Mice deficient in α-actinin-4 have severe glomerular disease

Dominantly inherited mutations in ACTN4, which encodes α-actinin-4, cause a form of human focal and segmental glomerulosclerosis (FSGS). By homologous recombination in ES cells, we developed a mouse model deficient in Actn4. Mice homozygous for the targeted allele have no detectable α-actinin-4 prot...

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Autores principales: Kos, Claudine H., Le, Tu Cam, Sinha, Sumita, Henderson, Joel M., Kim, Sung Han, Sugimoto, Hikaru, Kalluri, Raghu, Gerszten, Robert E., Pollak, Martin R.
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society for Clinical Investigation 2003
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Article
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC156110/
https://ncbi.nlm.nih.gov/pubmed/12782671
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200317988
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