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  • insulin secretion  (2)
  • 2′-bipyridyl)3Cl2  (1)
  • 6-Ketoprostaglandin F"1"α  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Enzyme immunoassay of 6-ketoprostaglandin F"1"α in a solid phase
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Lipids and Lipid Metabolism 836 (1985), S. 335-343 
    Details
    ISSN: 0005-2760
    Keywords: 6-Ketoprostaglandin F"1"α ; Enzyme immunoassay ; Prostaglandin ; Radioimmunoassay
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/0005-2760(85)90137-7
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Evidence that glucagon stimulates insulin secretion through its own receptor in rats (1995)
    Springer
    Diabetologia 38 (1995), S. 274-276 
    Details
    ISSN: 1432-0428
    Keywords: Key words Glucagon ; insulin secretion ; exendin (9 ; 39) ; GLP-1 ; pancreas perfusion.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Since glucagon-like peptide-1 (7–36) amide (7–37) (GLP-1) has been found to be a potent insulinotropic hormone, it has been postulated that glucagon stimulates insulin secretion from islet beta cells through the GLP-1 receptor. We therefore examined the effects of a GLP-1 receptor antagonist, exendin (9–39) amide, on glucagon- or GLP-1-stimulated insulin release from isolated perfused rat pancreas. When infusion of 100 nmol/l exendin (9–39) amide was started 5 min before that of 1 nmol/l glucagon, the stimulation of insulin release by glucagon was similar to that found in the control situation (preinfusion with vehicle alone). By contrast, when 0.3 nmol/l GLP-1 was used in the same experimental setting, exendin (9–39) amide clearly inhibited insulin release. These results indicate that glucagon stimulates insulin release mainly through glucagon receptors but not GLP-1 receptors on islet beta cells. [Diabetologia (1995) 38: 274–276]
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00400630
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Evidence that glucagon stimulates insulin secretion through its own receptor in rats (1995)
    Springer
    Diabetologia 38 (1995), S. 274-276 
    Details
    ISSN: 1432-0428
    Keywords: Glucagon ; insulin secretion ; exendin (9–39) ; GLP-1 ; pancreas perfusion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Since glucagon-like peptide-1 (7–36) amide (7–37) (GLP-1) has been found to be a potent insulinotropic hormone, it has been postulated that glucagon stimulates insulin secretion from islet beta cells through the GLP-1 receptor. We therefore examined the effects of a GLP-1 receptor antagonist, exendin (9–39) amide, on glucagon- or GLP-1-stimulated insulin release from isolated perfused rat pancreas. When infusion of 100 nmol/l exendin (9–39) amide was started 5 min before that of 1 nmol/l glucagon, the stimulation of insulin release by glucagon was similar to that found in the control situation (preinfusion with vehicle alone). By contrast, when 0.3 nmol/l GLP-1 was used in the same experimental setting, exendin (9–39) amide clearly inhibited insulin release. These results indicate that glucagon stimulates insulin release mainly through glucagon receptors but not GLP-1 receptors on islet beta cells.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00400630
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    Photoinduced electron transfer catalysis of titania particles modified with a Ru(2,2′-bipyridyl)3 2+-grafted polymer by visible light (2000)
    Springer
    Colloid & polymer science 278 (2000), S. 481-484 
    Details
    ISSN: 1435-1536
    Keywords: Key words Hybrid titania ; Photocatalysis ; Visible light ; Ru(2 ; 2′-bipyridyl)3Cl2 ; Polymer modification
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract  The preparation and photocatalysis of colloidal titania modified with Ru(2,2′-bipyridyl)3 2+-grafted polyacrylate were investigated. Visible light irradiation of the Ru(2,2′-bipyridyl)3 2+-tethered titania in pH 7.0 buffer solution gave electron transfer to methyl viologen to form the cation radical via electron migration from the Ru(II) complex to the titania surface.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s003960050543
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
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