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Clinical and functional impact of recurrent S1PR1 mutations in mantle cell lymphoma

S1PR1 mutations are present in 7.8% of patients with MCL and are significantly more frequent at relapse. S1PR1 mutations reduce expression of the S1PR1 receptor, which mediates migration towards the tissue-to-blood egress factor S1P in MCL. .

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Detalhes bibliográficos
Publicado no:Blood Adv
Main Authors: Wasik, Agata M., Wu, Chenglin, Mansouri, Larry, Rosenquist, Richard, Pan-Hammarström, Qiang, Sander, Birgitta
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5873236/
https://ncbi.nlm.nih.gov/pubmed/29549086
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2017014860
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