherichia coli (Q27681431) (← links)
- The 2.1 Å Resolution Structure of Cyanopindolol-Bound β1-Adrenoceptor Identifies an Intramembrane Na Ion that Stabilises the Ligand-Free Receptor (Q27682443) (← links)
- Structure of the human P2Y12 receptor in complex with an antithrombotic drug (Q27682517) (← links)
- Agonist-bound structure of the human P2Y12 receptor (Q27683598) (← links)
- Application of amphipols for structure-functional analysis of TRP channels (Q27690839) (← links)
- Structure-Based Sequence Alignment of the Transmembrane Domains of All Human GPCRs: Phylogenetic, Structural and Functional Implications (Q28551072) (← links)
- Sequence, structure and ligand binding evolution of rhodopsin-like G protein-coupled receptors: a crystal structure-based phylogenetic analysis (Q28649590) (← links)
- Serial femtosecond crystallography opens new avenues for Structural Biology. (Q30367012) (← links)
- The role of experimental and computational structural approaches in 7TM drug discovery. (Q30377191) (← links)
- The power of mass spectrometry in structural characterization of GPCR signaling. (Q30380212) (← links)
- Structure and function of serotonin G protein-coupled receptors. (Q30382524) (← links)
- Vibrational resonance, allostery, and activation in rhodopsin-like G protein-coupled receptors (Q30395265) (← links)
- Distinct activation modes of the Relaxin Family Peptide Receptor 2 in response to insulin-like peptide 3 and relaxin (Q33789816) (← links)
- Global fold of human cannabinoid type 2 receptor probed by solid-state 13C-, 15N-MAS NMR and molecular dynamics simulations (Q33809669) (← links)
- Allosteric sodium in class A GPCR signaling (Q33931569) (← links)
- Mechanistic insights into the allosteric modulation of opioid receptors by sodium ions (Q34041202) (← links)
- The recombinant expression systems for structure determination of eukaryotic membrane proteins (Q34090835) (← links)
- The platelet: life on the razor's edge between hemorrhage and thrombosis (Q34175105) (← links)
- Molecular signatures of G-protein-coupled receptors (Q34327700) (← links)
- Methods for recombinant expression and functional characterization of human cannabinoid receptor CB2. (Q34413054) (← links)
- Two disparate ligand-binding sites in the human P2Y1 receptor (Q34469331) (← links)
- Regulation of neutrophilic inflammation by proteinase-activated receptor 1 during bacterial pulmonary infection (Q34475362) (← links)
- Structural insights into µ-opioid receptor activation (Q34488374) (← links)
- Common variants in the human platelet PAR4 thrombin receptor alter platelet function and differ by race (Q34580117) (← links)
- Discovery of GPCR ligands for probing signal transduction pathways (Q34582707) (← links)
- Structure-based approaches to ligands for G-protein-coupled adenosine and P2Y receptors, from small molecules to nanoconjugates. (Q34676680) (← links)
- Development of a highly selective allosteric antagonist radioligand for the type 1 cholecystokinin receptor and elucidation of its molecular basis of binding (Q34785475) (← links)
- Proton transfer-mediated GPCR activation (Q34854983) (← links)
- Why we need many more G protein-coupled receptor structures (Q34981578) (← links)
- Thrombin promotes proliferation of human lung fibroblasts via protease activated receptor-1-dependent and NF-κB-independent pathways (Q35093428) (← links)
- Platelet specific promoters are insufficient to express protease activated receptor 1 (PAR1) transgene in mouse platelets (Q35168904) (← links)
- Peptide ligand recognition by G protein-coupled receptors (Q35179408) (← links)
- Parmodulins inhibit thrombus formation without inducing endothelial injury caused by vorapaxar (Q35197451) (← links)
- Distinct ETA receptor binding mode of macitentan as determined by site directed mutagenesis (Q35256194) (← links)
- GPCR crystallization using lipidic cubic phase technique (Q35271740) (← links)