@misc{Schoene1977,
  author    = {Sch{\"o}ne, Helmut C.},
  title     = {{\"U}ber die St{\"o}rwirkungen von Ger{\"a}uschen auf die unmittelbare Lernleistung bei verschiedenen Intelligenzgraden},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-54106},
  year      = {1977},
  abstract  = {Die Wirkung der Variablen ‚Intelligenz' und ‚Ger{\"a}uschintensit{\"a}t' auf die unmittelbare Lernleistung wurde mit zwei Tests untersucht. Dadurch sollten die „Stimulus trace"-Theorie (Ellis 1963) und die „neural theory" (Spitz 1963) bei 45 deutschen, lernbehinderten Kindern gepr{\"u}ft werden. Der „Stimulus trace"-Faktor ließ sich f{\"u}r Ger{\"a}uschreize nicht best{\"a}tigen. Es gab keinen Beweis f{\"u}r die G{\"u}ltigkeit der neuralen Theorie. Bei Erh{\"o}hung der Lautst{\"a}rke sank die Lernleistung in beiden Tests.},
  language  = {de}
}
@misc{KortPeterKoopmanschap1983,
  author    = {Kort, C. A. D. de and Peter, Martin G. and Koopmanschap, A. B.},
  title     = {Binding and degradation of juvenile hormone III by haemolymph proteins of the Colorado potato beetle: a re-examination},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-16777},
  year      = {1983},
  abstract  = {The haemolymph of the adult Colorado potato beetle, Lepinotarsa decemlineata Say, contains a high molecular weight (MW > 200,000) JH-III specific binding protein. The Kd value of the protein for racemic JH-III is 1.3 ± 0.2 × 10-7 M. It has a lower affinity for racemic JH-I and it does not bind JH-III-diol or JH-III-acid. The binding protein does discriminate between the enantiomers of synthetic, racemic JH-III as was determined by stereochemical anaysis of the bound and the free JH-III. Incubation of racemic JH-III with crude haemolymph results in preferential formation of (10S)-JH-III-acid, the unnatural configuration. The JH-esterase present in L. decemlineata haemolymph is not enantioselective. It is concluded that the most important function of the binding protein is that of a specific carrier, protecting the natural hormone against degradation by esterases. The carrier does not protect JH-I as efficiently as the lower homologue.},
  language  = {en}
}
@misc{ErdelenLaschewskyRingsdorfetal.1989,
  author    = {Erdelen, C. and Laschewsky, Andr{\´e} and Ringsdorf, H. and Schneider, J. and Schuster, A.},
  title     = {Thermal behaviour of polymeric Langmuir-Blodgett multilayers},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-17378},
  year      = {1989},
  abstract  = {Langmuir-Blodgett multilayers of hydrocarbon and fluorocarbon polymers with hydrophilic spacer, lipid-polyelectrolyte complexes and mesogenic polymers have been prepared. The thermal behaviour of the multilayers was studied by small angle X-ray scattering, IR and UV—visible spectroscopy. Good thermal stabilities were found for the various classes of polymers. In addition, for both complexed multilayers and mesogenic polymer films, reorientation processes were observed.},
  language  = {en}
}
@misc{PeterBoldtNiedersteinetal.1990,
  author    = {Peter, Martin G. and Boldt, Peter C. and Niederstein, Yvonne and Peter-Katalinić, Jasna},
  title     = {Synthesen von Galactose-Cluster-haltigen Steroid-Derivaten},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-16783},
  year      = {1990},
  abstract  = {The synthesis of galactose clusters that are linked to a steroid moiety by a peptide-like spacer unit is described. The galactose cluster is obtained by Koenigs-Knorr glycosylation of TRIS-Gly-Fmoc (2b) under Helferich conditions. Peptide and ester bonds are formed after activation of carboxylic acids as diphenylthiophene dioxide (TDO) esters. 6a is synthesized in a convergent way by coupling of (Ac4Gal)3-TRIS-Gly (3e) with cholesteryl TDO succinate (5b). Coupling of (Ac4Gal)3-TRIS-Gly hydrogen succinate (3f) with Gly-O-Chol (5d) by means of EEDQ yields 6d. Reaction of (Ac4Gal)3-TRIS-Gly-SUCC-O-TDO (3g) with 25-hydroxycholesterol leads in a linear sequence to the oxysterol derivative 6f. Selective cleavage of the acetyl groups from galactose units yields the known compound 6b and the new derivatives 6e and 6g.},
  language  = {de}
}
@article{GrielStroehlJeschkeitetal.1992,
  author    = {Griel, C. and Str{\"o}hl, D. and Jeschkeit, H. and Kleinpeter, Erich},
  title     = {Synthetische und NMR-spektroskopische Untersuchungen der Benzzyl-aminaddition an N-Maleyl- aminos{\"a}urederivaten},
  year      = {1992},
  language  = {de}
}
@article{Tristram1993,
  author    = {Tristram, Hildegard L. C.},
  title     = {"Metrische Motiviertheit in der {\"a}ltesten insularen Dichtung"},
  isbn      = {3-86057-090-0},
  year      = {1993},
