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Restriction-map variation with the yellow-achaete-scute region in five populations of Drosophila melanogaster 总被引:9,自引:0,他引:9
It has been proposed that the degree of recombination for a genomic region
will affect the level of both nucleotide heterozygosity and the density of
transposable elements. Both features of genomic diversity have been
examined in a number of recent reports for regions undergoing relatively
normal levels of recombination in Drosophila melanogaster. In this study
the genomic variation associated with yellow-achaete- scute loci located at
the tip of the X chromosome is examined by six- cutter restriction mapping.
In this region, as usual for regions adjacent to telomeres, crossing-over
is dramatically reduced, and published studies of visible mutants indicate
extremely little restriction-map variation. Eight six-cutter restriction
endonucleases were used to locate sequence variation in 14- and 16.5-kb
regions in 109 lines sampled from North America, Africa, and Europe. The
overall level of heterozygosity is estimated as 0.29%. Nine large
insertions, all presumed to be transposable elements, were observed.
Base-pair heterozygosity appears to be reduced compared with regions having
normal levels of recombination. The estimated heterozygosity is much higher
than reported in earlier studies of restriction-map variation among visible
mutations in the complex. The incidence of large insertions is not elevated
compared with that in other regions of the genome. This suggests that
asymmetric synapsis and exchange is not an important mechanism for the
elimination of transposable elements.
相似文献
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A total of 27Fusarium culmorum isolates from Germany and 41F. graminearum isolates from Kenya were investigated for aggressiveness and mycotoxin production on wheat ears. In addition, ergosterol content of the kernels from ears inoculated withF. graminearum was determined and theF. culmorum isolates were tested for mycotoxin productionin vitro. For both pathogens, isolates markedly differed in aggressiveness. 59% and 37% of theF. culmorum isolates produced NIV and DON, respectively,in vivo andin vitro. The DON-producing isolates also produced 3-acDONin vitro. The more aggressive isolates produced mainly DON while the less aggressive isolates produced mainly NIV. 12% and 85% of theF. graminearum isolates produced NIV and DON, respectively. The highly aggressive isolates produced higher amounts of DON, aggressiveness being highly correlated to DON content in the kernels. NIV-producing isolates were less aggressive. Ergosterol content of kernels was moderately correlated to aggressiveness but highly correlated to DON content. Disease severity was associated with kernel weight reduction. 相似文献
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Benjamin Wilde Marielle Thewissen Jan Damoiseaux Marc Hilhorst Pieter van Paassen Oliver Witzke Jan Willem Cohen Tervaert 《Arthritis research & therapy》2012,14(5):R227
Introduction
In autoimmune diseases, IL-17 producing T-cells (Th17), a pro-inflammatory subset of T-cells, are pathophysiologically involved. There is little knowledge on the role of Th17 cells in granulomatosis with polyangiitis (GPA). In the present study, we investigated Th17 cells, Tregs and subsets of circulating Th17 cells in GPA and related results to disease activity.Methods
42 GPA patients in remission, 18 with active disease and 14 healthy controls (HC) were enrolled. Th17 cells, their subsets and regulatory T-cells were determined by intracellular fluorescence activated cell sorter (FACS). Data are given as mean percentage ±SD of total T-helper-cells.Results
Th17 cells are expanded in active and quiescent GPA as compared to HC (1.7±1.4% vs. 0.7 ±0.3%, P = 0.006 and 1.9 ±1.5% vs. 0.7 ±0.3%, P<0.0001). Th17 expansion is stable over time and does not decline when remission is achieved. However, a negative association of Th17 cells and steroid dosage is observed (r=-0.46, P = 0.002). The Th17 expansion was not balanced by Tregs as indicated by skewed Th17/Treg ratios in active and quiescent GPA. Th17 subsets co-producing IFNγ or IL-10 are significantly increased in GPA. GPA patients in remission not receiving maintenance therapy have significantly more IL-10/IL-17A double positive T-cells than HC (0.0501 ±0.031% vs. 0.0282 ±0.016%, P = 0.007).Conclusions
We provide evidence for a persistent, unbalanced expansion of Th17 cells and Th17 subsets which seems to be independent of disease activity. Maintenance therapy reduces -but does not normalize- Th17 expansion. 相似文献65.
HJ de Jong SR Saldi OH Klungel RJ Vandebriel PC Souverein RH Meyboom JL Passier H van Loveren JW Tervaert 《PloS one》2012,7(7):e41289
Objective
To assess whether there is an association between statin use and the occurrence of polymyalgia rheumatic (PMR) in the spontaneous reporting database of the World Health Organisation (WHO).Methods
We conducted a case/non-case study based on individual case safety reports (ICSR) in the WHO global ICSR database (VigiBase). Case reports containing the adverse event term polymyalgia rheumatica (WHOART or MedDRA Preferred Term) were defined as cases. Non-cases were all case reports containing other adverse event terms. Each case was matched to five non-cases by age, gender, and time of reporting. Case reports regarding a statin as suspected or concomitant drug were identified using the Anatomical Therapeutic Chemical (ATC) classification. Multivariate logistic regression was used to calculate reporting odds ratios (RORs) with 95% confidence intervals (CI).Results
We identified 327 reports of PMR as cases and 1635 reports of other ADRs as non-cases. Among cases, statins were more frequently reported as suspected agent (29.4%) compared to non-cases (2.9%). After adjustment for several covariates, statins were significantly associated with reports of PMR (ROR 14.21; 95% CI 9.89–20.85).Conclusion
The results of this study lends support to previous anecdotal case reports in the literature suggesting that the use of a statin may be associated with the occurrence of PMR. Further studies are needed to study the strength of the association in more detail and to elucidate the underlying mechanism. 相似文献66.
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