International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors
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International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors. / Hamann, Jörg; Aust, Gabriela; Araç, Demet; Engel, Felix B; Formstone, Caroline; Fredriksson, Robert; Hall, Randy A; Harty, Breanne L; Kirchhoff, Christiane; Knapp, Barbara; Krishnan, Arunkumar; Liebscher, Ines; Lin, Hsi-Hsien; Martinelli, David C; Monk, Kelly R; Peeters, Miriam C; Piao, Xianhua; Prömel, Simone; Schöneberg, Torsten; Schwartz, Thue W; Singer, Kathleen; Stacey, Martin; Ushkaryov, Yuri A; Vallon, Mario; Wolfrum, Uwe; Wright, Mathew W; Xu, Lei; Langenhan, Tobias; Schiöth, Helgi B.
in: PHARMACOL RES, Jahrgang 67, Nr. 2, 04.2015, S. 338-67.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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T1 - International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors
AU - Hamann, Jörg
AU - Aust, Gabriela
AU - Araç, Demet
AU - Engel, Felix B
AU - Formstone, Caroline
AU - Fredriksson, Robert
AU - Hall, Randy A
AU - Harty, Breanne L
AU - Kirchhoff, Christiane
AU - Knapp, Barbara
AU - Krishnan, Arunkumar
AU - Liebscher, Ines
AU - Lin, Hsi-Hsien
AU - Martinelli, David C
AU - Monk, Kelly R
AU - Peeters, Miriam C
AU - Piao, Xianhua
AU - Prömel, Simone
AU - Schöneberg, Torsten
AU - Schwartz, Thue W
AU - Singer, Kathleen
AU - Stacey, Martin
AU - Ushkaryov, Yuri A
AU - Vallon, Mario
AU - Wolfrum, Uwe
AU - Wright, Mathew W
AU - Xu, Lei
AU - Langenhan, Tobias
AU - Schiöth, Helgi B
N1 - Copyright © 2015 by The American Society for Pharmacology and Experimental Therapeutics.
PY - 2015/4
Y1 - 2015/4
N2 - The Adhesion family forms a large branch of the pharmacologically important superfamily of G protein-coupled receptors (GPCRs). As Adhesion GPCRs increasingly receive attention from a wide spectrum of biomedical fields, the Adhesion GPCR Consortium, together with the International Union of Basic and Clinical Pharmacology Committee on Receptor Nomenclature and Drug Classification, proposes a unified nomenclature for Adhesion GPCRs. The new names have ADGR as common dominator followed by a letter and a number to denote each subfamily and subtype, respectively. The new names, with old and alternative names within parentheses, are: ADGRA1 (GPR123), ADGRA2 (GPR124), ADGRA3 (GPR125), ADGRB1 (BAI1), ADGRB2 (BAI2), ADGRB3 (BAI3), ADGRC1 (CELSR1), ADGRC2 (CELSR2), ADGRC3 (CELSR3), ADGRD1 (GPR133), ADGRD2 (GPR144), ADGRE1 (EMR1, F4/80), ADGRE2 (EMR2), ADGRE3 (EMR3), ADGRE4 (EMR4), ADGRE5 (CD97), ADGRF1 (GPR110), ADGRF2 (GPR111), ADGRF3 (GPR113), ADGRF4 (GPR115), ADGRF5 (GPR116, Ig-Hepta), ADGRG1 (GPR56), ADGRG2 (GPR64, HE6), ADGRG3 (GPR97), ADGRG4 (GPR112), ADGRG5 (GPR114), ADGRG6 (GPR126), ADGRG7 (GPR128), ADGRL1 (latrophilin-1, CIRL-1, CL1), ADGRL2 (latrophilin-2, CIRL-2, CL2), ADGRL3 (latrophilin-3, CIRL-3, CL3), ADGRL4 (ELTD1, ETL), and ADGRV1 (VLGR1, GPR98). This review covers all major biologic aspects of Adhesion GPCRs, including evolutionary origins, interaction partners, signaling, expression, physiologic functions, and therapeutic potential.
AB - The Adhesion family forms a large branch of the pharmacologically important superfamily of G protein-coupled receptors (GPCRs). As Adhesion GPCRs increasingly receive attention from a wide spectrum of biomedical fields, the Adhesion GPCR Consortium, together with the International Union of Basic and Clinical Pharmacology Committee on Receptor Nomenclature and Drug Classification, proposes a unified nomenclature for Adhesion GPCRs. The new names have ADGR as common dominator followed by a letter and a number to denote each subfamily and subtype, respectively. The new names, with old and alternative names within parentheses, are: ADGRA1 (GPR123), ADGRA2 (GPR124), ADGRA3 (GPR125), ADGRB1 (BAI1), ADGRB2 (BAI2), ADGRB3 (BAI3), ADGRC1 (CELSR1), ADGRC2 (CELSR2), ADGRC3 (CELSR3), ADGRD1 (GPR133), ADGRD2 (GPR144), ADGRE1 (EMR1, F4/80), ADGRE2 (EMR2), ADGRE3 (EMR3), ADGRE4 (EMR4), ADGRE5 (CD97), ADGRF1 (GPR110), ADGRF2 (GPR111), ADGRF3 (GPR113), ADGRF4 (GPR115), ADGRF5 (GPR116, Ig-Hepta), ADGRG1 (GPR56), ADGRG2 (GPR64, HE6), ADGRG3 (GPR97), ADGRG4 (GPR112), ADGRG5 (GPR114), ADGRG6 (GPR126), ADGRG7 (GPR128), ADGRL1 (latrophilin-1, CIRL-1, CL1), ADGRL2 (latrophilin-2, CIRL-2, CL2), ADGRL3 (latrophilin-3, CIRL-3, CL3), ADGRL4 (ELTD1, ETL), and ADGRV1 (VLGR1, GPR98). This review covers all major biologic aspects of Adhesion GPCRs, including evolutionary origins, interaction partners, signaling, expression, physiologic functions, and therapeutic potential.
KW - Animals
KW - Cell Adhesion
KW - Cell Adhesion Molecules
KW - Cell Membrane
KW - Cell Movement
KW - Cyclic AMP
KW - Humans
KW - International Agencies
KW - Ligands
KW - Models, Molecular
KW - Pharmacology
KW - Pharmacology, Clinical
KW - Protein Isoforms
KW - Receptors, G-Protein-Coupled
KW - Second Messenger Systems
KW - Signal Transduction
KW - Societies, Scientific
KW - Terminology as Topic
U2 - 10.1124/pr.114.009647
DO - 10.1124/pr.114.009647
M3 - SCORING: Journal article
C2 - 25713288
VL - 67
SP - 338
EP - 367
JO - PHARMACOL RES
JF - PHARMACOL RES
SN - 1043-6618
IS - 2
ER -