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  • 1
    In: Alternatives to Laboratory Animals, SAGE Publications, Vol. 26, No. 5 ( 1998-09), p. 619-626
    Type of Medium: Online Resource
    ISSN: 0261-1929 , 2632-3559
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1998
    detail.hit.zdb_id: 2390905-5
    SSG: 12,22
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  • 2
    In: Applied Spectroscopy, SAGE Publications, Vol. 52, No. 1 ( 1998-01), p. 17-21
    Abstract: An on-line near-infrared (NIR) spectroscopic method has been developed to determine in situ the endpoint of a bulk pharmaceutical hydrogenation reaction in a loop hydrogenator. This hydrogenation employs a 5% palladium-on-carbon catalyst with tetrahydrofuran (THF) as the reaction solvent. The traditional test for monitoring the endpoint of the hydrogenation is a gas chromatographic procedure that requires an estimated 60 min from the time a sample is taken to the point where the analysis results become available. The use of NIR spectroscopy in an on-line mode of operation allows spectra to be collected every 2 min and thereby significantly improves response time and result availability. The need for obtaining results in “real time” stems from the creation of undesired side products if the reaction is allowed to continue past the optimal endpoint. If the reaction is not stopped before these side products reach a level of approximately 0.8% (wt/wt), the batch requires additional purification at considerable time and cost. A partial least-squares model was constructed, validated, and successfully used to determine the endpoint of subsequent batches.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1998
    detail.hit.zdb_id: 1474251-2
    SSG: 11
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  • 3
    Online Resource
    Online Resource
    SAGE Publications ; 1999
    In:  Work, Employment and Society Vol. 13, No. 3 ( 1999-09), p. 503-524
    In: Work, Employment and Society, SAGE Publications, Vol. 13, No. 3 ( 1999-09), p. 503-524
    Abstract: This paper examines whether the supply side characteristics of the low paid are associated with the labour market wage setting institutions of five countries; Britain, Luxembourg, Germany, Spain and the USA, using the harmonised PAnel COmparability (PACO) data based on household panel studies and the Spanish European Household Panel survey. The age, education, marital status, children, lone parent status, household type, employment status of spouse, and housing tenure of the low paid are examined. The links between these characteristics, the low paid and labour market institutions are examined through multivariate analyses. Labour market wage setting institutions clearly influence the characteristics of the low paid and explain the variations in supply side, as well as demand side characteristics across countries.
    Type of Medium: Online Resource
    ISSN: 0950-0170 , 1469-8722
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1999
    detail.hit.zdb_id: 2000042-X
    SSG: 2
    SSG: 3,4
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  • 4
    Online Resource
    Online Resource
    SAGE Publications ; 1999
    In:  Psychological Science Vol. 10, No. 3 ( 1999-05), p. 263-266
    In: Psychological Science, SAGE Publications, Vol. 10, No. 3 ( 1999-05), p. 263-266
    Abstract: Research suggests that most people cannot tell from demeanor when others are lying. Such poor performance is typical not only of laypeople but also of most professionals concerned with lying. In this study, three professional groups with special interest or skill in deception, two law-enforcement groups and a select group of clinical psychologists, obtained high accuracy in judging videotapes of people who were lying or telling the truth about their opinions. These findings strengthen earlier evidence that some professional lie catchers are highly accurate, and that behavioral clues to lying are detectable in real time. This study also provides the first evidence that some psychologists can achieve high accuracy in catching lies.
    Type of Medium: Online Resource
    ISSN: 0956-7976 , 1467-9280
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1999
    detail.hit.zdb_id: 2022256-7
    SSG: 5,2
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  • 5
    Online Resource
    Online Resource
    SAGE Publications ; 1995
    In:  Urban Studies Vol. 32, No. 9 ( 1995-11), p. 1557-1568
    In: Urban Studies, SAGE Publications, Vol. 32, No. 9 ( 1995-11), p. 1557-1568
    Type of Medium: Online Resource
    ISSN: 0042-0980 , 1360-063X
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1995
    detail.hit.zdb_id: 5372-7
    detail.hit.zdb_id: 1482794-3
    SSG: 14
    SSG: 3,4
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  • 6
    Online Resource
    Online Resource
    SAGE Publications ; 1996
    In:  School Psychology International Vol. 17, No. 2 ( 1996-05), p. 171-186
    In: School Psychology International, SAGE Publications, Vol. 17, No. 2 ( 1996-05), p. 171-186
    Abstract: The higher rate ofjuvenile homicide among African-American males than among white males has led many to the assumption that blacks are more violent than whites and other racial/ethnic groups. The present study examines that hypothesis in the context of 3955 inner-city Miami boys who were surveyed over a three-year period from grades 6 and 7 to grades 8 and 9. Concurrent risk factors were more predictive than prospective risk factors in relation to self-reported violence in grades 8 and 9. A variety of familial, psychosocial, sociocultural and school-based risk factors for violence were examined. These included race/ethnicity, normative values, derogation (from self, teachers and parents), cocaine and crack use, marital and educational status of parents, grade in school, beliefs (on several levels) and behaviors (delinquency, response to anger, etc). Gun carrying at school was only slightly more prevalent among American blacks (6% for the partial school term) than among whites (4%) and boys of other races. White boys were more likely to carry knives than American blacks. Using a composite of violent behavior, no single racial group was more violent than another (F = .508,p = .83). Haitians, Caribbean blacks and Nicaraguans were more likely to be involved in gangs than other groups. Normlessness, low empathy, stealing, law-breaking and wanting to quit school and leave home function as a constellation of risk factors that appear to increase the likelihood of weapon carrying and interpersonal violence regardless of race/ethnicity. Other risk factors vary by race/culture group.
