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  • Polymer and Materials Science  (45)
  • Life Sciences  (6)
  • Mathematically Complete Language  (6)
  • 1
    ISSN: 1573-8787
    Schlagwort(e): Transparent Query Language ; Mathematically Complete Language ; Philosophically Closed Language ; SOLID Retrieval/Processing System
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Informatik
    Notizen: Abstract This part, PART IIB [2], of the document “HIGH-SPEED TOOLS FOR GLOBAL INFORMATION MANAGEMENT. II. Specifications and Uses of the Transparent Query Language (TQL)” [1–6] contains the specifications for the operations that provide the arithmetic capabilities for Transparent Query Language. PART IIB references PART IIA [1] and PART IIC [3]. Concise definitions of Transparent Query Language terms, Conclusions and Acknowledgments are given in PART IIF [6].
    Materialart: Digitale Medien
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  • 2
    ISSN: 1573-8787
    Schlagwort(e): Transparent Query Language ; Mathematically Complete Language ; Philosophically Closed Language ; SOLID Retrieval/Processing System
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Informatik
    Notizen: Abstract This part, PART IIC [3], of the document “HIGH-SPEED TOOLS FOR GLOBAL INFORMATION MANAGEMENT. II. Specifications and Uses of the Transparent Query Language (TQL)” [1–6] is a continuation of [2] and should be studied immediately after reading PART IIB [2]. It describes (i) the security system that can be easily invoked to deny unauthorized access to any item of information in any database; (ii) the special codes that can be used to specify virtually any degree of uncertainty; (iii) the registry numbers which terminate information paths; and (iv) the command structure for the Transportable Query Language. PART IIC references PART IIA [1], PART IIB [2], PART IID [4] and PART IIF [6]. Concise definitions of Transparent Query Language terms, Conclusions and Acknowledgments are given in PART IIF [6].
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  • 3
    ISSN: 1573-8787
    Schlagwort(e): Transparent Query Language ; Mathematically Complete Language ; Philosophically Closed Language ; SOLID Retrieval/Processing System
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Informatik
    Notizen: Abstract In the six parts of the document “HIGH-SPEED TOOLS FOR GLOBAL INFORMATION MANAGEMENT. II. Specifications and Uses of the Transparent Query Language (TQL)” [1–6], the Transparent Query Language (TQL) that is the mathematical basis for the SOLID Retrieval/Processing System [7] is described and its use demonstrated. TQL is directly responsible for the speed, versatility, security and information/question-type independence of the SOLID System. It can be viewed as a Mathematically Complete (or Philosophically Closed) [8] data structure or content/context independent language capable of describing individual or classes of descriptors in any combination with any degree of specificity. The security system is easily used to prevent unauthorized access to any item in any file. TQL is sufficiently general to be used outside the context of information retrieval. It is capable of concisely representing and manipulating a wide variety of time dependent or static numeric and non-numeric information. The six parts of this document [1–6], are as follows. The first part, PART IIA [1], contains a review of the literature and then introduces the Transparent Query Language. It references PART IIB [2], PART IIC [3], PART IID [4], PART IIE [5] and PART IIF [6]. Concise definitions of Transparent Query Language terms, Conclusions and Acknowledgments are given in PART IIF [6]. Section III in PART IIA [1] contains information for converting citations of sections and subsections in the original document to their locations in the partitioned document.
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  • 4
    ISSN: 1573-8787
    Schlagwort(e): Transparent Query Language ; Mathematically Complete Language ; Philosophically Closed Language ; SOLID Retrieval/Processing System
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Informatik
    Notizen: Abstract This part, PART IID [4], of the document “HIGH-SPEED TOOLS FOR GLOBAL INFORMATION MANAGEMENT. II. Specifications and Uses of the Transparent Query Language (TQL)” [1–6] is about normalization and manipulation of information representations. It references PART IIA [1], PART IIB [2] and PART IIC [3]. Concise definitions of Transparent Query Language terms, Conclusions and Acknowledgments are given in PART IIF [6].
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  • 5
    ISSN: 1573-8787
    Schlagwort(e): Transparent Query Language ; Mathematically Complete Language ; Philosophically Closed Language ; SOLID Retrieval/Processing System ; Sequel (SQL) ; Relational Algebra ; QUEL ; Query-By-Example (QBE)
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Informatik
    Notizen: Abstract In this part, PART IIE [5], of the document “HIGH-SPEED TOOLS FOR GLOBAL INFORMATION MANAGEMENT. II. Specifications and Uses of the Transparent Query Language (TQL)” [1–6] the conversion of queries coded in SQL, Relational Algebra, QUEL and Query-By-Examples (QBE) to TQL are demonstrated. PART IIE references PART IIA [1], PART IIB [2], PART IID [3] and PART IIF [6]. Concise definitions of Transparent Query Language terms, Conclusions and Acknowledgments are given in PART IIF [6].
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  • 6
    ISSN: 1573-8787
    Schlagwort(e): Transparent Query Language ; Mathematically Complete Language ; Philosophically Closed Language ; SOLID Retrieval/Processing System
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Informatik
    Notizen: Abstract This part, PART IIF [6], concludes the document “HIGH-SPEED TOOLS FOR GLOBAL INFORMATION MANAGEMENT. II. Specifications and Uses of the Transparent Query Language (TQL)” [1–6]. It describes novel applications of TQL, the key data structures, and contains a dictionary of Transparent Query Language terms. PART IIF references PART IIA [1], PART IIB [2], PART IIC [3], PART IID [4], and PART IIE [5] and contains Conclusions and Acknowledgements.
