Oval cell proliferation associated with the murine insertional mutation TgN737Rpw.

The Tg737 gene was identified by its direct association with a transgene-induced insertion mutation in the mouse. This mutation causes pleiotropic phenotypes including a syndrome similar to autosomal recessive polycystic kidney disease in humans. This syndrome, in addition to renal cyst formation, i...

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Main Authors: Richards, W. G., Yoder, B. K., Isfort, R. J., Detilleux, P. G., Foster, C., Neilsen, N., Woychik, R. P., Wilkinson, J. E.
Format: Artigo
Sprog:Inglês
Udgivet: 1996
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1865369/
https://ncbi.nlm.nih.gov/pubmed/8952527
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