  abstract  = {In the earliest recorded poetry of the Insular Celtic literature, the occurrence intra-linear phoneme recurrences in addition to the rather common feature of alliteration suggest that they served an indexical motivation of the metrical constraints. This is in particular suggested by the indexical use of personal names. This practice may perhaps even reach back to Continental Celtic metrical practices which already seem to bear witness of the use of such language skills. It is particularly interesting to note that the initial mutations of the lexemes do not obstruct indexicality. It is suggested that the orally trained poets may perhaps have received specific grammatical instructions as part of their prolongued poetic education.},
  language  = {de}
}
@article{Tristram1993,
  author    = {Tristram, Hildegard L. C.},
  title     = {Zwiebeln und W{\"o}rter : zum Sprachkontakt {\"u}ber den {\"A}rmelkanal},
  isbn      = {3-484-42911-9},
  year      = {1993},
  abstract  = {realisation in form of a retroflex is not only found in the English south West ('West Country burr'), but also across the English Channel in a well circumscribed area of Tr{\´e}gor in Brittany. Both areas also share other phonetic features such as sonorisation of word initial fricatives, epenthesis, surnames etc. How is this to be explained? Intensive mobility and trade across the sea suggest themselves as a possible answer. Travelling by sea, aided by expert knowledge of the seasonal currents and winds, was much quicker and efficient in former times than travelling across land. In this connection, the phenomenon of the "Johnnys de Roccoff" who traded Breton onions along the English coasts until very recently is pointed ou as a type of contact which may have transported phoneme realisations and lexis across the sea, forming a linguistic area with not much contact with their respective hinterlands in England and Brittany.},
  language  = {de}
}
@misc{PueschelKirchnerSchroederetal.1993,
  author    = {P{\"u}schel, Gerhard Paul and Kirchner, C. and Schr{\"o}der, A. and Jungermann, Kurt},
  title     = {Glycogenolytic and antiglycogenolytic prostaglandin E₂ actions in rat hepatocytes are mediated via different signalling pathways},
  url       = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-45853},
  year      = {1993},
  abstract  = {Prostaglandin E₂ has been reported both to stimulate glycogen-phosphorylase activity (glycogenolytic effect) and to inhibit the glucagon-stimulated glycogen-phosphorylase activity (antiglycogenolytic effect) in rat hepatocytes. It was the purpose of this study to resolve this apparent contradiction and to characterize the signalling pathways and receptor subtypes involved in the opposing prostaglandin E₂ actions. Prostaglandin E₂ (10 μM) increased glucose output, glycogen-phosphorylase activity and inositol trisphosphate formation in hepatocyte cell culture andor suspension. In the same systems, prostaglandin E₂ decreased the glucagon-stimulated (1 nM) glycogen-phosphorylase activity and cAMP formation. The signalling pathway leading to the glycogenolytic effect of PGE₂ was interrupted by incubation of the hepatocytes with 4P-phorbol 12-myristate 13-acetate (100 nM) for 10 min, while the antiglycogenolytic effect of prostaglandin E₂ was not attenuated. The signalling pathway leading to the antiglycogenolytic effect of prostaglandin E₂ was interrupted by an incubation of cultured hepatocytes with pertussis toxin (100 ng/ml) for 18 h, whereas the glycogenolytic effect of prostaglandin E₂ was enhanced. The EP₁/EP₃ prostaglandin-E₂-receptor-specific prostaglandin E₂ analogue Sulproston had a stronger glycogenolytic potency than the EP₃ prostaglandin-E₂-receptor-specific prostaglandin E₂ analogue Misoprostol. The antiglycogenolytic potency of both agonists was equal. It is concluded that the glycogenolytic and the antiglycogenolytic effects of prostaglandin E₂ are mediated via different signalling pathways in hepatocytes possibly involving EP₁ and EP₃ prostaglandin E₂ receptors, respectively.},
  language  = {en}
}
@article{SchellerWollenbergerSchubertetal.1993,
  author    = {Scheller, Frieder W. and Wollenberger, Ursula and Schubert, Florian and Pfeiffer, Dorothea and Markower, Alexander and McNeil, C. J.},
  title     = {Multienzyme biosensors : coupled enzyme reactions and enzyme activation},
  year      = {1993},
  language  = {en}
}
@article{SchellerKirsteinSchubertetal.1993,
  author    = {Scheller, Frieder W. and Kirstein, Dieter and Schubert, Florian and Pfeiffer, Dorothea and McNeil, C. J.},
  title     = {Enzymes in electrochemical biosensors},
  year      = {1993},
  language  = {en}
}