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Targeting tumors that lack methylthioadenosine phosphorylase (MTAP) activity: Current strategies

Many solid tumors and hematologic malignancies lack expression of the enzyme methylthioadenosine phosphorylase (MTAP), due either to deletion of the MTAP gene or to methylation of the MTAP promoter. In cells that have MTAP, its natural substrate, methylthioadenosine (MTA), generated during polyamine...

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Detalhes bibliográficos
Main Authors: Bertino, Joseph R, Waud, William R, Parker, William B, Lubin, Martin
Formato: Artigo
Idioma:Inglês
Publicado em: Landes Bioscience 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3084968/
https://ncbi.nlm.nih.gov/pubmed/21301207
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/cbt.11.7.14948
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