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L M Cherry 《Stain technology》1985,60(2):99-102
Immunofluorescent staining techniques using antitubulin antibody have been difficult to apply to meiotic tissue (testis) because of the large number of cell types present. Such techniques customarily use a fluorescent dye to counterstain nuclei, and this counterstain is hard to distinguish because of the fluorescence of the antitubulin. By counterstaining with dilute hematoxylin, we can photograph the same field using UV and then conventional illumination. This double photography allows us to identify precisely the many types of cells present, and it will be a useful tool for reexamining the staging of spermatogenesis. 相似文献
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Specificity of leucyl-tRNA and synthetase in plants 总被引:1,自引:0,他引:1
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J. Kitchin A. D. Borthwick A. C. Brodie P. C. Cherry A. J. Crame A. J. Pipe P. A. Procopiou M. A. Seaman J. P. Turnbull 《Bioorganic & medicinal chemistry》1995,3(12)
A novel series of tetrahydrobenzodioxinopyrroles has been identified as potent and selective α2-adrenoceptor antagonists. Convergent syntheses have been developed that allowed the preparation of analogues and their enantiomers. A compound of particular interest is the 5-fluoro substituted analogue (fluparoxan). 相似文献
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Vijayaganapathy Vaithilingam Cherry Fung Sabina Ratnapala Jayne Foster Vijesh Vaghjiani Ursula Manuelpillai Bernard E. Tuch 《PloS one》2013,8(3)
Xenotransplantation of microencapsulated fetal pig islet-like cell clusters (FP ICCs) offers a potential cellular therapy for type 1 diabetes. Although microcapsules prevent direct contact of the host immune system with the xenografted tissue, poor graft survival is still an issue. This study aimed to characterise the nature of the host immune cells present on the engrafted microcapsules and effects on encapsulated FP ICCs that were transplanted into immunocompetent mice. Encapsulated FP ICCs were transplanted into the peritoneal cavity of C57BL/6 mice. Grafts retrieved at days 1, 3, 7, 14 and 21 post-transplantation were analysed for pericapsular fibrotic overgrowth (PFO), cell viability, intragraft porcine gene expression, macrophages, myofibroblasts and intraperitoneal murine cytokines. Graft function was assessed ex vivo by insulin secretion studies. Xenogeneic immune response to encapsulated FP ICCs was associated with enhanced intragraft mRNA expression of porcine antigens MIP-1α, IL-8, HMGB1 and HSP90 seen within the first two weeks post-transplantation. This was associated with the recruitment of host macrophages, infiltration of myofibroblasts and collagen deposition leading to PFO which was evident from day 7 post-transplantation. This was accompanied by a decrease in cell viability and loss of FP ICC architecture. The only pro-inflammatory cytokine detected in the murine peritoneal flushing was TNF-α with levels peaking at day 7 post transplantation. This correlated with the onset of PFO at day 7 implying activated macrophages as its source. The anti-inflammatory cytokines detected were IL-5 and IL-4 with levels peaking at days 1 and 7, respectively. Porcine C-peptide was undetectable at all time points post-transplantation. PFO was absent and murine intraperitoneal cytokines were undetectable when empty microcapsules were transplanted. In conclusion, this study demonstrated that the macrophages are direct effectors of the xenogeneic immune response to encapsulated FP ICCs leading to PFO mediated by a combination of both pro- and anti-inflammatory cytokines. 相似文献
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Extraction of 14 teeth in six patients taking dicumarol caused no unusual bleeding. Discontinuance of dicumarol prior to dental extraction should not necessarily be a routine procedure; in certain persons with a demonstrated strong tendency to recurrent thrombosis, dicumarol should be continued, based on the decision that the danger of clotting without the drug is greater than the danger of bleeding with the drug. 相似文献
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