Ontology highlight
ABSTRACT:
OTHER RELATED OMICS DATASETS IN: GSE122352
INSTRUMENT(S): LTQ Orbitrap Velos
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Plasma Cell, Extracellular Exosome Assembly
DISEASE(S): Paroxysmal Nocturnal Hemoglobinuria
SUBMITTER: Pol Herrero
LAB HEAD: Irene Martínez Martínez
PROVIDER: PXD011768 | Pride | 2019-03-12
REPOSITORIES: pride
Action | DRS | |||
---|---|---|---|---|
P2838-TMT1-R1.msf | Msf | |||
P2838-TMT1-R1.raw | Raw | |||
P2838-TMT1-R2.msf | Msf | |||
P2838-TMT1-R2.raw | Raw | |||
P2838-TMT1-R3.msf | Msf |
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Scientific reports 20190305 1
Paroxysmal Nocturnal Hemoglobinuria (PNH) is a clonal disease of blood cells caused by the lack of glycosyl phosphatidyl inositol anchored proteins bound to the cell membrane. In consequence, erythrocytes lead to intravascular hemolysis upon complement activation, which promotes high risk of thrombosis, intravascular hemolytic anemia, and bone marrow failure in patients. The mechanisms of thrombosis in PNH are still poorly understood. Treatment with eculizumab reduces intravascular hemolysis and ...[more]