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Cited by 1,079

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

GABAB receptors function as a heteromeric assembly of the subunits GABABR1 and GABABR2

Jones, Kenneth A., Borowsky, Beth, Tamm, Joe A., Craig, Douglas A., Durkin, Margaret M., Dai, Meng, Yao, Wen-Jeng, Johnson, Mary, Gunwaldsen, Caryn, Huang, Ling-Yan, Tang, Cheng, Shen, Quanrong, Salon, John A., Morse, Kelley, Laz, Thomas, Smith, Kelli E., Nagarathnam, Dhanapalan, Noble, Stewart A., Branchek, Theresa A., Gerald, Christophe·1998·Nature
DOI 10.1038/25348
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Research works printed but not linked: 29

  1. Bowery, N. G. GABABreceptor pharmacology. Annu. Rev. Pharmacol. Toxicol. 33, 109–147 (1993). · DOI · Paper page
  2. Kaupmann, K.et al. Expression cloning of GABABreceptors uncovers similarity to metabotropic gutamate receptors. Nature 386, 239–246 (1997). · DOI · Paper page
  3. Hebert, T. E.et al. Apeptide derived from a beta2-adrenergic receptor transmembrane domain inhibits both receptor dimerization and activation. J. Biol. Chem. 271, 16384–16392 (1996). · DOI · Paper page
  4. Cvejic, S. & Devi, L. A. Dimerization of the delta opioid receptor: implication for a role in receptor internalization. J. Biol. Chem. 272, 26959–26964 (1997). · DOI · Paper page
  5. Maggio, R., Barbier, P., Fornai, F. & Corsini, G. U. Functional role of the third cytoplasmic loop in muscarinic receptor dimerization. J. Biol. Chem. 271, 31055–31060 (1996). · DOI
  6. Ciruela, F.et al. Immunological identification of A1 adenosine receptors in brain cortex. J. Neurosci. Res. 42, 818–828 (1995). · doi:10.1002/jnr.490420610
  7. Romano, C., Yang, W. L. & O'Malley, K. L. Metabotropic glutamate receptor 5 is a disulfide-linked dimer. J. Biol. Chem. 271, 28612–18616 (1996). · DOI · Paper page
  8. O'Hara, P. J.et al. The ligand-binding domain in metabotropic glutamate receptors is related to bacterial periplasmic binding proteins. Neuron 11, 41–52 (1998). · DOI · Paper page
  9. Bowery, N. G., Hudson, A. L. & Price, G. W. GABAAand GABABreceptor site distribution in the rat central nervous system. Neuroscience 20, 365–383 (1987). · DOI · Paper page
  10. North, R. A. Drug receptors and the inhibition of nerve cells. Br. J. Pharmacol. 98, 13–23 (1989). · DOI · Paper page
  11. Gahwiler, B. H. & Brown, D. A. GABAB-receptor-activated K+ current in voltage-clamped CA3 pyramidal cells in hippocampal cultures. Proc. Natl Acad. Sci. USA 82, 1558–1562 (1985). · DOI · Paper page
  12. Andrade, R., Malenka, R. C. & Nicoll, R. A. AG protein couples serotonin and GABABreceptors to the same channels in hippocampus. Science 234, 1261–1265 (1986). · DOI · Paper page
  13. Luscher, C., Jan, L. Y., Stoffel, M., Malenka, R. C. & Nicoll, R. A. Gprotein-coupled inwardly rectifying K+ channels (GIRKs) mediate postsynaptic but not presynaptic transmitter actions in hippocampal neurons. Neuron 19, 687–697 (1997). · DOI · Paper page
  14. Dascal, N.et al. Atrial G protein-activated K+ channel: expression cloning and molecular properties. Proc. Natl Acad. Sci. USA 90, 10235–10239 (1993). · DOI · Paper page
  15. Krapivinsky, G.et al. The G-protein-gated atrial K channel IKAChis a heteromultimer of two inwardly rectifying K channel proteins. Nature 374, 135–141 (1995). · DOI · Paper page
  16. Kubo, Y., Reuveney, E., Slesinger, P. A., Jan, Y. N. & Jan, L. Y. Primary structure and functional expression of a rat G-protein-coupled muscarinic potassium channel. Nature 364, 802–806 (1993). · DOI · Paper page
  17. Kaupmann, K.et al. Structure, pharmacology and chromosomal localization of GABA-B receptors. Soc. Neurosci. Abstr. 23, 954 (1997).
  18. Habert-Ortoli, E., Amiranoff, B., Loquet, I., Laburthe, M. & Mayaux, J. F. Molecular cloning of a functional human galanin receptor. Proc. Natl Acad. Sci. USA 91, 9780–9783 (1994). · DOI · Paper page
  19. Bon, C. & Galvan, M. Electrophysiological actions of GABABagonists and antagonists in rat dorso-lateral septal neurones in vitro. Br. J. Pharmacol. 118, 961–967 (1996). · DOI
  20. Seabrook, G. R., Howson, W. & Lacey, M. G. Electrophysiological characterization of potent agonists and antagonists at pre- and postsynaptic GABABreceptors on neurones in rat brain slices. Br. J. Pharmacol. 101, 949–957 (1990). · DOI
  21. Brugger, F., Wicki, U., Olpe, H. R., Froestl, W. & Mickel, S. The action of new potent GABABreceptor angtagonists in the hemisected spinal cord preparation of the rat. Eur. J. Pharmacol. 235, 153–155 (1993). · DOI
  22. Avissar, S., Amitai, G. & Sokolovsky, M. Oligomeric structure of muscarinic receptors is shown by photoaffinity labeling: subunit assembly may explain high- and low-affinity agonist states. Proc. Natl Acad. Sci. USA 80, 156–159 (1983). · doi:10.1073/pnas.80.1.156
  23. Wreggett, K. A. & Wells, J. W. Cooperativity manifest in the binding properties of purified cardiac muscarinic receptors. J. Biol. Chem. 270, 22488–22499 (1995). · DOI · Paper page
  24. Nimchinsky, E. A., Hof, P. R., Janssen, W. G. M., Morrison, J. H. & Schmauss, C. Expression of dopamine D3 receptor dimers and tetramers in brain and in transfected cells. J. Biol. Chem. 272, 29229–29237 (1998). · DOI · Paper page
  25. Smith, K. E.et al. Cloned human and rat galanin GALR3 receptors: pharmacology and activation of G-protein inwardly rectifying K+ channels. J. Cell Biol. 273, 23321–23326 (1998).
  26. Durkin, M. M.et al. Localization of messenger RNAs encoding three GABA transporters in rat brain: an in situ hybridization study. Brain Res. Mol. Brain Res. 33, 7–21 (1995). · DOI · Paper page
  27. Quick, M. W. & Lester, H. A. Methods for expression of excitability proteins in Xenopus oocytes. Methods Neurosci. 19, 261–279 (1994). · DOI
  28. Salon, J. A. & Owicki, J. C. Real-time measurements of receptor activity: applications of microphysiometric techniques to receptor biology. Methods Neurosci. 25, 201–233 (1995). · doi:10.1016/s1043-9471(05)80041-2
  29. Graham, J. in Centrifugation (The Practical Approach Series) (ed. Rickwood, D.) 161–182 (IRL, Oxford, 1984).

