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Scott syndrome erythrocytes contain a membrane protein capable of mediating Ca2+-dependent transbilayer migration of membrane phospholipids.

Phospholipid (PL) scramblase is a plasma membrane protein that mediates accelerated transbilayer migration of PLs upon binding Ca2+, facilitating rapid mobilization of phosphatidylserine to the cell surface upon elevation of internal Ca2+. In patients with Scott syndrome, a congenital bleeding disor...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Stout, J. G., Bassé, F., Luhm, R. A., Weiss, H. J., Wiedmer, T., Sims, P. J.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Society for Clinical Investigation 1997
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC508054/
https://ncbi.nlm.nih.gov/pubmed/9151796
Tagiau: Ychwanegu Tag
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