ライフサイエンスコーパス: morphometric

1 emporomandibular disorders, and craniofacial morphometrics.

2 ade synapsids and therapsids using geometric morphometrics.

3 onomy of S. saudiensis was re-examined using morphometrics.

4 e lower pharyngeal jaw (LPJ) using geometric morphometrics.

5 e extent and regional distribution of shared morphometric abnormalities between disorders remains unk

6 or each disorder to locate disorder-specific morphometric abnormalities.

7 dus preserves a foot that purportedly shares morphometric affinities with monkeys, but this interpret

8 itat-related variation in adult and immature morphometrics among diademed sifakas (Propithecus diadem

9 In this study, a series of morphometric analyses and biochemical assays, combined w

10 oxel-based pulsed arterial spin labeling and morphometric analyses and tested for association with CI

11 The use of geometric morphometric analyses corroborate the erection of the ne

12 ence for competitive exclusion; however, the morphometric analyses documented displacement in size of

13 nsional immunohistochemistry, histology, and morphometric analyses during aortic valve morphogenesis

14 Morphometric analyses further suggest that its dorsal an

15 rovide a standardized protocol for geometric morphometric analyses of 2D landmark data sets using a c

16 Morphometric analyses of choriocapillaris density (cross

17 Morphometric analyses of crania from these specimens rev

18 njury assessments often rely on conventional morphometric analyses of heart form and function.

19 Morphometric analyses of individual bony elements and th

20 Morphometric analyses of intravital video microscopy dat

21 er supported by functional morphological and morphometric analyses of its postcranium.

22 This kinematic pattern is mirrored in the morphometric analyses of metatarsal head shape.

23 Comparative morphometric analyses of the KNM-LH 1 cranium document t

24 Morphometric analyses of the outline of the first upper

25 Here, we address this deficiency with morphometric analyses of the postcrania of the two most

26 ormed magnetic resonance imaging (MRI)-based morphometric analyses of the postnatal human pons (0-18

27 Description and landmark-free morphometric analyses of the StW 573 atlas, along with o

28 Through in toto morphometric analyses of wild type and round egg mutants

29 he avian craniofacial skeleton, we conducted morphometric analyses on raptors, a polyphyletic group a

30 Immunohistochemistry and histological and morphometric analyses revealed a twofold increase in pro

31 Morphometric analyses revealed increased CD31(+) and Ki6

32 Morphometric analyses revealed that Treg depletion block

33 ecies have been named, our palaeogenomic and morphometric analyses support the idea that there was on

34 mission computerized tomography, and perform morphometric analyses to assess grey matter loss.

35 , we use multiscale population-growth and 3D-morphometric analyses to assess the spatiotemporal devel

36 We used quantitative morphometric analyses to evaluate both biopsy specimens.

37 We integrate class-wide geometric-morphometric analyses with evolutionary sequence analyse

38 We examined leaf shape using a variety of morphometric analyses, and complement this with a transc

39 Morphometric analyses, based on a quantification of the

40 Using statistical models and morphometric analyses, we demonstrate that the extinctio

41 Using three-dimensional kinematic and morphometric analyses, we show that humans push off with

42 nd essential dispersal niches defined by our morphometric analyses.

43 rscore the importance of size and scaling in morphometric analyses.

44 ogues using linear regressions and geometric morphometric analyses.

45 using mu-CT biomedical imaging and geometric morphometric analyses.

46 Histological sections were used for the morphometric analysis (number neutrophils and mononuclea

47 Histologic sections were used for the morphometric analysis (number of neutrophils and mononuc

48 Morphometric analysis also revealed endocrine cell alloc

49 ongitudinal magnetic resonance imaging-based morphometric analysis and survival.

50 Osseous morphometric analysis and tooth movement distance were e

51 The CAV development was evaluated with morphometric analysis at postoperation day 100.

52 3D geometric morphometric analysis correctly classifies 99.5% of the

53 Morphometric analysis demonstrated that the addition of

54 While highly variable, our results of morphometric analysis demonstrates that all Ch. stipae s

55 In study 2, Geometric Morphometric analysis did not reveal significant differe

56 ase using the Perth-Rotterdam Annotated Grid Morphometric Analysis for Cystic Fibrosis quantitative o

57 pled with the Perth-Rotterdam Annotated Grid Morphometric Analysis for Cystic Fibrosis scoring system

58 Subdivision-wise morphometric analysis found a significantly smaller medi

59 Finally, via a comparative morphometric analysis in lamprey, dogfish, zebrafish and

60 By applying a multi-scalar morphometric analysis in zebrafish embryos, we show that

61 Additional morphometric analysis indicated that DTI-derived normali

62 Here, we continue a morphometric analysis of >5,500 leaves representing 270

63 dy and mandible specimens were subjected for morphometric analysis of bone level.

