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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Bibliografiska uppgifter
I publikationen:	Mol Cell Biol
Huvudupphov:	Zanetti, Miriam, Braghetta, Paola, Sabatelli, Patrizia, Mura, Isabella, Doliana, Roberto, Colombatti, Alfonso, Volpin, Dino, Bonaldo, Paolo, Bressan, Giorgio M.
Materialtyp:	Artigo
Språk:	Inglês
Utgiven:	Taylor & Francis 2004
Ämnen:	Mammalian Genetic Models with Minimal or Complex Phenotypes
Länkar:	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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