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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Detalles Bibliográficos
Publicado en:	Mol Cell Biol
Autores principales:	Zanetti, Miriam, Braghetta, Paola, Sabatelli, Patrizia, Mura, Isabella, Doliana, Roberto, Colombatti, Alfonso, Volpin, Dino, Bonaldo, Paolo, Bressan, Giorgio M.
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	Taylor & Francis 2004
Materias:	Mammalian Genetic Models with Minimal or Complex Phenotypes
Acceso en línea:	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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EMILIN-1 Deficiency Induces Elastogenesis and Vascular Cell Defects

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