ライフサイエンスコーパス: microarchitecture

1 has been exceedingly useful in imaging cell microarchitecture.

2 s a key inhibitory signal governing skeletal microarchitecture.

3 TEM showed normal microarchitecture.

4 le thymus with preservation of normal thymic microarchitecture.

5 gans and for the maintenance of their proper microarchitecture.

6 not sufficient to establish normal cellular microarchitecture.

7 cient (LTalpha-/-) mice show altered splenic microarchitecture.

8 reveal an emerging LCIC modular-extramodular microarchitecture.

9 gration in a porous environment with a given microarchitecture.

10 hysiologically relevant cell combination and microarchitecture.

11 eflecting subtle local differences in tissue microarchitecture.

12 ere deficits in cortical and trabecular bone microarchitecture.

13 ral density and trabecular and cortical bone microarchitecture.

14 ere accompanied by restoration of their bone microarchitecture.

15 re associated with decrements in the left PC microarchitecture.

16 of femur bone mineral density and trabecular microarchitecture.

17 A, generally preserving ECM's components and microarchitecture.

18 aging to obtain information about the tissue microarchitecture.

19 e trabeculae, suggesting disruption of their microarchitecture.

20 g the generation of secondary lymphoid organ microarchitectures.

21 how coacervates evolve into intricate solid microarchitectures.

22 onstrate its utility for creating complex 3D microarchitectures.

23 ale filaments into complex three-dimensional microarchitectures.

24 The battery microarchitecture affords trade-offs between power and e

25 ne, we compiled a reference for myofibrillar microarchitecture among myocardial subtypes in vivo and

26 abecular bone score, which helps assess bone microarchitecture and adds value to standard bone densit

27 ls in relation to blood flow dynamics, organ microarchitecture and cellular phenotype.

28 s to generate tissue constructs with tunable microarchitecture and complexity.

29 e abilities, explained by defective cortical microarchitecture and excitation/inhibition imbalance.

30 8, and 56 days of treatment, to measure bone microarchitecture and extract RNA for microarray analyse

31 tal N-cadherin is required for normal marrow microarchitecture and for hematopoiesis.

32 4-dimensional methodologies for elucidating microarchitecture and function of the reconstructed micr

33 gnment resulted in severe disruption of cell microarchitecture and greater EMT.

34 T) tissue characterized by marked defects in microarchitecture and HEV.

35 e of the byssal cuticle were explored in its microarchitecture and in the cuticular protein, mcfp-1.

36 ilencing in HEp3-hi/diss cells modulated the microarchitecture and integrity of the angiogenic vascul

37 rcuits, but the functional structure of this microarchitecture and its relation to behaviour are poor

38 Poor bone microarchitecture and low bone strength are likely to co

39 pamycin (mTOR), thus maintaining proper bone microarchitecture and mass.

40 oxidative stress, leading to changes in bone microarchitecture and material properties and thus bone

41 techniques that directly measure trabecular microarchitecture and mechanical properties of bone at a

42 Microarchitecture and mechanical properties of young, tr

43 oping both high-resolution imaging of the LC microarchitecture and next-generation, deep-scanning OCT

44 Cartilage degeneration, subchondral bone microarchitecture and the expression of adrenoreceptors,

45 to suggest that the effects of aging on the microarchitecture and the function of the splenic margin

46 spite persistent decrease in BMD, trabecular microarchitecture and tissue quality remain normal in lo

47 was sufficiently high to visualize scaffold microarchitecture and to detect major anatomical feature

48 challenges associated with finding the right microarchitectures and ECM compositions for optimal tiss

49 position rate (MAR), improved the trabecular microarchitecture, and decreased bone turn over markers

50 s, Peyer's patches, and an organized splenic microarchitecture, and have a profound defect in T cell-

51 GC treatment reduced trabecular bone mass, microarchitecture, and the degree of bone mineralization

52 However, these three-dimensional microarchitectures are significantly limited by their sc

53 but for the maintenance of aspects of their microarchitecture as well.

54 of articular cartilage and subchondral bone microarchitecture associated with OA.

55 Estradiol deficiency disrupted cortical microarchitecture at peripheral sites.

56 MD and geometry at the radius and tibia, and microarchitecture at the tibia.

57 year study to evaluate changes in bone mass, microarchitecture, biomechanical competence, and remodel

58 Each domain is characterized by a microarchitecture built of a definite mineral assemblage

59 easured volumetric BMD (vBMD), geometry, and microarchitecture by high-resolution peripheral quantita

60 etition in the context of the water column's microarchitecture calls for new ecological frameworks, s

61 l-resolution 3-T MR images of proximal femur microarchitecture can allow detection of lower elastic m

62 Our key insight is that the battery microarchitecture can concurrently optimize ion and elec

63 s involved in the regulation of the synovial microarchitecture, cell populations contributing to the

64 t MGUS patients have altered trabecular bone microarchitecture compared with controls.

