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See detailn-InGaAs Schottky Diode with Current Transport along 2DEG Channel
Kordoš, P.; Marso, Michel UL; Fox, A. et al

in Electronics Letters (1992), 28(1992), 1689-1690

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See detailSchottky Contacts on n-In0.53Ga0.47As with Enhanced Barriers by Counter-Doped Interfacial Layers,
Kordoš, P.; Marso, Michel UL; Meyer, R. et al

in IEEE Transactions on Electron Devices (1992), 39(1992), 1970-1972

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See detailIn vivo analysis of functional domains from villin and gelsolin.
Finidori, J.; Friederich, Evelyne UL; Kwiatkowski, D. J. et al

in The Journal of cell biology (1992), 116(5), 1145-55

Transfected CV1 cells were used to compare the in vivo effects of various domains of villin and gelsolin. These two homologous actin modulating proteins both contain a duplicated severin-like sequence ... [more ▼]

Transfected CV1 cells were used to compare the in vivo effects of various domains of villin and gelsolin. These two homologous actin modulating proteins both contain a duplicated severin-like sequence. Villin has in addition a carboxy-terminal domain, the headpiece, which accounts for its bundling activity. The effects of the villin-deleted mutants were compared with those of native villin. Our results show that essential domains of villin required to induce the growth of microvilli and F-actin redistribution are present in the first half of the core and in the headpiece. We also show that the second half of the villin core cannot be exchanged by its homolog in gelsolin. When expressed at high levels of CV1 cells, full length gelsolin completely disrupted stress fibers without change of the cell shape. Addition of the villin headpiece to gelsolin had no effect on the phenotype induced by gelsolin alone. Expression of the first half of gelsolin induced similar modifications as capping proteins and rapid cell mortality; this deleterious effect on the cell structure was also observed when the headpiece was linked to the first half of gelsolin. In cells expressing the second half of gelsolin, a dotted F-actin staining was often seen. Moreover elongated dorsal F-actin structures were observed when the headpiece was linked to the second gelsolin domain. These studies illustrate the patent in vivo severing activity of gelsolin as well as the distinct functional properties of villin core in contrast to gelsolin. [less ▲]

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See detailFamille de courbes hyperelliptiques de genre g munies d'une classe de diviseurs rationnels d'ordre 2g^2+4g+1
Leprévost, Franck UL

in Séminaire de Théorie des Nombres (1992), 116

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See detailLes polarisations de Vergne dans une algèbre de Lie exponentielle
Molitor-Braun, Carine UL

in Travaux Mathématiques (1992), 4

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See detailSequence analysis of polymerase chain reaction amplified t(14;18) chromosomal breakpoints in formalin fixed, paraffin wax embedded follicular lymphoma.
Volkenandt, M.; Koch, O.; Fanin, R. et al

in Journal of clinical pathology (1992), 45(3), 210-2

AIMS: To determine whether junctional sequences of rearranged chromosomes can be amplified by use of the polymerase chain reaction (PCR) and whether direct sequence analysis of the PCR products is ... [more ▼]

AIMS: To determine whether junctional sequences of rearranged chromosomes can be amplified by use of the polymerase chain reaction (PCR) and whether direct sequence analysis of the PCR products is possible, using DNA from formalin fixed, paraffin wax embedded biopsy specimens. METHODS: DNA was extracted from paraffin wax embedded, formalin fixed lymphoma specimens, and junctional sequences of rearranged chromosomes were amplified by the PCR. The products were used as templates for asymmetrical PCR. Subsequently, direct sequence analysis was performed using the chain termination method. RESULTS: Formalin fixed, paraffin wax embedded biopsy specimens and PCR amplification could be used to determine the nucleotide sequences of junctional regions of rearranged chromosomes t(14;18) from patients with follicular lymphoma. CONCLUSION: The identification of junctional sequences of the translocation in follicular lymphoma provides a molecular "fingerprint" of t(14;18) of the lymphoma of an individual patient and can be used for the detection of clone specific DNA in any biopsy tissue obtained from the patient. The strategy used for rapid sequence analysis of PCR amplified DNA sequences will be useful in many areas of molecular pathology. [less ▲]

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See detailPurification and molecular cloning of the APO-1 cell surface antigen, a member of the tumor necrosis factor/nerve growth factor receptor superfamily. Sequence identity with the Fas antigen
Oehm, A.; Behrmann, Iris UL; Falk, W. et al

in Journal of Biological Chemistry (1992), 267(15), 10709-15

The APO-1 antigen as defined by the mouse monoclonal antibody anti-APO-1 was previously found to be expressed on the cell surface of activated human T and B lymphocytes and a variety of malignant human ... [more ▼]

The APO-1 antigen as defined by the mouse monoclonal antibody anti-APO-1 was previously found to be expressed on the cell surface of activated human T and B lymphocytes and a variety of malignant human lymphoid cell lines. Cross-linking of the APO-1 antigen by anti-APO-1 induced programmed cell death, apoptosis, of APO-1 positive cells. To characterize the APO-1 cell surface molecule and to better understand its role in induction of apoptosis, the APO-1 protein was purified to homogeneity from membranes of SKW6.4 B lymphoblastoid cells by solubilization with sodium deoxycholate, affinity chromatography with anti-APO-1 antibody, and reversed phase high performance liquid chromatography. Each purification step was followed by an APO-1-specific solid phase enzyme-linked immunosorbent assay using the monoclonal antibody anti-APO-1. In sodium dodecyl sulfate-polyacrylamide gel electrophoresis, the APO-1 antigen was found to be a membrane glycoprotein of 48-kDa. Endoproteinase-cleaved peptides of the APO-1 protein were subjected to amino acid sequencing, and corresponding oligonucleotides were used to identify a full-length APO-1 cDNA clone from an SKW6.4 cDNA library. The deduced amino acid sequence of APO-1 showed sequence identity with the Fas antigen, a cysteine-rich transmembrane protein of 335 amino acids with significant similarity to the members of the tumor necrosis factor/nerve growth factor receptor superfamily. The APO-1 antigen was expressed upon transfection of APO-1 cDNA into BL60-P7 Burkitt's lymphoma cells and conferred sensitivity towards anti-APO-1-induced apoptosis to the transfectants. [less ▲]

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See detailBanken und Wirtschaftskreislauf: Makroökonomische Konsequenzen einer Portfoliotheorie des Giralgeldangebotes
Klump, Rainer UL

in Jahrbucher für Nationalokonomie und Statistik (1992)

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See detailSchottky Barrier Height Enhancement on n-In0.53Ga0.47As
Kordoš, P.; Marso, Michel UL; Meyer, R. et al

in Journal of Applied Physics (1992), 72(1992), 2347-2355

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See detailMultiple Invariance ESPRIT
Swindlehurst, A.; Ottersten, Björn UL; Roy, R. et al

in IEEE Transactions on Signal Processing (1992), SP-40(4), 867881

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See detail«Slechtsprekenden en hardhorigen»
Roelens, Nathalie UL

in ALW-Cahier (1992)

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See detail«Le mode d'existence sémiotique des passions»
Roelens, Nathalie UL

in Scripta Semiotica (1992)

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See detailStates and traits in psychological assessment.
Steyer, Rolf; Ferring, Dieter UL; Schmitt, Manfred J.

in European Journal of Psychological Assessment (1992), 8(2)

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See detailVom Vorteil, ein Außenseiter zu sein
Steffgen, Georges UL

in Sportpsychologie (1992), 6(1), 22-23

Im Sport beobachtet man häufig das Phänomen, daß Außenseiter „übermächtige“ Gegner schlafen. Gibt es dafür eine plausible Erklärung?

