Concurrent down-regulation of IP prostanoid receptors and the alpha-subunit of the stimulatory guanine-nucleotide-binding protein (Gs) during prolonged exposure of neuroblastoma x glioma cells to prostanoid agonists. Quantification and functional im (Q42798728)

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scientific article published on July 15, 1992

Language	Label	Description	Also known as
English	Concurrent down-regulation of IP prostanoid receptors and the alpha-subunit of the stimulatory guanine-nucleotide-binding protein (Gs) during prolonged exposure of neuroblastoma x glioma cells to prostanoid agonists. Quantification and functional im	scientific article published on July 15, 1992

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scholarly article

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Europe PubMed Central

PMC publication ID

7 November 2017

Concurrent down-regulation of IP prostanoid receptors and the alpha-subunit of the stimulatory guanine-nucleotide-binding protein (Gs) during prolonged exposure of neuroblastoma x glioma cells to prostanoid agonists. Quantification and functional im (English)

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

Concurrent down-regulation of IP prostanoid receptors and the alpha-subunit of the stimulatory guanine-nucleotide-binding protein (Gs) during prolonged exposure of neuroblastoma x glioma cells to prostanoid agonists. Quantification and functional implications (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1379045

20 September 2022

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McKenzie FR

3

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7 November 2017

E. J. Adie

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1379045

20 September 2022

I. Mullaney

2

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20 September 2022

F. R. McKenzie

3

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20 September 2022

G. Milligan

4

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20 September 2022

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publication date

1 July 1992

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7 November 2017

15 July 1992

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National Center for Biotechnology Information

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1379045

20 September 2022

number of pages

8

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full work available at URL

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1379045/?tool=EBI

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20 September 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1379045/pdf/?tool=EBI

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20 September 2022

https://europepmc.org/articles/PMC1132820

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1379045

20 September 2022

https://europepmc.org/articles/PMC1132820?pdf=render

Portable Document Format

online access status

content deliverer

Europe PubMed Central

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1379045

20 September 2022

Biochemical Journal

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7 November 2017

285 ( Pt 2)

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Europe PubMed Central

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7 November 2017

529-536

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

A highly sensitive adenylate cyclase assay

1 reference

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1 reference

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G proteins: transducers of receptor-generated signals

1 reference

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Human cDNA clones for four species of G alpha s signal transduction protein

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Molecular basis for two forms of the G protein that stimulates adenylate cyclase

1 reference

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Molecular mechanisms of receptor desensitization using the beta-adrenergic receptor-coupled adenylate cyclase system as a model

1 reference

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The inhibitory guanine nucleotide-binding protein (Ni) purified from bovine brain is a high affinity GTPase.

1 reference

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Chronic ethanol causes heterologous desensitization of receptors by reducing alpha s messenger RNA.

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Antibodies which recognize the C-terminus of the inhibitory guanine-nucleotide-binding protein (Gi) demonstrate that opioid peptides and foetal-calf serum stimulate the high-affinity GTPase activity of two separate pertussis-toxin substrates

1 reference

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Foetal-calf serum stimulates a pertussis-toxin-sensitive high-affinity GTPase activity in rat glioma C6 BU1 cells

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A selective binding site for 3H-NECA that is not an adenosine A2 receptor

1 reference

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Mutations of GS alpha designed to alter the reactivity of the protein with bacterial toxins. Substitutions at ARG187 result in loss of GTPase activity

1 reference

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Increase in Gs and cyclic AMP generation in HIT cells. Evidence that the 45-kDa alpha-subunit of Gs has greater functional activity than the 52-kDa alpha-subunit

1 reference

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Guanine nucleotide-binding proteins and cellular control

1 reference

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27 May 2018

Guanine-nucleotide-binding proteins expressed in rat white adipose tissue. Identification of both mRNAs and proteins corresponding to Gi1, Gi2 and Gi3.

1 reference

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27 May 2018

Persistent activation of the alpha subunit of Gs promotes its removal from the plasma membrane

1 reference

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27 May 2018

Ethanol increases extracellular adenosine by inhibiting adenosine uptake via the nucleoside transporter.

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Secretin receptors in the neuroglioma hybrid cell line NG108-15. Characterization and regulation of their expression

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Prostaglandin E1-mediated, cyclic AMP-independent, down-regulation of Gs alpha in neuroblastoma x glioma hybrid cells.

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Delta-opioid-receptor-mediated inhibition of adenylate cyclase is transduced specifically by the guanine-nucleotide-binding protein Gi2

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Biphasic regulation of adenylate cyclase by cholera toxin in neuroblastoma x glioma hybrid cells is due to the activation and subsequent loss of the alpha subunit of the stimulatory GTP binding protein (GS).

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Reticulocyte lysates synthesize an active alpha subunit of the stimulatory G protein Gs

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Catecholamine-stimulated GTPase cycle. Multiple sites of regulation by beta-adrenergic receptor and Mg2+ studied in reconstituted receptor-Gs vesicles

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Development of opiate receptors and GTP-binding regulatory proteins in neonatal rat brain

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Identifiers

10.1042/BJ2850529

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

7 November 2017

ResearchGate publication ID

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