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Metadata

Authors
Jones, K. A., Borowsky, B., Tamm, J. A., Craig, D. A., Durkin, M. M., Dai, M., Yao, W.-J., Johnson, M., Gunwaldsen, C., Huang, L.-Y., Tang, C., Shen, Q., Salon, J. A., Morse, K., Laz, T., Smith, K. E., Nagarathnam, D., Noble, S. A., Branchek, T. A., & Gerald, C.
Venue
Nature
Publisher
Springer Science and Business Media LLC
Published
1998-12
Volume
396
Issue
6712
Pages
674-679
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
DOI
10.1038/25348
OpenAlex
W2110469184
Cited by
1,079
References
1
FWCI
24.87
Type
journal article
Language
en
Open access
closed
Licence
www.springer.com/tdm (tdm)

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CoChat. (2026). Citation check: GABAB receptors function as a heteromeric assembly of the subunits GABABR1 and GABABR2. https://app.cochat.ai/papers/10.1038/25348
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Jones, K. A., Borowsky, B., Tamm, J. A., Craig, D. A., Durkin, M. M., Dai, M., Yao, W.-J., Johnson, M., Gunwaldsen, C., Huang, L.-Y., Tang, C., Shen, Q., Salon, J. A., Morse, K., Laz, T., Smith, K. E., Nagarathnam, D., Noble, S. A., Branchek, T. A., & Gerald, C. (1998). GABAB receptors function as a heteromeric assembly of the subunits GABABR1 and GABABR2. Nature. https://doi.org/10.1038/25348

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.