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  • SAGE Publications  (7)
  • 1990-1994  (7)
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  • SAGE Publications  (7)
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  • 1990-1994  (7)
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  • 1
    Online Resource
    Online Resource
    SAGE Publications ; 1993
    In:  Australian Journal of Education Vol. 37, No. 2 ( 1993-08), p. 198-211
    In: Australian Journal of Education, SAGE Publications, Vol. 37, No. 2 ( 1993-08), p. 198-211
    Abstract: Television is often accused of undermining children's academic achievement. This paper investigates two explanations which frequently accompany such a claim. The displacement hypothesis predicts that the time children spend with television is taken from activities that are more beneficial to school performance. The distraction hypothesis suggests that children's cumulative exposure to the structure of television—its pace, format, etc.–engenders an intolerance for the pace of schooling. A review of research on television viewing, time displacement, and academic performance fails to find any support for the displacement hypothesis. A review of studies relevant to the distraction hypothesis, however, uncovers mixed findings. This paper presents analyses of data gathered from school children in South Africa.
    Type of Medium: Online Resource
    ISSN: 0004-9441 , 2050-5884
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1993
    detail.hit.zdb_id: 2420054-2
    SSG: 5,3
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  • 2
    Online Resource
    Online Resource
    SAGE Publications ; 1990
    In:  Studia Liturgica Vol. 20, No. 2 ( 1990-09), p. 201-218
    In: Studia Liturgica, SAGE Publications, Vol. 20, No. 2 ( 1990-09), p. 201-218
    Type of Medium: Online Resource
    ISSN: 0039-3207 , 2517-4797
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1990
    detail.hit.zdb_id: 2941104-X
    SSG: 1
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  • 3
    Online Resource
    Online Resource
    SAGE Publications ; 1993
    In:  Journal of Histochemistry & Cytochemistry Vol. 41, No. 1 ( 1993-01), p. 57-70
    In: Journal of Histochemistry & Cytochemistry, SAGE Publications, Vol. 41, No. 1 ( 1993-01), p. 57-70
    Abstract: Pulmonary surfactant is thought to be internalized and processed for reuse by alveolar Type II cells. In the present study we followed the internalization and intracellular trafficking of purified surfactant protein A (SP-A) by primary cultures of alveolar Type II cells. Internalization of native rat SP-A was compared with that of recombinant rat and human SP-A isolated from a patient with alveolar proteinosis. All SP-A species were conjugated with colloidal gold for visualization by electron microscopy. The gold conjugates were biologically active, as demonstrated by inhibition of phospholipid secretion from alveolar Type II cells. The SP-A-gold conjugates were internalized to lamellar bodies (LB) via the endosomal system, which included both electron-lucent and -dense multivesicular bodies. Labeling of LB was time dependent, and after 7 hr 30-40% of these organelles were labeled. Alkylation of SP-A greatly reduced internalization, as did an excess of non-conjugated SP-A. No qualitative differences in uptake were observed with the three forms of SP-A. The percent of labeled LB was similar (30-40%) after 7 hr of internalization with the three species of SP-A. The recombinant SP-A produced using a baculovirus vector lacked hydroxyproline and had an altered oligosaccharide, but these features did not affect its internalization or the rate of LB labeling. Internalization of the gold-conjugated SP-A and endocytosis of the fluid-phase marker Lucifer Yellow were related to the shape of Type II cells. Both uptake of SP-A, which is receptor mediated, and fluid-phase endocytosis were found to be less active in the flattened than in the rounded cells. Therefore, cell shape and hence cytoskeletal organization may play an important role in SP-A recycling. However, it is possible that both morphology and decreased endocytosis are independent manifestations related to the loss of differentiated function of cultured Type II cells.
    Type of Medium: Online Resource
    ISSN: 0022-1554 , 1551-5044
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1993
    detail.hit.zdb_id: 1421306-0
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    SAGE Publications ; 1993
    In:  Journal of Histochemistry & Cytochemistry Vol. 41, No. 12 ( 1993-12), p. 1823-1832
    In: Journal of Histochemistry & Cytochemistry, SAGE Publications, Vol. 41, No. 12 ( 1993-12), p. 1823-1832
    Abstract: The multifunctional adhesive glycoprotein vitronectin (VN) undergoes a unique conformational transition from the plasma form into a multimeric form that represents the reactive heparin-binding form. In this study we investigated the interaction of multimeric vitronectin (VNmult) or VN-gold conjugates (which are equivalent in biochemical properties) with confluent and subconfluent monolayers of porcine endothelial cells. Time-dependent direct binding of radiolabeled VNmult to the luminal face of endothelial cells at 37 degrees C was observed which was competed by heparin, whereas plasma VN showed hardly any binding. At 4 degrees C binding of VNmult remained cell-associated, whereas after 6 hr at 37 degrees C a major portion of the ligand was translocated through cells and was associated with the subcellular matrix. Cytochemical studies with VN-gold conjugates were performed to demonstrate uptake of VNmult. At 4 degrees C only surface decoration of cells with gold label was seen, which was totally reversible in the presence of heparin. Subsequent incubation for various time intervals at 37 degrees C revealed disappearance of gold label from the surface and accumulation of conjugates in a perinuclear distribution inside the cells as judged both by electron microscopy and after silver enhancement by light microscopy. Cross-sections of endothelial cells demonstrated the inclusion of VN-gold conjugates in coated pits, endosomes, and in lysosomal compartments close to the nucleus. Within 2-6 hr a portion of VN-gold conjugates had accumulated with proteoglycans at the matrix face. These data provide strong evidence for specific routing of a portion of VNmult from the circulation into extravascular spaces, where the protein is believed to fulfill major adhesive and regulatory functions particularly as co-factor in plasminogen activation and immune defense.