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See detailQuestions actuelles en droit allemand des sociétés : de quoi nourrir la réflexion au sein d'un droit belge en mutation
Corbisier, Isabelle UL

in Revue Pratique des Sociétés Civiles et Commerciales (1992), (3), 153-209

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See detailThe molecular and genetic analysis of mouse development.
Gossler, A.; Balling, Rudi UL

in European Journal of Biochemistry (1992), 204(1), 5-11

This review describes some recent advances in the molecular-genetic analysis of mouse development. Reversed genetics and gene assignment have been used to isolate genes affected in developmental mutations ... [more ▼]

This review describes some recent advances in the molecular-genetic analysis of mouse development. Reversed genetics and gene assignment have been used to isolate genes affected in developmental mutations. The establishment of a high-density molecular-genetic map promises to facilitate cloning of additional genes with developmental functions. Based on molecular, biochemical or other biological criteria many mouse genes that code for transcriptional regulators, growth-factor-like molecules and their receptors have been isolated. The role of these genes during development can be analysed in vivo after producing targeted mutations. Mutations can be generated by homologous recombination in the genome of embryonic stem cells and can then be introduced into the mouse germ line by means of germ-line chimaeras. Additional approaches employing stem cells to identify and mutate putative developmental genes are coming into use. [less ▲]

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See detailno-bridge of drosophila melanogaster, - portrait of a structural brain mutant of the central complex
Strauß, Roland; Hanesch, Ulrike UL; Kinkelin, Martin et al

in Journal of Neurogenetics (1992), 8

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See detailNatural polyamines stimulate G-proteins
Bueb, Jean-Luc UL; Da Silva, A.; Mousli, M. et al

in Biochemical Journal (1992), 282 (Pt 2)

The natural polyamines spermine and spermidine, the biosynthetic precursor putrescine and their analogues cadaverine and tyramine stimulate the GTPase activity of purified GTP-binding proteins (Go/Gi ... [more ▼]

The natural polyamines spermine and spermidine, the biosynthetic precursor putrescine and their analogues cadaverine and tyramine stimulate the GTPase activity of purified GTP-binding proteins (Go/Gi) from calf brain reconstituted into phospholipid vesicles. The order of potency was spermine greater than spermidine greater than putrescine = cadaverine greater than tyramine. The physiological relevance of this observation was assessed, showing the same order of potency of polyamines in the stimulation of peritoneal and tracheal rat mast cells. The activation of rat mast cells by polyamines was inhibited by benzalkonium chloride or by a 2 h pretreatment of the cells with pertussis toxin. The increase in inositol phosphates evoked by polyamines was also inhibited by pertussis toxin. Therefore we propose that intracellular polyamines might control the basal level of second messengers and modulate extracellular signals transduced through G-protein-coupled receptors. [less ▲]

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See detailClinical and laboratory features of type 1 diabetic children at the time of diagnosis
Levy-Marchal, C.; Papoz, L.; De Beaufort, Carine UL et al

in Diabetic Medicine: A Journal of the British Diabetic Association (1992), 9

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See detailDevelopment of the skeletal system.
Balling, Rudi UL; Lau, C. F.; Dietrich, S. et al

in Ciba Foundation Symposium (1992), 165

The analysis of the development of the skeletal system has been greatly facilitated by the availability of a large number of mouse mutants with skeletal defects. Whereas for many of these mutants a ... [more ▼]

The analysis of the development of the skeletal system has been greatly facilitated by the availability of a large number of mouse mutants with skeletal defects. Whereas for many of these mutants a description of the main phenotypic abnormalities is known, molecular insight into the ontogeny of the skeletal system is limited. One of the few skeletal mutants for which the molecular basis is known is undulated. These mice have a defect in the differentiation of the sclerotome and Pax-1, a mouse paired-box containing gene, has been identified as a candidate gene for this mutation. A molecular analysis of three independent undulated alleles revealed that in each case the Pax-1 gene is affected. One of the alleles could be classified as a null allele, in which the Pax-1 gene is deleted. A phenotypic analysis shows that Pax-1 is required for proper differentiation of intervertebral discs and vertebral bodies. [less ▲]

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See detailWHATS IN A GENOME
BORK, P.; OUZOUNIS, C.; SANDER, C. et al

in Nature (1992), 358(6384), 287-287

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See detailAnalysis of Subspace Fitting and ML Techniques for Parameter Estimation from Sensor Array Data
Ottersten, Björn UL; Viberg, M.; Kailath, T.

in IEEE Transactions on Signal Processing (1992), SP-40

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See detailFremdenfeindliche Gewalt: Entwicklung, Strukturen, Eskalationsprozesse
Willems, Helmut UL

in Gruppendynamik (1992), 23. Jg(4), 433-448

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See detailBarcelona '92 - Psychologische Betreuung einer Olympia-Delegation
Steffgen, Georges UL

in Sportpsychologie (1992), 6(4), 29-30

In seiner Funktion als beratender Psychologe des Olympischen Komitees von Luxemburg (C.O.S.L.) hat der Autor die luxemburgische Olympia Delegation bei den Olympischen Spielen in Barcelona begleitet. Im ... [more ▼]

In seiner Funktion als beratender Psychologe des Olympischen Komitees von Luxemburg (C.O.S.L.) hat der Autor die luxemburgische Olympia Delegation bei den Olympischen Spielen in Barcelona begleitet. Im Rahmen des vorliegenden Erfahrungsberichtes zeigt er seine Aktivitäten im Vorfeld wie auch während der Olympischen Spiele auf. [less ▲]

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See detailTheoretische Pedagogiek (De AERA Annual Meeting: Chicago 1991)
Miedema, S.; Biesta, Gert UL

in Pedagogische Studiën: Tijdschrift voor Onderwijskunde en Opvoedkunde (1992), 68

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See detailBonAccord: un nouveau didacticiel de traduction semi-intelligent
Weber, Jean-Jacques UL

in Bulletin Nouvelles Technologies et Education (1992), 7

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See detailAn actin-binding site containing a conserved motif of charged amino acid residues is essential for the morphogenic effect of villin.
Friederich, Evelyne UL; Vancompernolle, K.; Huet, C. et al

in Cell (1992), 70(1), 81-92

The actin-binding protein villin induces microvillus growth and reorganization of the cytoskeleton in cells that do not normally produce this protein. Transfection of mutagenized villin cDNAs into CV-1 ... [more ▼]

