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Träfflista för sökning "WFRF:(Bjartell A) srt2:(1995-1999)"

Sökning: WFRF:(Bjartell A) > (1995-1999)

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1.
  • Christensson, A, et al. (författare)
  • The significance of serpins in the regulation of proteases in the male genital tract
  • 1997
  • Ingår i: Advances in Experimental Medicine and Biology. - Boston, MA : Springer US. - 0065-2598. ; 425, s. 76-163
  • Forskningsöversikt (refereegranskat)abstract
    • The male genital tract is rich in proteases, delivered by the male accessory sex glands, that are delicately balanced in their action by serpins, non-serpin class protease inhibitors and other regulatory mechanisms. Still, the biological function of the serpins and their target enzymes in the male genital tract and possible involvement in the regulation of normal reproductive function mainly remains to be elucidated. However, it is important with careful control of the catalytic activity of serine proteases, in particular in the different extracellular compartments, where they may produce significant potential hazards for biological structures. Immunochemical measurements of the serine protease prostate-specific antigen (PSA) in serum have gained widespread use in the monitoring and detection of prostate cancer. Moreover, the rapidly growing body of data on the disease-related variations in the proportion of different forms of PSA in serum which relate to the covalent complex formation between the serpin α1-antichymotrypsin and PSA has significantly improved the diagnostic specificity in blood testing for early detection of prostate cancer.
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2.
  • Bjartell, A., et al. (författare)
  • Time-resolved fluorescence imaging (TRFI) for direct immunofluorescence of PSA and alpha-1-antichymotrypsin in prostatic tissue sections
  • 1999
  • Ingår i: Prostate Cancer and Prostatic Diseases. - : Springer Science and Business Media LLC. - 1365-7852 .- 1476-5608. ; 2:3, s. 140-147
  • Tidskriftsartikel (refereegranskat)abstract
    • We have developed a direct immunofluorescence technique utilising chelates of the lanthanide ions europium and terbium conjugated to monoclonal IgGs (Mabs) against prostate-specific antigen (PSA) and alpha-1- antichymotrypsin (ACT) for the detection and quantification on the same tissue section. Strong signals without disturbance from tissue autofluorescence were demonstrated in paraffin sections of ten benign and six malignant prostate tissue specimens. The signal intensity increased linearly with the amount of labelled Mab until epitope saturation began. The highest concentrations of bound IgG in tissue sections were 27.3 fmol/pixel for ACT and 7.2 for PSA. Time-resolved fluorescence imaging (TRFI) offers an attractive method for histochemical studies based on specific and quantitative detection of fluorescent lanthanide chelates.
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3.
  • He, X., et al. (författare)
  • The gene encoding vitamin K-dependent anticoagulant protein C is expressed in human male reproductive tissues
  • 1995
  • Ingår i: Journal of Histochemistry and Cytochemistry. - : SAGE Publications. - 0022-1554 .- 1551-5044. ; 43:6, s. 563-570
  • Tidskriftsartikel (refereegranskat)abstract
    • Protein C is a vitamin K-dependent protein circulating in plasma as a zymogen to an anticoagulant serine protease. After its activation, protein C cleaves and inactivates coagulation factors Va and VIIIa. Human protein C is synthesized in liver and undergoes extensive post-translational modification during its synthesis. Recently, the protein C inhibitor was demonstrated to be synthesized in several organs of the human male reproductive tract. Moreover, vitamin K-dependent protein S, which functions as a co-factor to activated protein C, was found to be synthesized in the Leydig cells of human testis. The aim of this study was to elucidate whether the protein C gene is also expressed in the male reproductive system. Specific immunostaining of protein C was found in Leydig cells of human testis, in the excretory epithelium of epididymis, and in some epithelial glands of the prostate, whereas no immunostaining was detected in seminal vesicles. Northern blotting and non-radioactive in situ hybridization demonstrated protein C mRNA in Leydig cells, in the excretory epithelium of epididymis, and in some of the epithelial glands of the prostate. The mRNA was distributed perinuclearly and the localization was in accordance with the specific immunostaining for protein C. The epithelium of epididymis was also found to contain both protein S mRNA and immunoreactivity. The demonstration of both protein C and protein S immunoreactivities, as well as their mRNAs, in male reproductive tissues suggests as yet unknown local functions for these proteins.
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4.
  • Weiber, H., et al. (författare)
  • Immunohistochemical and in situ hybridization studies of β- microseminoprotein in the human gastric mucosa
  • 1997
  • Ingår i: Histochemical Journal. - 0018-2214. ; 29:11-12, s. 839-845
  • Tidskriftsartikel (refereegranskat)abstract
    • β-Microseminoprotein is a 10-kDa disulphide-rich protein with unknown function which is present in the mucus of the airways, gastrointestinal tract and urogenital tract. In this paper, an investigation of the distribution of β-microseminoprotein in the human stomach is reported. Immunohistochemistry and in situ hybridization were used. β-Microseminoprotein was found to be localized mainly in the antrum part of the stomach and in two types of cells. Cells of the most abundant type (designated M-cells) were the neutral mucin- containing cells in the bottom part of the gastric glands and the surface epithelium. Virtually all these cells contained both β-microseminoprotein mRNA and protein product. Cells of the second type (designated E-cells) were found in a zone one-third up from the bottom of the gastric glands, where gastric endocrine cells are located. The E-cells were fewer than the M-cells and usually solitary. They seemed to have a high concentration of protein compared with their low mRNA level. The majority of the E-cells contained chromogranin A and gastrin. The observations made have implications for the understanding of the differentiation of the mucosal cells in the antrum of the stomach and form a basis for future studies of β-microseminoprotein in gastric disease.
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