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Internal ribosome entry site of bFGF is the target of thalidomide for IMiDs development in multiple myeloma

Although new analogues of immunomodulatory drugs (IMiDs) are being developed for MM, the molecular mechanism of these drugs remains unclear. In the current study, we used MM cell lines as a model to investigate the molecular mechanism of thalidomide and to compare its potency with IMiDs such as poma...

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Autori principali: Lien, I-Chia, Horng, Lin-Yea, Hsu, Pei-Lun, Wu, Chia-Ling, Sung, Hui-Ching, Wu, Rong-Tsun
Natura: Artigo
Lingua:Inglês
Pubblicazione: Impact Journals LLC 2014
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4091528/
https://ncbi.nlm.nih.gov/pubmed/25053990
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