The actin-binding protein villin induces microvillus growth and reorganization of the cytoskeleton in cells that do not normally produce this protein. Transfection of mutagenized villin cDNAs into CV-1 cells was used to show that a conserved, COOH-terminally located cluster of charged amino acid residues (KKEK) is crucial for the morphogenic activity of villin in vivo. In vitro experiments with a 22 amino acid synthetic peptide corresponding to this region of villin provide evidence that this motif is part of an F-actin-binding site that induces G-actin to polymerize. Chemical cross-linking of actin to this peptide, the effects of amino acid substitutions in peptides, and the behavior of villin variants further corroborate the participation of the KKEK sequence in actin contacts. [less ▲]

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See detailMolecular biology of oncogenes and cardiovascular hypertrophy.
Neyses, Ludwig UL; Vetter, H.

in Journal of hypertension (1992), 10(12), 1447-52

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See detailPax1, a member of the paired box-containing class of developmental control genes, is mapped to human chromosome 20p11.2 by in situ hybridization (ISH and FISH).
Schnittger, S.; Rao, V. V.; Deutsch, U. et al

in Genomics (1992), 14(3), 740-4

Pax-1, a member of a murine multigene family, belongs to the paired box-containing class of developmental control genes first identified in Drosophila. The Pax-1 gene encodes a sequence-specific DNA ... [more ▼]

Pax-1, a member of a murine multigene family, belongs to the paired box-containing class of developmental control genes first identified in Drosophila. The Pax-1 gene encodes a sequence-specific DNA-binding protein with transcriptional activating properties and has been found to be mutated in the autosomal recessive mutation undulated (un) on mouse chromosome 2 with vertebral anomalies along the entire rostrocaudal axis. By radioactive in situ hybridization (ISH) using a fragment from the murine Pax-1 paired box that is almost identical to the respective sequences from the cognate human gene HuP48 and fluorescence in situ hybridization (FISH) using a complete mouse Pax-1 cDNA, we have assigned the human homologue of murine Pax-1, the PAX1 locus, to chromosome 20p. The map position of PAX1 after FISH (FL-pter value of 0.34 +/- 0.04) corresponds to band p11.2. These results confirm the exceptional homology between human chromosome 20 and the distal segment of mouse chromosome 2, extending from bands F to G, and add PAX1 to the group of genes on 20p like PTPA, PRNP, SCG1, BMP2A, which are located in proximity on both chromosomes. [less ▲]

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See detail[Potassium restriction and essential hypertension].
Neyses, Ludwig UL

in Deutsche medizinische Wochenschrift (1946) (1992), 117(35), 1341

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See detailCOMPREHENSIVE SEQUENCE-ANALYSIS OF THE 182 PREDICTED OPEN READING FRAMES OF YEAST CHROMOSOME-III
BORK, P.; OUZOUNIS, C.; SANDER, C. et al

in Protein Science: A Publication of the Protein Society (1992), 1(12), 1677-1690

With the completion of the first phase of the European yeast genome sequencing project, the complete DNA sequence of chromosome III of Saccharomyces cerevisiae has become available (Oliver, S.G., et al ... [more ▼]

With the completion of the first phase of the European yeast genome sequencing project, the complete DNA sequence of chromosome III of Saccharomyces cerevisiae has become available (Oliver, S.G., et al., 1992, Nature 357, 38-46). We have tested the predictive power of computer sequence analysis on the 176 probable protein products of this chromosome, after exclusion of six problem cases. When the results of database similarity searches are pooled with prior knowledge, a likely function can be assigned to 42% of the proteins, and a predicted three-dimensional structure to a third of these (140% of the total). The function of the remaining 58% remains to be determined. Of these, about one-third have one or more probable transmembrane segments. Among the most interesting proteins with predicted functions are a new member of the type X polymerase family, a transcription factor with an N-terminal DNA-binding domain related to GAL4, a ''fork head'' DNA-binding domain previously known only in Drosophila and in mammals, and a putative methyltransferase. Our analysis increased the number of known significant sequence similarities on chromosome III by 13, to now 67. Although the near 40% success rate of identifying unknown protein function by sequence analysis is surprisingly high, the information gap between known protein sequences and unknown function is expected to widen and become a major bottleneck of genome projects in the near future. Based on the experience gained in this test study, we suggest that the development of an automated computer workbench for protein sequence analysis must be an important item in genome projects. [less ▲]

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See detailTorsion sur des familles de courbes de genre g
Leprévost, Franck UL

in Manuscripta Mathematica (1992), 75

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See detailMontesquieu face au mariage. Alliances matrimoniales entre noblesse de robe et négociants à Bordeaux au début du XVIIIe siècle
Voss, Peter UL

in Revue Historique de Bordeaux et du Département de la Gironde (1992), 34(2), 41-54

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See detailString branchings on complex tori and algebraic representations of generalized Krichever-Novikov algebras
Ruffing, Andreas; Deck, Thomas; Schlichenmaier, Martin UL

in Letters in Mathematical Physics (1992), 26(1), 23-32

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See detailNeurokinin A-like immunoreactivity in articular afferents of the cat
Hanesch, Ulrike UL; Heppelmann, Bernd; Schmidt, Robert

in Brain Research (1992), 586

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See detailTableau des délais d'action en matière de garantie des immeubles vendus ou construits
Ravarani, Georges UL

in Pasicrisie Luxembourgeoise: Recueil Trimestriel de la Jurisprudence Luxembourgeoise (1992), 28

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See detailLa loi du 5 août 1991 sur la protection de la concurrence économique
Corbisier, Isabelle UL

in Le droit des affaires = Het ondernemingsrecht (1992), 24

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See detailNicotinamid
De Beaufort, Carine UL

in Diabetes, prevention and therapy (1992), 6

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See detailDie historische Bäderarchitektur des Ostseebades Sellin auf Rügen - wertvolles Kapitel für die Entwicklung des Fremdenverkehrs
Helfer, Malte UL

in Greifswalder Beiträge zur Regional-, Freizeit- und Tourismusforschung (1992), 3

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See detailWaardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene.
Tassabehji, M.; Read, A. P.; Newton, V. E. et al

in Nature (1992), 355(6361), 635-6

Waardenburg's syndrome (WS) is an autosomal dominant combination of deafness and pigmentary disturbances, probably caused by defective function of the embryonic neural crest. We have mapped one gene for ... [more ▼]

