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1  support its function as an energy-dependent aminophospholipid translocase.
2 embrane surface, but can interfere with both aminophospholipid translocase activity and calcium-induc
3 erstood but has been associated with loss of aminophospholipid translocase activity and nonspecific f
4 uld affect PS appearance, either by altering aminophospholipid translocase activity or phospholipid f
5 arance in the plasma membrane outer leaflet, aminophospholipid translocase activity ultimately modula
6 ibited despite DNA fragmentation and loss of aminophospholipid translocase activity, the latter demon
7  RBC and that it correlates with the loss of aminophospholipid translocase activity, the only common
8 de of PS appearance depended on the level of aminophospholipid translocase activity.
9  to severe cellular damage and impairment of aminophospholipid translocase activity.
10 hich can be exacerbated by the inhibition of aminophospholipid translocase activity.
11 ent of spin-labeled PS was used to determine aminophospholipid translocase activity.
12  consists of 12 members that encode putative aminophospholipid translocases (ALA1-12).
13 it is thought that declining activity of the aminophospholipid translocase and calcium-mediated, nons
14 lic Ca2+ in concert with inactivation of the aminophospholipid translocase and is inhibited by calciu
15 tosis, the appearance of PS followed loss of aminophospholipid translocase and was accompanied by non
16 transporters involved in PS externalization, aminophospholipid translocase (APLT) and phospholipid sc
17              PS distribution is regulated by aminophospholipid translocase (APLT), which maintains PS
18  cytosolic leaflet of the plasma membrane by aminophospholipid translocase (APLT).
19                                              Aminophospholipid translocases (APLTs) are defined prima
20 rnalization was accompanied by inhibition of aminophospholipid translocase (APT).
21 s encoding P-type ATPases that are potential aminophospholipid translocases (APTs): DRS2, NEO1, and t
22 ter the decline in PS inward movement by the aminophospholipid translocase as measured by the uptake
23   The recently cloned gene for the mammalian aminophospholipid translocase belongs to this new subfam
24  is an essential P-type ATPase and potential aminophospholipid translocase (flippase) in the Drs2p fa
25 ntegral membrane P-type ATPase and potential aminophospholipid translocase (or flippase).
26 the inactivation of the transmembrane enzyme aminophospholipid-translocase (or flippase) by HNE and a
27                     Our results suggest that aminophospholipid translocases play an important role in
28 s2p/Swa3p is a P-type ATPase and a potential aminophospholipid translocase that localizes to the tran
29 activity in concert with inactivation of the aminophospholipid translocase, there is no evidence indi
30 ate-labeled annexin V, (ii) PS uptake by the aminophospholipid translocase using [6-[(7-nitrobenz-2-o
31 e inner leaflet of the plasma membrane by an aminophospholipid translocase, which has now been cloned

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