The molecular basis for paroxysmal nocturnal hemoglobinuria
- 1 October 1993
- journal article
- review article
- Published by Wiley in Transfusion
- Vol. 33 (10), 852-873
- https://doi.org/10.1046/j.1537-2995.1993.331094054626.x
Abstract
No abstract availableThis publication has 100 references indexed in Scilit:
- The urokinase receptor and regulation of cell surface plasminogen activationCell Differentiation and Development, 1990
- The Ca-MOv18 molecule, a cell-surface marker of human ovarian carcinomas, is anchored to the cell membrane by phosphatidylinositolBiochemical and Biophysical Research Communications, 1990
- Dynamics and longevity of the glycolipid-anchored membrane protein, Thy-1.The Journal of cell biology, 1990
- Analysis of PI (phosphatidylinositol)‐anchoring antigens in a patient of paroxysmal nocturnal hemoglobinuria (PNH) reveals deficiency of 1F5 antigen (CD59), a new complement‐regulatory factorFEBS Letters, 1990
- Paroxysmal nocturnal hemoglobinuria and the transfusion of washed red cells. A myth revisitedTransfusion, 1989
- Complete deficiency of 20 KDa homologous restriction factor (HRF20) and restoration with purified HRF20Biochemical and Biophysical Research Communications, 1989
- A family showing inheritance of the Inab phenotypeTransfusion, 1988
- Decay accelerating factor of complement is anchored to cells by a C-terminal glycolipidBiochemistry, 1986
- A hydrophobic dimer of acetylcholinesterase from Torpedo californica electric organ is solubilized by phosphatidylinositol-specific phospholipase CNeuroscience Letters, 1983
- A possible null phenotype in the Cromer blood group complexTransfusion, 1982