Waardenburg's syndrome (WS) is an autosomal dominant combination of deafness and pigmentary disturbances, probably caused by defective function of the embryonic neural crest. We have mapped one gene for WS to the distal part of chromosome 2. On the basis of their homologous chromosomal location, their close linkage to an alkaline phosphatase gene, and their related phenotype, we suggested that WS and the mouse mutant Splotch might be homologous. Splotch is caused by mutation in the mouse Pax-3 gene. This gene is one of a family of eight Pax genes known in mice which are involved in regulating embryonic development; each contains a highly conserved transcription control sequence, the paired box. Here we show that some families with WS have mutations in the human homologue of Pax-3. Mutations in a related gene, Pax-6, which, like Pax-3, has both a paired box and a paired-type homeobox sequence, cause the Small-eye mutation in mice and aniridia in man. Thus mutations in the Pax genes are important causes of human developmental defects. [less ▲]

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See detailThe Development of the Preverbal Markers in St-Louis-Creole: The Formation of a TMA-System
Ehrhart, Sabine UL

in Language Sciences (1992), 14(3), 233-247

St-Louis-Creole or Tayo is spoken by the people of the St-Louis tribe in New Caledonia. Our data stem from several months of fieldwork in 1989 and 1990 with some Melanesian families of the tribe. All the ... [more ▼]

St-Louis-Creole or Tayo is spoken by the people of the St-Louis tribe in New Caledonia. Our data stem from several months of fieldwork in 1989 and 1990 with some Melanesian families of the tribe. All the phrases and structures we quote in this article can be placed in a communicative and syntactic context. [less ▲]

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See detailEnhancement of the Schottky Barrier Height on n-InGaAs by Thin InP Interlayers
Kordoš, P.; Marso, Michel UL; Lüth, H.

in Journal of Electrical Engineering (1992), 44(1992), 367-371

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See detailSELECTION OF REPRESENTATIVE PROTEIN DATA SETS
HOBOHM, U.; SCHARF, M.; Schneider, Reinhard UL et al

in Protein Science: A Publication of the Protein Society (1992), 1(3), 409-417

The Protein Data Bank currently contains about 600 data sets of three-dimensional protein coordinates determined by X-ray crystallography or NMR. There is considerable redundancy in the data base, as many ... [more ▼]

The Protein Data Bank currently contains about 600 data sets of three-dimensional protein coordinates determined by X-ray crystallography or NMR. There is considerable redundancy in the data base, as many protein pairs are identical or very similar in sequence. However, statistical analyses of protein sequence-structure relations require nonredundant data. We have developed two algorithms to extract from the data base representative sets of protein chains with maximum coverage and minimum redundancy. The first algorithm focuses on optimizing a particular property of the selected proteins and works by successive selection of proteins from an ordered list and exclusion of all neighbors of each selected protein. The other algorithm aims at maximizing the size of the selected set and works by successive thinning out of clusters of similar proteins. Both algorithms are generally applicable to other data bases in which criteria of similarity can be defined and relate to problems in graph theory. The largest nonredundant set extracted from the current release of the Protein Data Bank has 155 protein chains. In this set, no two proteins have sequence similarity higher than a certain cutoff (30% identical residues for aligned subsequences longer than 80 residues), yet all structurally unique protein families are represented. Periodically updated lists of representative data sets are available by electronic mail from the file server "netserv @ embl-heidelberg.de." The selection may be useful in statistical approaches to protein folding as well as in the analysis and documentation of the known spectrum of three-dimensional protein structures. [less ▲]

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See detailIncidence of childhood-onset insulin-dependent diabetes mellitus: the EURODIAB ACE Study
Green, A.; Patterson, C.C.; Gale, E.A. et al

in Lancet (1992), 339(8798), 905-909

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See detail«Nez à nez avec l'humour»
Roelens, Nathalie UL

in Poétique (1992)

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See detailPsychophysical examination of pain induced by defined CO2 pulses applied to the nasal mucosa
Anton, Fernand UL; Euchner, Ingrid; Handwerker, Hermann-Otto

in Pain (1992), 49(1), 53-60

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See detailDie Korrektion verwahrloster Kinder im Königreich Württemberg zu Beginn des 19. Jahrhunderts
Priem, Karin UL

in Zeitschrift für Wurttembergische Landesgeschichte (1992), 51

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See detailInteractions between Earth and ocean tides
Francis, Olivier UL

in Marées Terrestres Bulletin d'Informations (1992), 112

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See detailThe methodology of mental stress testing in cardiovascular research.
Steptoe, Andrew; Vögele, Claus UL

in Circulation (1991), 83(Suppl II), 14-24

Many issues related to the selection, reliability, and validity of mental stress testing in cardiovascular research are discussed. Five categories of mental stress testing are distinguished: problem ... [more ▼]

Many issues related to the selection, reliability, and validity of mental stress testing in cardiovascular research are discussed. Five categories of mental stress testing are distinguished: problem-solving tasks, information-processing tasks, psychomotor tasks, affective conditions, and aversive or painful conditions. A series of practical and theoretical criteria are outlined for the selection of appropriate tests, and the measurement of a range of dependent variables is emphasized. The temporal stability of cardiovascular responses to mental stress tests is examined through an analysis of test-retest correlations (weighted for sample size) in 28 comparisons with intervals between sessions varying from 1 day to more than 1 year. Heart rate reactions to tasks show an average-weighted Z of 0.732 +/- 0.031 (r = 0.62), with Z = 0.575 +/- 0.034 (r = 0.52) for systolic blood pressure and Z = 0.313 +/- 0.035 (r = 0.30) for diastolic blood pressure. It is argued that the validity of mental stress tests can be judged in relation to several different aspects, specifically, methodological, ecological, diagnostic, prognostic, and therapeutic validities. The nature of these standards is described, and pertinent literature is presented. [less ▲]

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See detailBarrier Height Enhancement of n-In0.53Ga0.47As Schottky Diodes Grown by MOCVD Technique
Kordoš, P.; Marso, Michel UL; Meyer, R. et al

in Electronics Letters (1991), 27(1991), 1759-1760

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See detailStress e disturbi cardiovasculari. Problemi metodologici nell'utilizo della tecnica dello stress mentale (Mental Stress Test)
Pruneti, Carlo A.; Vögele, Claus UL; Steptoe, Andrew

in Medicina Psicosomatica (1991), 36

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See detailgl(∞) and geometric quantization
Bordemann, Martin UL; Hoppe, Jens; Schaller, Peter et al

in Communications in Mathematical Physics (1991), 138(2), 209-244

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See detailEndothelins: functional and autoradiographic studies in guinea pig trachea
Tschirhart, Eric UL; Drijfhout, J. W.; Pelton, J. T. et al

in Journal of Pharmacology and Experimental Therapeutics (1991), 258(1), 381-7

The presence of binding sites for [125I]endothelin-1 and the contractile activities of endothelins (ETs) and sarafotoxin S6b and the endothelin fragment ET(16-21) were investigated in guinea pig trachea ... [more ▼]

