Upregulation of Checkpoint Ligand Programmed Death-Ligand 1 in Patients with Paroxysmal Nocturnal Hemoglobinuria Explained by Proximal Complement Activation
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare hemolytic disease driven by impaired complement regulation. Mutations in genes encoding the enzymes that build the GPI anchors are causative, with somatic mutations in the gene occurring most frequently. As a result, the important membrane-bound co...
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Veröffentlicht in: | The Journal of immunology (1950) 2022-03, Vol.208 (5), p.1248-1258 |
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Sprache: | eng |
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