64 Morphometric analysis of bone loss was performed.

65 MVD was scored by digital morphometric analysis of CD31-stained whole tumour secti

66 of this surprising observation, we combined morphometric analysis of cells and their subcellular com

67 provided descriptive information, a thorough morphometric analysis of end-stage CF lung disease is la

68 A morphometric analysis of glomeruli obtained during nephr

69 In addition, morphometric analysis of leaves showed that polyploidy a

70 In parallel we performed a morphometric analysis of mossy fiber synapses following

71 ceous unit, we carried out three-dimensional morphometric analysis of paired PP and nonlesional psori

72 A three-dimensional morphometric analysis of presynaptic glutamatergic bouto

73 Morphometric analysis of renal parenchyma can predict no

74 ective on this debate through a 3D geometric morphometric analysis of shape covariation between the t

75 We present a squamate-wide, high-density morphometric analysis of the skull across 181 modern and

76 Morphometric analysis of the whole-heart sections demons

77 I postprocessing technique, implemented in a morphometric analysis program (MAP), to facilitate detec

78 Morphometric analysis revealed greater bone loss in DM+P

79 Morphometric analysis revealed that neurons with a highe

80 Morphometric analysis was performed by measuring epithel

81 ng was evaluated by serial echocardiography, morphometric analysis, and histology.

82 Using a combination of morphometric analysis, neuroanatomical tract-tracing, an

83 orrelation of findings with current standard morphometric analysis.

84 rison subjects by subdivision-wise classical morphometric analysis.

85 captured by a deformation-based 3D geometric morphometric analysis.

86 tellite markers accompanied by the geometric morphometrics analysis of wing venation, we have reveale

87 Here we gathered morphometric and biomechanical data on the presacral ver

88 ging tool for identifying and characterizing morphometric and connectivity brain changes occurring wi

89 effects of PTH(1-34) and loading on the bone morphometric and densitometric properties in ovariectomi

90 However, morphometric and echocardiographic analysis revealed mas

91 psychosis spectrum symptoms and review brain morphometric and functional alterations as well as genet

92 psies were collected and processed for histo-morphometric and immunohistochemical evaluation to deter

93 Interactions with physical morphometric and lithological factors were generally of

94 Both morphometric and metagenomic analyses have raised questi

95 ecimens from the mandible were processed for morphometric and microcomputed tomography examination of

96 By genetic manipulation in vivo and by using morphometric and molecular analyses, such as immunofluor

97 We present findings from morphometric and neurocognitive analyses of 1381 subject

98 evolution of this anatomical region using 3D morphometric and phylogenetically-informed evolutionary

99 ts from the mucosal biopsies and analyzed by morphometric and polymerase chain reaction analyses.

100 The present study analyzes morphometric and stereological estimators in the whole A

101 aller than both the La and Ba nuclei in both morphometric and stereological estimators.

102 By analysing morphometric and stress results in the context of the co

103 This integrative analysis of morphometric and transcriptomic data predicted YY1 as on

104 However, morphometric and ultrastructural analyses show an altere

105 and lung tissue were collected at birth for morphometric and Western blot measurements of HIF-1a, HI

106 poise reproductive tracts using 2D geometric morphometrics and 3D models of the vaginal lumen and inf

107 Geometric morphometrics and analyses of traditional measurements y

108 ic had a significant negative effect on bird morphometrics and blood calcium levels and a positive re

109 of living and fossil deer using 3D geometric morphometrics and cladistics.

110 Airway morphometrics and inflammation were similar in viral and

111 Here we combine geometric morphometrics and maximum-likelihood analysis to show th

112 Morphometrics and modeling analyses of the jaws of Mesoz

113 Here we use geometric morphometrics and phenotypic matrix statistics to compar

114 ology, geochemistry, archeobotany, geometric morphometrics and photogrammetry, here we present eviden

115 Here, using geometric morphometrics and phylogenetic comparative methods in a

116 by urinary androgen profiles, birth weights, morphometrics, and behaviour.

