ライフサイエンスコーパス: sheet-like

1 ctofilin to form filament bundles as well as sheet-like, 2D crystalline assemblies, which may represe

2 ma membrane, expected for an NPF that builds sheet-like actin-based protrusions.

3 ly morphologies for such systems: cube-like, sheet-like, and cylinder-like.

4 th an extramuscular free tendon as well as a sheet-like aponeurosis.

5 ), reveals that the superficial position and sheet-like architecture of the viscerosensory column in

6 FGFs especially FGF8 promoted sheet-like architecture, cell proliferation, and surviva

7 ubcellular organelle composed of tubules and sheet-like areas of membrane connected at junctions.

8 ith a hydrophilic core, consisting of a beta-sheet-like arrangement of constituent helix 1 components

9 esulting in a highly interconnected, stable, sheet-like arrangement.

10 ed solubility, resulting in micrometer-scale sheet-like assemblies that were one peptide-length thick

11 Epithelial tissues are lined with a sheet-like basement membrane (BM) extracellular matrix a

12 ronment around cells, while others provide a sheet-like basement membrane scaffold beneath epithelial

13 Whereas some stroma thylakoids form solid, sheet-like bridges between adjacent grana, others exhibi

14 ks with distinct structural organizations in sheet-like cell protrusions.

15 nana, low pigment levels also correlate with sheet-like chitin structures as opposed to rod-like stru

16 ated, and some connected to needle-shaped or sheet-like cholesterol crystals.

17 py which lead to the formation of plate- and sheet-like colloidal nanomaterials.

18 yielded peptides 3a-c that preferred a beta-sheet-like conformation.

19 nto single-, double-, and triple-strand beta-sheet-like conformations.

20 The sheet-like crystalline I-TTA COF shows better electrocat

21 nd oxidative polymerization of dopamine into sheet-like crystalline structure are enabled by the effe

22 rprisingly, ab1C neurons featured flattened, sheet-like dendrites-distinct from the cylindrical branc

23 To engineer heterotelechelic PPVs in a sheet-like design, we engineer an iterative one-pot cros

24 forms primarily by the injection of vertical sheet-like dykes, some tens of kilometres long.

25 ntributions to control transformation of the sheet-like equatorial band into a ribbon-like contractil

26 of ER tubules will lead to the formation of sheet-like ER, the action of atlastin GTPases must be ti

27 The thick sheet-like extracellular matrix (mesoglia) of the diplob

28 nt membrane is a dense, highly cross-linked, sheet-like extracellular matrix that underlies all epith

29 each end of the dimer, forming a short beta-sheet-like feature with an N-terminal segment of the par

30 stals to thermodynamically stable cross-beta-sheet-like fibrils by a de novo designed heptapeptide.

31 one segment promotes self-assembly into beta-sheet-like filaments.

32 Basement membrane (BM), a sheet-like form of extracellular matrix, surrounds most

33 The basement membrane is a specialized sheet-like form of the extracellular matrix that provide

34 h2) whose ER membrane is mostly present in a sheet-like form.

35 n walls constitute a completely new class of sheet-like functional material.

36 We propose that sheet-like geometries for the cool gas in the CGM can re

37 -driven reaction products consist of layered sheet-like hydrocarbon structures and nanosized carbon c

38 he G-strand in the V-set domain forming beta-sheet-like hydrogen bonds with the glycerol side chain o

39 oposed mode of stabilization exploits a beta-sheet-like hydrogen-bonding array to cooperatively inter

40 Although the beta sheet-like interactions contribute to the stability of t

41 interactions stabilize local structure, as B-sheet-like interactions were identified via circular dic

42 edom of chain segments and local-scale, beta-sheet-like interactions were sensitive to the patchiness

43 characteristic novel phenotype consisting of sheet-like invaginations of the sarcolemma.

44 remarkable t-system remodeling, particularly sheet-like invaginations of the sarcolemma.

45 e investigate how the WAVE complex organizes sheet-like lamellipodia.

46 the WAVE complex instructs the formation of sheet-like lamellipodia.

47 dings suggest that evolutionary expansion of sheet-like, laminated brain regions requires a concomita

48 Three major classes are spinels, sheet-like layered structures, and three-dimensional net

49 le, where the oil remained connected in thin sheet-like layers in the narrower regions of the pore sp

50 Lamellipodia are sheet-like, leading edge protrusions in firmly adherent

51 e polymer backbone is sufficient to induce B-sheet-like local structure akin to the FF copolymers; ho

52 c copolymers were synthesized that exhibit B-sheet-like local structure upon collapsing into single-c

53 ted a histologic pattern of interstitial and sheet-like lymphocytic infiltrates associated with a hig

54 like intercapsomer joints, and abundant beta-sheet-like mainchain:mainchain intermolecular interactio

55 Tumours growing in a sheet-like manner on the surface of organs and tissues w

56 in the absence of ectoderm formed continuous sheet-like masses of cartilage.

