EMILIN-1 Deficiency Induces Elastogenesis and Vascular Cell Defects
EMILINs constitute a family of genes of the extracellular matrix with high structural similarity. Four genes have been identified so far in human and mouse. To gain insight into the function of this gene family, EMILIN-1 has been inactivated in the mouse by gene targeting. The homozygous animals wer...
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| Publicado no: | Mol Cell Biol |
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| Principais autores: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Taylor & Francis
2004
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC343785/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/14701737/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/MCB.24.2.638-650.2004 |
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