@article{KlotzLohseSchwabeetal.1989,
  author    = {Klotz, Karl-Norbert and Lohse, M. J. and Schwabe, U. and Cristalli, G. and Vittori, S. and Grifantini, M.},
  title     = {2-Chloro-N\(^6\)-[\(^3\)H]cyclopentyladenosine ([\(^3\)H]CCPA) - a high affinity agonist radioligand for A\(_1\) adenosine receptors},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-60328},
  year      = {1989},
  abstract  = {The tritiated analogue of 2-chloro-N6-cyclopentyladenosine (CCPA), an adenosine derivative with subnanomolar affinity and a 10000-fold selectivity for A1 adenosine receptors, has been examined as a new agonist radioligand. [3H]CCP A was prepared with a specifi.c radioactivity of 1.58 TBqjmmol ( 43 Ci/mmol) and bound in a reversible manner to A1 receptors from rat brain membranes with a high affinity K0 -value of 0.2 nmol/1. In the presence of GTP a K0 -value of 13 nmol/1 was determined for the low affinity state for agonist binding. Competition of several adenosine receptor agonists and antagonists for [3H]CCPA binding to rat brain membranes confrrmed binding to an A1 receptor. Solubilized A1 receptors bound [3H]CCPA with similar affinity for the high affinity state. At solubilized receptors a reduced association rate was observed in the presence of MgC12, as has been shown for the agonist [ 3H]N6-phenylisopropyladenosine ([3H]PIA). [3H]CCPA was also used for detection of A1 receptors in rat cardio myocyte membranes, a tissue with a very low receptor density. A K0 -value of 0.4 nmol/1 and a Bmax-value of 16 fmol/ mg protein was determined in these membranes. In human platelet membranes no specific binding of [3H]CCPA was measured at concentrations up to 400 nmoljl, indicating that A2 receptors did not bind [3H]CCPA. Based on the subnanomolar affinity and the high selectivity for A1 receptors [ 3H]CCPA proved to be a useful agonist radioligand for characterization of A 1 adenosine receptors also in tissues with very low receptor density.},
  subject      = {Toxikologie},
  language  = {en}
}
@incollection{Wehgartner1989,
  author    = {Wehgartner, Irma},
  title     = {346. Ger{\"a}tteil mit Panskopf - 347. Rechteckige Reliefplatte mit J{\"u}nglingsb{\"u}ste - 348. Reliefmedaillon mit Gorgoneion - 350. Schale - 351. Miniaturgef{\"a}ß - 352. Fig{\"u}rlicher Gef{\"a}ßhenkel in Gestalt eines Eros als Akrobat (?) - 362. Griffspiegel - 363. Ger{\"a}tteil - 364. Zwei hohle Halbkugeln (Rassel ?) - 365. Anh{\"a}nger in Form eines Vogels},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-129393},
  publisher      = {Universit{\"a}t W{\"u}rzburg},
  year      = {1989},
  abstract  = {Katalogbeitr{\"a}ge},
  subject      = {Kiseleff, Alexander},
  language  = {de}
}
@article{ChristlBrunnRothetal.1989,
  author    = {Christl, Manfred and Brunn, E. and Roth, W. R. and Lennartz, H.-W.},
  title     = {7-Methyl- and 7-Phenylcyclohepta-1,3,5-trienes from Benzvalene Via 3,3a,4,5,6,6a-Hexahydro-4,5,6-methenocyclopentapyrazoles and Tetracyclo[4.1.0.0\(^{2,4}\).0\(^{3,5}\)]heptanes},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-58471},
  year      = {1989},
  abstract  = {No abstract available},
  subject      = {Organische Chemie},
  language  = {en}
}
@article{GilmoreCruzRodzLeimeisterWaechteretal.1989,
  author    = {Gilmore, Michael S. and Cruz-Rodz, Armando L. and Leimeister-W{\"a}chter, Michaela and Kreft, J{\"u}rgen and Goebel, Werner},
  title     = {A Bacillus cereus cytolytic determinant, cereolysin AB, which comprises the phospholipase C and sphingomyelinase genes: nucleotide sequence and genetic linkage},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-60588},
  year      = {1989},