65 composed of multiple materials within porous microarchitectures designed for specific shape change st

66 e accompanied with restoration of their bone microarchitecture, determined by microcomputed tomograph

67 Our results demonstrate that these microarchitectures form due to self-organization of the

68 odel that explains how the bundle's specific microarchitecture gives rise to its exquisite mechanosen

69 studied because its biologically controlled microarchitecture gives rise to remarkable strength and

70 ssessing several advantages such as tailored microarchitecture, high-throughput capability, coculture

71 of articular cartilage and subchondral bone microarchitecture in a mouse model of human OA.

72 mance of OCME as a means to visualize tissue microarchitecture in benign and malignant human breast t

73 out functions essential for a proper splenic microarchitecture in both hemopoietic and non-hemopoieti

74 port in osteoblasts normalizes bone mass and microarchitecture in murine CF.

75 n summary, the effect of spaceflight on bone microarchitecture in ovariectomized rats was bone-and bo

76 alcin levels and improved long bone mass and microarchitecture in SAMP-6 senescent osteopenic mice.

77 which could be used to improve bone mass and microarchitecture in the aging skeleton.

78 ce a day for 28 days) improved bone mass and microarchitecture in the lumbar spine and femur in F508d

79 G could have been due to the altered splenic microarchitecture in these mice.

80 14-day spaceflight on bone mass, density and microarchitecture in weight bearing (femur and humerus)

81 of 3 functionally distinct types of lymphoid microarchitectures in the inflamed synovium: ectopic GCs

82 bute to the emergence of functional columnar microarchitectures in the mature neocortex.

83 which promoted bone formation, improved bone microarchitecture, increased bone mass and enhanced mech

84 a polyphenols in achieving better bone mass, microarchitecture integrity, and bone strength, which ar

85 Disruption of tissue microarchitecture is an early step in pancreatic tumorig

86 of specific B cell subsets within the immune microarchitecture is essential to ensure successful cogn

87 icantly less trabecular bone, the trabecular microarchitecture is more fragmented, and the diaphyseal

88 ering scaffolds with native-like biology and microarchitectures is a prerequisite for stem cell media

89 ion of hierarchy in conch shell's multiscale microarchitectures is explicated.

90 When studying apatite mineral microarchitecture, mineral distributions or mineralizati

91 The microarchitecture of a hair cell synapse may be such tha

92 oton calcium imaging to study the functional microarchitecture of both neurons in the mouse dorsal IC

93 ic computational principle in organizing the microarchitecture of cell assemblies that would readily

94 The microarchitecture of different components of the extrace

95 Altered microarchitecture of secondary lymphoid organs in mutant

96 es with p52 homodimers, share defects in the microarchitecture of secondary lymphoid organs.

97 sh the epithelial barrier and regenerate the microarchitecture of the lung.

98 Alterations in the microarchitecture of the posterior cingulum (PC), a whit

99 faces and are associated with changes in the microarchitecture of the root surface consistent with de

100 sociated with the so-called crossed lamellar microarchitecture of the shell, which provides for 'chan

101 redundant, in particular, in supporting the microarchitecture of the spleen and in host defense.

102 Microarchitectures of R, such as dimer racks, would effe

103 the evolution of next-generation bio-derived microarchitectures, probes for cellular/biochemical proc

104 hat receptor-effector specificity requires a microarchitecture provided by the SNARE complex during v

105 and immunized immediately with SRBC, splenic microarchitecture remained disturbed and there was no Ig

106 that where composed of native-like cellular microarchitectures resembling vascularized and bone marr

107 e defect in lymph node formation and splenic microarchitecture seen in LT-deficient mice is recapitul

108 ecause it is associated with changes in bone microarchitecture, strength, and clinical fractures.

109 Many brain regions contain subnuclear microarchitectures, such as the matrix-striosome organiz

110 igher bone mass and strength and better bone microarchitecture than in vehicle-treated mice.

111 e mass and improves the disturbances in bone microarchitecture that characterize established and adva

112 le for both formation and maintenance of SLO microarchitecture; their expression of lymphotoxin alpha

113 generate 3D collagen gels of varying matrix microarchitectures to characterize their regulation of 3

114 shape transformations to complex multipodal microarchitectures under continuous blue light.

115 Bone microarchitecture was assessed in 100 men.

116 Furthermore, the splenic marginal zone microarchitecture was substantially disturbed, adversely

117 The general-purpose microarchitecture we demonstrate supports workflows with

118 understand the behavior of the 3D composite microarchitectures, we carry out high fidelity computati

119 Images of proximal femur microarchitecture were obtained by using a high-spatial-

120 t-effective approach to fabricate an arrayed microarchitecture with an ultra-high aspect ratio using

121 ent, disarranging extracellular matrix (ECM) microarchitecture, with downregulation of secreted prote

122 smooth macroscale to the heterogeneous local microarchitecture, with emphasis on maps of the visual a

123 rmation analyses revealed distinct chromatin microarchitectures, with a more compact structure charac

124 Designing cellular materials with a specific microarchitecture would allow one to exploit the structu

125 ld tissue engineering, the evolution of bone microarchitecture, wound healing, and tumor growth.