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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 32 (1960), S. 1289-1292 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-184X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Two urease-positiveVibrio spp. were isolated from a brown shark (Carcharhinus plumbeus) that died in captivity at a national aquarium. Morphological, biochemical, and molecular genetic studies revealed one of the isolates to beV. damsela; the other isolate was unique and has been classified asV. carchariae sp. nov. BothV. damsela andV. carchariae were found to be virulent for spiny dogfish (Squalus acanthias), causing death in less than 18 hours after intraperitoneal injection of ca. 4×106 cells.V. damsela was strongly cytotoxic for Y1 adrenal cell monolayers;V. carchariae exhibited weak cytotoxicity for Y1 cells.V. damsela contained cryptic plasmids and both isolates were urease positive.V. carchariae was able to utilize urea as sole source of carbon and nitrogen.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Blackwell Science Ltd/Inc.
    Wound repair and regeneration 12 (2004), S. 0 
    ISSN: 1524-475X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Excessive scarring is a significant clinical problem. p21, a cyclin-dependent kinase inhibitor, blocks cell cycle progression and attenuates proliferation of various cell types. Our in vitro rAd-p21 dose response studies of primary human dermal fibroblasts showed a 3–80 fold reduction of cell proliferation as measured by BrdU incorporation at doses of 1 × 108−3 × 109 PN/mL, respectively. Further, rAd-p21 at 3 × 109 PN/mL showed a 2-fold less procollagen I (PIP) production when compared to control virus. These in vitro data demonstrate that rAd-p21 significantly attenuates fibroproliferation and procollagen production in the target cells. In vivo, a rat PVA sponge model was used. rAd-p21, at doses of 1 × 109, 1 × 1010 and 5 × 1010 PN was delivered into sponges that had previously been treated with a granulation tissue stimulator, rAd-PDGF-B. Results showed that sponges receiving rAd-PDGF-B alone had the highest % granulation fill (40–60% fill area). Sponges that were treated with rAd-PDGF-B for the first injection followed by rAd-p21 on a second injection showed a dose-dependent decrease in % granulation fill as rAd-p21 doses increased (p 〈 0.001). On day 5 post-injection, IHC staining identified p21 protein expression only in sponges receiving rAd-p21. In addition, the quantitative measurement of cells labeled by BrdU or Ki67 demonstrated that rAd-p21 significantly attenuated cell proliferation when compared to rAd-PDGF alone in this model (p 〈 0.01). In another in vivo experiment, a rabbit excessive scar model was used. rAd-p21, at a dose of 2 × 109 PN/wound was intradermally injected into the rabbit ear wounds that had previously been treated with PDGF-BB protein. Preliminary data showed that scar thickness in rAd-p21 treated wounds was significantly decreased in comparison to wounds treated with the control virus (p 〈 0.05). These data suggest that rAd-p21 is effective in attenuating scars in the rabbit ear excessive scar model. Our in vitro and in vivo data support the further exploration of rAd-p21 as a useful therapeutic candidate for hyperproliferative diseases in patients.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Blackwell Science Ltd/Inc.
    Wound repair and regeneration 12 (2004), S. 0 
    ISSN: 1524-475X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Excessive scarring is a significant clinical problem, resulting in both adverse tissue form and function and the goal of therapeutic interventions is to reduce and prevent excessive scarring. We have demonstrated that a recombinant adenovirus containing the cyclin-dependent kinase inhibitor p21 (rAd-p21), inhibited scar formation by blocking cell cycle progression and attenuated cell proliferation at the wound site (Perkins et al 2002). Recently, we have shown rAd-p21 specific antiproliferative effects on granulation tissue in vivo(Gu, et al, manuscript submitted). Safety parameters using rAd-p21 for anti-scarring may include effects on wound strength and dehiscence of the wound. We tested effects of rAd-p21 on wound strength in vivo using tensile strength as an endpoint and included comparisons with other clinically relevant antiproliferative agents. Specifically, rAd-p21 at doses from 1 × 107 to 3.8 × 1010 particle (PN) per incision was administered intradermally to linear rat incisions and assayed 14–28 days post treatment. rAd-p21 mildly reduced tensile strength at high doses (≥3 × 1010PN), whereas low to moderate doses (1 × 107 to 1 × 1010PN) had no effect. Interestingly, all rAd-p21 treated wounds regained tensile strength indistinguishable from vehicle control, 4 weeks after treatment, suggesting that rAd-p21 wounds recover with time. An adenovirus control vector, not containing a gene (rAd-Empty), showed subtle reduction of tensile strength that was only statistically significant at day 21. This suggests that delivery of rAd-Empty alone in the wound has little effect on wound strength. Triamcinolone at 5 mg/mL/wound, 5-FU at 10 mg/mL/wound, and low doses of MMC did not significantly reduce tensile strength, although high doses of MMC (0.2 mg/mL/wound) severely reduced tensile strength which failed to recover after 28 days. Morphological analysis of all groups revealed necrosis only in the MMC treatment. This data suggests that rAd-p21 may reduce the hyperproliferative status in excessive scar formation with minimal effects on wound strength.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Blackwell Science Ltd/Inc.
