ライフサイエンスコーパス: lateral movement

1 or =2 cm, and in 4% there was > or =4 cm of lateral movement.

2 o relatively static and exhibit virtually no lateral movement.

3 helical axis was calculated from a simulated lateral movement.

4 e proteins encounter cytoplasmic barriers to lateral movement.

5 cto-myosin contractility induces their rapid lateral movement.

6 otion modes-walking, crawling, swinging, and lateral movement.

7 y ~3 angstrom and accompanied by significant lateral movements.

8 dynamic movement of AMPA receptors occurs by lateral movement across the surface of neurons.

9 The blockage of this ion channel's lateral movement affects the killing potential of CAR T

10 , forming a molecular lattice that restricts lateral movement and endocytosis of glycoproteins.

11 kinds of tracks, defining stalls, reversals, lateral movement, and forward movement.

12 hered at these sites, gradually clustered by lateral movement, and subsequently initiated filopodia f

13 The barriers to lateral movement are dynamic, discontinuous, and low in

14 The models suggest predominantly lateral movement around Asp(204) and rotational movement

15 ard deviation of lane position, a measure of lateral movements away from the center of the lane, duri

16 nvaded cells, and to be capable of extensive lateral movement between cells.

17 ion of AT(1)-R, including internalization or lateral movement between plasma membrane compartments in

18 mal perception of surface roughness requires lateral movement between skin and surface, suggesting th

19 ndergoes ~3- to 5- angstrom transitional and lateral movements during depolarization, which are coupl

20 int allows the stator to bend to accommodate lateral movements during the activity of the catalytic d

21 Lateral movement, either via diffusion or active transpo

22 Barriers to lateral movement (>3 times the continuous resistance) we

23 ch the mode shift is attributable to a slow, lateral movement in S4 that is triggered by the initial

24 of the surface VSG coat, which displays both lateral movement in the plane of the membrane and variat

25 uired for oligomerization, which include the lateral movement of a key amphipathic helix.

26 igitate into a hydrophobic pocket created by lateral movement of a Pru B-hairpin with an exposed end

27 nsmits a positional signal, CR4 promotes the lateral movement of aleurone signaling molecules between

28 nsulin-induced internalization of AMPARs, or lateral movement of AMPARs to extrasynaptic sites.

29 Although the lateral movement of anterior mitral leaflet is limited b

30 A lateral movement of at least two strands neighbored in s

31 igh actin-ezrin intensity area restricts the lateral movement of BCRs upon stimulation, consequently

32 heir relationship to "rafts." We studied the lateral movement of different membrane molecules thought

33 ntegrases, suggesting an evolution involving lateral movement of DNA among species.

34 our observations support the hypothesis that lateral movement of filopodia is caused by retrograde fl

35 contamination relative to the reconstructed lateral movement of groundwater over the same period.

36 t is consistent with the previously observed lateral movement of HIV into the virological synapse.

37 curs through a ledge mechanism involving the lateral movement of ledges on the close-packed {111} ato

38 n local curvature of the membrane affect the lateral movement of lipids, affecting the biophysical pr

39 or function of the YSL2 appears to be in the lateral movement of metals in the vasculature.

40 teriorly; finally, the axial push drives the lateral movement of midline PSM cells to maintain PSM gr

41 s produced by individual actin filaments and lateral movement of molecular complexes must all be inco

42 Depletion of Caldesmon results in aberrant lateral movement of myosin-II filaments along actin bund

43 be used to better leverage the differential lateral movement of particles with different sizes as th

44 ize the endodermal epithelium to promote the lateral movement of pouch-forming cells.

45 Whereas lateral movement of proteins in this lipid bilayer is po

46 tinal and forebrain precursors suggests that lateral movement of retinal precursors is responsible fo

47 king S5 and S2, which not only restricts the lateral movement of S5 but also prevents substrate from

48 lesterol and 25-hydroxycholesterol block the lateral movement of sterol regulatory element-binding pr

49 translocation states of RNAP by restricting lateral movement of TEC along the DNA register.

50 a solvent during matrix application reduces lateral movement of the analyte.

51 ant widening (4 A) of the tetramer caused by lateral movement of the C domains.

52 nding hemi-neuromeres which results from the lateral movement of the germband halves during spider em

53 acing GltPh conformations are nonconductive, lateral movement of the glutamate transport domain from

54 The responses to lateral movement of the jaw were similar across all trea

55 No lateral movement of the layers was observed during this

56 s between Msh2-Msh6 and DNA are dominated by lateral movement of the protein along the helical axis a

57 from the source, while allowing significant lateral movement of the receiver on the WiGL (Wireless G

58 S4 during activation are rigidly coupled to lateral movement of the S4-S5 linker, which could induce

59 en together, these data suggest that a large lateral movement of the S5 helix is not required for sub

60 Flagellar bending and lateral movement of the sperm head during [Ca(2+)](i) pe

61 y draws heart and liver ROI and corrects for lateral movement of the subject.

62 ransport domain across the membrane, and the lateral movement of this domain results in anion channel

63 junction and in doing so, likely changes the lateral movement of Tpm3.1 across the actin surface resu

64 itions from a closed to open conformation by lateral movement of two groups of AHs, exposing a large

65 ace on the disk membrane, by restricting the lateral movement of, and hence the rate of encounters be

66 usion time, whereas down-regulation promoted lateral movements of filopodia.

67 These results suggest that lateral movements of synaptic vesicles are restricted se

68 g/relaxation of the F bridge correlates with lateral movements of the RNA 3' terminus.

69 ndings suggest that the mental simulation of lateral movements, reflecting immature neurocognitive sc

70 molecules docked at the membrane where their lateral movement slowed and then ceased as Gag assembled

71 filopodia induces a rapid and highly ordered lateral movement, "surfing" toward the cell body before

72 haracter of BPs, revealing rigid and limited lateral movements under magnetic field pulses as well as

73 in to be in each child's repertoire, and the lateral movement was goal-directed (used to hit a plasti

74 linking of Qa-2 molecules, the resistance to lateral movement was that expected of monomeric lipid-an

75 The CD99-blocked PMN exhibited dynamic lateral movement within endothelial cell junctions, indi