ライフサイエンスコーパス: microarchitecture

1 ays a decisive role in bone mass accrual and microarchitecture.

2 of femur bone mineral density and trabecular microarchitecture.

3 aging to obtain information about the tissue microarchitecture.

4 e trabeculae, suggesting disruption of their microarchitecture.

5 has been exceedingly useful in imaging cell microarchitecture.

6 s a key inhibitory signal governing skeletal microarchitecture.

7 cer by palpation), and (iv) altered physical microarchitecture.

8 TEM showed normal microarchitecture.

9 le thymus with preservation of normal thymic microarchitecture.

10 gans and for the maintenance of their proper microarchitecture.

11 reduced cortical porosity and improved bone microarchitecture.

12 not sufficient to establish normal cellular microarchitecture.

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

14 protein aggregates or disruption of the lens microarchitecture.

15 bone mineral density and impaired trabecular microarchitecture.

16 ne mineral density and deterioration of bone microarchitecture.

17 severity and deficits in periarticular bone microarchitecture.

18 KI) mice exhibit no significant loss of bone microarchitecture.

19 he preservation of femoral and alveolar bone microarchitecture.

20 oisson's ratios via the deformation of their microarchitecture.

21 perfusion significantly disrupted glomerular microarchitecture.

22 lactational SSRI exposure on C57BL6 pup bone microarchitecture.

23 fferences in the composition of white matter microarchitecture.

24 ghly continuous and homogeneous pore network microarchitecture.

25 den and hierarchical implants with bone-like microarchitecture.

26 rough exploration of exhaustively labeled 3D microarchitecture.

27 ochemistry to examine the juxtaparanode LGI3 microarchitecture.

28 last markers, and trabecular bone volume and microarchitecture.

29 ity ratios consistent with a blocky gradient microarchitecture.

30 is hard to reasonably characterize cortical microarchitecture.

31 ribrosa defects (FLCDs), and lamina cribrosa microarchitecture.

32 ere accompanied by restoration of their bone microarchitecture.

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

34 reveal an emerging LCIC modular-extramodular microarchitecture.

35 gration in a porous environment with a given microarchitecture.

36 hysiologically relevant cell combination and microarchitecture.

37 eflecting subtle local differences in tissue microarchitecture.

38 ere deficits in cortical and trabecular bone microarchitecture.

39 ral density and trabecular and cortical bone microarchitecture.

40 re associated with decrements in the left PC microarchitecture.

41 onstrate its utility for creating complex 3D microarchitectures.

42 ale filaments into complex three-dimensional microarchitectures.

43 g the generation of secondary lymphoid organ microarchitectures.

44 how coacervates evolve into intricate solid microarchitectures.

45 g several of the sleep macroarchitecture and microarchitecture abnormalities.

46 res to LSD significantly altered gray matter microarchitecture across much of the brain.

47 an adults to investigate how sleep depth and microarchitecture affect auditory encoding.

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

49 significant regional differences in the lung microarchitecture among all DAD-causing entities.

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

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

52 complex interactions between the lymph node microarchitecture and antitumor immune surveillance, def

53 anical testing revealed that trabecular bone microarchitecture and bone mechanical properties were im

54 ial in less than 4 h, while preserving plant microarchitecture and branching vascular network.

55 ls induced severe bone deterioration at both microarchitecture and cellular levels.

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

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

58 ation, underscoring the critical role of ECM microarchitecture and dynamics in megakaryocyte function

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

60 8, and 56 days of treatment, to measure bone microarchitecture and extract RNA for microarray analyse

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

62 4-dimensional methodologies for elucidating microarchitecture and function of the reconstructed micr

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

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

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

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

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

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

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

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

71 microenvironment by taking advantage of the microarchitecture and mechanical forces to efficiently i

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

73 Microarchitecture and mechanical properties of young, tr

74 Tissue microarchitecture and mechanics are important in develop

75 The phenomenon is microarchitecture and microrotation field independent.

76 the brain would suggest altered gray matter microarchitecture and neuroplasticity.