    Wound repair and regeneration 12 (2004), S. 0 
    ISSN: 1524-475X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Research on abnormal scarring, such as excessive scars, has been hampered by the lack of relevant animal models. Recent studies suggest that TGF-β1, PDGF-BB and FGF-2 are stimulators of fibrosis or scarring. We developed a rabbit ear cutaneous excessive scarring model using the growth factor stimulators TGF-β1 (0.25, 0.5 or 1 μg per wound), PDGF-BB (1, 2 or 3 μg per wound) and FGF-2 (0.5, 1, 3 or 5 μg per wound). Three 8-mm diameter wounds were created on each ear in NZW rabbits (n = 6 wounds). The test growth factors were injected intradermally immediately after wounding. Controls consisted of PBS, BSA and wounding only without injections. Scar thickness of wounds was measured with a micrometer at days 14 and continued twice a week thereafter until sacrifice at day 28. Results showed that the greatest measurement of elevated scars was observed at day 14. Significant differences of scar thickness were observed in TGF-β1 at a dose of 0.25 μg, PDGF-BB at a dose of 3 μg, and FGF-2 at a dose of 3 μg per wound groups when compared to PBS and wounding only groups (p 〈 0.05). Interestingly, BSA, a protein stabilizer for TGF-β1 and FGF-2 proteins, also significantly elevated scar thickness at day 14 over PBS alone (p 〈 0.05). Trichrome stained tissue sections on day 28 showed an increase in cellularity and thicker epithelium in all doses of TGF-β1, PDGF-BB and FGF-2 protein treated groups when compared to wounding only, PBS or BSA treatments. In general, FGF-2 treated wounds showed more vascularity than TGF-β1 and PDGF-BB treated wounds. By contrast, PDGF-BB treated wounds showed richer collagen deposition than TGF-β1 and FGF-2 treated wounds. Results from these studies demonstrated that TGF-β1, PDGF-BB and FGF-2 contributed to the scar formation in the rabbit ear scar model. BSA may contribute in stimulating scar formation in the early stage of wound healing in this model. Enhancing elevated scar formation in the rabbit ear model will be useful in evaluating anti-scarring agents for excessive scars such as hypertrophic scars and keloids.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Luminescence 60-61 (1994), S. 32-35 
    ISSN: 0022-2313
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Luminescence 60-61 (1994), S. 32-35 
    ISSN: 0022-2313
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1438-3888
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract TwoVibrio species identified asV. damsela and a new sucrose-positiveVibrio sp.,V. carchariae sp. nov., were simultaneously isolated from a brown shark which died while being held in captivity at a large aquarium. Pathogenicity studies were subsequently conducted using a variety of elasmobranchs, including smooth dogfish and lemon sharks. Both bacterial strains proved pathogenic, causing death in nearly all of the elasmobranch hosts challenged. Virulence studies revealed that both bacterial strains were cytotoxic for Y-1 mouse adrenal cells. TheV. damsela strain was highly cytotoxic causing Y-1 cellular damage at culture supernatant dilutions up to 1 : 128. Both strains were hemolytic, but neither exhibited the Kanagawa phenomenon. They were both capable of urea hydrolysis, an interesting trait, considering that elasmobranchs retain large (ca 300 milliosmolal) urea concentration in their tissue.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Methods in cell science 6 (1980), S. 85-90 
    ISSN: 1573-0603
    Keywords: Y1 cells ; bacterial enterotoxins ; Vibrio cholerae ; enterotoxigenic bacteria ; Y1 assay
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Specific standard steps are described for the implementation of the Y1 mouse adrenal tumor cell line in evaluating the production of bacterial enterotoxins and cytotoxins. The importance of standardization of methods for Y1 cell culture, preparation of test materials, and interpretation of results is emphasized. Rationale for utilization of the Y1 cell assay and difficulties of application are discussed. Adaptations for research purposes and potential applications are described.
    Type of Medium: Electronic Resource
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