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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

50 Their sheet-like structure derives from two independent polyme

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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