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  Stable expression of cloned rat GABAA receptor subunits in a human kidney cell line

Hamilton, B. J., Lennon, D. J., Im, H. K., Im, W. B., Seeburg, P. H., & Carter, D. B. (1993). Stable expression of cloned rat GABAA receptor subunits in a human kidney cell line. Neuroscience Letters, 153(2), 206-209. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/7687050.

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Alternativer Titel : Stable expression of cloned rat GABAA receptor subunits in a human kidney cell line

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NeurosciLett_153_1993_206.pdf (beliebiger Volltext), 288KB
 
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http://doi.org/10.1016/0304-3940(93)90323-D (beliebiger Volltext)
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 Urheber:
Hamilton, B. J., Autor
Lennon, D. J., Autor
Im, H. K., Autor
Im, W. B., Autor
Seeburg, Peter H.1, Autor           
Carter, D. B., Autor
Affiliations:
1Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Max Planck Society, ou_1497704              

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 Zusammenfassung: A predominant form of the GABAA/benzodiazepine receptor-Cl- channel complex is believed to consist of three different 48-55 kDa subunits (alpha, beta, gamma) with unknown stoichiometry. Plasmids containing the rat GABAA receptor cDNAs coding for alpha 1, beta 2, and gamma 2 were co-transfected, along with a plasmid encoding G418 resistance, into human embryonic kidney cells previously transformed with Adenovirus 5 (HEK-293) [J. Gen. Virol., 36 (1977) 59-72]. Four percent of the G418 resistant colonies were found to express mRNA for all three of the GABAA subunits constitutively. A single cell clone derived from one of the alpha 1 beta 2 gamma 2 expressors has demonstrated stable electrophysiological characteristics over 25 passages. The GABA-activated Cl- current in this cell line is blocked by picrotoxin and bicuculline, and is modulated by a variety of agonist and inverse agonist ligands including diazepam, Ro 154513, zolpidem, and beta-CCE. The cell line has been used successfully over a 12-month period as a screen for novel drugs modulating GABA-mediated polarization of neuronal cells.

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Sprache(n): eng - English
 Datum: 1993-01-211992-05-111993-01-211993-04-30
 Publikationsstatus: Erschienen
 Seiten: 4
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: eDoc: 666787
URI: https://www.ncbi.nlm.nih.gov/pubmed/7687050
Anderer: 4052
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Titel: Neuroscience Letters
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Amsterdam : Elsevier
Seiten: - Band / Heft: 153 (2) Artikelnummer: - Start- / Endseite: 206 - 209 Identifikator: ISSN: 0304-3940
CoNE: https://pure.mpg.de/cone/journals/resource/954925512448