117 cell-selective markers, confocal microscopy, morphometrics, and electrophysiology were used to examin

118 Using a high-dimensional geometric morphometric approach, we quantified the shape of the sk

119 eir chewing kinematics; we also used various morphometric approaches based on microtomography to exam

120 MA patients and controls, using quantitative morphometric approaches on immunohistochemically labeled

121 t form at the macromorphological scale using morphometric approaches quantifies what is commonly refe

122 In this review, we explore morphometric approaches used to perform whole-plant phen

123 Morphometric assessments, expression analysis, blood pre

124 a method to detect subtle changes in nuclear morphometrics at single-cell resolution by combining flu

125 Morphometric atlases enable precise quantification of sh

126 mbined approach, involving ecophysiological, morphometric, biochemical, and molecular analyses, has b

127 In morphometric brain analysis, we serendipitously found a

128 Here, we demonstrate how geometric morphometrics can be applied in order to overcome these

129 We show TB morphometrics can be determined within lesion pathology,

130 ation accuracy and further enables automated morphometric cell classifications in multi-population bi

131 in and eosin (H&E) and subjected to detailed morphometric cellular analysis, using a commercial digit

132 pathogenesis of MCI in connection with brain morphometric change.

133 This study investigated subcortical morphometric changes 6 months after switching treatment

134 rize the metabolomic, pathophysiological and morphometric changes associated with AVNFH providing ins

135 ecade, several studies have identified brain morphometric changes in ET, but these changes remain poo

136 at shape asymmetries, potentially induced by morphometric changes in subnuclei, rather than size asym

137 Shape analysis revealed pronounced morphometric changes in the anterior hippocampus and bas

138 skeletal dimensions combined with localized morphometric changes may underlie the facial phenotype s

139 Morphometric changes were absent across time in controls

140 e correlated with clinical, biochemical, and morphometric characteristics.Broad ranges of cellular ch

141 These results suggest that morphometric characterization can serve as a simple read

142 The authors performed morphometric comparison of the microstructurally informe

143 Nerve diameter was measured as a morphometric criterion.

144 vian skull using high-dimensional 3D surface morphometric data across a broad phylogenetic sample enc

145 Cell densities were correlated with morphometric data for the same animals, and the spatial

146 evolution of the salamander using geometric morphometric data from 148 species spanning the order's

147 We collected morphometric data from sifakas at Tsinjoarivo, Madagasca

148 Here we combine morphometric data from the fossil record of the ubiquito

149 Obtaining morphometric data on free-ranging marine megafauna is di

150 he digital micrographs, along with other non-morphometric data to predict pregnancy.

151 Brain morphometric data were employed to create multivariate p

152 in reflex distances 1 and 2 and other facial morphometric data.

153 e modern phylogenetic tools and 3D geometric morphometric datasets to examine adaptive zone shifts in

154 3D morphometrics derived from these specimens and a sample

155 Thus, morphometric differences between compartmentalized ORNs

156 Our results highlight a strong morphometric distinction between Mesolithic hunter-gathe

157 gical disease modeling, however canine brain morphometric diversity creates computational and statist

158 henotype, we performed unbiased quantitative morphometric electron microscopic studies of biopsied ki

159 Morphometric evaluation of ABL was conducted and express

160 Morphometric evaluation of lung changes and lung elastin

161 Morphometric evaluation of small airways revealed increa

162 Lastly, through application of 3D morphometric facial surface analysis, our results suppor

163 a unique or overlapping difference for each morphometric feature.

164 machine learning to test whether cerebellar morphometric features could robustly predict general cog

165 ifferent classifiers that is feed with novel morphometric features extracted from the digital microgr

166 Morphometric features of brain ageing in dogs, like huma

167 ex processes can be uniquely captured in the morphometric features of stained tissue specimens.

168 y was to correlate clinical, histologic, and morphometric features of the liver in children with extr

169 Correlation of histologic and morphometric features of the liver with outcome has not

170 es related to suicidal risk, including brain morphometric features, leading to an elaborate suicide r

171 we combined three dimensional (3D) geometric morphometrics, finite element modelling and phylogenetic

172 f traditional surface markers on independent morphometric frameworks permits more sensitive and autom

173 providing detailed individual life-history, morphometric, genetic, reproductive and disease data.

174 Digital anatomy and computed morphometrics have provided major advances in this field

175 Morphometric, histologic, and molecular analyses demonst

176 Visual and morphometric histological analyses at basal, midventricu

177 3D morphometrics hold great promise for GSSCP classificatio

178 We here evaluated morphometric, immunohistochemical and messenger RNA (mRN

179 utomated neuroimaging methods for cerebellar morphometrics in 417 individuals to (1) localize normati

180 six segmental bronchi were evaluated for CT morphometric indices of bronchial wall thickness (BWT) a

181 ed by correlative analysis with the computed morphometric indices.

