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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, Vol. 67, No. 2, 04.2015, p. 338-67.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Hamann, J, Aust, G, Araç, D, Engel, FB, Formstone, C, Fredriksson, R, Hall, RA, Harty, BL, Kirchhoff, C, Knapp, B, Krishnan, A, Liebscher, I, Lin, H-H, Martinelli, DC, Monk, KR, Peeters, MC, Piao, X, Prömel, S, Schöneberg, T, Schwartz, TW, Singer, K, Stacey, M, Ushkaryov, YA, Vallon, M, Wolfrum, U, Wright, MW, Xu, L, Langenhan, T & Schiöth, HB 2015, 'International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors', PHARMACOL RES, vol. 67, no. 2, pp. 338-67. https://doi.org/10.1124/pr.114.009647

APA

Hamann, J., Aust, G., Araç, D., Engel, F. B., Formstone, C., Fredriksson, R., Hall, R. A., Harty, B. L., Kirchhoff, C., Knapp, B., Krishnan, A., Liebscher, I., Lin, H-H., Martinelli, D. C., Monk, K. R., Peeters, M. C., Piao, X., Prömel, S., Schöneberg, T., ... Schiöth, H. B. (2015). International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors. PHARMACOL RES, 67(2), 338-67. https://doi.org/10.1124/pr.114.009647

Vancouver

Hamann J, Aust G, Araç D, Engel FB, Formstone C, Fredriksson R et al. International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors. PHARMACOL RES. 2015 Apr;67(2):338-67. https://doi.org/10.1124/pr.114.009647

Bibtex

@article{cd38f63cd51a4fc69f62a7e6abf8cf1f,
title = "International Union of Basic and Clinical Pharmacology. XCIV. Adhesion G protein-coupled receptors",
abstract = "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.",
keywords = "Animals, Cell Adhesion, Cell Adhesion Molecules, Cell Membrane, Cell Movement, Cyclic AMP, Humans, International Agencies, Ligands, Models, Molecular, Pharmacology, Pharmacology, Clinical, Protein Isoforms, Receptors, G-Protein-Coupled, Second Messenger Systems, Signal Transduction, Societies, Scientific, Terminology as Topic",
author = "J{\"o}rg Hamann and Gabriela Aust and Demet Ara{\c c} and Engel, {Felix B} and Caroline Formstone and Robert Fredriksson and Hall, {Randy A} and Harty, {Breanne L} and Christiane Kirchhoff and Barbara Knapp and Arunkumar Krishnan and Ines Liebscher and Hsi-Hsien Lin and Martinelli, {David C} and Monk, {Kelly R} and Peeters, {Miriam C} and Xianhua Piao and Simone Pr{\"o}mel and Torsten Sch{\"o}neberg and Schwartz, {Thue W} and Kathleen Singer and Martin Stacey and Ushkaryov, {Yuri A} and Mario Vallon and Uwe Wolfrum and Wright, {Mathew W} and Lei Xu and Tobias Langenhan and Schi{\"o}th, {Helgi B}",
note = "Copyright {\textcopyright} 2015 by The American Society for Pharmacology and Experimental Therapeutics.",
year = "2015",
month = apr,
doi = "10.1124/pr.114.009647",
language = "English",
volume = "67",
pages = "338--67",
journal = "PHARMACOL RES",
issn = "1043-6618",
publisher = "Academic Press Inc.",
number = "2",

}

RIS

TY - JOUR

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 -