Expansion of T helper type 17 lymphocytes in patients with chronic granulomatous disease

Hyper-immunoglobulin (Ig)E syndrome (HIES) is a primary immunodeficiency associated with mutations in STAT3 resulting in impaired development of T helper type 17 (Th17) lymphocytes. HIES patients with a reduced frequency of Th17 cells present with infections caused by Staphylococcus aureus and/or Ca...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Horváth, R, Rožková, D, Lašt'ovička, J, Poloučková, A, Sedláček, P, Šedivá, A, Špíšek, R
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Blackwell Science Inc 2011
विषय:
Translational Studies
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC3193916/
https://ncbi.nlm.nih.gov/pubmed/21910722
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2249.2011.04449.x
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