  abstract  = {A cloned cytolytic determinant from the genome of Bacillus cereus GP-4 has been characterized at the molecular Ievel. Nucleotide sequence determination revealed the presence of two open reading frames. 8oth open reading frames were found by deletion and complementation analysis to be necessary for expression of the hemolytic phenotype by Bacillus subtilis and Escherichia coli hosts. The 5' open reading frame was found to be nearly identical to a recently reported phospholipase C gene derived from a mutant B. cereus strain which overexpresses the respective protein, and it conferred a lecithinase-positive phenotype to the B. subtilis host. The 3' open reading frame encoded a sphingomyelinase. The two tandemly encoded activities, phospholipase C and sphingomyelinase, constitute a biologically functional cytolytic determinant of B. cereus termed cereolysin AB.},
  subject      = {Biologie},
  language  = {en}
}
@misc{HuenigWehner1989,
  author    = {H{\"u}nig, Siegfried and Wehner, Ingeborg},
  title     = {A convenient synthesis of 2,2',6,6'-Tetramethyl-4,4'-bipyridine and its oxidation to 2,2',6,6'-Tetracarboxy-4,4'-bipyridine},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-32005},
  year      = {1989},
  abstract  = {No abstract available},
  language  = {en}
}
@article{GesslerThomasCouillinetal.1989,
  author    = {Gessler, Manfred and Thomas, G. H. and Couillin, P. and Junien, C. and McGillivray, B. C. and Hayden, M. and Jaschek, G. and Bruns, G. A.},
  title     = {A deletion map of the WAGR region on chromosome II},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-59255},
  year      = {1989},
  abstract  = {The WAGR (Wilms tumor, aniridia, genitourinary anomalies, and mental retardation) region has been assigned to chromosome 11p13 on the basis of overlapping constitutional deletions found in affected individuals. We have utilized 31 DNA probes which map to the WAGR deletion region, together with six reference loci and 13 WAGR-related deletions, to subdivide this area into 16 intervals. Specific intervals have been correlated with phenotypic features, leading to the identification of individual subregions for the aniridia and Wilms tumor loci. Delineation, by specific probes, of multiple intervals above and below the critical region and of five intervals within the overlap area provides a framework map for molecular characterization of WAGR gene loci and of deletion boundary regions.},
  subject      = {Biochemie},
  language  = {en}
}
@article{GesslerBruns1989,
  author    = {Gessler, Manfred and Bruns, G. A. P.},
  title     = {A physical map around the WAGR complex on the short arm of chromosome 11},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-59246},
  year      = {1989},
  abstract  = {A long-range restriction map of part of the short arm of ehromosome 11 including the WAGR region has been constructed using pulsed-field gel electrophoresis and a number of infrequently cutting restriction enzymes. A total of 15.4 Mbp has been mapped in detall, extending from proximal 11p14 to the distal part of 11p12. The map localizes 35 different DNA probes and reveals at least nine areas with features eharaeteristle of BTF islands, some of which may be candidates for the different loci underlying the phenotype of the WAGR syndrome. This map will furthermore allow screening of DNA from individuals with WAGR-related phenotypes and from Wilms tumors for associated chromosomal rearrangements.},
  subject      = {Biochemie},
  language  = {en}
}
@article{LambrechtFeifelWagnerRoederetal.1989,
  author    = {Lambrecht, G. and Feifel, R. and Wagner-R{\"o}der, M. and Strohmann, C. and Zilch, H. and Tacke, Reinhold and Waelbroeck, M. and Christophe, J. and Boddeke, H. and Mutschler, E.},
  title     = {Affinity profiles of hexahydro-sila-difenidol analogues at muscarinic receptor subtypes},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-63979},
  year      = {1989},
