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

The family of CD1 molecules is structurally similar to MHC class I molecules, but the 2 protein families mediate fundamentally different immune functions. MHC class I molecules present peptides to T cells, whereas CD1 molecules present lipids to natural killer T cells and other CD1-restricted T cell...

Täydet tiedot

Bibliografiset tiedot
Päätekijät:	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
Aineistotyyppi:	Journal article
Kieli:	English
Julkaistu:	Elsevier 2016

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

Julkaistu 2016

Journal article

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 Tekijä 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

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