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The Heterozygous Disproportionate Micromelia (Dmm) Mouse: Morphological Changes in Fetal Cartilage Precede Postnatal Dwarfism and Compared With Lethal Homozygotes Can Explain the Mild Phenotype

The disproportionate micromelia (Dmm) mouse has a mutation in the C-propeptide coding region of the Col2a1 gene that causes lethal dwarfism when homozygous (Dmm/Dmm) but causes only mild dwarfism observable ∼1-week postpartum when heterozygous (Dmm/+). The purpose of this study was 2-fold: first, to...

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Detalhes bibliográficos
Main Authors: Seegmiller, Robert E., Bomsta, Brandon D., Bridgewater, Laura C., Niederhauser, Cindy M., Montaño, Carolina, Sudweeks, Sterling, Eyre, David R., Fernandes, Russell J.
Formato: Artigo
Idioma:Inglês
Publicado em: Histochemical Society 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2569899/
https://ncbi.nlm.nih.gov/pubmed/18678883
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1369/jhc.2008.951673
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