The presence of binding sites for [125I]endothelin-1 and the contractile activities of endothelins (ETs) and sarafotoxin S6b and the endothelin fragment ET(16-21) were investigated in guinea pig trachea. ETs and sarafotoxin S6b (0.1-100 nM) induced potent contractile responses in guinea pig trachea with EC50 values ranging from 1.57 to 12.97 nM. Epithelium removal increased the potencies of ET-1, ET-2 and S6b, but not that of ET-3, and maximal responses to ET-1 and ET-2 were also increased. Effects of epithelium removal were partially mimicked by phosphoramidon (10 microM), an enkephalinase inhibitor, suggesting that enkephalinase (EC.3.4.24.11.) is able to degrade ET-1 and ET-2. ET-3-induced contractions were not affected by phosphoramidon. Autoradiographic studies suggested the presence of at least two specific binding sites for [125]ET-1 in guinea pig airway smooth muscle. The correlation between Kd and EC50 values suggests that the binding sites identified in the airway smooth muscle represent functional receptors for ETs. ET(16-21) and ET(16-21)-NH2 were less potent agonists than the ETs in guinea pig trachea and 10 microM ET(16-21) was unable to inhibit [125I]ET-1 binding in guinea pig airway smooth muscle. Therefore, these results suggest that the C-terminal hexapeptide of ET-1 cannot be used to classify ET receptors in guinea pig trachea. [less ▲]

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See detailWetenschapspedagogiek. Over de pedagogische bijdrage aan het wetenschapstheoretisch debat.
Biesta, Gert UL; Miedema, S.

in Comenius (1991), 11(1), 20-36

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See detailEvidence for the interaction of mast cell-degranulating peptide with pertussis toxin-sensitive G proteins in mast cells
Mousli, M.; Bronner, C.; Bueb, Jean-Luc UL et al

in European Journal of Pharmacology (1991), 207(3), 249-55

K(+)-channel blocker properties have been reported for mast cell-degranulating peptide (MCD) in the central nervous system, but its action mechanism in mast cells remains unknown. We studied the effect of ... [more ▼]

K(+)-channel blocker properties have been reported for mast cell-degranulating peptide (MCD) in the central nervous system, but its action mechanism in mast cells remains unknown. We studied the effect of MCD on the membrane potential of rat peritoneal mast cells using the fluorescent probe bis-oxonol. Unexpectedly, MCD induced a decrease in bis-oxonol fluorescence, in a rapid and then a slower phase, suggesting hyperpolarization of mast cells. Other K(+)-channel blockers, tetraethylammonium and 4-aminopyridine, did not significantly modify the bis-oxonol fluorescence and did not alter the effect of MCD. The late phase of bis-oxonol fluorescence decrease was inhibited by ouabain and by potassium deprivation, whereas histamine release was not affected. The first phase of putative hyperpolarization induced by MCD coincided with histamine release and with the generation of inositol polyphosphates. Prior treatment of the cells with pertussis toxin inhibited these effects of MCD. MCD stimulated the GTPase activity of purified G proteins (G0/Gi) in a concentration-dependent manner. These results indicate that the effect of MCD on mast cells is unrelated to K+ channels but that it is relevant to the activation of pertussis toxin-sensitive G proteins leading to the activation of phospholipase C. A direct interaction of MCD with G proteins is proposed, which, unlike mastoparan, does not require positive cooperativity. [less ▲]

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See detailMolecular basis for cellular effects of naturally occurring polyamines
Bueb, Jean-Luc UL; Mousli, M.; Landry, Y.

in Agents and Actions (1991), 33(1-2), 84-7

The naturally occurring polyamines, putrescine, spermidine and spermine, and the analogue cadaverine, induce a dose-dependent histamine release from rat peritoneal mast cells. Spermine was the most active ... [more ▼]

The naturally occurring polyamines, putrescine, spermidine and spermine, and the analogue cadaverine, induce a dose-dependent histamine release from rat peritoneal mast cells. Spermine was the most active among these polycationic metabolites, followed by spermidine and putrescine. The histamine release was inhibited by a 2 h pretreatment of the cells with pertussis toxin (100 ng/ml), demonstrating the involvement of a pertussis toxin-sensitive GTP-binding regulatory protein during the exocytotic process. Experiments performed with purified Go/Gi proteins reconstituted into phospholipid vesicles showed a direct stimulation of GTPase activity by the polyamines. This direct stimulation of G proteins and the consequent activation of the coupled effectors may represent a new mechanism of action for natural polyamines controlling receptor-dependent processes. [less ▲]

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See detailAnspruch und Wirklichkeit. Theodor W. Adornos Beitrag zur 'Rettung' Stefan Georges
Heimböckel, Dieter UL

in Castrvm peregrini : Zeitschrift für Literatur, Kunst- und Geistesgeschichte (1991), CXCVI-CXCVII

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See detailSubspace Based Detection for Linear Structural Relations
Viberg, M.; Ottersten, Björn UL; Kailath, T.

in Journal of Combinatorics, Information and System Sciences (1991), 16(2-3), 170189

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See detailLa propriété de Wiener
Molitor-Braun, Carine UL

in Travaux Mathématiques (1991), 3

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See detailDATABASE OF HOMOLOGY-DERIVED PROTEIN STRUCTURES AND THE STRUCTURAL MEANING OF SEQUENCE ALIGNMENT
SANDER, C.; Schneider, Reinhard UL

in Proteins (1991), 9(1), 56-68

The database of known protein three-dimensional structures can be significantly increased by the use of sequence homology, based on the following observations. (1) The database of known sequences ... [more ▼]

The database of known protein three-dimensional structures can be significantly increased by the use of sequence homology, based on the following observations. (1) The database of known sequences, currently at more than 12,000 proteins, is two orders of magnitude larger than the database of known structures. (2) The currently most powerful method of predicting protein structures is model building by homology. (3) Structural homology can be inferred from the level of sequence similarity. (4) The threshold of sequence similarity sufficient for structural homology depends strongly on the length of the alignment. Here, we first quantify the relation between sequence similarity, structure similarity, and alignment length by an exhaustive survey of alignments between proteins of known structure and report a homology threshold curve as a function of alignment length. We then produce a database of homology-derived secondary structure of proteins (HSSP) by aligning to each protein of known structure all sequences deemed homologous on the basis of the threshold curve. For each known protein structure, the derived database contains the aligned sequences, secondary structure, sequence variability, and sequence profile. Tertiary structures of the aligned sequences are implied, but not modeled explicitly. The database effectively increases the number of known protein structures by a factor of five to more than 1800. The results may be useful in assessing the structural significance of matches in sequence database searches, in deriving preferences and patterns for structure prediction, in elucidating the structural role of conserved residues, and in modeling three-dimensional detail by homology. [less ▲]

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See detailValidity of the interaction model of anger: Studies in management and competitive sport
Steffgen, Georges UL; Schwenkmezger, Peter

in German Journal of Psychology (1991)

