ライフサイエンスコーパス: hourglass

1 g spheres, ellipsoids, capped cylinders, and hourglasses.

2 ompanied by loss of septin subunits from the hourglass and reorganization of the remaining subunits i

3 We found that both the hourglass and ring filament assemblies have sub-resoluti

4 vo, but the filament organization within the hourglass and ring structures is controversial.

5 Septin filaments form ordered hourglass and ring-shaped structures in close apposition

6 t Saccharomyces cerevisiae, septins form an 'hourglass' at the mother-bud neck before cytokinesis, wh

7 pteridine ring of the substrate, DHF, at the hourglass center of the pore, holds the reactants in pla

8 electron microscopy, we find that the early hourglass consists of septin double filaments oriented a

9 aried; however, 19 patients (68%) showed an "hourglass" contour, with midventricular hypertrophy prod

10 arger plaques, severe curvature, complete or hourglass deformities, then incision or excision of the

11 res shorten the penis and do not correct the hourglass deformity.

12 The front funnel is of the novel "hourglass" design that efficiently accumulates ions and

13 xplore the possible functional dependence of hourglass domains in adjacent subunits, we prepared a se

14 Besides the hourglass fermion, another surface of KHgX manifests a t

15 These 'hourglass' fermions are formed in the large-gap insulato

16 The hourglass figures appear to result from the deposition o

17 The hourglass filaments have an additional degree of symmetr

18 the membrane, forming an aqueous pore ("the hourglass") flanked by the corresponding B and E residue

19 nit containing an aqueous pore likened to an hourglass formed by obversely arranged tandem repeats.

20 The age of the hourglass glacier, considered to be inactive and slowly

21 rock glaciers in Tharsis and of a piedmont ('hourglass') glacier at the base of a 3-km-high massif ea

22 We found that the hourglass is made of filaments aligned along the yeast b

23 yonic gene expression analysis identified an hourglass-like divergence of turtle and chicken embryoge

24 ilibration, the water-filled pore adopted an hourglass-like shape as headgroups of ceramides and phos

25 ion of experimental observations such as the hourglass magnetic dispersion and the Yamada plot of inc

26 echanistic explanation for the developmental hourglass model in the dipteran lineage.

27 According to the hourglass model, body plan conservation would depend on

28 he recently described transcriptome "inverse hourglass" model for animal embryogenesis, suggesting bo

29 provide an epigenetic underpinning for the 'hourglass' model.

30 number therefore violates the 'developmental hourglass' model.

31 The hourglass nanocrystals are formed in a three-step thermo

32 The hourglass nanocrystals are then shown to readily self-as

33 vely - a pattern resembling the evolutionary hourglass pattern observed during embryogenesis in anima

34 at interareal differences exhibit a temporal hourglass pattern, dividing the human neocortical develo

35 The hourglass patterns found in herbivory-induced defense re

36 These timelines unfold congruent hourglass patterns in rates of appearance of domain stru

37 ce heights observed and may also explain the hourglass phenomenon observed by optical microscopy.

38 Thus, although hourglass pore-forming domains are not points of subunit

39 tion spectrum of the cuprates: the X-shaped 'hourglass' response and the resonance mode in the superc

40 The septin hourglass scaffolds the asymmetric localization of many

41 While these phylo-onto correlations have an hourglass shape in Deuterostomia, Ecdysozoa, plants and

42 This suggests that the hourglass shape of aquaporins could be the result of a n

43 cifically examine whether the characteristic hourglass shape of aquaporins may arise from a geometric

44 narrow constriction at the center, like the hourglass shape of its internal surface.

45 es a natural explanation for the distinctive hourglass shape of the magnetic spectrum previously obse

46 The channel has an hourglass shape with a narrow constriction approximately

47 e remarkable for the formation of a distinct hourglass shape within the crystals that develops after

48 d ruthenium nanocrystals with a well-defined hourglass shape.

49 they undergo a transition from a non-dynamic hourglass-shaped assembly to two separate rings, at the

50 If water molecules were confined within an hourglass-shaped cavity (with a central radius of 3 A in

51 into the pore ring, the constriction of the hourglass-shaped channel.

52 tely 63 nm in diameter, which fuse by way of hourglass-shaped intermediates into wide ( approximately

53 These vesicles fuse with each other to form hourglass-shaped intermediates, which become wide (appro

54 as the pore-lining inner helix, creating an hourglass-shaped ion permeation pathway in the channel t

55 An initial hourglass-shaped lipid structure, the fusion stalk, is f

56 61alpha, consists of two halves that form an hourglass-shaped pore with a constriction in the middle

57 complex consists of two halves that form an hourglass-shaped pore with a constriction in the middle

58 esidues that would form a constriction in an hourglass-shaped pore.

59 ding sites within the 15-angstrom neck of an hourglass-shaped pore.

60 ntacting monolayers become continuous via an hourglass-shaped structure called a stalk.

61 After vesicle fusion, hourglass-shaped vesicle intermediates are stretched to

62 The balloon-expandable, stainless steel, hourglass-shaped, coronary-sinus reducing device creates

63 Hourglasses-shaped ceramic- resin bond specimens were pr

64 a solid empirical basis for theories of the hourglass spectrum built on short-range, quasi-static, s

65 across the water layer and developed into an hourglass structure consistent with a postulated membran

66 Bow-tie or hourglass structure is a common architectural feature fo

67 copy of AQP1 previously revealed the central hourglass structure surrounded by six transmembrane heli

68 whose dispersion relation is shaped like an hourglass; surface bands connect one hourglass to the ne

69 e of Neuron that the human neocortex has an "hourglass" temporal gene expression pattern with robust

70 In the late hourglass, these double filaments are connected by perio

71 During the transition from hourglass to rings the filaments rotate through 90 degre

72 We previously reported that during the hourglass to rings transition septin filaments change th

73 like an hourglass; surface bands connect one hourglass to the next in an unbreakable zigzag pattern.

74 Live-cell imaging studies indicate that the hourglass-to-double ring transition is accompanied by lo

75 g displacement can open the channel into an 'hourglass' with a ring of hydrophobic residues at its co

76 ow sand can stream through the orifice of an hourglass yet support one's weight on the beach; how it