    Type of Medium: Online Resource
    ISSN: 0022-1554 , 1551-5044
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1993
    detail.hit.zdb_id: 1421306-0
    SSG: 12
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  • 5
    Online Resource
    Online Resource
    SAGE Publications ; 1991
    In:  Journal of Histochemistry & Cytochemistry Vol. 39, No. 10 ( 1991-10), p. 1385-1394
    In: Journal of Histochemistry & Cytochemistry, SAGE Publications, Vol. 39, No. 10 ( 1991-10), p. 1385-1394
    Abstract: We investigated the distribution of thrombospondin-specific binding sites and the uptake of thrombospondin-gold conjugates in cultured porcine endothelial cells by light and electron microscopy. Colloidal gold marker and silver enhancement techniques were applied for cytochemical detection of monomeric thrombospondin and fragments of thrombospondin. Thrombospondin binds to granular and fibrillar structures and to sites of cell-cell contact on the cell surface, as indicated by many proteoglycan-cuprolinic blue precipitates. Cell migration tracks on the culture dish bottom are most heavily stained. Labeling of intact thrombospondin and of proteolytic fragments of thrombospondin with colloidal gold followed by silver intensification enables one to detect its binding and uptake in endothelial cells. Binding to the cell surface and uptake of thrombospondin-gold particles was inhibited by heparin but not by hyaluronic acid or chondroitin sulfate. The heparin binding region at the N-terminal end of the thrombospondin molecule proved to be essential for cell surface binding. Gold-conjugated thrombospondin fragments devoid of the heparin binding region were not internalized. After 60 min incubation at 37 degrees C, thrombospondin-gold particles accumulated in the lysosomal compartment close to the nucleus. In the presence of monensin and ammonium chloride, vesicles in this area are swollen and the concentration of particulate marker is reduced. Binding and uptake of thrombospondin by vascular endothelial cells appears to require linkage of the heparin binding region of the thrombospondin molecule to coated pits and heparan sulfate-rich molecules as receptors. Colloidal gold conjugation of thrombospondin fragments proved to be useful for cytochemical characterization of molecular domains.
    Type of Medium: Online Resource
    ISSN: 0022-1554 , 1551-5044
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1991
    detail.hit.zdb_id: 1421306-0
    SSG: 12
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  • 6
    Online Resource
    Online Resource
    SAGE Publications ; 1990
    In:  Journalism Quarterly Vol. 67, No. 4 ( 1990-12), p. 732-739
    In: Journalism Quarterly, SAGE Publications, Vol. 67, No. 4 ( 1990-12), p. 732-739
    Abstract: Three mailings of a six-page survey questionnaire to a circulation-weighted newspaper sample group of 540 editors in 1987 resulted in a final response rate of 51.6%. Follow-up study with nonresponders did not find any regional variations in nonreponse, but did discover that editors from smaller, noncorporate newspapers were more likely to respond. Among reasons given for nonresponse were lack of time—especially from editors of larger newspapers—and complaints that the survey was too long. Some editors said they received too many mail questionnaires.
    Type of Medium: Online Resource
    ISSN: 0022-5533
    RVK:
    RVK:
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1990
    detail.hit.zdb_id: 2070253-X
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  • 7
    Online Resource
    Online Resource
    SAGE Publications ; 1990
    In:  Healthcare Management Forum Vol. 3, No. 1 ( 1990-04), p. 13-18
    In: Healthcare Management Forum, SAGE Publications, Vol. 3, No. 1 ( 1990-04), p. 13-18
    Abstract: Constraints on resources push hospitals into strategic planning. Although this process is accelerating in the United States, Canadian hospitals need to approach planning according to the provincial structure. This study included a literature and policy review as well as interviews of key stakeholders. Decisions toward centralized planning versus hospital-initiated development were found to depend on the availability of planning and policy staff, and the views of the elected representatives. Implications for Canadian health care planners were offered.
    Type of Medium: Online Resource
    ISSN: 0840-4704 , 2352-3883
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1990
    detail.hit.zdb_id: 2552324-7
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