182 etry (DTBM), a novel technique that extracts morphometric information from diffusion data, to investi

183 Here, we report detailed morphometric, isotopic, and genetic analyses of Zhur tha

184 ess of their humerus was measured using a 3D morphometric mapping approach and compared with 23 free-

185 Combined with machine learning, morphometric markers form intuitive visualizations of no

186 ing reveals robust and distinct patterns of 'morphometric' markers for each major cell type.

187 Morphometric measurement demonstrated lumenal narrowing

188 Morphometric measurements also included percentages of a

189 Periodontitis was assessed by bone morphometric measurements and histomorphometry of block

190 ed heritability analyses on global and local morphometric measurements derived from brain structural

191 Our results suggest that morphometric measurements of brain volume could be a pro

192 We performed morphometric measurements of external and internal genit

193 Morphometric measurements of portal tract structures wer

194 FG following CG definition) as well as gyral morphometric measurements of the affected gyri.

195 Morphometric measurements showed increased mandibular le

196 Body condition, based on morphometric measurements, had a nonsignificant decreasi

197 ontaminants in European starlings, including morphometric measurements, immunotoxicology, oxidative s

198 e than 100 mitochondria-level and cell-level morphometric measurements.

199 at term regardless of labor status; however, morphometric measures (width and depth) were higher in t

200 Support vector machines determined whether morphometric measures at baseline predicted ECT-related

201 luten-targeting proteases, to reduce mucosal morphometric measures in biopsy specimens from patients

202 ics were significantly different across five morphometric measures used in this study (p <= 0.0001).

203 were dramatic species differences in several morphometric measures, electromyograms provided strong e

204 ent cancer diagnosis employs various nuclear morphometric measures.

205 Here, we apply morphometric, mechanistic, and macroevolutionary analyse

206 er group from this large set by developing a morphometric method based on experimental footprints.

207 completed with a specific computer-assisted morphometric method to quantify bronchial and alveolar s

208 Geometric morphometric methods and principal components analysis w

209 aonic and Meroitic, by means of 3D geometric morphometric methods, in order to assess shape variation

210 pared to extant angel sharks using geometric morphometric methods, within a phylogenetic framework, w

211 re analyzed by biochemical, immunologic, and morphometric methods.

212 Yet, a morphometric model integrating evolutionary, development

213 Multisite voxel- and region-based morphometric MRI analysis was conducted in 73 depressed

214 aitlisted for LT were analyzed by applying 6 morphometric muscle scores, including 2 density indices

215 aluated interindividual heterogeneity within morphometric networks and across the whole-brain organiz

216 rticipants' structural MRI, we first derived morphometric networks and extracted grey matter volume i

217 heterogeneity in grey matter volumes across morphometric networks and in the whole-brain grey matter

218 BP, combining geometric morphometrics numerical taxonomy, ancient mitochondrial

219 Here, we used morphometrics of skull isosurfaces derived from 374 pedi

220 The only method of determining colony morphometrics of TB infection in a tissue in situ is two

221 orrelation between body size, morphology and morphometrics of the spinning apparatus and the spinning

222 y computed tomography combined with detailed morphometrics, offering new imaging and computational to

223 se is uniquely associated with disruption of morphometric organization.

224 ve-crest modulation of tissue thickness as a morphometric parameter that can, together with the curva

225 However, the morphometric parameter values were higher with the doses

226 taxa based on the relationship between three morphometric parameters (length, width and depth) and su

227 adulteration and check the applicability of morphometric parameters and DNA barcoding to detect the

228 The morphometric parameters did not discriminate the adulter

229 Twenty-four morphometric parameters measured from 286 canine brain m

230 sed on inter-regional similarity of multiple morphometric parameters measured using multimodal MRI.

231 The morphometric parameters of P. elaeisis exposed to the do

232 The morphometric parameters of the villi, crypts, muscular l

233 In this study, we investigate new US morphometric parameters to quantify bone regeneration in

234 macular changes with visual acuity and other morphometric parameters were assessed by means of linear

235 MCTS systems, whereas traditional size-based morphometric parameters were inconclusive.

236 Radiographs are used to measure the most morphometric parameters.

237 d quantified from the US and CT data using 3 morphometric parameters: the new-bone bulk (NBB), new-bo

238 We measured the morphometric parameters; wood density and sizes of the x

239 pathology, which enable mining of subvisual morphometric phenotypes and might, ultimately, improve p

240 to 71 diverse clinical samples, single-cell morphometric profiling reveals robust and distinct patte

241 519 features were incorporated, summarising morphometric properties of the retinal vasculature, vari

242 ly distributed in the femoral head, and bone morphometric properties were determined in each region.