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

78 d three-dimensional model of atrial anatomy, microarchitecture and patchy fibrosis.

79 omote rapid reconstitution of normal hepatic microarchitecture and reparation of the gut-liver barrie

80 inal morphogenesis establishes 3D epithelial microarchitecture and spatially organized crypt-villus c

81 lls (OCPs) and its contribution to long bone microarchitecture and strength are unclear.

82 ployed cryo-based methods that preserved the microarchitecture and the cellular/molecular integrity o

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

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

85 A more precise definition of the microarchitecture and three-dimensional structure of the

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

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

88 mutations on bone biology, we compared bone microarchitecture and turnover in an ageing series of wi

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

90 we present a hybrid adhesive that integrates microarchitectures and macroscopic nonlinear cut archite

91 y was to compare the bone augmentation, bone microarchitecture, and biodegradation rate of additional

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

93 Volumetric bone mineral density (BMD), microarchitecture, and estimated bone strength of the di

94 diol suppression therapy preserves BMD, bone microarchitecture, and estimated strength, and is likely

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

96 ations in bone quality including remodeling, microarchitecture, and mineralization.

97 was associated with higher BMD, better bone microarchitecture, and no different BMSi but poorer phys

98 d by changes in cortical thickness, cortical microarchitecture, and resting-state low-frequency oscil

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

100 laboratory parameters, bone mineral density, microarchitecture, and vertebral fractures were assessed

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

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

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

104 Estradiol deficiency disrupted cortical microarchitecture at peripheral sites.

105 imaging was feasible for visualizing tissue microarchitecture at the surface of resected tissues and

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

107 ry of bone strength, density, and trabecular microarchitecture at the weight-bearing tibia, commensur

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

109 nistration (5 mg/kg) improved the trabecular microarchitecture, bone mineral density, and strength, a

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

111 es the regeneration of functional intestinal microarchitecture by controlling basolateral fluid flow

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

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

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

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

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

117 The relationship between LNneg size, LNneg microarchitecture, clinicopathological variables, and OS

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

119 indings also suggest the possibility that WM microarchitecture could serve as a novel treatment targe

120 materials and 3D printed piezoceramics with microarchitectures create opportunities for miniaturized

121 otential tumor-host interactions, and tissue microarchitecture, derived from morphologically resolved

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

123 omposite hydrogels with precisely engineered microarchitectures designed to optimize the acidic micro

124 Bone microarchitecture deteriorated, mainly in the trabecular

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

126 embrane fluidity and maintenance of membrane microarchitecture, directly impacting on GPCR stability,

127 ental lines), as well as of the cranial bone microarchitecture (e.g., diploic channels), our synchrot

128 iofabrication techniques to build complex 3D microarchitectures essential for guiding cell growth and

129 We analysed sleep macroarchitecture and microarchitecture features and measured sleep homoeostas

130 The impact of tau pathology on sleep microarchitecture features, including slow oscillations,

131 osteoporosis, with many studies focusing on microarchitecture for fracture prediction.

132 century to provide measures of BMD and bone microarchitecture for the purposes of clinical practice

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

134 ent investigated (i.e., cortical morphology, microarchitecture, function).

135 Recognizing the crucial importance of the microarchitecture-function relationship is pivotal for u

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

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

138 This specific microarchitecture guides megakaryocyte maturation and in

139 er, it remains unknown which effect collagen microarchitecture has on myofibroblast differentiation.

