المؤلفون: M'Kadmi, Céline, Leyris, Jean-Philippe, Onfroy, Lauriane, Galés, Céline, Saulière, Aude, Gagne, Didier, Damian, Marjorie, Mary, Sophie, Maingot, Mathieu, Denoyelle, Séverine, Verdié, Pascal, Fehrentz, Jean-Alain, Martinez, Jean, Baneres, Jean-Louis, Marie, Jacky

المساهمون: Institut des Biomolécules Max Mousseron Pôle Chimie Balard (IBMM), Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), Institut des Neurosciences de Montpellier (INM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Centre Hospitalier Régional Universitaire Montpellier (CHRU Montpellier), Institut des Maladies Métaboliques et Cardiovasculaires (I2MC), Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)

المصدر: ISSN: 0021-9258.

مصطلحات موضوعية: G protein-coupled receptor (GPCR), bioluminescence resonance energy transfer (BRET), cell signaling, ghrelin, hormone receptor, signaling bias, GHS-R1a, growth hormone secretagogue receptor type 1a, GH, growth hormone, GPCR, G protein-coupled receptor, IP1, inositol 1-phosphate, SRE, serum-responsive element, BRET, bioluminescence resonance energy transfer, HTRF, homogenous time resolved fluorescence, GTP␥S, guanosine 5Ј-O-(3-thiotriphosphate), ANOVA, analysis of variance, SPA, substance P analog, IP, inositol phosphate, G protein, G protein subtypes

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26363071; hal-03564155; https://hal.umontpellier.fr/hal-03564155Test; https://hal.umontpellier.fr/hal-03564155/documentTest; https://hal.umontpellier.fr/hal-03564155/file/1-s2.0-S0021925820494724-main.pdfTest; PUBMED: 26363071; PUBMEDCENTRAL: PMC4646384

الإتاحة: https://doi.org/10.1074/jbc.M115.659250Test
https://hal.umontpellier.fr/hal-03564155Test
https://hal.umontpellier.fr/hal-03564155/documentTest
https://hal.umontpellier.fr/hal-03564155/file/1-s2.0-S0021925820494724-main.pdfTest

المؤلفون: Hatakeyama, Masanori, Kawahara, Atsuo, Mori, Hisashi, Shibuya, Hiroshi, Taniguchi, Tadatsugu

المصدر: Proceedings of the National Academy of Sciences of the United States of America, 1992 Mar . 89(6), 2022-2026.

الوصول الحر: https://www.jstor.org/stable/2358635Test

المؤلفون: Xie, Y, Tan, E.-J, Wee, S, Manser, E, Lim, L, Koh, C.-G

المساهمون: DEPT OF PHARMACOLOGY

المصدر: Unpaywall 20201031

مصطلحات موضوعية: phosphatase, phosphatase POPX2, protein Cdc42, protein mDia1, Rac1 protein, Rho guanine nucleotide binding protein, RhoA guanine nucleotide binding protein, serum response factor, transcription factor, unclassified drug, actin polymerization, article, cell adhesion, cell motility, controlled study, cytoskeleton, human, human cell, priority journal, protein analysis, protein binding, protein function, protein protein interaction, serum responsive element, stress fiber, transcription regulation, Animals, Biological Transport, Carrier Proteins, Immunoprecipitation

العلاقة: Xie, Y, Tan, E.-J, Wee, S, Manser, E, Lim, L, Koh, C.-G (2008). Functional interactions between phosphatase POPX2 and mDia modulate RhoA pathways. Journal of Cell Science 121 (4) : 514-521. ScholarBank@NUS Repository. https://doi.org/10.1242/jcs.013557Test; https://scholarbank.nus.edu.sg/handle/10635/181025Test

الإتاحة: https://doi.org/10.1242/jcs.013557Test
https://scholarbank.nus.edu.sg/handle/10635/181025Test

المؤلفون: Jean-Louis Banères, Lauriane Onfroy, Jean-Philippe Leyris, Mathieu Maingot, Pascal Verdié, Jean Martinez, Aude Saulière, Céline Galés, Marjorie Damian, Jean-Alain Fehrentz, Céline M'Kadmi, Didier Gagne, Séverine Denoyelle, Jacky Marie, Sophie Mary

المساهمون: Institut des Biomolécules Max Mousseron [Pôle Chimie Balard] (IBMM), Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie du CNRS (INC)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), Institut des Neurosciences de Montpellier (INM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Institut des Maladies Métaboliques et Cardiovasculaires (I2MC), Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Universitaire de Toulouse (CHU Toulouse), Herrada, Anthony

المصدر: Journal of Biological Chemistry
Journal of Biological Chemistry, 2015, 290 (45), pp.27021-27039. ⟨10.1074/jbc.M115.659250⟩

