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  • 1
    Online Resource
    Online Resource
    Munich : [High Performance Space Structure Systems GmbH]
    Keywords: Forschungsbericht
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (17 Seiten, 1,04 MB)
    Edition: Issue: 1, dated 31.07.2020
    Language: German
    Note: Förderkennzeichen BMWi 50RK1904 , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden , Sprache der Zusammenfassungen: Deutsch, Englisch
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  • 2
    Online Resource
    Online Resource
    Munich : High Performance Space Structure Systems GmbH
    Keywords: Forschungsbericht
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (28 Seiten, 2,16 MB) , Illustrationen, Diagramme
    Edition: Erste Ausgabe
    Language: German
    Note: Förderkennzeichen BMWi 50YB1649 , Weitere Autoren dem Berichtsblatt entnommen , Unterschiede zwischen dem gedruckten Dokument und der elektronischen Ressource können nicht ausgeschlossen werden , Sprache der Zusammenfassung: Deutsch, Englisch
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 82 (1959), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    The @journal of child psychology and psychiatry 30 (1989), S. 0 
    ISSN: 1469-7610
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine , Psychology
    Notes: Abstract In a syndrome validation study, four groups of patients suffering from conversion disorders, anxiety states, obsessive-compulsive disorder and emotional disorders, as well as a healthy control group, were compared. The following Findings emerged: besides female preponderance and greater age, a higher rate of low SES subjects and social migration patients suffering from conversion disorders displayed a greater proportion of psychiatric and medical diseases in their parental heritage.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary The serum-calcium of the rat is regulated by the antagonistic hormones parathyroid hormone and thyrocalcitonin. The intake of calcium with the food also has an effect in certain limits. Cautery of the thyroid gland is an unspecific stimulus for TCT-secretion. The hormone is producing a rapid decrease of the serum-calcium, but the following increase of the mineral depends upon the parathyroid glands. Hypercalcemia is the specific stimulus for TCT-secretion. In thyroidectomized animals the adminstration of calcium produces a higher and more prolonged increase in calcium. The absence of the thyroid gland can be substituted by administration of exogenous TCT. There is no evidence for a “TCT-releasing-factor”. Exogenous TCT has a larger effect when it is given intravenously. Repeated application of the factor has an additive affect. Exogenous (heterologous) and endogenous TCT probably have the same mechanism of action. The influences of parathyroid hormone on the serum-calcium may be neutralized by TCT in every phase of efficiency.
    Notes: Zusammenfassung Der Ca-Spiegel der Ratte wird von den antagonistischen Hormonen Parathormon und Thyreocalcitonin gesteuert, daneben hat die Ca-Zufuhr mit der Nahrung in gewissen Grenzen eine Bedeutung. Die TCT-Sekretion wird unspezifisch durch Schilddrüsenkauterisierung angeregt. Das Hormon ruft einen prompten Ca-Abfall hervor, der Wiederanstieg des Minerals ist von den Nebenschilddrüsen abhängig. Den physiologischen Reiz für die TCT-Ausschüttung stellt die Hypercalciämie dar. Ca-Gabe ruft bei schilddrüsenlosen Tieren einen erhöhten und verlängerten Ca-Anstieg hervor, der Schilddrüsenausfall läßt sich durch exogene TCT-Zufuhr substituieren. Ein „TCT-releasing-factor” der Epithelkörperchen wird nicht ersichtlich. Exogenes TCT wirkt bei intravenöser Gabe stärker als bei subcutaner. Mehrfache Applikation führt zu einer Summierung der Effekte. Exogenes (artfremdes) und endogenes TCT sind gleichartig wirksam. Parathormoneinflüsse auf den Ca-Spiegel können in jeder Wirkungsphase durch TCT neutralisiert werden.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The (ν5-C5H5)(L)(RN3R)Ni and (ν5-C5H5)(PPh3)(RN3R)Pd compounds, with L = PPh3, CO, CNR′, and RN3R = diaryltriazenido anion, were prepared. The bonding mode of the triazenido ligand is monodentate in the (ν5-C5H5)(PPh3)(RN3R)M phosphine compounds. The carbonyl and isonitrile groups are inserted into the nickel-nitrogen bond and a five-membered heteronuclear ring is formed in (ν5-C5-C5H5)(L)(RN3R)Ni, when L= CO and CNR′. Most compounds are fluxional, involving site exchange of the triazenidoaryl-groupsvia intermediates with a chelating bonding mode of the triazenido ligand. The (ν5-C5H5)(PPh3)(RN3R)Ni compound shows anomalous solution paramagnetism, that is correlated with the fluxional mechanism. The temperature dependence of contact shifts in the n.m.r. spectrum was determined and ΔE-values were calculated.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The complexes (η 5-C5H5)L(RN3R′)Fe, where L = PPh3, P(OMe)3, P(OPh)3 or CO and R,R′=p-MeC6H4 orp-ClC6H4, have been prepared by reaction of suitable iron halides with Ag(RN3R′). The mechanism of formation of the Fe(RN3R′) group is thought to involve, initially, an Fe-Ag bond. The bonding mode of the triazenido ligand is chelating in a six coordinate configuration. The spectroscopic results are discussed in relation to variations in the environment of the metal atom.