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

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

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

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

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

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

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

147 We examined bone strength, density, and microarchitecture in seventeen astronauts (14 males; mea

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

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

150 sleep, but whether and how they affect sleep microarchitecture in the setting of tauopathy is unknown

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

152 14-day spaceflight on bone mass, density and microarchitecture in weight bearing (femur and humerus)

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

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

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

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

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

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

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

160 l modeling further suggest that the beetle's microarchitecture is optimized toward maximizing the fir

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

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

163 The hippocampus has a specialized microarchitecture, is situated at the nexus of multiple

164 lous bone, a naturally occurring lightweight microarchitectured material, resistance to fatigue failu

165 Microarchitectured materials achieve superior mechanical

166 Although ultralightweight microarchitectured materials can have high stiffness and

167 atigue life, with consequences to the use of microarchitectured materials in durable devices and to h

168 echanical performance of cancellous bone and microarchitectured materials is enhanced by aligning str

169 When studying apatite mineral microarchitecture, mineral distributions or mineralizati

170 educed bone mineral density (BMD), poor bone microarchitecture/mineralization, and/or diminished bone

171 ntifying volumetric bone mineral density and microarchitecture necessary for early diagnosis of bone

172 omic phenotypes including body weight, tibia microarchitecture, neurodevelopment, adult cognition, an

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

174 This microarchitecture of bone offers a unique geometry where

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

176 ore pronounced in females than in males, the microarchitecture of both the interparietal bone and bod

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

178 Altered microarchitecture of collagen type I is a hallmark of wo

179 ely, we reveal a notably distinct functional microarchitecture of critical metabolism-regulatory neur

180 The microarchitecture of different components of the extrace

181 analyses of decellularised matrices revealed microarchitecture of differing fibre density and express

182 aches to investigate the hypothesis that the microarchitecture of fibrillar collagen networks mechani

183 Ultrastructural alterations in the stromal microarchitecture of grafted corneas provide evidence of

184 Our study reveals the molecular microarchitecture of human carotid artery plaques, using

185 e flexibility and toughness derived from the microarchitecture of its exoskeleton.

186 ible to non-destructively resolve/verify the microarchitecture of pterosaur bone not previously seen

187 Altered microarchitecture of secondary lymphoid organs in mutant

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

189 Observations of the humeral microarchitecture of stem-tetrapods, batrachians, and am

190 composition, cell-cell contact partners and microarchitecture of such iHALT structures in mice were

191 owth of apatite nanocrystals, recreating the microarchitecture of the different anatomical regions of

192 ugh age-related changes were observed in the microarchitecture of the femur, tibia, vertebra, and bas

193 In addition, there may be remodeling of the microarchitecture of the lamina, resulting in more varia

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

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

196 uccal and palatal surfaces and preserved the microarchitecture of the remaining bone, decreased TNF-a

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

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

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

200 tic visual stimulus space and map functional microarchitecture of thousands of neurons with single-ce

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

202 of artificial IDPs as well as the available microarchitectures of this class of biocompatible IDPs,

203 BP-POZ in vitro maintained collagen microarchitecture per two-photon microscopy despite AGE

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

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

206 ur findings suggest that changes of collagen microarchitecture regulate myofibroblast differentiation

207 ory activity, control sleep architecture and microarchitecture, regulate responsiveness to sensory st

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

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

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

211 naive mice is sufficient to change the sleep microarchitecture similar to stress.

212 ilities for producing periodic and aperiodic microarchitectures spanning four orders of magnitude fro

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

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

215 teoclast cells, which promotes a strong bone microarchitecture, suggesting that complement pathways m

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

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

218 rd-shelled prey specialists, possess unusual microarchitecture that controls tooth erosion in a way t

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

220 of tauopathy on sleep macroarchitecture and microarchitecture throughout aging remains unknown.

221 dently related to decrements in white matter microarchitecture throughout the brain.

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

223 The formation of intricate microarchitectures typically requires sophisticated fabr

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

225 Bone microarchitecture was assessed in 100 men.

226 mental patterning of cortical morphology and microarchitecture was explained by age, sex, and puberta

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

228 The general-purpose microarchitecture we demonstrate supports workflows with

229 I ratio as a noninvasive measure of cortical microarchitecture, we systematically compared depth-depe

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

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

232 yeloid compartment results in a reduced bone microarchitecture, whereas gain-of-function TTP knock-in

233 n at the macroscale by combining shell-based microarchitecture with an additively manufactured medium

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

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

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

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

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

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