ライフサイエンスコーパス: hourglass

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

2 ion, but not RNA editing or a 'developmental hourglass,' act in concert to shape its transcriptome du

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

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

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

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

7 diversity of architectures including rings, hourglasses, and gauzes.

8 ments at the outer zones of the transitional hourglass, as well as in the double ring.

9 hourglass during the cell cycle and controls hourglass assembly and stability, especially for the dau

10 inding and phosphorylation to control septin hourglass assembly and stability.

11 the myosin-II heavy chain Myo1 to the septin hourglass at the bud neck prior to cytokinesis, but the

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

13 er higher-order structures, such as rings or hourglasses, at the cell division site in fungal and ani

14 This study paves the way for incorporating hourglass based oscillators to be used as building block

15 d Shs1) localize to the bud neck and form an hourglass before cytokinesis that acts as a scaffold for

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

17 Spitting is controlled by an 'hourglass' circuit motif: parallel neural pathways conve

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

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

20 de SV-informative signals and uses a stacked hourglass convolutional neural network to predict the ty

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

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

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

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

25 17], specifically associates with the septin hourglass during the cell cycle and controls hourglass a

26 twork analysis framework referred to as the "hourglass effect".

27 racting domain destabilizes the transitional hourglass, especially at the mother side, with partial l

28 ies of the M(1) and R phases of VO(2) in an "hourglass" fashion through the relaxation of interstitia

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

30 the exotic properties of Kramers nodal-line/hourglass fermions.

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

32 The hourglass figures appear to result from the deposition o

33 The hourglass filaments have an additional degree of symmetr

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

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

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

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

38 netic groups adopt the unique aquaporin-like hourglass helical fold.

39 Here we tested the presence of a molecular hourglass in the brown algae, a eukaryotic lineage that

40 on to enable timely remodeling of the septin hourglass into a double ring.

41 ase, enables timely remodeling of the septin hourglass into a double ring.

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

43 The hourglass is remodeled into a double ring that sandwiche

44 in Fir1 to the peripheral side of the septin hourglass just before its transformation into the double

45 pheral nerve pathologies in NA, most notably hourglass-like constrictions.

46 lla We further discuss patterns that suggest hourglass-like developmental divergence early and late i

47 ge antisymmetric spin-orbit couplings and by hourglass-like dispersions.

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

49 rectional electron jets can be formed by the hourglass-like magnetic configuration of the structure.

50 idopsis seed life cycle, revealing a reverse hourglass-like phylotranscriptome pattern.

51 Arabidopsis thaliana are known to follow an hourglass-like phylotranscriptomic pattern (with higher

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

53 of transcriptional conservation to identify hourglass-like stages during inflorescence development.

54 florescences are most different during their hourglass-like stages of development, following an inver

55 are reports that they might exhibit a basic, hourglass-like timekeeping mechanism(7-9).

56 ve twisting and swelling with the so-called "hourglass-like" constriction sign.

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

58 nd damping offered by the various classes of hourglass metastructures.

59 This hourglass-mimicking biosensor could separate ~95% target

60 An hourglass-mimicking biosensor was developed to detect ta

61 The hourglass model can be used to inform operational tools,

62 Here, we propose an hourglass model compatible with all existing data, provi

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

64 The hourglass model is a popular evo-devo model depicting th

65 stages of development, following an inverse-hourglass model of development.

66 The hourglass model of embryonic evolution depicts how devel

67 at the onset of gastrulation, supporting the hourglass model of phylotypic stage conservation.

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

69 eflected the upper half of the developmental hourglass model.

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

71 number therefore violates the 'developmental hourglass' model.

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

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

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

75 the phononic systems, we have predicted the hourglass nodal net TPs in TeO(3), as well as the clean

76 The hourglass organization of the connectome suggests that C

77 idence for the generality of a developmental hourglass pattern across complex multicellular eukaryote

78 oss Physcomitrium patens identify an inverse hourglass pattern across plant phyla, as in animals.

79 morphological complexities, we uncovered an hourglass pattern during embryogenesis in morphologicall

80 e for ancient/conserved genes manifesting an hourglass pattern during mid-embryogenesis.

81 However, whether the hourglass pattern is an intrinsic feature of all complex

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

83 Transcriptomic analyzes reveal an hourglass pattern of gene expression during plant and an

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

85 g different animal phyla describe an inverse hourglass pattern, where expression is correlated during

86 al structural features of the ONH) formed an hourglass pattern, with most of them located within the

87 The hourglass patterns found in herbivory-induced defense re

88 ally found in animal embryos(5-8), molecular hourglass patterns have recently been proposed for land

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

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

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

92 A dual hourglass recruitment pattern transferred scale-free pro

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

94 The septin hourglass scaffolds the asymmetric localization of many

95 l regions between constrictions to a smooth, hourglass shape as the nucleus passed through the center

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

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

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

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

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

101 These studies reveal an hourglass shape of the podosome actin core, a protruding

102 of the surface, while stability requires an hourglass shape with a "waist" and whose curvature excee

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

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

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

106 We propose a novel hourglass shaped lattice metastructure that takes advant

107 Six new classes of hourglass shaped lattice metastructures have been develo

108 to the available lumens, forming transient "hourglass"-shaped steric locks onto the surrounding coll

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

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

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

112 neous nucleation, involving the formation of hourglass-shaped crystalline nuclei that conceive at eit

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

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

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

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

117 This channel forms a hydrophilic, hourglass-shaped membrane channel, with a lateral gate t

118 tal-enriched gas at 10,000 kelvin through an hourglass-shaped nebula that resembles an evacuated and

119 61alpha, consists of two halves that form an hourglass-shaped pore with a constriction in the middle

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

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

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

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

124 ated conical filament to a lower-resistance, hourglass-shaped structure is driven by the synergistic

125 Hourglass-shaped translocation conduits for two cargo co

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

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

128 Hourglasses-shaped ceramic- resin bond specimens were pr

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

130 We introduce the hourglass stigma model, a theory-informed conceptualisat

131 Septins form an hourglass structure at the bud neck of yeast cells that

132 septins are assembled into a highly ordered hourglass structure at the division site [13] is largely

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

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

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

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

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

138 king zonal architecture for the transitional hourglass that pre-patterns two cytokinetic structures-a

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

140 How septin architecture is remodeled from an hourglass to a double ring during cytokinesis in fungal

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

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

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

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

145 Here, we show that during the hourglass-to-double-ring transition in budding yeast, se

146 at the network stochasticity follows an anti-hourglass trajectory, and such a pattern supports Raff's

147 the architecture and stability of the septin hourglass until it dissociates from the bud neck at the

148 The core neurons at the hourglass waist represent the information bottleneck of

149 is feedforward flow traverses a small core ("hourglass waist") that consists of 10-15 interneurons.

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

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