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Sökning: WFRF:(Widell S)

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  • Shev, S, et al. (författare)
  • Second-generation hepatitis C Elisa antibody tests confirmed by the four-antigen recombinant immunoblot assay correlate well with hepatitis C viremia and chronic liver disease in Swedish blood donors
  • 1993
  • Ingår i: Vox Sanguinis. - 1423-0410. ; 65:1, s. 32-37
  • Tidskriftsartikel (refereegranskat)abstract
    • Seventy-three Swedish blood donors (52 men, 21 women; median age 36 years) repeatedly reactive for hepatitis C antibodies (anti-HCV C-100-3) were tested with a second-generation (2nd-gen) anti-HCV Elisa and a 4-band recombinant immunoblot assay (RIBA 2). These results were correlated to serum alanine aminotransferase (S-ALAT), liver morphology and viremia as detected by 'nested' polymerase chain reaction (PCR) based on primers from a 5'-noncoding sequence of the HCV genome. Thirty-five of 46 (76%) donors with positive 2nd-gen Elisa tests confirmed by RIBA 2 were PCR positive whereof 27 had histological findings compatible with chronic persistent hepatitis (CPH) and 7 had chronic active hepatitis (CAH). Ten of 56 (18%) 2nd-gen Elisa-positive donors were RIBA 2 negative (or indeterminate) and none of these had chronic hepatitis nor were PCR positive. Seventeen of 73 (23%) donors were 1st-gen Elisa positive but 2nd-gen Elisa negative. All of these were PCR negative and only 1 (6%) had chronic hepatitis (CPH). An elevated S-ALAT level (reference < 0.7 mu kat/l) was found in 26 2nd-gen Elisa and RIBA 2-positive donors of which 18 had CPH and 7 had CAH and all 25 were PCR positive. A normal S-ALAT level was found in 9 of 34 (26%) donors with chronic hepatitis (all had CPH) and positive PCR. We have found that blood donors with positive 2nd-gen anti-HCV Elisa tests confirmed by RIBA-2 and especially with a concomitant elevated S-ALAT are highly likely to be viremic as demonstrated by PCR and to have chronic hepatitis.
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3.
  • Simmonds, P, et al. (författare)
  • Consensus proposals for a unified system of nomenclature of hepatitis C virus genotypes
  • 2005
  • Ingår i: Hepatology. - : Ovid Technologies (Wolters Kluwer Health). - 1527-3350 .- 0270-9139. ; 42:4, s. 962-973
  • Tidskriftsartikel (refereegranskat)abstract
    • International standardization and coordination of the nomenclature of variants of hepatitis C virus (HCV) is increasingly needed as more is discovered about the scale of HCV-related liver disease and important biological and antigenic differences that exist between variants. A group of scientists expert in the field of HCV genetic variability, and those involved in development of HCV sequence databases, the Hepatitis Virus Database (Japan), euHCVdb (France), and Los Alamos (United States), met to re-examine the status of HCV genotype nomenclature, resolve conflicting genotype or subtype names among described variants of HCV, and draw up revised criteria for the assignment of new genotypes as they are discovered in the future. A comprehensive listing of all currently classified variants of HCV incorporates a number of agreed genotype and subtype name reassignments to create consistency in nomenclature. The paper also contains consensus proposals for the classification of new variants into genotypes and subtypes, which recognizes and incorporates new knowledge of HCV genetic diversity and epidemiology. A proposal was made that HCV variants be classified into 6 genotypes (representing the 6 genetic groups defined by phylogenetic analysis). Subtype name assignment will be either confirmed or provisional, depending on the availability of complete or partial nucleotide sequence data, or remain unassigned where fewer than 3 examples of a new subtype have been described. In conclusion, these proposals provide the framework by which the HCV databases store and provide access to data on HCV, which will internationally coordinate the assignment-of-new genotypes and subtypes in the future.
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  • Brändström, U., et al. (författare)
  • Results from the intercalibration of optical low light calibration sources 2011
  • 2012
  • Ingår i: Geoscientific Instrumentation, Methods and Data Systems. - : Copernicus GmbH. - 2193-0856 .- 2193-0864. ; 1:1, s. 43-51
  • Tidskriftsartikel (refereegranskat)abstract
    • Following the 38th Annual European Meeting onAtmospheric Studies by Optical Methods in Siuntio in Finland,an intercalibration workshop for optical low light calibrationsources was held in Sodankyl¨a, Finland. The mainpurpose of this workshop was to provide a comparable scalefor absolute measurements of aurora and airglow. All sourcesbrought to the intercalibration workshop were compared tothe Fritz Peak reference source using the Lindau CalibrationPhotometer built by Wilhelm Barke and Hans Lauche in1984. The results were compared to several earlier intercalibrationworkshops. It was found that most sources were fairlystable over time, with errors in the range of 5–25 %. To furthervalidate the results, two sources were also intercalibratedat UNIS, Longyearbyen, Svalbard. Preliminary analysis indicatesagreement with the intercalibration in Sodankyl¨a withinabout 15–25 %.
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  • Petersen-Mahrt, S.K., et al. (författare)
  • Effects of UV‐B radiation and nitrogen starvation on enzyme activities in isolated plasma membranes of Euglena gracilis
  • 1995
  • Ingår i: Physiologia Plantarum. - : Wiley. - 0031-9317 .- 1399-3054. ; 95, s. 515-522
  • Tidskriftsartikel (refereegranskat)abstract
    • Circadian rhythms are characteristic of many physiological and biochemical processes in the freshwater flagellate Euglena gracilis. Earlier, we found that the rhythms of photosynthesis, phototaxis and cell shape followed the same pattern in control organisms, but were differently affected by stress such as UV‐B irradiation and nitrogen deficiency. Here we extend our studies to use isolated plasma membranes to characterize the rhythms of some plasma membrane‐bound enzymes. Also, we wanted to see whether stress‐induced changes of these rhythms could be detected at the subcellular level and possibly be coupled to the changes seen in photosynthesis, phototaxis and cell shape. The isolation of plasma membranes using aqueous polymer two‐phase partitioning was successful, as judged by the large enrichment of the plasma membrane‐marker 5′‐nucleotidase, and the difference in the polypeptide pattern compared with the microsomal fraction from which it was prepared.
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