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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Hlavní autoři: Zanetti, Miriam, Braghetta, Paola, Sabatelli, Patrizia, Mura, Isabella, Doliana, Roberto, Colombatti, Alfonso, Volpin, Dino, Bonaldo, Paolo, Bressan, Giorgio M.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Society for Microbiology 2004
Témata:
Mammalian Genetic Models with Minimal or Complex Phenotypes
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC343785/
https://ncbi.nlm.nih.gov/pubmed/14701737
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.24.2.638-650.2004
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