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  • Annual Reviews  (3)
  • English  (3)
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  • Annual Reviews  (3)
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  • English  (3)
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  • 1
    Online Resource
    Online Resource
    Annual Reviews ; 2002
    In:  Annual Review of Biophysics and Biomolecular Structure Vol. 31, No. 1 ( 2002-06), p. 97-119
    In: Annual Review of Biophysics and Biomolecular Structure, Annual Reviews, Vol. 31, No. 1 ( 2002-06), p. 97-119
    Abstract: ▪ Abstract  Flow cytometers make homogeneous real-time measurements of ligand-receptor interactions and, simultaneously, the physiological responses of cells. Their multiparameter capabilities are also useful in resolving multicomponent assemblies or in developing multiplexed assays. Recent advances suggest that these approaches can be extended in several important ways. Sample delivery in the millisecond time domain is applicable to the analysis of complex binding kinetics and reaction mechanisms. The homogeneous discrimination of free components and particle-based assemblies can be extended into the micromolar concentration range. Measurements can be made of molecular assemblies among proteins, DNA, RNA, lipids, and carbohydrates on beads. The topography and assembly of components within cells can be evaluated with resonance energy transfer. Temperature dependence can be evaluated with Peltier temperature control. Many assembly endpoints can be assessed through new tools for high-throughput flow cytometry using plate-based assay formats and small volume samples.
    Type of Medium: Online Resource
    ISSN: 1056-8700 , 1545-4266
    URL: Issue
    RVK:
    RVK:
    Language: English
    Publisher: Annual Reviews
    Publication Date: 2002
    detail.hit.zdb_id: 2434740-1
    detail.hit.zdb_id: 1473778-4
    SSG: 12
    Location Call Number Limitation Availability
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  • 2
    Online Resource
    Online Resource
    Annual Reviews ; 2008
    In:  Annual Review of Physiology Vol. 70, No. 1 ( 2008-03-01), p. 165-190
    In: Annual Review of Physiology, Annual Reviews, Vol. 70, No. 1 ( 2008-03-01), p. 165-190
    Abstract: Steroids play an important role in the regulation of normal physiology and the treatment of disease. Steroid receptors have classically been described as ligand-activated transcription factors mediating long-term genomic effects in hormonally regulated tissues. It is now clear that steroids also mediate rapid signaling events traditionally associated with growth factor receptors and G protein–coupled receptors. Although evidence suggests that the classical steroid receptors are capable of mediating many of these events, more recent discoveries reveal the existence of transmembrane receptors capable of responding to steroids with cellular activation. One such receptor, GPR30, is a member of the G protein–coupled receptor superfamily and mediates estrogen-dependent kinase activation as well as transcriptional responses. In this review, we provide an overview of the evidence for the cellular and physiological actions of GPR30 in estrogen-dependent processes and discuss the relationship of GPR30 with classical estrogen receptors.
    Type of Medium: Online Resource
    ISSN: 0066-4278 , 1545-1585
    URL: Issue
    RVK:
    Language: English
    Publisher: Annual Reviews
    Publication Date: 2008
    detail.hit.zdb_id: 1474465-X
    SSG: 12
    Location Call Number Limitation Availability
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  • 3
    Online Resource
    Online Resource
    Annual Reviews ; 2023
    In:  Annual Review of Pharmacology and Toxicology Vol. 63, No. 1 ( 2023-01-20), p. 295-320
    In: Annual Review of Pharmacology and Toxicology, Annual Reviews, Vol. 63, No. 1 ( 2023-01-20), p. 295-320
    Abstract: The actions of estrogens and related estrogenic molecules are complex and multifaceted in both sexes. A wide array of natural, synthetic, and therapeutic molecules target pathways that produce and respond to estrogens. Multiple receptors promulgate these responses, including the classical estrogen receptors of the nuclear hormone receptor family (estrogen receptors α and β), which function largely as ligand-activated transcription factors, and the 7-transmembrane G protein–coupled estrogen receptor, GPER, which activates a diverse array of signaling pathways. The pharmacology and functional roles of GPER in physiology and disease reveal important roles in responses to both natural and synthetic estrogenic compounds in numerous physiological systems. These functions have implications in the treatment of myriad disease states, including cancer, cardiovascular diseases, and metabolic disorders. This review focuses on the complex pharmacology of GPER and summarizes major physiological functions of GPER and the therapeutic implications and ongoing applications of GPER-targeted compounds.
    Type of Medium: Online Resource
    ISSN: 0362-1642 , 1545-4304
    URL: Issue
    RVK:
    Language: English
    Publisher: Annual Reviews
    Publication Date: 2023
    detail.hit.zdb_id: 1474461-2
    SSG: 15,3
    Location Call Number Limitation Availability
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