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See detailSeparate elements cause lineage restriction and specify boundaries of Hox-1.1 expression.
Puschel, A. W.; Balling, Rudi UL; Gruss, P.

in Development (1991), 112(1), 279-87

The Hox genes are a class of putative developmental control genes that are thought to be involved in the specification of positional identity along the anteroposterior axis of the vertebrate embryo. It is ... [more ▼]

The Hox genes are a class of putative developmental control genes that are thought to be involved in the specification of positional identity along the anteroposterior axis of the vertebrate embryo. It is apparent from their expression pattern that their regulation is dependent upon positional information. In a previous analysis of the Hox-1.1 promoter in transgenic mice, we identified sequences that were sufficient to establish transgene expression in a specific region of the embryo. The construct used, however, did not contain enough regulatory sequences to reproduce all aspects of Hox-1.1 expression. In particular, neither a posterior boundary nor a restriction of expression to prevertebrae was achieved. Here we show correct regulation by Hox-1.1 sequences in transgenic mice and identify the elements responsible for different levels of control. Concomitant with the subdivision of mesodermal cells into different lineages during gastrulation and organogenesis, Hox-1.1 expression is restricted to successively smaller sets of cells. Distinct elements are required at different stages of development to execute this developmental programme. One position-responsive element (130 bp nontranslated leader) was shown to be crucial for the restriction of expression not only along the anteroposterior axis of the embryo, setting the posterior border, but also along the dorsoventral axis of the neural tube and to the lineage giving rise to the prevertebrae. Thus, Hox-1.1 expression is established in a specific region of the embryo and in a specific lineage of the mesoderm by restricting the activity of the promoter by the combined effect of several regulatory elements. [less ▲]

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See detailCRABP and the teratogenic effects of retinoids
Balling, Rudi UL

in Trends in Genetics (1991), (7), 279-287

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See detailStructure, expression and chromosomal location of the Oct-4 gene.
Yeom, Y. I.; Ha, H. S.; Balling, Rudi UL et al

in Mechanisms of Development (1991), 35(3), 171-9

The map position of Oct-4 on mouse chromosome 17 is between Q and T regions in the Major Histocompatibility Complex (MHC), and it is physically located within 35 kb of a class I gene. Several Oct-4 ... [more ▼]

The map position of Oct-4 on mouse chromosome 17 is between Q and T regions in the Major Histocompatibility Complex (MHC), and it is physically located within 35 kb of a class I gene. Several Oct-4-related genes are present in the murine genome; one of them maps to chromosome 9. The genomic structure and sequence of Oct-4 determined in t-haplotypes reveals five exons, and shows no significant changes in the t12 mutant haplotype making it unlikely that Oct-4 and the t12 early embryonic lethal are the same gene. By in situ hybridization, detectable onset of zygotic Oct-4 expression does not occur until compaction begins at 8-cells, suggesting that there might be other regulatory factors responsible for initiating Oct-4 expression. [less ▲]

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See detailAnalysen der Bedeutungsstrukturen alltagssprachlicher Emotionswörter: Grundzüge eines Verfahrens, exemplarische Anwendung, Implikationen für die Forschung zu spezifischen Emotionen
Neppl, Rainer; Boll, Thomas UL

in Sprache und Kognition (1991), 10(2), 85-96

The paper presents a procedure that uses speech analysis to assess the meaning structures in natural-language emotion terms. It is noted that most psychological research on specific emotions is based on a ... [more ▼]

The paper presents a procedure that uses speech analysis to assess the meaning structures in natural-language emotion terms. It is noted that most psychological research on specific emotions is based on a structuring of the emotion domain provided by natural-language emotion terms, and that the vagueness and inconsistencies of natural-language emotion terms is frequently problematic. The proposed procedure assumes that the use of natural-language emotion terms in the attribution of emotions to self and others is guided by rules, that these rules can be reconstructed, and that the outcome of this reconstruction can be described as an (abstract) structure. The general procedure for obtaining these structures (explicit meaning structures) is described and illustrated with the German emotion term "Empoerung" (moral indignation). Then possible applications of the procedure and the explicit meaning structures are discussed: explicit meaning structures as (1) a reference point for intercultural emotion research, (2) as a starting point for differentiating empirical and pseudo-empirical questions, (3) for defining and operationalizing the object of research, and (4) for generating hypotheses on conditions, consequences, and possibilities of modifying specific emotions. [less ▲]

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See detailIncidence du diabète insulino-dépendant, survenant avant l’âge de 20 ans en France
Levy-Marchal, C.; Pappoz, L.; De Beaufort, Carine UL et al

in Pediatrie (1991), 46

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See detailÄrger lass nach - Ärger auf der Trainerbank
Steffgen, Georges UL

in Sportpsychologie (1991), 5(3), 14-17

Nicht nur Fußballspieler, sondern auch Trainer sind während eines Spiels emotional belastet. Im Leistungssport werden jedoch psychoregulative Fertigkeiten bisher meist nur von Sportlern gefordert. Im ... [more ▼]

Nicht nur Fußballspieler, sondern auch Trainer sind während eines Spiels emotional belastet. Im Leistungssport werden jedoch psychoregulative Fertigkeiten bisher meist nur von Sportlern gefordert. Im folgenden wird aus sportpsychologischer Sicht das Problem von Trainern mit Ärgersituationen umrissen und auf angemessene Umgangsweisen eingegangen. [less ▲]

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See detailInhibition of endothelin-1 induced myocardial protein synthesis by an antisense oligonucleotide against the early growth response gene-1.
Neyses, Ludwig UL; Nouskas, J.; Vetter, H.

in Biochemical and biophysical research communications (1991), 181(1), 22-7

We explored the role of the recently discovered "early growth response gene-1 (Egr-1)" in the induction of myocardial protein synthesis by endothelin-1. Endothelin-1 stimulated protein synthesis (i.e. 3H ... [more ▼]

We explored the role of the recently discovered "early growth response gene-1 (Egr-1)" in the induction of myocardial protein synthesis by endothelin-1. Endothelin-1 stimulated protein synthesis (i.e. 3H-phenylalanine incorporation) in isolated adult rat cardiomyocytes more than 2-fold. Addition of a 15mer Egr-1 antisense oligodeoxyribonucleotide complementary to the first 5 codons of the Egr-1 mRNA completely blocked endothelin-induced protein synthesis. A single base mismatch in the oligonucleotide sequence abolished the inhibitory effect. T3-induced stimulation of protein synthesis was unaffected by the antisense oligonucleotide. These results indicate that the Egr-1 gene product is involved (putatively as a third messenger) in the signal transduction cascade initiated by endothelin-1 which eventually culminates in the induction of cardiac protein synthesis. [less ▲]