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  • 7
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Human fibrinogen was treated with thrombin in the presence of fibrinoligase (Factor XIIIa) and calcium ion at pH 8.5, ionic strength 0.45, and the ensuing polymerization was interrupted at various time intervals (t) both before and after the clotting time (tc) by solubilization with a solution of sodium dodecyl sulfate and urea. Aliquots of the solubilized protein were subjected to gel electrophoresis on polyacrylamide gels after disulfide reduction by dithiothreitol and on agarose gels without reduction. The degree of γ-γ ligation was determined from the former. The latter provided the size distribution of ligated end-to-end sequences produced by splitting the ligated staggered overlapped oligomers down the middle, for degrees of polymerization, x, from 1 to 10. Addition of fibrinoligase (in which the activating thrombin had been inhibited by p-nitrophenyl-p′-guanidinobenzoate, NPGB) to Kabi fibrinogen showed the presence of small amounts of ligatable oligomers. Addition of fibrinoligase to a polymerizing mixture in which the action of thrombin had been stopped before clotting by NPGB produced the same distribution of ligated end-to-end sequences that was obtained when fibrinoligase was originally present, at least for reaction times up to 0.7 of the clotting time. The kinetics of γ-γ ligation by fibrinoligase acting on a polymerized mixture stabilized by NPGB were followed. The reaction was first order in the concentration of ligatable γ-γ junctions and the initial velocity was proportional to the enzyme concentration. The time evolution of size distribution of ligated end-to-end sequences agreed with a theory based on random ligation of ligatable junctions.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Biopolymers 21 (1982), S. 2265-2277 
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Human fibrinogen was treated with thrombin in the presence of fibrinoligase (Factor XIIIa) and calcium ion at pH 8.5, ionic strength 0.45, and the ensuing polymerization was interrupted at various time intervals (t) both before and after the clotting time (tc) by solubilization with a solution of sodium dodecylsulfate and urea. Aliquots of the solubilized protein were subjected to gel electrophoresis on polyacrylamide gels after disulfide reduction by dithiothreitol and on agarose gels without reduction. The degree of γ-γ ligation was determined from the former and the size distribution of ligated oligomers, for degree of polymerization x from 1 to 10, from the latter. In some experiments, thrombin was inhibited, after partial polymerization, by p-nitrophenyl-p′-guanidinobenzoate. From these, it was concluded that for thrombin concentration ≤0.013 units/mL and fibrinoligase ≥30 mg/L, oligomer assembly is rapid compared with peptide A release and ligation is rapid compared with assembly. Under these conditions, the theory of the first paper of this series describes rather well the time dependences of the degree of γ-γ ligation, the weight fractions of monomer and small oligomers, and the number- and weight-average degrees of polymerization after solubilization of the staggered overlapped assemblies, each of which splits to give two strands of end-to-end ligated oligomers. The theory assumes that the second A peptide is released by thrombin more rapidly than the first by a factor q, which, from the experimental data, is determined to be 16. The subsequent assembly into staggered overlapped oligomers follows the statistics of linear polycondesation taking into account the presence of both difunctional and monofunctional combining units. For higher thrombin or lower fibrinoligase concentrations, ligation fails to keep pace with oligomer assembly, and the size distributions after solubilization show a higher proportion of very small and a lower proportion of larger ligated oligomers, owing to separation of the staggered overlapped assemblies into smaller fragments.
    Zusätzliches Material: 10 Ill.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Biopolymers 25 (1986), S. 1337-1344 
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Soluble fibrin oligomers were formed by reacting fibrinogen with thrombin under fine clotting conditions where the action of thrombin is the rate-determining step for polymerization, and by inhibiting the reaction shortly before gelation. Oligomeric fibrin was separated from unreacted fibrinogen and small oligomers by gel permeation chromatography. Electron microscopy revealed that the largest soluble fibrin oligomers resemble the protofibrils present in fine clots, but are somewhat shorter and entirely lack the twisted, trifunctional junctions that contribute to the elastic properties of fine clots. When thrombin was added to the soluble fibrin oligomers, polymerization resumed and clots were formed at a more rapid rate than from fibrinogen at the same concentration and resulted in a less-opaque clot under coarse clotting conditions. The results confirm a prediction of a theory for the polymerization of fibrin and provide additional evidence that the final state of a coarse fibrin clot depends on the mobility of protofibrils during its formation.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 10
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The desire to replace the amide backbone of renin inhibitors with a new scaffold led us to explore vinylogous amides (enaminones). An initial attempt proved unsuccessful, a result explained after the fact via docking experiments. Based on this lesson, we designed a different vinylogous amide scaffold which incorportated one or more pyrrolinone rings into the backbone. Three of the four compounds gave IC50s in the 0.6 to 18 μM range. These compounds did not inhibit HIV-1 protease. Taken together, the results reported herein provide insights into the role of hydrogen bonding and steric interactions for binding to renin. © 1994 John Wiley & Sons, Inc.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
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