  abstract  = {In an attempt to assess the structural requirements of hexahydro-sila-difenidol for potency and selectivity, a series of analogues modified in the amino group and the phenyl ring were investigated for their affinity to muscarinic M1- (rabbit vas deferens), Mr (guinea-pig atria) and Mr (guinea-pig ileum) receptors. All compounds were competitive antagonists in the three tissues. Their affinities to the three muscarinic receptor subtypes differed by more than two orders of magnitude and the observed receptor selectivities were not associated with high affinity. The pyrrolidino and hexamethyleneimino analogues, compounds substituted in the phenylring with a methoxy group or a chlorine atom as weil as p-fluoro-hexahydro-difenidol displayed the same affinity profile as the parent compound, hexahydro-sila-difenidol: M1 = M3 > M2 • A different selectivity patternwas observed for p-fluoro-hexahydro-sila-difenidol: M3 > M1 > M2 • This compound exhibited its highest affinity for M3-receptors in guinea-pig ileum (pA 2 = 7.84), intermediate affinity for M1-receptors in rabbit vas deferens (pA 2 = 6.68) and lowest affinity for the Mrreceptors in guinea-pig atria (pA 2 = 6.01). This receptor selectivity profile of p-fluoro-hexahydro-sila-difenidol was confirmed in ganglia (M1), atria (M2 ) and ileum (M 3 ) of the rat. Furthermore, dose ratios obtained with either pirenzepine (Mt) or hexahydrosila- difenidol (M2 and M3) and the p-fluoro analogue used in combination suggested that the antagonism was additive, implying mutual competition with a single population of muscarinic receptor subtypes. These results indicate that p-fluoro-hexahydro-sila-difenidol represents a valuable tool for characterization of muscarinic receptor subtypes.},
  subject      = {Anorganische Chemie},
  language  = {en}
}
@incollection{HommersAnderson1989,
  author    = {Hommers, Wilfried and Anderson, Norman A.},
  title     = {Algebraic schemes in legal thought and in everyday morality},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-44015},
  publisher      = {Universit{\"a}t W{\"u}rzburg},
  year      = {1989},
  abstract  = {No abstract available},
  subject      = {Kriminalpsychologie / Aufsatzsammlung},
  language  = {en}
}
@article{SchmollHoschuetzkyMorschhaeuseretal.1989,
  author    = {Schmoll, T. and Hosch{\"u}tzky, H. and Morschh{\"a}user, J. and Lottspeich, F. and Jann, K. and Hacker, J{\"o}rg},
  title     = {Analysis of genes coding for the Sialic acid-binding adhesin and two other minor fimbrial subunits of the S-fimbrial adhesin determinant of Escherichia coli},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-59585},
  year      = {1989},
  abstract  = {The S flmbrial adhesln (Sfa) enables Esch richla colito attach to slalfc acld-containing receptor molecules of eukaryotJc cells. As prevlously reported, the genetlc determinant coding for the Sfa of an E. co/1 06 strain was cloned, the gene codlng for the major fimbrfal subunit was ldentlfled and sequenced and th.e S speclflc adhesin was detected. Here we present evidence that ln addltlon to the major subunit proteln SfaA three other minor subunit proteins, SfaG (17 kD), SfaS (14kD) and SfaH (31 kD) can be isolated from the S..speclfic flmbrial adhesln complex. The genes coding for these minor subunits were ldenblied, mutagenlzed separately and sequenced. Using haemagglutlnatton tests. electron-microscopy and quantitative ELISA assays with monoclonal anti-SfaA and anti-SfaS antlbodles the functlons of the minor subunlts were determined. lt was determlned that SfaS ls ldentlcal to the S-specific adhesln; whlch also plays a role ln deterrninatlon of the degree of fimbri· ation ofthe cell. The mlnor subunit SfaH also had some Jnfluence on the Ievei of fimbrlation of the cell. while StaG ls necessary for full expression of S·specific binding. lt was further shown that the amino-terminal proteln sequence of the isolated SfaS profein was identJcal to the proteln sequence calculated from the DNA sequence of the sfaS gene locus.},
  subject      = {Infektionsbiologie},
  language  = {en}
}