Dysregulation of interleukin 5 expression in familial eosinophilia

BACKGROUND: Familial eosinophilia (FE) is a rare autosomal dominant inherited disorder characterized by the presence of lifelong peripheral eosinophilia (>1500/μL). Mapped to chromosome 5q31-q33, the genetic cause of FE is unknown, and prior studies have failed to demonstrate a primary abnormalit...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Allergy
Päätekijät: Babu, Senbagavalli Prakash, Chen, Yun-Yun K., Bonne-Annee, Sandra, Yang, Jun, Maric, Irina, Myers, Timothy G., Nutman, Thomas B., Klion, Amy D.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2017
Aiheet:
Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5546948/
https://ncbi.nlm.nih.gov/pubmed/28226398
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/all.13146
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia