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A pathway in quiescent cells that controls p27(Kip1) stability, subcellular localization, and tumor suppression

We have created two knock-in mouse models to study the mechanisms that regulate p27 in normal cells and cause misregulation of p27 in tumors: p27(S10A), in which Ser10 is mutated to Ala; and p27(CK–), in which point mutations abrogate the ability of p27 to bind cyclins and CDKs. These two mutant all...

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Detalhes bibliográficos
Main Authors: Besson, Arnaud, Gurian-West, Mark, Chen, Xueyan, Kelly-Spratt, Karen S., Kemp, Christopher J., Roberts, James M.
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2006
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1356100/
https://ncbi.nlm.nih.gov/pubmed/16391232
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gad.1384406
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