Transcriptomic insights into the role of the spleen in a mouse model of Wiskott‑Aldrich syndrome

Wiskott-Aldrich syndrome (WAS) is a rare X-linked primary immunodeficiency characterized by microthrombocytopenia, eczema, recurrent infection and increased incidence of autoimmune disorders and malignancy. WAS is caused by mutations in the was gene, which is expressed exclusively in hematopoietic c...

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Detalles Bibliográficos
Autores principales: Liang, Fangfang, Yang, Jun, Gan, Qian, Xia, Yu, Wang, Linlin, Huang, Yanyan, Peng, Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798154/
https://www.ncbi.nlm.nih.gov/pubmed/36605531
http://dx.doi.org/10.3892/etm.2022.11763

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798154/
https://www.ncbi.nlm.nih.gov/pubmed/36605531
http://dx.doi.org/10.3892/etm.2022.11763

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