Quantitative measurement of estrogen-induced ERK 1 and 2 activation via multiple membrane-initiated signaling pathways. - Wikidata - awgldk - TriplyDB

Quantitative measurement of estrogen-induced ERK 1 and 2 activation via multiple membrane-initiated signaling pathways.

Quantitative measurement of estrogen-induced ERK 1 and 2 activation via multiple membrane-initiated signaling pathways.

http://www.wikidata.org/entity/Q33947416

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Endocrine disruption via estrogen receptors that participate in nongenomic signaling pathways Membrane estrogen receptor-alpha levels predict estrogen-induced ERK1/2 activation in MCF-7 cells Xenoestrogens at picomolar to nanomolar concentrations trigger membrane estrogen receptor-alpha-mediated Ca2+ fluxes and prolactin release in GH3/B6 pituitary tumor cells Xenoestrogen-induced ERK-1 and ERK-2 activation via multiple membrane-initiated signaling pathways.Bisphenol S disrupts estradiol-induced nongenomic signaling in a rat pituitary cell line: effects on cell functions The roles of membrane estrogen receptor subtypes in modulating dopamine transporters in PC-12 cells 17beta-estradiol-mediated neuroprotection and ERK activation require a pertussis toxin-sensitive mechanism involving GRK2 and beta-arrestin-1 Nongenomic mechanisms of physiological estrogen-mediated dopamine efflux.Proliferative and anti-proliferative effects of dietary levels of phytoestrogens in rat pituitary GH3/B6/F10 cells - the involvement of rapidly activated kinases and caspases.Sex differences in estrogen receptor subcellular location and activity in lung adenocarcinoma cells Nongenomic signaling pathways of estrogen toxicity.NAD-dependent isocitrate dehydrogenase as a novel target of tributyltin in human embryonic carcinoma cells Click synthesis of estradiol-cyclodextrin conjugates as cell compartment selective estrogens Quantitative changes in intracellular calcium and extracellular-regulated kinase activation measured in parallel in CHO cells stably expressing serotonin (5-HT) 5-HT2A or 5-HT2C receptors.Combinations of physiologic estrogens with xenoestrogens alter calcium and kinase responses, prolactin release, and membrane estrogen receptor trafficking in rat pituitary cells.Estrogens of multiple classes and their role in mental health disease mechanisms.Direct estradiol and diethylstilbestrol actions on early- versus late-stage prostate cancer cells.Insulin-like growth factor-I E-peptide activity is dependent on the IGF-I receptor.Combinations of physiologic estrogens with xenoestrogens alter ERK phosphorylation profiles in rat pituitary cells.Alkylphenol xenoestrogens with varying carbon chain lengths differentially and potently activate signaling and functional responses in GH3/B6/F10 somatomammotropes Estradiol effects on the dopamine transporter - protein levels, subcellular location, and function.Xenoestrogens are potent activators of nongenomic estrogenic responses.International Union of Basic and Clinical Pharmacology. XCVII. G Protein-Coupled Estrogen Receptor and Its Pharmacologic Modulators Estrogen- and xenoestrogen-induced ERK signaling in pituitary tumor cells involves estrogen receptor-α interactions with G protein-αi and caveolin I.Controllable drug uptake and nongenomic response through estrogen-anchored cyclodextrin drug complex Nongenomic actions of low concentration estrogens and xenoestrogens on multiple tissues.Non-genomic effects of xenoestrogen mixtures.Mixtures of xenoestrogens disrupt estradiol-induced non-genomic signaling and downstream functions in pituitary cells.Nongenomic actions of estradiol compared with estrone and estriol in pituitary tumor cell signaling and proliferation.Synthesis and characterization of bioactive tamoxifen-conjugated polymers.Estradiol activates mast cells via a non-genomic estrogen receptor-alpha and calcium influx.Key developments in endocrine disrupter research and human health.Membrane estrogen receptor-alpha-mediated nongenomic actions of phytoestrogens in GH3/B6/F10 pituitary tumor cells.Estrogen Regulation of MicroRNA Expression Toxicological mechanism of endocrine disrupting chemicals:is estrogen receptor involved?Molecular pathways: environmental estrogens activate nongenomic signaling to developmentally reprogram the epigenome.Rapid actions of xenoestrogens disrupt normal estrogenic signaling Estrogenic endocrine-disrupting chemicals: molecular mechanisms of actions on putative human diseases.Membrane lipid rafts and estrogenic signalling: a functional role in the modulation of cell homeostasis.MAPK and NF-κB pathways are involved in bisphenol A-induced TNF-α and IL-6 production in BV2 microglial cells.

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P2860

Quantitative measurement of estrogen-induced ERK 1 and 2 activation via multiple membrane-initiated signaling pathways.

http://www.wikidata.org/entity/Q33947416

description

2004 nî lūn-bûn

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2004 թուականի Մարտին հրատարակուած գիտական յօդուած

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2004 թվականի մարտին հրատարակված գիտական հոդված

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2004年の論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年論文

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2004年论文

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Quantitative measurement of es ...... -initiated signaling pathways.

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Bahiru Gametchu

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Cheryl S Watson

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Nataliya N Bulayeva

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P2860

Cloning, expression, and characterization of a membrane progestin receptor and evidence it is an intermediary in meiotic maturation of fish oocytes

Nongenotropic, sex-nonspecific signaling through the estrogen or androgen receptors: dissociation from transcriptional activity

Linkage of rapid estrogen action to MAPK activation by ERalpha-Shc association and Shc pathway activation

Heparin-binding EGF-like growth factor and ErbB signaling is essential for heart function

Estrogen-induced activation of Erk-1 and Erk-2 requires the G protein-coupled receptor homolog, GPR30, and occurs via trans-activation of the epidermal growth factor receptor through release of HB-EGF

The specificities of protein kinase inhibitors: an update

Interaction of oestrogen receptor with the regulatory subunit of phosphatidylinositol-3-OH kinase

Epitope-dependent localization of estrogen receptor-alpha, but not -beta, in en face arterial endothelium.

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10.1016/J.STEROIDS.2003.12.003

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3

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69

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8628761

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15072920

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