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See detailJugend zwischen Märkten und Verbänden
Willems, Helmut UL; Eckert, Roland; Drieseberg, Drieseberg

in Deutsche Jugend: Zeitschrift für die Jugendarbeit (1991), (10), 435-442

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See detailPrévalence du diabète insulino-dépendant chez les enfants scolarisés de 6 a 16 ans en Lorraine
De Beaufort, Carine UL; Cecchi-Tenerini, R.; Clerc, R. et al

in Archives Françaises de Pédiatrie (1991), 48

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See detailG-proteins as targets for non-immunological histamine releasers
Mousli, M.; Bueb, Jean-Luc UL; Rouot, B. et al

in Agents and Actions (1991), 33(1-2), 81-3

The molecular mechanism of action of several non-immunological histamine releasers has been investigated using pertussis toxin which interfers, via ADP-ribosylation, with some G-proteins. Pertussis toxin ... [more ▼]

The molecular mechanism of action of several non-immunological histamine releasers has been investigated using pertussis toxin which interfers, via ADP-ribosylation, with some G-proteins. Pertussis toxin (100 ng/ml) inhibited histamine release induced by compound 48/80, substance P, mastoparan, peptide 401, bradykinin and spermine showing that a G-protein sensitive to pertussis toxin was involved in the non-immunological histamine release. All these compounds directly activate purified G-proteins. The sensitivity to pertussis toxin of this direct stimulatory effect was demonstrated for compound 48/80, mastoparan and substance P. Altogether these results suggest that a direct activation of G-protein might be the molecular mechanism of action of histamine secretagogues acting through a pertussis toxin sensitive G-protein and in this way mimic agonist-ligand receptor interaction. [less ▲]

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See detailSome Results of Heterogeneous Data Inversions for Oceanic Tides
Jourdin, F.; Francis, Olivier UL; Vincent, P. et al

in Journal of Geophysical Research (1991), 96(B12), 20267-20288

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See detailMethodisch handelen. Over de betekenis voor de radiologische beroepspraktijk.
Biesta, Gert UL

in Gamma. (1991), 41(2), 42-49

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See detailActivation of Gi-like proteins, a receptor-independent effect of kinins in mast cells
Bueb, Jean-Luc UL; Mousli, M.; Bronner, C. et al

in Molecular Pharmacology (1991), 38(6), 816-22

The peptide hormones bradykinin and kallidin (Lys-bradykinin), as well as their analogues [des-Arg9]-bradykinin, a selective B1 agonist, [des-Arg9,Leu8]-bradykinin, a selective B1 antagonist, and [Thi5,8 ... [more ▼]

The peptide hormones bradykinin and kallidin (Lys-bradykinin), as well as their analogues [des-Arg9]-bradykinin, a selective B1 agonist, [des-Arg9,Leu8]-bradykinin, a selective B1 antagonist, and [Thi5,8,D-Phe7]-bradykinin and D-Arg0-[Hyp3,D-Phe7]-bradykinin, two selective B2 antagonists, induced rapid histamine release from purified rat peritoneal mast cells. In contrast, the N-terminal fragment bradykinin-(1-5) was inactive. These peptides also activate the GTPase activity of GTP-binding proteins (G proteins) (Go/Gi) purified from calf brain, with an order of potency identical to that observed on mast cells, [Thi5,8,D-Phe7]-bradykinin much greater than kallidin greater than bradykinin greater than D-Arg0-[Hyp3,D-Phe7]-bradykinin greater than [des-Arg9]-bradykinin greater than [des-Arg9,Leu8]-bradykinin greater than bradykinin-(1-5). This correlation suggested that G proteins are the targets of kinins in mast cells. Accordingly, the concomitant increase in inositol trisphosphates and release of histamine elicited by kinins were inhibited by pertussis toxin pretreatment of mast cells. The inhibitory effect of benzalkonium chloride showed that the G proteins involved belong to the Gi type. GTPase activity was measured in the supernatant of homogenized mast cells but not in the membranous fraction. This activity was stimulated by kinins and by the venom peptide mastoparan. The potency of peptides was similar to that observed with purified bovine G proteins. Sodium dodecyl sulfate-gel electrophoresis of mast cell supernatant revealed pertussis toxin-induced ADP-ribosylation of two proteins, in the Mr 41,000 and 40,000 range, i.e., similar to purified alpha-subunits of Gi1 and Gi2 or Gi3 subtypes. The data support the proposal that bradykinin and analogues act like mastoparan, substance P, and compound 48/80, interacting first with sialic acid residues of the cell surface and then with Gi-like proteins, inducing phospholipase C activation and intracellular calcium mobilization. [less ▲]

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See detailGaInAs Camel transistors With Current Gain Above 6 at Room Temperature
Marso, Michel UL; Zwinge, G.; Grützmacher, D. et al

in Electronics Letters (1991), 27(1991), 335-337

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See detailCentral projections of trigeminal primary afferents innervating the nasal mucosa: a horseradish peroxidase study in the rat
Anton, Fernand UL; Peppel, Petra

in Neuroscience (1991), 41(2-3), 617-628

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See detailKalium-Restriktion und essentielle Hypertonie
Neyses, Ludwig UL

in Deutsche Medizinische Wochenschrift (1946) (1991), (116), 2417-2248

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See detailPerformance Analysis of the Total Least Squares ESPRIT Algorithm
Ottersten, Björn UL; Viberg, M.; Kailath, T.

in IEEE Transactions on Signal Processing (1991), SP-39

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See detailZur inhaltlichen Bestimmung und Erfassung von Lebensqualität um Umfeld schwerer körperlicher Erkrankungen.
Filipp, Sigrun-Heide; Ferring, Dieter UL

in Praxis der Klinischen Verhaltensmedizin und Rehabilitation (1991)

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See detailIncidence of insulin dependent diabetes in children of school age in Lorraine
De Beaufort, Carine UL; Cecchi-Tenerini, R.; Clerc, R. et al

in Archives Françaises de Pédiatrie (1991), 48(3), 228

[No abstract available]

Detailed reference viewed: 54 (1 UL)
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See detailUtilisation de médicaments anti-diabétiques au Grand Duché de Luxembourg
De Beaufort, Carine UL; Michel, G.; Haas, N. et al

in Bulletin de la Société des Sciences Médicales du Grand-Duché de Luxembourg (1991), 2

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See detailM2 World Ocean Tide from Tide Gauge Measurements
Francis, Olivier UL; Mazzega, P.

in Geophysical Research Letters (1991), 18(6), 1167-1170

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See detailSensor Array Processing Based on Subspace Fitting
Viberg, M.; Ottersten, Björn UL

in IEEE Transactions on Signal Processing (1991), SP-39(5), 11101121

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See detailMortalité par accident dans les mines de charbon en Belgique aux XIXe-XXe siècles
Leboutte, René UL

in Revue du Nord (1991), LXXIII, 293

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See detailTheoretische Pedagogiek (De AERA Annual Meeting: Chicago 1991).
Miedema, S.; Biesta, Gert UL

in Pedagogische Studiën: Tijdschrift voor Onderwijskunde en Opvoedkunde (1991), 68

