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Journal Article
Molecular and Cellular Biology, ISSN 0270-7306, 04/2002, Volume 22, Issue 8, pp. 2871 - 2881
Journal Article
ELIFE, ISSN 2050-084X, 06/2019, Volume 8
Adgrg6 (Gpr126) is an adhesion class G protein-coupled receptor with a conserved role in myelination of the peripheral nervous system. In the zebrafish,... 
GPR56/ADGRG1 | IN-VITRO | INNER-EAR | REGENERATION | DISTINCT | BIOLOGY | PROTEIN-COUPLED RECEPTORS | EXTRACELLULAR-MATRIX | MECHANISMS | SCHWANN-CELLS | AGONIST | Gene expression | Myelin proteins | G proteins | G protein-coupled receptors | Schwann cells | Nervous system | Drug development | Embryos | Inner ear | Myelin basic protein | Morphogenesis | Proteins | Myelination | Alleles | Extracellular matrix | Software | Libraries | Versican
Journal Article
Biochemical Journal, ISSN 0264-6021, 09/2005, Volume 390, Issue 3, pp. 749 - 759
MSK (mitogen- and stress-activated protein kinase) 1 and MSK2 are kinases activated downstream of either the ERK (extracellular-signal-regulated kinase) 1/2 or... 
Nurr1 | Nur77 | p38 | Mitogen- and stress-activated protein kinase (MSK) | Nor1 | Extracellular-signal-regulated kinase (ERK) | mitogen-and stress-activated protein kinase (MSK) | NEGATIVE INHIBITOR | ACTIVATED PROTEIN-KINASE | STRESS-INDUCED PHOSPHORYLATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | ELEMENT-BINDING PROTEIN | NERVE GROWTH-FACTOR | extracellular-signal-regulated kinase (ERK) | MEMBRANE DEPOLARIZATION | NGFI-B | EMBRYONIC STEM-CELLS | GENE-EXPRESSION | NF-KAPPA-B | Tetradecanoylphorbol Acetate | Ribosomal Protein S6 Kinases - metabolism | Nuclear Receptor Subfamily 4, Group A, Member 1 | Nuclear Receptor Subfamily 4, Group A, Member 2 | MAP Kinase Signaling System | CREB-Binding Protein - metabolism | Mitogen-Activated Protein Kinase Kinases - metabolism | Ribosomal Protein S6 Kinases, 90-kDa - metabolism | Receptors, Thyroid Hormone - genetics | Fibroblasts | Transcription, Genetic | Promoter Regions, Genetic | Cells, Cultured | Receptors, Cytoplasmic and Nuclear - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Tumor Necrosis Factor-alpha | Epidermal Growth Factor | Mice, Knockout | Animals | Anisomycin | Receptors, Steroid - genetics | Ribosomal Protein S6 Kinases, 90-kDa - genetics | Mice | Ribosomal Protein S6 Kinases - genetics | TCR, T-cell receptor | AP-1, activator protein-1 | EGF, epidermal growth factor | NGFI-B, NGF-induced B factor | TNF, tumour necrosis factor α | NGF, nerve growth factor | CRE, cAMP response element | MEF2D, myocyte-enhancer-binding factor 2D | mitogen- and stress-activated protein kinase (MSK) | ATF1, activating transcription factor-1 | ERK, extracellular-signal-regulated kinase | PKI, PKA inhibitor | DMEM, Dulbecco's modified Eagle's medium | CREB, CRE-binding protein | MEF, murine embryonic fibroblast | NBRE, NGFI-B response element | MSK, mitogen- and stress-activated protein kinase | MAPK, mitogen-activated protein kinase | PKA, protein kinase A
Journal Article
Biochemical Journal, ISSN 0264-6021, 09/2005, Volume 390, Issue 3, pp. 749 - 759
Journal Article
Nature, ISSN 0028-0836, 05/2017, Volume 545, Issue 7652, pp. 112 - 115
Protease-activated receptors ( PARs) are a family of G-proteincoupled receptors ( GPCRs) that are irreversibly activated by proteolytic cleavage of the N... 
PHENIX | THROMBIN | CRYSTAL-STRUCTURE | MULTIDISCIPLINARY SCIENCES | Allosteric Regulation - drug effects | Benzyl Alcohols - chemistry | Allosteric Site - drug effects | Humans | Receptor, PAR-2 - metabolism | Imidazoles - chemistry | Models, Molecular | Crystallography, X-Ray | Antibodies, Blocking - pharmacology | Imidazoles - pharmacology | Benzimidazoles - chemistry | Receptor, PAR-2 - chemistry | Immunoglobulin Fab Fragments - pharmacology | Receptor, PAR-2 - antagonists & inhibitors | Signal Transduction - drug effects | Antibodies, Blocking - chemistry | Immunoglobulin Fab Fragments - chemistry | Benzyl Alcohols - pharmacology | Benzimidazoles - pharmacology | Ligands | Benzodioxoles - chemistry | Kinetics | Benzodioxoles - pharmacology | Physiological aspects | Cell receptors | Allosteric proteins | Cytochrome | Residues | G protein-coupled receptors | Peptides | Molecular structure | Hydrogen | Homology | Antagonists | Hydrophobicity | Hydrogen bonding | Optimization | Proteins | Lipophilic | Allosteric properties | Imidazole | Cleavage | Inhibition | Thromboembolism | Lysozyme | Hydrogen ion concentration | Deoxyribonucleic acid--DNA | Cultivation | Architecture | Fab | Crystals | Crystallization | Pharmacology | Inflammation | Glycosylation | Computer programs | Chemistry | Diffraction | Antagonist drugs | Lysine | Isoforms | Computer applications | Mutation | Internet | Receptor mechanisms | Binding sites | Glutamine | Cancer
Journal Article
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