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The synthesis and properties of the [(η5-C5H5)L(RN3R)CoIII]PF6 complexes, with L = PEt3, PPh3, P(OMe)3 or P(OPh)3, are reported. A six coordinate configuration containing a chelating triazenido ligand is proposed which is isostructural with the known complexes of iron and nickel. The spectroscopic properties of the isoelectronic Co and Fe complexes, (η5-C5H5)L(RN3R)M, are compared in relation to the charge on the central metal atom. The complex with L = CO could not be prepared, but the carbonyl inserted product (η5-C5H5)(L{RNNN(R)C(O)}Co was isolated. In one of the reactions, the novel ring-bound triphenylphosphine complex, [η5-C5H5)(η5-C5H4PPh3)CoIII](PF6)2, was isolated as a side product. The mechanism of this reaction is discussed.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Medical microbiology and immunology 50 (1905), S. 324-330 
    ISSN: 1432-1831
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Acta diabetologica 9 (1972), S. 865-899 
    ISSN: 1432-5233
    Keywords: cAMP ; Chlorpropamide ; Diabetes ; Glibenclamide ; Glibornuride ; Glucagon ; Insulin ; Methylxanthines ; Sulphonylureas ; Tolbutamide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Résumé A présent, il est certain que les sulfanilurées exerçent essentiellement leur action au niveau du pancréas, stimulant la sécrétion insulinique et interdisant la sécrétion du glucagone. Dès la découverte des substances hypoglycemisantes par la voie orale, le développement de nouvelles sulfanilurées encore plus fortes a fait l'objet d'un très vif intérêt. Tout récemment, par la synthèse d'un nouveau composé plus puissant appartenant au groupe des sulfanilurées — la glibenclamide (HB 419, Daonil®) —, des progrès encourageants ont été réalisés, notamment en ce qui concerne le traitment du diabète chez les individus d'un âge mûr. Nombre de patients dépendant de l'insuline atteints de cette forme de diabète peuvent être traités en effet avec de la glibenclamide. Parfois, il se peut que des hypoglycemies masquées se manifestent, ce qui témoigne de l'activité intense de cette substance. La glibenclamide se diversifie des autres sulfanilurées du fait des différentes modalités qui provoquent la sécrétion d'insuline. Cette substance agit également synergiquement avec le glucose stimulant cette sécrétion. Aucun autre médicament hypoglycemisant ne permet, chez l'animal aussi bien que chez l'homme, d'accroître dans une mesure autant considérable la tolérance des glycides. La glibenclamide semble exercer son influence au niveau de la cellule B sur le même récepteur ou avec le même mécanisme agissant avec le glucose.
    Abstract: Resumen Actualmente se considera como un hecho cierto que las sulfanilureas actúan principalmente a nivel del áncreas estimulando la secreción insulínica e inhibendo la de glucagón. Desde la época en que fueron descubiertas las substancias hipoglicémicas orales, ha sido objeto de vivo interés el desarrollo de sulfanilureas nuevas y más potentes. Recientemente, a través de la síntesis de un compuesto muy potente perteneciente al grupo de las sulfanilureas — la glibenclamida (HB 419, Daonil®) —, se han realizado progresos alentadores sobre todo en el tratamiento de la diabetes de la edad madura. En efecto, muchos enfermos insulinodependientes afectos de dicho tipo de diabetes pueden pasar a la glibenclamida. A veces se pueden virificar hipoglicemias disfrazadas, que prueban la intensa actividad de esta substancia. La glibenclamida se diferencia de las demás sulfanilureas por las diversas modalidades con que provoca la secreción de insulina. Además, actúa sinérgicamente con la glucosa en el stímulo de dicha secreción. Ningún otro producto hipoglicémico es capaz, tanto en el hombre como en el animal, de aumentar en medida tan notable la tolerancia glucídica. La glibenclamida parace actuar a nivel de la célula B en el mismo receptor o con el mismo mecanismo con que actúa la glucosa.
    Notes: Riassunto Attualmente, è considerato un fatto certo che le sulfaniluree agiscano principalmente a livello del pancreas, stimolando la secrezione insulinica ed inibendo quella del glucagone. Sin dall'epoca della scoperta degli ipoglicemizzanti orali, lo sviluppo di nuove e più efficaci sulfaniluree è stato oggetto di vivo interesse. Recentemente, attraverso la sintesi di un nuovo ed assai efficace composto appartenente al gruppo delle sulfaniluree — la glibenclamide (HB 419, Daonil®) —, incoraggianti progressi sono stati compiuti, soprattutto nel trattamento del diabete dell'età matura. Molti pazienti insulino-dipendenti affetti da tale tipo di diabete possono essere infatti passati alla glibenclamide. Talvolta possono verificarsi ipoglicemie mascherate, a dimostrazione dell'intensa attività di questa sostanza. La glibenclamide si differenzia dalle altre sulfaniluree per le diverse modalità con cui provoca la secrezione di insulina. Essa agisce inoltre sinergicamente con il glucosio nello stimolare tale secrezione. Nessun altro farmaco ipoglicemizzante è capace, sia nell'animale che nell'uomo, di aumentare in misura altrettanto notevole la tolleranza glicidica. La glibenclamide sembra agire a livello della cellula B sullo stesso recettore o con il medesimo meccanismo con cui agisce il glucosio.
    Type of Medium: Electronic Resource
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