Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipids
about
c-Abl tyrosine kinase binds and phosphorylates phospholipid scramblase 1Deciphering the plasma membrane hallmarks of apoptotic cells: phosphatidylserine transverse redistribution and calcium entryBeyond apoptosis: the mechanism and function of phosphatidylserine asymmetry in the membrane of activating mast cellsStimulation of phosphatidylserine biosynthesis and facilitation of UV-induced apoptosis in Chinese hamster ovary cells overexpressing phospholipid scramblase 1IgE receptor type I-dependent tyrosine phosphorylation of phospholipid scramblaseStructure and expression of the murine phosphatidylserine synthase-1 gene.Membrane lipid interactions in intestinal ischemia/reperfusion-induced InjuryInvolvement of the Na+/H+ exchanger in membrane phosphatidylserine exposure during human platelet activation.Phospholipid scramblase 1 mediates type i interferon-induced protection against staphylococcal α-toxinPhospholipid scramblase 1 is required for β2-glycoprotein I binding in hypoxia and reoxygenation-induced endothelial inflammationPhospholipid scramblase 1 (PLSCR1) in villous trophoblast of the human placenta.N-terminal proline-rich domain is required for scrambling activity of human phospholipid scramblases.Microvesicle release is associated with extensive protein tyrosine dephosphorylation in platelets stimulated by A23187 or a mixture of thrombin and collagen.Involvement of sodium in early phosphatidylserine exposure and phospholipid scrambling induced by P2X7 purinoceptor activation in thymocytes.Involvement of ABCB1 and ABCC1 transporters in sea urchin Echinometra lucunter fertilization.The single C-terminal helix of human phospholipid scramblase 1 is required for membrane insertion and scrambling activity.Impaired redistribution of aminophospholipids with distinctive cell shape change during Ca2+-induced activation of platelets from a patient with Scott syndrome.
P2860
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P2860
Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipids
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on May 1997
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Scott syndrome erythrocytes co ...... tion of membrane phospholipids
@en
Scott syndrome erythrocytes co ...... ion of membrane phospholipids.
@nl
type
label
Scott syndrome erythrocytes co ...... tion of membrane phospholipids
@en
Scott syndrome erythrocytes co ...... ion of membrane phospholipids.
@nl
prefLabel
Scott syndrome erythrocytes co ...... tion of membrane phospholipids
@en
Scott syndrome erythrocytes co ...... ion of membrane phospholipids.
@nl
P2093
P2860
P356
P1476
Scott syndrome erythrocytes co ...... tion of membrane phospholipids
@en
P2093
P2860
P304
P356
10.1172/JCI119397
P407
P577
1997-05-01T00:00:00Z