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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 67 (1984), S. 113-122 
    ISSN: 1432-2242
    Keywords: Mice ; Selection ; Growth ; Genetic correlation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Four lines of mice were formed from a common base population and selected for 37 generations for either increased 3-week weight (weaning weight), 6-week weight, 3–6 week gain, or maintained as a randomly bred control line. Realised heritability estimates for short-term (long-term) responses were 0.33±0.20 (0.07±0.10), 0.46±0.14 (0.26±0.09), 0.36±0.14 (0.24±0.11) for 3-week weight, 6-week weight and 3–6 week gain, respectively. Realised genetic correlations estimated from short-term (long-term) responses were 0.23±0.08 (0.35±0.10) between 3-week weight and 3–6 week gain; 0.82±0.04 (0.58±0.08) between 3-week weight and 6-week weight; and 0.81±0.04 (0.97±0.04) between 3–6 week gain and 6-week weight. The genetic correlation between 3-week weight and 6-week weight was asymmetric with a greater correlated response for 3-week weight when selecting for 6-week weight (1.06) than vice versa (0.63).
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 1982-12-24
    Description: Evidence for the binding of 5,5-diphenylhydantoin and glucocorticoids to a common receptor is presented for pulmonary and hepatic cytosols and thymocytes of A/J female mice. The 5,5-diphenylhydantoin-protein complex is absorbed by DNA cellulose, and is incorporated into nuclei, 5,5-Diphenylhydantoin, like glucocorticoids, inhibits the production of prostaglandins in thymocytes. Thus a common receptor is probably responsible for the inhibitory and teratogenic effects of these drugs.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Katsumata, M -- Gupta, C -- Baker, M K -- Sussdorf, C E -- Goldman, A S -- DE-4622/DE/NIDCR NIH HHS/ -- DE-5041/DE/NIDCR NIH HHS/ -- DE-5592/DE/NIDCR NIH HHS/ -- New York, N.Y. -- Science. 1982 Dec 24;218(4579):1313-5.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/6897299" target="_blank"〉PubMed〈/a〉
    Keywords: 6-Ketoprostaglandin F1 alpha/biosynthesis ; Animals ; Binding, Competitive ; Cleft Palate/chemically induced ; Dexamethasone/metabolism ; Liver/metabolism ; Lung/metabolism ; Mice ; Phenytoin/*metabolism ; Prostaglandins/*biosynthesis ; Receptors, Glucocorticoid/*metabolism ; Receptors, Steroid/*metabolism ; Thromboxane B2/biosynthesis
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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