Tricyclic antidepressants and mecamylamine bind to different sites in the human alpha4beta2 nicotinic receptor ion channel. (Q36160970)

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19 January 2020

title

Tricyclic antidepressants and mecamylamine bind to different sites in the human alpha4beta2 nicotinic receptor ion channel (English)

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Katarzyna M Targowska-Duda

19 January 2020

author

3

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19 January 2020

Krzysztof Jóźwiak

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19 January 2020

author name string

Hugo R Arias

1

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19 January 2020

Avraham Rosenberg

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19 January 2020

Dominik Feuerbach

4

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19 January 2020

Ruin Moaddel

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19 January 2020

Irving W Wainer

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publication date

17 March 2010

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International Journal of Biochemistry & Cell Biology

19 January 2020

published in

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19 January 2020

volume

42

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19 January 2020

issue

6

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19 January 2020

page(s)

1007-1018

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Different interaction between tricyclic antidepressants and mecamylamine with the human alpha3beta4 nicotinic acetylcholine receptor ion channel.

19 January 2020

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Study of the calcium dynamics of the human alpha4beta2, alpha3beta4 and alpha1beta1gammadelta nicotinic acetylcholine receptors

2 October 2017

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2 October 2017

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Nicotinic acetylcholine receptors as targets for antidepressants.

2 October 2017

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Analysis of mecamylamine stereoisomers on human nicotinic receptor subtypes

2 October 2017

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M2 mutations of the nicotinic acetylcholine receptor increase the potency of the non-competitive inhibitor phencyclidine

2 October 2017

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Unmasking the functions of the chromaffin cell alpha7 nicotinic receptor by using short pulses of acetylcholine and selective blockers.

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Differentiation of the open and closed states of the ionic channels of nicotinic acetylcholine receptors by tricyclic antidepressants

2 October 2017

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2 October 2017

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2 October 2017

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Probing the structure of the affinity-purified and lipid-reconstituted torpedo nicotinic acetylcholine receptor

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23 September 2018

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12 December 2020

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Inhibition of 22Na influx by tricyclic and tetracyclic antidepressants and binding of [3H]imipramine in bovine adrenal medullary cells

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Identification of the sites of incorporation of [3H]ethidium diazide within the Torpedo nicotinic acetylcholine receptor ion channel

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12 December 2020

Snake venom toxins, unlike smaller antagonists, appear to stabilize a resting state conformation of the nicotinic acetylcholine receptor

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10.1016/J.BIOCEL.2010.03.002

Identifiers

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release_g6txqcogfbhw3cvur3pe43x6ju

19 January 2020

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19 January 2020

PubMed publication ID

20223294

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