Antagonistic property of buprenorphine for putative epsilon-opioid receptor-mediated G-protein activation by beta-endorphin in pons/medulla of the mu-opioid receptor knockout mouse. (Q34159292)

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English	Antagonistic property of buprenorphine for putative epsilon-opioid receptor-mediated G-protein activation by beta-endorphin in pons/medulla of the mu-opioid receptor knockout mouse.	scientific article

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15 December 2019

Antagonistic property of buprenorphine for putative epsilon-opioid receptor-mediated G-protein activation by beta-endorphin in pons/medulla of the mu-opioid receptor knockout mouse (English)

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15 December 2019

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Frank Scott Hall

4

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15 December 2019

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H Mizoguchi

1

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15 December 2019

H-E Wu

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15 December 2019

M Narita

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15 December 2019

I Sora

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15 December 2019

G R Uhl

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15 December 2019

H Nagase

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15 December 2019

L F Tseng

8

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1 January 2002

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15 December 2019

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15 December 2019

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15 December 2019

3

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15 December 2019

715-721

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15 December 2019

The role of amino-terminal sequence of beta-endorphin and dynorphin in the determination of opiate receptor type selectivity.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Autoradiography of [3H]β-endorphin binding in brain

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

inferred from DOI database lookup

3H-beta-endorphin binding in rat brain

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

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Norbinaltorphimine, a selective kappa-opioid receptor antagonist, induces an itch-associated response in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Activation of G-proteins in the mouse pons/medulla by beta-endorphin is mediated by the stimulation of mu- and putative epsilon-receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

inferred from DOI database lookup

The mu-opioid receptor gene-dose dependent reductions in G-protein activation in the pons/medulla and antinociception induced by endomorphins in mu-opioid receptor knockout mice

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

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Absence of G-protein activation by mu-opioid receptor agonists in the spinal cord of mu-opioid receptor knockout mice

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Binaltorphimine and nor-binaltorphimine, potent and selective kappa-opioid receptor antagonists

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Naltrindole, a highly selective and potent non-peptide delta opioid receptor antagonist

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

inferred from DOI database lookup

mu-Opioid receptor-stimulated guanosine-5'-O-(gamma-thio)-triphosphate binding in rat thalamus and cultured cell lines: signal transduction mechanisms underlying agonist efficacy

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Opiate receptor knockout mice define mu receptor roles in endogenous nociceptive responses and morphine-induced analgesia

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Spinal analgesic actions of the new endogenous opioid peptides endomorphin-1 and -2.

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Beta-endorphin-(1-27) antagonizes beta-endorphin- but not morphine-, D-Pen2-D-Pen5-enkephalin- and U50, 488H-induced analgesia in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

inferred from DOI database lookup

A potent and selective endogenous agonist for the mu-opiate receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0306-4522%2802%2900486-4

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0306-4522(02)00486-4

1 reference

Europe PubMed Central

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15 December 2019

1 reference

Europe PubMed Central

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15 December 2019

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