نتائج البحث - "Ee Von Moo"

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دورية أكاديمية

Rules and mechanisms governing G protein coupling selectivity of GPCRs

المؤلفون: Ikuo Masuho, Ryoji Kise, Pablo Gainza, Ee Von Moo, Xiaona Li, Ryosuke Tany, Hideko Wakasugi-Masuho, Bruno E. Correia, Kirill A. Martemyanov

المصدر: Cell Reports, Vol 42, Iss 10, Pp 113173- (2023)

مصطلحات موضوعية: CP: Cell biology, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2211124723011853; https://doaj.org/toc/2211-1247

URL الوصول: https://doaj.org/article/9dcef49af9894a03b9baf4ad1e758c40

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Delineation of the GPR15 receptor-mediated Gα protein signalling profile in recombinant mammalian cells

المؤلفون: Yufang Deng, Ee Von Moo, Claudia Victoria Pérez Almería, Patrick R. Gentry, Line Vedel, Jesper M. Mathiesen, Hans Bräuner‐Osborne

المساهمون: AIMMS, Medicinal chemistry

المصدر: Basic and Clinical Pharmacology and Toxicology, 131(2), 104-113. Wiley-Blackwell
Deng, Y, Moo, E V, Pérez Almería, C V, Gentry, P R, Vedel, L, Mathiesen, J M & Bräuner-Osborne, H 2022, ' Delineation of the GPR15 receptor-mediated Gα protein signalling profile in recombinant mammalian cells ', Basic and Clinical Pharmacology and Toxicology, vol. 131, no. 2, pp. 104-113 . https://doi.org/10.1111/bcpt.13738
Deng, Y, Moo, E V, Almería, C V P, Gentry, P R, Vedel, L, Mathiesen, J M & Bräuner-Osborne, H 2022, ' Delineation of the GPR15 receptor-mediated Gα protein signalling profile in recombinant mammalian cells ', Basic and Clinical Pharmacology and Toxicology, vol. 131, no. 2, pp. 104-113 . https://doi.org/10.1111/bcpt.13738

مصطلحات موضوعية: Mammals, Pharmacology, Gα protein, General Medicine, Toxicology, Receptors, G-Protein-Coupled, second messenger, Pertussis Toxin, SDG 3 - Good Health and Well-being, GTP-Binding Proteins, Animals, GPR15, BRET, signalling, Signal Transduction

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34653d98d74e3978578f3737bf61e97b
https://hdl.handle.net/1871.1/123ae551-44fd-47ff-8167-d15bad897b87

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Endocytic proteins mediating GPR15 receptor internalization provide insight into the underlying mechanisms

المؤلفون: Yufang Deng, Ee Von Moo, Asuka Inoue, Hans Bräuner‐Osborne

المصدر: Deng, Y, Von Moo, E, Inoue, A & Braeuner-Osborne, H 2023, ' Endocytic proteins mediating GPR15 receptor internalization provide insight into the underlying mechanisms ', FEBS Letters, vol. 597, no. 11, pp. 1528-1540 . https://doi.org/10.1002/1873-3468.14622

مصطلحات موضوعية: COUPLED RECEPTORS, Biophysics, Cell Biology, ADAPTER, AP-2, Biochemistry, GRKs, internalization, CAVEOLAE, CLATHRIN, Structural Biology, dynamin, Genetics, GPR15, caveolin, BETA-ARRESTINS, PHOSPHORYLATION, Molecular Biology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::250e66898784d48118ebe2ec5639e9d0
https://doi.org/10.1002/1873-3468.14622

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Migration mediated by the oxysterol receptor GPR183 depends on arrestin coupling but not receptor internalization

المؤلفون: Viktoria M. S. Kjær, Viktorija Daugvilaite, Tomasz M. Stepniewski, Christian M. Madsen, Astrid S. Jørgensen, Kaustubh R. Bhuskute, Asuka Inoue, Trond Ulven, Tau Benned-Jensen, Siv A. Hjorth, Gertrud M. Hjortø, Ee Von Moo, Jana Selent, Mette M. Rosenkilde

المصدر: Science Signaling. 16

مصطلحات موضوعية: Cell Biology, Molecular Biology, Biochemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::274d2a351b8b56396567f2da3b82dab5
https://doi.org/10.1126/scisignal.abl4283

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Arrestin-Dependent and -Independent Internalization of G Protein–Coupled Receptors: Methods, Mechanisms, and Implications on Cell Signaling

المؤلفون: Thor C. Møller, Ee Von Moo, Jeffrey R. van Senten, Hans Bräuner-Osborne

المصدر: Moo, E V, Van Senten, J R, Bräuner-osborne, H & Møller, T C 2021, ' Arrestin-Dependent and-Independent Internalization of G Protein–Coupled Receptors: Methods, Mechanisms, and Implications on Cell Signaling ', Molecular Pharmacology, vol. 99, no. 4, pp. 242-255 . https://doi.org/10.1124/molpharm.120.000192
Molecular Pharmacology