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The mouse tail model in dermatology : a histological study on the effects of crude coal tar and isoquinolineSmith, Catherine Claire January 1987 (has links)
This study involves a morphological and histological investigation of normal mouse tail skin and its response to crude coal tar and isoquinoline (a major constituent of coal tar). Mouse tail skin is unusual in that it undergoes both parakeratotic and orthokeratotic keratinization in adjacent sites. The former develops without a granular layer and resembles psoriasis, while the latter, with a granular layer, resembles normal human skin. Based on this property, mouse tail skin has frequently been used as a model for psoriasis but in spite of this, an integrated, detailed picture of its structure has not previously been described. This was achieved in this study by using a range of complementary techniques: light microscopy of embedded and frozen material, scanning and transmission electron microscopy, quantitative image analysis and autoradiography. Such a study may help to elucidate the mechanism of both orthokeratotic and parakeratotic keratinization. Coal tar has been used extensively in the treatment of psoriasis and is safe and effective. However, it is cosmetically unappealing, its mechanism of action is unknown and its efficacy varies with its composition which is extremely heterogeneous. Isoquinoline may significantly contribute to its anti-psoriatic properties. The mode of action of these substances as modifiers of the keratinization process may be clarified by studying their effects on the model. Both substances induced granular layer formation in previously parakeratotic areas, with concommitant development of an orthokeratotic stratum corneum, a desirable property in a potential anti-psoriatic. However, they also induced epidermal thickening and hyperkeratosis. The effects on the pilosebaceous unit were strikingly different: coal tar caused metaplasia of sebaceous glands with follicular hyperkeratosis and hair loss while isoquinoline caused sebaceous gland hypertrophy. Isoquinoline also caused far more epidermal irritation than coal tar, and caused damage to the basal lamina and dermal collagen. The irritant effects were modified to some extent by hydrocortisone cream but this also reduced granular layer induction. These studies suggest that isoquinoline may act on parakeratotic epidermis in a similar way to coal tar. It has the advantages of being a cleaner substance, with a more consistent action. However, its usefulness may be limited by its irritancy.
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A study of the antigens in bullous pemphigoidCook, A. L. January 1988 (has links)
No description available.
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The role of tumour necrosis factor-alpha 9TNF-#alpha# and other cytokines in the celluar immunopathology of psoriasisEttehadi, Parisa January 1997 (has links)
No description available.
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The molecular genetics of familial psoriasisMatthews, Deborah Anne January 1997 (has links)
No description available.
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The role of arthropod vectors in the epidemiology of lumpy skin diseaseChihota, Charles Munyaradzi January 2000 (has links)
No description available.
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Radiochemical neutron activation analysis of copper and molybdenum in human tissuesCurley, R. K. January 1987 (has links)
No description available.
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Psoriasis : the role of the keratinocyteSt. George-Smith, Stephen January 2000 (has links)
No description available.
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The detection of lumpy skin disease virus in samples of experimentally infected cattle using different diagnostic techniquesTuppurainen, Eeva S. M. January 2004 (has links)
Thesis (MSc. (Vet. Trop. Diseases))--University of Pretoria, 2004. / Includes bibliographical references.
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Mechanisms by which lumpy skin disease virus is shed in semen of artificially infected bullsAnnandale, Cornelius Henry. January 2006 (has links)
Thesis (MMedVet (Reproduction))--University of Pretoria, 2006. / Includes bibliographical references.
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The demonstration of lumpy skin disease virus in semen of experimentally infected bulls using different diagnostic techniquesBagla, Victor P. January 2006 (has links)
Thesis (MSc. (Veterinary Science))--University of Pretoria, 2006. / Includes bibliographical references.
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