    Type of Medium: Online Resource
    ISSN: 0143-0343 , 1461-7374
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1996
    detail.hit.zdb_id: 2060753-2
    SSG: 5,2
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  • 7
    In: The Linacre Quarterly, SAGE Publications, Vol. 64, No. 4 ( 1997-11), p. 3-31
    Type of Medium: Online Resource
    ISSN: 0024-3639 , 2050-8549
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1997
    detail.hit.zdb_id: 2560599-9
    SSG: 1
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  • 8
    In: Alternatives to Laboratory Animals, SAGE Publications, Vol. 26, No. 1_suppl ( 1998-03), p. 131-183
    Abstract: Results from tests on the Multicentre Evaluation of In Vitro Cytotoxicity (MEIC) reference chemicals 31–50 in 67 different in vitro toxicity assays are presented in this paper as a prerequisite to in vitro/in vivo comparisons for all MEIC in vitro toxicity data in forthcoming papers, i.e. the final MEIC evaluation of the relevance of the tests. With the aim of increasing knowledge about the relative significance of some in vitro methodological factors, the strategies and methods of the preceding parts in the MEIC series (Parts II and III) were again employed to enable comparative cytotoxicity analysis of the new in vitro results presented in this paper. A principal components analysis (PCA) of the results from tests of the 20 chemicals in 67 assays demonstrated a dominating first component describing as much as 74% of the variance in the toxicity data, indicating a similar ranking of the cytotoxicities of the chemicals in most of the tests. The influence on the general variability of the results of a few, key methodological factors was also evaluated by using linear regression comparisons of the results of all pairs of methods available in the study, i.e. methods which were similar in all respects except for the factor being analysed. Results from this “random probe” analysis were: a) the cytotoxicities of 11 of the 20 chemicals increased considerably with exposure time ( 〉 10 times over 4–168 hours); b) in general, human cell line toxicity was well predicted by cytotoxicity in animal cells; c) prediction of human cell line toxicity by most ecotoxicological tests was only fairly good; d) 14 comparisons of similar assays with different cell lines showed similar toxicities (mean R 2 = 0.83); e) nine comparisons of similar assays employing different primary cultures and cell lines shared similar toxicities (mean R 2 = 0.71); and f) 16 comparisons of similar assays with different growth/viability endpoints showed similar toxicities (mean R 2 = 0.71). Results b, d, e and f must contribute to the PCA-documented high general similarity of the in vitro toxicity data. Results a and c, together with factors which were not analysed, such as different protocols and inter-laboratory variability of tests, could explain the 26% dissimilarity. To provide background information to the planned final MEIC evaluation of the relevance of the 61 methods in which all 50 chemicals have been tested, an additional PCA was made of the 50 chemical-61 assay in vitro database (from Parts II and III and the present paper). This supplementary PCA demonstrated an 80% similarity of results. Compared with the previous analysis of the tests of the first 30 MEIC reference chemicals (MEIC Part III), the present analysis of the tests of the last 20 MEIC chemicals indicates a somewhat higher variation in the results. Correspondingly, some deviating endpoint measurements and cell line responses were demonstrated by the pairwise comparisons in the present study. As a result, the analysis revealed a high correlation (R 2 = 0.73) between the average human cell line toxicity and the results from a new protein denaturation test. These preliminary results suggest that intracellular protein denaturation may be a frequently occurring mechanism in basal cytotoxicity.
