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  • Artikel: DFG Deutsche Nationallizenzen  (45)
  • Cell & Developmental Biology  (38)
  • Transparent Query Language  (7)
  • 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
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    Cell Motility and the Cytoskeleton 25 (1993), S. 87-104 
    ISSN: 0886-1544
    Schlagwort(e): polymerization ; solation ; gelation ; α-actinin ; gelsolin ; calcium ; Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie , Medizin
    Notizen: We describe a cellular automaton model of the actin cytoskeleton. The model incorporates spatial and temporal behavior at the macomolecular level and is relevant to the viscous nonequilibrium conditions suspected to occur in vivo. The model include cation and nucleotide binding to actin monomers, actin nucleation and polymerization into filaments, coss-linking with α-actinin, monomer sequestration with pfilin, filament severing, capping and nucleation with gelsolin, binding of profilin and gelsolin to membrane-bound phosphatidylinositide biphosphate (PIP2), and regulation of coss-linking and severing by changing calcium levels. We derive (1) equations for the molecular trnslation and rotation probabilities required for the cellular automaton simulation in terms of molecular size, shape, cytoplasmic viscosity, and temperature; and (2) equations for the binding probabilities of adjacent molecules in terms of experimentally determined reaction rate constants. The model accurately captures the known characteristics of actin polymerization and subsequent ATP hydrolysis under different cation and nucleotide conditions. An examination of gelation and sol-gel transitions resulting from calcium regulation of α-actinin and gelsolin predicts an inhomogeneous distribution of bound α-actinin and F-actin. The double-bound α-actinin (both ends bound to F-actin) is tightly bunched, while single-bound α-actinin is moderately bunched and unbound α-actinin is homogeneously distributed. The spatial organization of the α-actinin is quantified using estimates of fractal dimension. The simulation results also suggest that actin/α-actinin gels may shift from an isotropic to an amorphous phase after shortening of filaments. The gel-sol transition of the model shows excellent agreement with the present theory of polymer gels. The close correspondence of the model's predictions with previous experimental and theoretical results suggests that the model may be pertinent to better understanding the spatial and temporal properties of complex cytoskeletal processes. © 1993 Wiley-Liss, Inc.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Molecular Reproduction and Development 26 (1990), S. 248-252 
    ISSN: 1040-452X
    Schlagwort(e): Microfilaments ; Pinocytosis ; Amino acids ; Defolliculation ; Pigment ; Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: Defolliculated fully grown oocytes of Xenopus laevis were treated with cytochalasin D (10 μg/ml) and their protein synthesis was studied by labelling with S-35 methionine. This treatment brought about an alteration in pigment pattern as well as a reduction in amino acid uptake by the oocytes. However, the radioactive amino acid taken by cytochalasin-treated oocytes was incorporated into protein in the same proportion as in untreated oocytes. These results suggested that subcortical pigment distribution and amino acid uptake in fully grown oocytes were microfilament-dependent processes, whereas protein synthesis in the oocyte was not.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Molecular Reproduction and Development 36 (1993), S. 7-15 
    ISSN: 1040-452X
    Schlagwort(e): Intercellular coupling ; Connexin32 ; Connexin43 ; Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: The connexins constitute a family of proteins that make up the intercellular membrane channels of gap junctions. We had previously reported the presence of two members of this protein family, connexins 32 and 43, in mouse one-cell zygotes (Barron et al., Dev Genet 10:318-323, 1989; Valdimarsson et al., Mol Reprod Dev 30:18-26, 1991), implying that both must be present in the mature oocyte and could be involved in mediating the intercellular coupling that occurs between the oocyte and cumulus granulosa during oogenesis. In the present report we provide evidence for this, based on an analysis of the cumulus-oocyte complex (COC) using reverse transcription-polymerase chain reaction (RT-PCR) and immunocytochemistry with a confocal microscope. Transcripts of both connexin32 (Cx32) and connexin43 (Cx43) were detected by RT-PCR in both components of the COC. Cx32 mRNA in the oocyte declined precipitously following human chorionic gonadotropin (hCG) stimulation of pregnant mare serum gonadotropin (PMSG)-primed ovaries, whereas there was no obvious change in Cx43 mRNA. Peptide-specific antibodies against both connexins provided diffuse cytoplasmic staining of oocytes as well as some punctate staining near the oocyte surface, which could not be unequivocally resolved as cumulus-oocyte gap junctions. However, the two antibodies did provide clear evidence of Cx32 and Cx43 in gap junction-like structures between cumulus cells. We could find no evidence of the incorporation of the oocyte's store of Cx32 into gap junctions during postfertilization development. These findings make it very likely that intercellular coupling within the COC involves at least three types of gap junction channels (32-32, 32-43, 43-43), only one of which (43-43) is retained by the preimplantation embryo. © 1993 Wiley-Liss, Inc.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Molecular Reproduction and Development 30 (1991), S. 18-26 
    ISSN: 1040-452X
    Schlagwort(e): Gap junction protein ; Gene expression ; Compaction ; Life and Medical Sciences ; Cell & Developmental Biology
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Biologie
    Notizen: De novo assembly of gap junctions begins during compaction in the eight-cell stage of mouse development, and intercellular coupling mediated by gap junctions appears to be required for maintenance of the compacted state. We have begun to explore the expression of the family of genes encoding the connexins, the proteins that form the gap junction channels. We recently reported that a protein with antigenic and size similarity with connexin32, the rat liver gap junction protein, is inherited as an oogenetic product by the mouse zygote, but its gene appears not to be transcribed prior to implantation (Barron et al., Dev Genet 10:318-323, 1989). Here we report that another member of this gene family, connexin43, is transcribed by the embryonic genome from shortly after the time of genomic activation. As revealed by Northern blotting, connexin43 mRNA is absent from ovulated oocytes, becomes detectable in the 4-cell stage, and accumulates steadily thereafter to reach a maximum in blastocysts. In contrast, no transcripts of connexin26 could be detected in any preimplantation stage. A protein with antigenic and size similarity with connexin43 from rat heart was found by Western blotting to accumulate from the four-cell stage onward. Immunofluorescence analysis with embryo whole mounts was used to demonstrate that this protein is incorporated into punctate interblastomeric foci during compaction, consistent with its assembly into gap junction plaques. We conclude that connexin43 is one member of the connexin gene family whose zygotic expression is critical for preimplantation morphogenesis.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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