コーパス検索結果 (left1)
通し番号をクリックするとPubMedの該当ページを表示します
2 The estimated free energy of binding of a DPPS lipid to the second binding site is around -8.8 kca
3 s of the incubation of BBR3464 with DPPA and DPPS correspond to chloride displacement and formation o
5 tached with nearly equal coverage to OPN and DPPS surfaces alone, suggesting that the preferential se
6 s demonstrated that lateral proton fluxes at DPPS are significant, but the lateral proton diffusion c
7 lity to test whether and how the HBR-derived DPPS is affected by the presence and movement of threate
8 DL-alpha-phosphatidyl-L-serine, dipalmitoyl (DPPS) or zwitterionic L-alpha-phosphatidylcholine, dipal
10 holine (DPPC)/dipalmitoylphosphatidylserine (DPPS) (3:1:1 molar ratio) bilayers using (2)H-NMR and sp
12 one and two dipalmitoylphosphatidylserines (DPPS) in a dipalmitoylphosphatidylcholine (DPPC) bilayer
13 es to negatively charged phospholipids DPPA, DPPS, and DPPG were slightly lower in a 100 mM chloride
14 f the negatively charged phospholipids DPPA, DPPS, and DPPG with the highly positively charged platin
16 r DPPA was the phosphate oxygen, whereas for DPPS, a binding site of the nitrogen of the serine side
18 ows flying towards the participant result in DPPS expansion, an effect directionally-tuned towards th
20 ing body posture, we show that the extent of DPPS asymmetry is defined in an earth-centred coordinate
22 line (DPPC), dipalmitoyl phosphatidylserine (DPPS), dipalmitoyl phosphatidylethanolamine (DPPE), or d
24 entropy of negatively charged phospholipids DPPS, DPPA, and DPPG were changed upon reaction with the
25 In contrast, the two acidic phospholipids, DPPS and DPPA, caused a dose-dependent increase in both
27 ized the fine-grained geometry of the face's DPPS by recording the enhancement of the blink reflex el
31 STATEMENT The defensive peripersonal space (DPPS) has a crucial role for survival, and its modulatio
34 pain, affects defensive peripersonal space (DPPS), the portion of space surrounding the body within
35 ferred to as a defensive peripersonal space, DPPS), as well as stimulus movement and probability of s
37 when the hand of the participant enters the DPPS of another individual, either in egocentric or in a
41 threatening stimulus is delivered inside the DPPS, subcortical defensive responses like the hand-blin
42 en that TN is unilateral, in TN patients the DPPS of the face might not be horizontally symmetric as
43 All these findings provide evidence that the DPPS is dynamically shaped by predictive mechanisms run
45 on COM crystals and suppresses attachment to DPPS, suggesting a link between OPN and reduced attachme
46 omes was higher than the ratio of BBR3464 to DPPS liposomes, and similar differences were seen for BB