ライフサイエンスコーパス: cellular protrusion

1 ntracellular domain of CD44 to the posterior cellular protrusion.

2 nside, and budded from the tip of these thin cellular protrusions.

3 budding sites at the tip or side of the long cellular protrusions.

4 ollicular epithelium and (2) the dynamics of cellular protrusions.

5 mbrane tension in the control of actin-based cellular protrusions.

6 cal adhesions, with concomitant increases in cellular protrusions.

7 auses membrane ruffling and the formation of cellular protrusions.

8 ctural rigidity of most cells or support new cellular protrusions.

9 s well as filopodia, lamellipodia, and other cellular protrusions.

10 erogeneous and exhibit different patterns of cellular protrusions.

11 on and cytoskeletal activity, which underlie cellular protrusions.

12 cylindrical and linear diffusion modes along cellular protrusions.

13 gions of dynamic actin remodeling, including cellular protrusions and cell-cell and cell-matrix junct

14 tracellular bacterial movement, formation of cellular protrusions and cell-to-cell spread.

15 Mutant ENCCs show undirected cellular protrusions and disrupted directional and chain

16 in the cytoskeleton, specifically diminished cellular protrusions and expression of the BLBC-associat

17 us, Rhes promotes the biogenesis of TNT-like cellular protrusions and facilitates the cell-cell trans

18 al Hh receptor Patched is localized in these cellular protrusions and Hh reception takes place in mem

19 tors can be used to control the formation of cellular protrusions and how the range of achievable str

20 polarity (PCP) organizes the orientation of cellular protrusions and migratory activity within the t

21 gy characterized by the formation of dynamic cellular protrusions and the assembly of discrete aggreg

22 bundles believed to mediate the formation of cellular protrusions and to provide mechanical support t

23 na/VASP proteins to promote the formation of cellular protrusions and to stimulate invasive migration

24 ion correlated with the dynamic formation of cellular protrusions and was dependent upon cell-to-cell

25 shows that phagocytic spreading is driven by cellular protrusion, and that the extent of spreading is

26 e reduction, a rounded cell shape, decreased cellular protrusions, and a higher nuclear/cytoplasmic r

27 imulated N-cadherin reorganization into thin cellular protrusions, and decreased N-cadherin adhesion.

28 wnian kinetics on flattened membranes and on cellular protrusions, and does not transfer between cell

29 and activity, enhanced PI3K distribution to cellular protrusions, and increased AKT activation in in

30 Actin-based cellular protrusions are a ubiquitous feature of cell mo

31 Actin-based cellular protrusions are an ubiquitous feature of cells,

32 sitive curvature associated with the tips of cellular protrusions as intuitively expected.

33 ar, posits that receptor activation promotes cellular protrusion at the leading edge.

34 nsion in wild-type embryos reveals elaborate cellular protrusions at ND tips that are not detected in

35 (ROS) production, cell-matrix adhesion, and cellular protrusions at the leading edge of migrating ce

36 regulates the localization of some mRNAs at cellular protrusions but the underlying mechanisms and f

37 in filaments and microtubules create diverse cellular protrusions, but intermediate filaments, the st

38 Numerous RNAs are enriched within cellular protrusions, but the underlying mechanisms are

39 e signaling pathways are thought to generate cellular protrusions by modulating the activity of downs

40 Filopodia are slender cellular protrusions containing parallel actin bundles i

41 the G protein-coupled receptor at actin-rich cellular protrusions containing VASP, a filopodial marke

42 Cellular protrusions controlled by Eph/Ephrin signaling

43 Cellular protrusions create complex cell surface topogra

44 The data indicate that beta-Pix-dependent cellular protrusions drive and coordinate collective mig

45 high levels in leading edge cells and their cellular protrusions during the morphogenetic process of

46 Dynamic and oriented cellular protrusions emanating from the socket cell, the

47 elial tip cells use dactylopodia as the main cellular protrusion for invasion into nonvascular extrac

48 form necessary for the maintenance of stable cellular protrusions generated by actin polymerization f

49 how Arg stimulates actin polymerization and cellular protrusion has not yet been fully elucidated.

