10 research outputs found
Mis casos clínicos de especialidades odontológicas
Libro que muestra la atención de casos clínicos particulares referente a las diferentes especialidades odontológicasLibro que muestra la atención de casos clínicos particulares referente a las diferentes especialidades odontológicasUniversidad Autónoma de Campeche
Universidad Autónoma del Estado de Hidalgo
Universidad Autónoma del Estado de Méxic
Privatisation and quasi-markets
Paper presented at the EACES First Trento Workshop, University of Trento (IT), 1-2 Mar 1991Available from British Library Document Supply Centre- DSC:8490.3304(7) / BLDSC - British Library Document Supply CentreSIGLEGBUnited Kingdo
Immunolocalization of α-tubulin (green) of control, T<sub>4</sub> and DHT treated parasites.
<p>Phase contrast of the control sections of the slides obtained by Tissue-Teck fixing are shown in upper panel from left to right, control (C), testosterone (T<sub>4</sub>) and dihydrotestosterone (DHT). In lower panel, green tiny spots are produced by the specific binding of the anti-α-tubulin stained with alexa-488 antibody to cytoskeletal α-tubulin. Tubulin protein inside the bladder wall and at the level of the tegument in the tissue of control parasites and those treated with T<sub>4</sub> and DHT. Scale bar corresponds to 10 μm.</p
Immunolocalization of F-actin (red) of control, T<sub>4</sub> and DHT treated parasites.
<p>Phase contrast of the control sections of the slides obtained by Tissue-Teck fixing are shown in upper panel from left to right, control (C), testosterone (T<sub>4</sub>) and dihydrotestosterone (DHT). In lower panel, red tiny spots are produced by the specific binding of the anti-α-tubulin stained with rhodamine-coupled phalloidin to cytoskeletal F-actin. F-actin proteins inside the bladder wall and at the level of the tegument in the tissue of control parasites and those treated with T<sub>4</sub> and DHT. Scale bar corresponds to 10 μm.</p
Specific expression of actin, tubulin and myosin in <i>Taenia crassiceps</i> cysticerci by flow cytometry.
<p>Dot plot depicted in Fig 1 (A), represents size and complexity of the <i>T</i>. <i>crassiceps</i> cells used for staining and detection of cytoskeletal proteins. FACS analysis of parasitic actin (B and C), tubulin (D and E) and myosin (F and G). Histograms (B, D and F) show a representative experiment of actin, tubulin and myosin-detection. Pink line: Unstained cells cultured in the presence of vehicle; Purple line: Unspecific secondary staining from FITC- (Sec Ab); Green line: Actin (B), Tubulin (D) or Myosin (F) specific expression in unstimulated cells cultured in the presence of vehicle; Light blue: Actin (A), Tubulin (C) or Myosin (E) specific expression in T4-stimulated cells; and Orange line: Actin (A), Tubulin (C) or Myosin (E) specific expression in DHT-stimulated cells. Panels (C, E and G) show the relative expression in steroid-treated and control cells. Relative expression was calculated according to: MFI of actin, tubulin or myosin stained cells / MFI secondary antibody stained cells. Data show the mean ± SE of five independent experiments.</p
Immunolocalization of nuclei after staining with DAPI of control, T<sub>4</sub>- and DHT-treated cysticerci.
<p>Phase contrast of the control sections of the slides obtained by Tissue-Teck fixing are shown in upper panel from left to right, control (C), testosterone (T<sub>4</sub>) and dihydrotestosterone (DHT). In lower panel, DAPI was used to detect nuclei in frozen tissue sections fixed with Tissue-Teck. Treatment with both steroids induced changes in the distribution of nuclei, which also affected the morphology of FCs. Cysticerci were observed under an SEM Zeiss DSM-950 after five days of treatment with 50 μg/ml of each steroid. Scale bar corresponds to 10 μm.</p
Docking of testosterone or dihydrotestosterone to actin, tubulin and myosin.
<p>Dihydrotestosterone (green or red) and testosterone (cyan) docking to actin (A and D), myosin VIb (B and E) and tubulin (C and F). We show the higher affinity sites according to neural-network scoring.</p
Confocal microscopy depicting flame cells of control, T<sub>4</sub> and DHT-treated parasites.
<p>Phase contrast of the control sections of the slides obtained by Tissue-Teck fixing are shown in upper panel from left to right, control (C), testosterone (T<sub>4</sub>) and dihydrotestosterone (DHT). In lower panel, flame cells of control, cysticerci treated with T<sub>4</sub> and DHT are presented. The normal number and distribution of flame cells is observed in control, while in those parasites exposed to T<sub>4</sub> and those exposed to DHT there is a decreased and disrupted pattern of flame cells. Scale bar corresponds to 10 μm.</p