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- W2149377487 abstract "dickkopf (dkk) genes encode a small family of secreted Wnt antagonists, except for dkk3, which is divergent and whose function is poorly understood. Here, we describe the generation and characterization of dkk3 mutant mice. dkk3-deficient mice are viable and fertile. Phenotypic analysis shows no major alterations in organ morphology, physiology, and most clinical chemistry parameters. Since Dkk3 was proposed to function as thyroid hormone binding protein, we have analyzed deiodinase activities, as well as thyroid hormone levels. Mutant mice are euthyroid, and the data do not support a relationship of dkk3 with thyroid hormone metabolism. Altered phenotypes in dkk3 mutant mice were observed in the frequency of NK cells, immunoglobulin M, hemoglobin, and hematocrit levels, as well as lung ventilation. Furthermore, dkk3-deficient mice display hyperactivity." @default.
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- W2149377487 date "2006-03-01" @default.
- W2149377487 modified "2023-10-17" @default.
- W2149377487 title "Generation and Characterization of <i>dickkopf3</i> Mutant Mice" @default.
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- W2149377487 doi "https://doi.org/10.1128/mcb.26.6.2317-2326.2006" @default.
- W2149377487 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/1430294" @default.
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