    Type of Medium: Online Resource
    ISSN: 0261-1929 , 2632-3559
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1998
    detail.hit.zdb_id: 2390905-5
    SSG: 12,22
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  • 9
    In: Alternatives to Laboratory Animals, SAGE Publications, Vol. 24, No. 1_part_1 ( 1996-06), p. 273-311
    Abstract: Results from tests of the first 30 MEIC reference chemicals in 68 different toxicity assays are presented as a prerequisite to subsequent in vitro/in vivo comparisons of acute toxicity data. A comparative cytotoxicity study was also carried out. Firstly, the variability of all of the results was analysed by using principal components analysis (PCA), analyses of variance (ANOVAs) and pairwise comparisons of means according to Tukey's method. The first PCA component described 80% of the variance of all of the cytotoxicity data. Tukey's ANOVA indicated a similar sensitivity for the assays, of approximately 80%. Secondly, the influence of five major methodological components on the general variability of the results was evaluated by linear regression and ANOVA linear contrast analyses. The findings were that: a) the toxicity of many chemicals increased with exposure time; b) in general, human cytotoxicity was predicted well by animal cytotoxicity tests; c) this prediction was poor for two chemicals; d) the prediction of human cytotoxicity by the ecotoxicological tests was only fairly good; e) one organotypic endpoint used, i.e. contractility of muscle cells, gave different results to those obtained according to viability/growth toxicity criteria; f) twelve comparisons of similar test systems involving different cell types (including highly differentiated cells) showed similar toxicities regardless of cell type; and g) nine out often comparisons of test systems with identical cell types and exposure times revealed similar toxicities, regardless of the viability or growth endpoint measurement used. Factors b, f and g must be the main causes of the remarkable similarity between the total results, while factors a, c, d and e, together with other minor factors that were not analysed, contributed to the 20% dissimilarity. The findings strongly support the basal cytotoxicity concept, and will facilitate future in vitro toxicity testing.
    Type of Medium: Online Resource
    ISSN: 0261-1929 , 2632-3559
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1996
    detail.hit.zdb_id: 2390905-5
    SSG: 12,22
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  • 10
    In: American Journal of Rhinology, SAGE Publications, Vol. 12, No. 4 ( 1998-07), p. 293-300
    Abstract: This was a double-blind, randomized, placebo-controlled, multicenter, parallel study comparing the effectiveness, at recommended doses, of an extended-release formulation of brompheniramine maleate and terfenadine in the treatment of allergic rhinitis. Subjects with symptoms of seasonal and/or perennial allergic rhinitis received brompheniramine 12 mg (n = 106), 8 mg (n = 105), terfenadine 60 mg (n = 106), or placebo (n = 53) twice daily for 14 days. On treatment days 3, 7, and 14, symptom severity ratings (i.e., rhinorrhea, sneezing, nasal congestion, itchy nose, eyes or throat, excessive tearing, postnasal drip) were completed by the physician; subjects and physicians each completed a global efficacy evaluation. Brompheniramine 12 mg and 8 mg and terfenadine were more effective than placebo (p ≤ 0.05) on the physicians’ global; brompheniramine 12 mg was more effective than terfenadine (p ≤ 0.05) on days 7 and 14 and brompheniramine 8 mg on day 3. On the subjects’ global evaluation, brompheniramine 12 mg and 8 mg and terfenadine were more effective than placebo (p ≤ 0.05); brompheniramine 12 mg was more effective than terfenadine (p ≤ 0.05) on days 7 and 14 and brompheniramine 8 mg on day 3. In general, brompheniramine 8 mg was comparable to terfenadine. On days 3 and 7, the total symptom and total nasal symptom severity scores for subjects receiving brompheniramine 12 mg were significantly more improved than for placebo (p 〈 0.05); terfenadine was not different from placebo; brompheniramine 12 mg was significantly better than terfenadine on day 7 (p 〈 0.05) for reducing total symptom severity and on days 3, 7, and 14 for reducing total nasal symptom severity. Adverse experiences were reported by 155 (41.9%) of the 370 subjects enrolled in the study. The overall rate of adverse experiences in the brompheniramine 12 mg treatment group (57.5%) was significantly greater (p 〈 0.05) than for brompheniramine 8 mg (38.1%), terfenadine (31.1%), and placebo (39.6%). In conclusion, an extended-release formulation of brompheniramine 12 mg or 8 mg bid alleviates allergic rhinitis symptoms and brompheniramine 12 mg provides significantly better relief of these symptoms than terfenadine 60 mg bid.
    Type of Medium: Online Resource
    ISSN: 1050-6586 , 1539-6290
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1998
    detail.hit.zdb_id: 2083922-4
    detail.hit.zdb_id: 2554548-6
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