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del Barco Barrantes, I.* ; Montero-Pedrazuela, A.* ; Guadano-Ferraz, A.* ; Obregon, M.J.* ; de Mena, R.M.* ; Gailus-Durner, V. ; Fuchs, H. ; Franz, T.J.* ; Kalaydjiev, S.* ; Klempt, M.* ; Hölter, S.M. ; Rathkolb, B.* ; Reinhard, C. ; de Escobar, G.M.* ; Bernal, J.* ; Busch, D.H.* ; Wurst, W. ; Wolf, E.* ; Schulz, S. ; Shtrom, S.* ; Greiner, E.* ; Hrabě de Angelis, M. ; Westphal, H.* ; Niehrs, C.*

Generation and characterization of dickkopf3 mutant mice.

Mol. Cell. Biol. 26, 2317-2326 (2006)
Verlagsversion DOI PMC
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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
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
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
ISSN (print) / ISBN 0270-7306
e-ISSN 1098-5549
Zeitschrift Molecular and Cellular Biology
Quellenangaben Band: 26, Heft: 6, Seiten: 2317-2326 Artikelnummer: , Supplement: ,
Verlag American Society for Microbiology (ASM)