Titlebook: Welfare Aspects of Transgenic Animals; Proceedings EC-Works L. F. M. Zutphen,M. Meer Conference proceedings 1997 Springer-Verlag Berlin Hei

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Growth Hormone Overproduction in Transgenic Mice: Phenotypic Alterations and Deduced Animal Models,s. In the early 1980s, transfer of growth hormone (GH) fusion genes to the germ-line of mice demonstrated that foreign genetic information may be stably integrated and expressed to yield a biologically active product, as evidenced by markedly stimulated growth of these mice. Consequently, GH structu

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Use of Transgenic Animals and Welfare Implications,er States and into the potential effects of transgenesis on the health and welfare of the animals. Screening of the Medline database revealed data for quantifying research with transgenic animals and for estimating the number of institutes working with these animal models. Questionnaires have been s

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Transgenic Animals: The Need for Ethical Dialogue,uch factual information as possible about animal biotechnology, called here the information approach..The main aim of this paper is to argue that the information approach cannot stand alone, and to present a broader approach, the approach of ethical dialogue, which explicitly takes value questions i

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Legislation on Transgenic Animals in Europe,ts of this new technology which need specific consideration, such as the regulation and control of animal welfare. In this overview, current regulations in Europe, dealing with transgenic animals, will be presented. Emphasis will be put on the welfare aspects..On the basis of the information present

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The Utrecht Workshop on Welfare Aspects of Transgenic Animals,cs and genetical changes achieved through traditional selective breeding. The opponents of this view argued that the changes brought about by transgenics are less predictable, much more rapid and in some cases much more debilitating. The point was made that genes from different species may have been

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Conference proceedings 1997A frag­ ments into a mouse zygote in the early 1980s. New well-defined animal models, developed either by micro injection techniques or by homologous recombination in embryonic stem (ES) cells, have become widely available and several classical animal models have now been replaced by these transgeni

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foreign DNA frag­ ments into a mouse zygote in the early 1980s. New well-defined animal models, developed either by micro injection techniques or by homologous recombination in embryonic stem (ES) cells, have become widely available and several classical animal models have now been replaced by these