50 m, which may be relevant to a broad range of cellular protrusions, illustrates that membrane remodeli

51 Cilia are hair-like cellular protrusions important in many aspects of eukary

52 nt the dynamic behaviors and morphologies of cellular protrusions in different tissue contexts.

53 sh PGC migration depends on the formation of cellular protrusions in form of blebs, a type of protrus

54 and performance objectives, of non-canonical cellular protrusions in general.

55 colocalizes with both SCRIB and VANGL1 along cellular protrusions in metastatic breast cancer cells,

56 e motors move efficiently toward the tips of cellular protrusions in the presence of blue light, and

57 taneously observe Cdc42 and Rac1 activity in cellular protrusions, indicating that Rac1 but not Cdc42

58 cell function in the root, how the growth of cellular protrusions induces local tension, and how the

59 ll to cell via tunneling nanotube (TNT)-like cellular protrusions, interacts with dysfunctional mitoc

60 shown by loss of villi, tubule dilation, and cellular protrusions into the tubule lumen, was unambigu

61 Polarised targeting of diverse mRNAs to cellular protrusions is a hallmark of cell migration.

62 been linked to the formation of proteolytic cellular protrusions known as invadopodia, undergoes an

63 , which could have relevance for the role of cellular protrusions like microvilli.

64 n the correct formation of other actin-based cellular protrusions (microchaetae and macrochaetae).

65 Regulation of cellular protrusions, movement and intercalation within

66 Before establishing communication, cellular protrusions must find their target cell.

67 roglial gene expression with upregulation of cellular protrusion/neuritogenic pathways, concurrently

68 ected with wild-type ARF6, and resembled the cellular protrusions observed in cells expressing the GT

69 e the functional role of RNA localization at cellular protrusions of migrating mesenchymal cells, usi

70 te the size and architecture of the TNT-like cellular protrusions of the distal tip cell (DTC), the g

71 te the size and architecture of the TNT-like cellular protrusions of the distal tip cell (DTC), the g

72 cal and experimental study of the coiling of cellular protrusions on fibers of different geometry.

73 ics and find that the structured ECM orients cellular protrusions parallel to the ECM.

74 Bleb-type cellular protrusions play key roles in a range of biolog

75 legant studies have revealed the specialized cellular protrusions, proteases, and distinct modes of m

76 Cellular protrusion rate, protrusion orientation, speed

77 ed for all orientations of stress fibers and cellular protrusions relative to the stretch direction,

78 protein, induces the biogenesis of TNT-like cellular protrusions, "Rhes tunnels," through which Rhes

79 ls in tissue also communicate via long, thin cellular protrusions, such as airinemes in zebrafish.

80 and randomizes the orientation of polarized cellular protrusions, suggesting that integrin-fibronect

81 nerate is regulated by the primary cilium, a cellular protrusion that serves as a sensitive sensory o

82 1alpha- and miR-205-dependent suppression of cellular protrusions that are required to initiate colle

83 ll-contact-dependent filamentous-actin-based cellular protrusions that can connect two or more cells

84 This co-movement likely depends on epidermal cellular protrusions that directly contact pObs only whe

85 Filopodia are slender cellular protrusions that dynamically extend and retract

86 ey their microenvironment by forming dynamic cellular protrusions that enable chemotaxis, contacts wi

87 ocytosis fuels generation of large, invasive cellular protrusions that expand tiny basement membrane

88 ia are highly specialized small antenna-like cellular protrusions that extend from the cell surface o

89 sion was evaluated in invadopodia, which are cellular protrusions that form the invasive tips of canc

90 l is traversed by hundreds of extremely long cellular protrusions that maintain long-term contacts be

91 Blebs are spherical cellular protrusions that occur in many physiological si

92 Membrane blebs are specialized cellular protrusions that play diverse roles in processe

93 n SCLC cells in culture and in vivo can grow cellular protrusions that resemble axons.

94 0-mum diameter) vesicles, derived from bulky cellular protrusions, that contain metalloproteinases, R

95 1 enhances the formation of various types of cellular protrusions through directly targeting and down

96 led that activation induced the formation of cellular protrusions tipped with MHC class I protein.

97 Measurements done on nonmoving cellular protrusion tips showed no pair-correlation at t

98 The recent discovery of cellular protrusions - tumor microtubes - connecting can