57 ect endothelial cells; (2) vascular drift, a sheet-like medial translocation of the entire vascular p

58 trate the striking envelopment of T cells by sheet-like membrane extensions derived from mature dendr

59 Sheet-like membrane protrusions at the leading edge, ter

60 runk neural crest cells from a non-segmental sheet like migration mode to a segmental stream migratio

61 ients inhibited sprouting, promoting instead sheet-like migration analogous to vessel dilation.

62 for neural crest cells to transition from a sheet-like migration behavior to migrating as a segmenta

63 he amyloid and is necessary to establish the sheet-like morphology of the assemblies.

64 -COF, with a hexagonal layered structure and sheet-like morphology, is synthesized.

65 rated membrane, (3) solvated proteins with a sheet-like nanomaterial, (4) solvated proteins with a sh

66 m shaping is used to create a highly uniform sheet-like observation volume that enables the detection

67 tyrosine melanin is present in solution as a sheet-like particle with a mean thickness of 12.5 A and

68 asticity over time and minimally invade in a sheet-like pattern.

69 ere, we demonstrate that OPTN and NDP52 form sheet-like phase-separated condensates with liquid-like

70 ixed membrane-nanomaterial system, and (6) a sheet-like polymer with gaseous solvent.

71 e nanomaterial, (4) solvated proteins with a sheet-like polymer, (5) a mixed membrane-nanomaterial sy

72 de and expand into the cardiac jelly to form sheet-like projections.

73 tes actin nucleation via the Arp2/3 complex, sheet-like protrusions are still observed in ARP2-null,

74 Lamellipodia are sheet-like protrusions formed during migration or phagoc

75 ical ring-like origami objects, a tile-based sheet-like ribbon, and a 3D crystalline tensegrity motif

76 align well across parallel and antiparallel sheets, like rungs on a ladder.

77 These high-aspect ratio sheet-like solids come in a wide array of chemical compo

78 upport the formation of disordered, non-beta-sheet-like soluble molten oligomers as early intermediat

79 While the NH...O H-bonding facilitates beta-sheet-like stacking along one direction, weak CH...N H-b

80 d structures, in particular, those emulating sheet-like structural aspects using poly(p-phenyleneviny

81 l folded structure rearranges to form a beta-sheet like structure showing that the collision induces

82 rared measurements indicate only 20-26% beta-sheet-like structure at 5 degrees C for Betanova and 42-

83 that beta barrels begin to fold into a beta-sheet-like structure before they are integrated into the

84 Their sheet-like structure derives from two independent polyme

85 y uniform and periodic in-plane with stacked sheet-like structure in the out-of-plane direction.

86 owever, the protein is more dynamic, and the sheet-like structure increases both by lengthening of th

87 The simple cellular basis and sheet-like structure of Arabidopsis integuments make the

88 ly intermediates, we propose that CA forms a sheet-like structure that associates with the condensed

89 over a 3-eV range when moving from a planar sheet-like structure to increasingly coiled conformation

90 d the conserved YKTEL motif forms a parallel sheet-like structure with the C terminus of this domain.

91 ochiral azapeptide counterparts adopt a beta-sheet-like structure, which is less favorable compared t

92 by the coexistence of a 3(1)(PII) and a beta-sheet-like structure.

93 is used to assemble epithelial cells into a sheet-like structure.

94 their C-terminal, self-assemble to form beta-sheet like structures upon mixing.

95 y, while both parallel and antiparallel beta-sheet-like structures are realized.

96 sembled in water to create fiber and fibrous sheet-like structures as observed by cryo-TEM, and the i

97 atocyte-rMVEC coculture while they formed 2D sheet-like structures in rMVEC monoculture.

98 : (1) microtubules initiate via rectangular, sheet-like structures that grow faster the larger they b

99 e BChl c molecules formed folded or twisted, sheet-like structures with a lamellar spacing of approxi

100 d-like structures further aggregate, forming sheet-like structures with a mean thickness of 51 A.

101 of the hydrogelators affords helical or beta-sheet-like structures.

102 turbulent topology, towards two-dimensional sheet-like structures.

103 efined one-dimensional aggregation into beta-sheet-like superstructures in the presence of a central

104 tional surfaces and opens up applications in sheet-like systems across scales.

105 lay critical roles in this transition from a sheet-like to a stream-like mode of migration, yet the e

106 is supported by dynamic simulations showing sheet-like transient electron or hole wave functions in

107 Furthermore, a beta-sheet-like transition that is observed when Cu ions are