مصطلحات موضوعية: MESH: Signal Transduction, Arrestins, Pharmacology, MESH: Drug Design, Ligands, Biochemistry, GHS-R1a, homogenous time resolved fluorescence, MESH: Receptors, Ghrelin, GPCR, MESH: Structure-Activity Relationship, [CHIM] Chemical Sciences, MESH: Ligands, Receptor, Receptors, Ghrelin, beta-Arrestins, bioluminescence resonance energy transfer (BRET), ANOVA, MESH: Kinetics, GTP␥S, Growth hormone secretion, GH, MESH: GTP-Binding Protein alpha Subunits, Gq-G11, ghrelin, MESH: HEK293 Cells, signaling bias, bioluminescence resonance energy transfer, SRE, MESH: Arrestins, Signal transduction, HTRF, hormones, hormone substitutes, and hormone antagonists, Signal Transduction, serum-responsive element, Cell signaling, analysis of variance, MESH: GTP-Binding Proteins, inositol phosphate, G protein, MAP Kinase Signaling System, Inositol Phosphates, G protein-coupled receptor (GPCR), G protein subtypes, Biology, Structure-Activity Relationship, GTP-binding protein regulators, MESH: beta-Arrestins, GTP-Binding Proteins, guanosine 5Ј-O-(3-thiotriphosphate), mental disorders, Arrestin, Inverse agonist, Humans, cell signaling, [CHIM]Chemical Sciences, G protein-coupled receptor, Molecular Biology, substance P analog, growth hormone secretagogue receptor type 1a, MESH: Humans, MESH: MAP Kinase Signaling System, IP1, Cell Biology, hormone receptor, MESH: Inositol Phosphates, Kinetics, HEK293 Cells, inositol 1-phosphate, Drug Design, IP, growth hormone, GTP-Binding Protein alpha Subunits, Gq-G11, BRET, SPA

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c4d0d6af27d5751b836d84dcea5c49eTest
https://hal.umontpellier.fr/hal-03564155/documentTest

المؤلفون: Elsy Edouard, Sonia Do Carmo, Louis-Charles Levros, Philippe Legault, Eric Rassart, Cyndia Charfi

المصدر: Biochimica et Biophysica Acta. Molecular Cell Research

مصطلحات موضوعية: Apolipoprotein D, APEX-1, Poly (ADP-Ribose) Polymerase-1, Kif4, Kinesin family member 4, GRE, Glucocorticoid responsive element, Mice, 0302 clinical medicine, Gene expression, Ifi204, Interferon-inducible protein 204, IFI204, DNA-(Apurinic or Apyrimidinic Site) Lyase, EBS, Ets-Binding site, EMSA, Electrophoretic Mobility Shift Assay, Nuclear protein, Promoter Regions, Genetic, CBF-A, CArG-box Binding Factor A (CBF-A), Regulation of gene expression, Mitogen-Activated Protein Kinase 1, 0303 health sciences, Gene knockdown, Mitogen-Activated Protein Kinase 3, ERK1/2, Cell Cycle, Nuclear Proteins, Poly(ADP-ribose) Polymerases, Rbp1, Ribosome-binding protein 1, DNA binding proteins, SRE, Serum responsive element, HnRNP, Heterogeneous nuclear ribonucleoprotein, Cellular stress, PARP-1, Cell Growth Processes, Biology, DNA-binding protein, Catalysis, Article, Parp-1, Poly(ADP-ribose) polymerase-1, 03 medical and health sciences, Enzyme activator, BUB-3, Budding Uninhibited by Benzimidazole 3, Animals, Humans, Electrophoretic mobility shift assay, Apolipoproteins D, Molecular Biology, 030304 developmental biology, Glycoproteins, Kif4, Apolipoprotein D (apoD), Membrane Transport Proteins, Cell Biology, Molecular biology, Enzyme Activation, apoD, apolipoprotein D, Gene Expression Regulation, Growth arrest, NIH 3T3 Cells, BUB-3, KifC1, Kinesin family member C1, HnRNP-U, 030217 neurology & neurosurgery, Transcription Factors, APEX-1, Apurinic/Apyrimidinic Endonuclease-1

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04d0f54ed8bbfc8144901d32b212164eTest

المؤلفون: Marc Lipinski, Laura Magnaghi-Jaulin, Hiroshi Masutani, Annick Harel-Bellan

المصدر: FEBS Letters. (3):247-251

مصطلحات موضوعية: Serum Response Factor, DNA, Complementary, Blotting, Western, Molecular Sequence Data, Restriction Mapping, Biophysics, Biology, Biochemistry, Cell Line, Structural Biology, Serum responsive element, Proto-Oncogene Proteins, Serum response factor, Tumor Cells, Cultured, Genetics, Transcriptional regulation, Humans, RNA, Messenger, ets-Domain Protein Elk-4, Northern blot, Molecular Biology, Gene, Transcription factor, ets-Domain Protein Elk-1, ELK-1, Base Sequence, SAP-1, Nuclear Proteins, RNA, Cell Biology, Serum responsive factor, Blotting, Northern, Molecular biology, DNA-Binding Proteins, Blot, Cell culture, Electrophoresis, Polyacrylamide Gel, HeLa Cells, Transcription Factors

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::215c07b0a1430fbd7e8e4ea45708b4d7Test