Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence

Complete human CD1a deficiency on Langerhans cells due to a rare point mutation in the coding sequence

अन्य संस्करण दिखाएं (1)

CD1a molecules on skin Langerhans cells that present self and microbial lipids to T cells have been implicated in the maintenance of skin barrier function. We identified two healthy Vietnamese siblings with a complete lack of surface CD1a expression. Both individuals showed a rare single nucleotide...

पूर्ण विवरण

ग्रंथसूची विवरण
मुख्य लेखकों: Cerny, D, Thi Le, D, The, T, Zuest, R, Kg, S, Velumani, S, Khor, C, Mori, L, Simmons, C, Poidinger, M, Zolezzi, F, Ginhoux, F, Haniffa, M, Wills, B, Fink, K
स्वरूप: Journal article
प्रकाशित: Elsevier 2016

समान संसाधन