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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Опубликовано в::	Mol Cell Biol
Главные авторы:	Zanetti, Miriam, Braghetta, Paola, Sabatelli, Patrizia, Mura, Isabella, Doliana, Roberto, Colombatti, Alfonso, Volpin, Dino, Bonaldo, Paolo, Bressan, Giorgio M.
Формат:	Artigo
Язык:	Inglês
Опубликовано:	Taylor & Francis 2004
Предметы:	Mammalian Genetic Models with Minimal or Complex Phenotypes
Online-ссылка:	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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