243 Trabecular metaphyseal and cortical midshaft morphometric properties, and bone mineral content (BMC)

244 We performed morphometric quantification of the capillary network ove

245 reduced interstitial fibrosis as assessed by morphometric quantification of the collagen proportional

246 Morphometric quantification using the lysosomal marker p

247 d changes in liver fibrosis, as evidenced by morphometric quantitation of Sirius Red staining and inc

248 llected and analyzed in immunohistochemical, morphometric, real-time polymerase chain reaction, and w

249 he growing tip of the duct, and incorporates morphometrics, region-specific proliferation and apoptos

250 We demonstrate that morphometric regional boundaries correspond to mapped ge

251 een facilitated through the growing field of morphometrics, representing the conversion of shapes and

252 Instead, morphometrics revealed alterations in both basal and api

253 Changes in morphometric ridge parameters were evaluated as a second

254 lable for the meta-analysis of surface-based morphometric (SBM) studies to effectively characterize w

255 The observed shared morphometric signature of these disorders showed little

256 We used morphometric similarity analysis of MRI data as a marker

257 ychosis was associated with globally reduced morphometric similarity in all three studies.

258 Morphometric similarity mapping provides a novel, robust

259 an, one macaque), we find that the resulting morphometric similarity networks (MSNs) have a complex t

260 ctonic divisions, and greater inter-regional morphometric similarity was associated with stronger int

261 MSNs with tract-tracing data confirmed that morphometric similarity was related to axonal connectivi

262 cortical map of case-control differences in morphometric similarity was spatially correlated with co

263 overexpressed in cortical areas with reduced morphometric similarity were significantly up-regulated

264 tern of case-control differences in regional morphometric similarity, which was significantly reduced

265 d the measurement of ART was performed using morphometric software.

266 Images were segmented by using voxel-based morphometric software.

267 iffusing in synthetic cells parameterized by morphometric statistics are then iterated to fit experim

268 Prior morphometric studies have frequently reported volumetric

269 parasitic nematode species by morphology and morphometric studies is very difficult because of high m

270 Blood biochemistry and morphometric studies of internal organs revealed no pron

271 study reports a meta-analysis of voxel-based morphometric studies of patients with major depressive d

272 Morphometric studies showed that a subset of these patie

273 cotton, but through pioneering chimeric and morphometric studies, it has contributed to fundamental

274 We present the first geometric morphometric study using ontogenetic series of dog and w

275 ough a multidisciplinary study that combines morphometrics, taphonomy, stable isotopes, radiocarbon d

276 methods of biomedical imaging and geometric morphometrics to analyze changes in pelvic morphology fr

277 sing corolla tube measurements and geometric morphometrics to quantify petal shape.

278 on study for molar shape and used 3D surface morphometrics to quantify subtle variation between indiv

279 France (SWF) and Moravia, using 3D geometric morphometrics to test for human group affinities.

280 cological niche modeling [ENM] and geometric morphometrics) to test two hypotheses: given their behav

281 ethod recently incorporated in the geometric morphometric toolkit that complements previous approache

282 Our results suggest that male rhesus macaque morphometric traits are either not under selection, or a

283 impacts on yield, quality and end-use, grain morphometric traits remain an important goal for modern

284 We found that variation in most male morphometric traits was heritable, but found no evidence

285 ntenance of variation in male rhesus macaque morphometric traits which may be subject to sexual selec

286 After adjustment for sex, age, ACR, and each morphometric variable at baseline, an increase in ACR du

287 GFR was not associated with changes in these morphometric variables after additionally adjusting for

288 in adults, stunting in immatures); selected morphometric variables can thus be useful at gauging vul

289 n this proof-of-principle study, IRC-derived morphometric variables correlated well with treatment-na

290 Here, we jointly analyse genetic and morphometric variation in the house mice (Mus musculus d

291 predictive of adult phenotypes and that SAM morphometric variation is associated with genes not prev

292 Morphometric variations associated with each risk factor

293 RDN may precede the established clinical and morphometric vascular changes caused by DM and represent

294 other long-lived organisms will show similar morphometric "warning signs" (wasting in adults, stuntin

295 3D geometric morphometrics was used to analyze GSSCP shape and size.

296 Using geometric morphometrics, we assess the morphology of the mandibula

297 rements and three-dimensional (3D) geometric morphometrics, we show that ant social parasite worker m

298 Finite Element Analysis and Geometric Morphometrics were employed to analyse chewing biomechan

299 rocomputed tomography scans and 3D geometric morphometrics were used to quantify shape and functional

300 their regions of interest and corresponding morphometrics, while embracing cortical variability.