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See detailControlled noxious chemical stimuation: reponses of rat trigeminal brainstem neurons to CO2 pulses applied to the naal mucosa
Anton, Fernand UL; Peppel, Petra; Euchner, Ingrid et al

in Neuroscience Letters (1991), 123(2), 208-211

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See detailBinding characteristics of [125I]endothelin-1 in guinea-pig trachea and its displacement by endothelin-1, endothelin-3 and endothelin (16-21)
Tschirhart, Eric UL; Pelton, J. T.; Jones, C. R.

in Agents and Actions. Supplements (1991), 31

The presence of binding sites for endothelin-1 (ET-1) and endothelin-3 (ET-3) in airway epithelium, submucosa and smooth muscle of guinea-pig trachea was investigated using in vitro autoradiography. We ... [more ▼]

The presence of binding sites for endothelin-1 (ET-1) and endothelin-3 (ET-3) in airway epithelium, submucosa and smooth muscle of guinea-pig trachea was investigated using in vitro autoradiography. We also examined the ability of the C-terminal hexapeptide of endothelin, ET(16-21) to inhibit specific [125I]ET-1, binding. ET-1 appeared to bind to a single class of binding sites (nH not different from unity). In contrast, nH values for ET-3 displacement of [125I]ET-1 specific binding were different from unity, suggesting that these peptides bound to more than one site. ET (16-21) did not affect [125I]ET-1 binding. The present results suggest that the binding sites identified in guinea pig airway smooth muscle may be related to receptors mediating contractile responses to the endothelins. [less ▲]

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See detailModelle der dreimodalen Faktorenanalyse: formale Eigenschaften, theoretische Zusammenhänge und ihre Implikationen für das Konzept individueller Differenzen
Krolak-Schwerdt, Sabine UL

in Psychologische Beiträge (1991), 133

The present paper is concerned with methods of three-mode factor analysis to obtain a dimensional representation of three-way data. Classifying the methods by the number of derived spaces and their ... [more ▼]

The present paper is concerned with methods of three-mode factor analysis to obtain a dimensional representation of three-way data. Classifying the methods by the number of derived spaces and their interrelations yields two distinct classes of models: CANDECOMP (Carroll & Chang, 1970), PARAFAC (Harshman, 1976) and SUMMAX (Orlik, 1980) rest on a basic trilinear decornposition of the data defining a separate space for each mode, whereas Tucker's (1964a thrce-mode factor analysis and SUMMA X in its extended form use a quadeilinear model specifying an additional core matrix. Associated with the current classification are different properties of the two model classes which refer to the number of substantial dimensions, their interpretation and the orientation of dimensions which is subject to rotations within the quadrilinear dass and uniquely determined by trilinear methods. Considering the different characteristics of the methods, formal relations between the classes have been found under very restrictive conditions only. However, there exist some general connections between trilinear and quadrilinear models. CANDECOMP and PARAFAC derive from the trilinear SUMMAX model by rescaling and permutation of axes, and the methodological link between the Tucker model and SUMMAX is given by orthogonal rotations of the SUMMAX configuration. These relationships are shown in an empirical example and their implications for the distinct concepts of individual differences within the two classes of methods are discussed. [less ▲]

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See detailDetection and Estimation in Sensor Arrays Using Weighted Subspace Fitting
Viberg, M.; Ottersten, Björn UL; Kailath, T.

in IEEE Transactions on Signal Processing (1991), SP-39(11), 24362449

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See detailPax: a murine multigene family of paired box-containing genes.
Walther, C.; Guenet, J. L.; Simon, D. et al

in Genomics (1991), 11(2), 424-34

A murine multigene family has been identified that shares a conserved sequence motif, the paired box, with developmental control and tissue-specific genes of Drosophila. To date five murine paired box ... [more ▼]

A murine multigene family has been identified that shares a conserved sequence motif, the paired box, with developmental control and tissue-specific genes of Drosophila. To date five murine paired box-containing genes (Pax genes) have been described and one, Pax-1, has been associated with the developmental mutant phenotype undulated. Here we describe the paired boxes of three novel Pax genes, Pax-4, Pax-5, and Pax-6. Comparison of the eight murine paired domains of the mouse, the five Drosophila paired domains, and the three human paired domains shows that they fall into six distinct classes: class I comprises Pox meso, Pax-1, and HuP48; class II paired, gooseberry-proximal, gooseberry-distal, Pax-3, Pax-7, HuP1, and HuP2; class III Pax-2, Pax-5, and Pax-8; class IV Pax-4; class V Pox neuro; and class VI Pax-6. Pax-1 and the human gene HuP48 have identical paired domains, as do Pax-3 and HuP2 as well as Pax-7 and HuP1, and are likely to represent homologous genes in mouse and man. Identical intron-exon structure and extensive sequence homology of their paired boxes suggest that several Pax genes represent paralogs. The chromosomal location of all novel Pax genes and of Pax-3 and Pax-7 has been determined and reveals that they are not clustered. [less ▲]

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See detailc-Fos immunoreactivity in rat brainstem neurons following noxious chemical stimulation of the nasal mucosa
Anton, Fernand UL; Herdegen, Thomas; Peppel, Petra et al

in Neuroscience (1991), 41(2-3), 629-641

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See detailSubstance P and calcitonin gene-related peptide immunoreactivity in primary afferent neurons of the cat`s knee joint
Hanesch, Ulrike UL; Heppelmann, Bernd; Schmidt, Robert

in Neuroscience (1991), 45

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See detailSelective implication of thromboxane A2 and PAF-acether in two guinea pig anaphylactic models
Bertrand, C.; Tschirhart, Eric UL; Landry, Y.

in Agents and Actions. Supplements (1991), 31

In an IgE and an IgG model of anaphylaxis in the guinea pig, we investigated the role of prostanoids and PAF-acether in the tracheal response in vitro to immunochallenge. Indomethacin (10(-6) M ... [more ▼]

In an IgE and an IgG model of anaphylaxis in the guinea pig, we investigated the role of prostanoids and PAF-acether in the tracheal response in vitro to immunochallenge. Indomethacin (10(-6) M) potentiated the antigen-induced contraction in both models suggesting the synthesis of relaxant prostaglandins during the anaphylactic phenomenon. UK-38,485 (10(-5) M), a thromboxane (TxA2) synthetase inhibitor, did not modify the tracheal response in the IgE model. In the IgG model, this drug reduced the response of the tracheal strips to antigen. Ro 19-3704 (10(-6) M) and BN 52021 (10(-5) M), two potent PAF antagonists, reduced antigen-induced contraction of the tracheal strips in the IgE model. These two drugs did not modify the contractile response in the IgG model. These results indicate that PAF-acether and TxA2 play a role in the IgE and IgG model of anaphylaxis, respectively. [less ▲]

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