A TMEM16F point mutation causes an absence of canine platelet TMEM16F and ineffective activation and death-induced phospholipid scrambling.
about
Exposure of phosphatidylserine on the cell surfaceCombined Quantification of the Global Proteome, Phosphoproteome, and Proteolytic Cleavage to Characterize Altered Platelet Functions in the Human Scott Syndrome.Anoctamins/TMEM16 Proteins: Chloride Channels Flirting with Lipids and Extracellular Vesicles.
P2860
A TMEM16F point mutation causes an absence of canine platelet TMEM16F and ineffective activation and death-induced phospholipid scrambling.
description
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name
A TMEM16F point mutation cause ...... duced phospholipid scrambling.
@en
type
label
A TMEM16F point mutation cause ...... duced phospholipid scrambling.
@en
prefLabel
A TMEM16F point mutation cause ...... duced phospholipid scrambling.
@en
P2093
P2860
P356
P1476
A TMEM16F point mutation cause ...... duced phospholipid scrambling.
@en
P2093
J A McCardle
J L Catalfamo
M B Brooks
R MacNguyen
P2860
P304
P356
10.1111/JTH.13157
P577
2015-09-28T00:00:00Z