ライフサイエンスコーパス: mediolateral

1 stinct axes: dorsoventral, proximodistal and mediolateral.

2 ic cue' (anteroposterior, + 6.0%, P < 0.001; mediolateral, - 2.1%, P = 0.022) conditions.

3 ic cue' (anteroposterior, + 3.0%, P = 0.001; mediolateral, - 4.2%, P < 0.001) and 'stretch tall plus

4 n the lateral shift of the carotid foramina, mediolateral abbreviation of the lateral tympanic, and a

5 ) proteins that regulate cell elongation and mediolateral alignment.

6 cated coefficients of high magnitude in both mediolateral (all cases range 0.71-0.78) and anteroposte

7 o cooperating signals that operate along the mediolateral and anteroposterior axes of the neural plat

8 M), center of pressure (CP) dynamics (in the mediolateral and anteroposterior directions), and foot c

9 l CT images were evaluated for tilt angle in mediolateral and anteroposterior directions, CT appearan

10 Mediolateral and anteroposterior tilt angle, degree of p

11 he superficial dorsal and ventral horns, the mediolateral and central canal regions.

12 functions during vascular development and in mediolateral and dorsiventral patterning of maize leaves

13 pathway, optic tract, olivary pretectal, and mediolateral and dorsolateral geniculate nuclei.

14 CR(-)/mGluR1alpha(+) UBCs differed along the mediolateral and dorsoventral axes of the folium.

15 sion and indentation tests were performed in mediolateral and dorsoventral direction to determine You

16 ly within domains that are restrained in the mediolateral and dorsoventral directions.

17 ocaudal clones being more constrained in the mediolateral and dorsoventral directions.

18 Arrays were restricted in the mediolateral and dorsoventral planes but could span up t

19 highly structured spatial distributions with mediolateral and dorsoventral positional biases.

20 th the size of the injection site, and their mediolateral and dorsoventral positions change as the in

21 that TRMs impact organ shape along both the mediolateral and proximo-distal axes of growth.

22 gonal coordinated biases in planar polarity: mediolateral and proximodistal.

23 Compartmentation along both the mediolateral and rostrocaudal axes might be linked mecha

24 k-reared axons' terminal zones are normal in mediolateral and rostrocaudal extent despite the lack of

25 The striatal projections follow mediolateral and rostrocaudal gradients that correspond

26 entral plane of the dorsal horn according to mediolateral and segmental locations, a finding that was

27 spatially organized along the dorsoventral, mediolateral, and anteroposterior striatal axis.

28 ensive rostrocaudal (two or three segments), mediolateral, and dorsoventral (reaching laminae III-IV)

29 (unloading phase) were found to be primarily mediolateral, and of significantly reduced amplitude (me

30 delta-protocadherins along the dorsoventral, mediolateral, and rostrocaudal dimensions at intermediat

31 lateral AL tract and to a lesser extent the mediolateral antennal lobe tract.

32 Annular area and mediolateral, anteroposterior, and high (superior)-low (

33 ), and more circular with decreased ratio of mediolateral/anteroposterior (1.11+/-0.09 versus 1.32+/-

34 ne triggering the emergence of the discrete, mediolateral anthocyanin stripe in the M. verbenaceus le

35 e caudal belt, the caudomedial area, and the mediolateral area, stained more darkly, especially for p

36 ning and coordination of adaxial-abaxial and mediolateral axes 713 VI.

37 , and normal craniocaudal, dorsoventral, and mediolateral axes are re-established.

38 f 870 genes along the anterior-posterior and mediolateral axes of the cranial neural plate and reprod

39 along the anteroposterior, dorsoventral, and mediolateral axes with target capture enrichment sequenc

40 nner ear (dorsoventral, anteroposterior, and mediolateral axes) as a function of time indicate a line

41 which is ordered along both rostrocaudal and mediolateral axes, in the orientation found in wild-type

42 coarse pattern along its anteroposterior and mediolateral axes, this basis is progressively refined b

43 terned along proximodistal, dorsoventral and mediolateral axes.

44 directions, e.g., along the rostrocaudal and mediolateral axes.

45 the dorsoventral than in the rostrocaudal or mediolateral axes.

46 leads to abortion of blade expansion in the mediolateral axis and disruption of vein patterning.

47 s reveals that cells are polarized along the mediolateral axis and exhibit protrusive activity.

48 in how adaxial-abaxial polarity patterns the mediolateral axis and subsequent lateral expansion of le

49 tterning cerebellum foliation throughout the mediolateral axis and that act late in development.

50 ented cellular aggregates arranged along the mediolateral axis are the patterning element most common

51 on of the dermomyotome is greatest along its mediolateral axis coincident with the dorsalward and ven

52 the presence of coarse somatotopy along the mediolateral axis in PPC.

53 The dermomyotome is then patterned along its mediolateral axis into medial, central and lateral compa

54 orient their stereociliary bundles along the mediolateral axis of the cochlea.

55 translation of the loaded indenter along the mediolateral axis of the disc.

56 ody axis terminate in different areas in the mediolateral axis of the DON, the first electrosensory p

57 he location of the cells of origin along the mediolateral axis of the entorhinal cortex.

58 Furthermore, the mediolateral axis of the ganglion is linked to both deve

59 metric stripe that lies at the middle of the mediolateral axis of the neural plate.

60 nal ganglion cell axon termination along the mediolateral axis of the superior colliculus.

61 he direction of the trajectory of the PL and mediolateral axis was used to represent the direction of

62 oventral axis, pump-handle rotation around a mediolateral axis, and caliper rotations around a cranio

63 ontralateral eye were commonly fused along a mediolateral axis, rostral to which were large and somet

64 al manner with SLIT to pattern the planarian mediolateral axis, while WNT11-2 patterns the posterior

65 ior sites, which were often skewed along the mediolateral axis.

66 ern truncations that are primarily along the mediolateral axis.

67 rent areas or fields of the cortex along the mediolateral axis.

68 ession is observed throughout the cerebellar mediolateral axis.

69 ation were distributed more evenly along the mediolateral axis.

70 l structures on kidney positioning along the mediolateral axis.

71 extension of RGC axon branches important for mediolateral axon targeting in the formation of retinoco

72 Injections in PMD labeled neurons across a mediolateral belt of posterior parietal cortex extending

73 Declines in mediolateral bending strength of the lower limb bones an

74 We found a strong mediolateral bias in fusion timing; however, at a cellul

75 s arrangement is achieved without any direct mediolateral bias other than that which is provided by t

76 At adulthood, gentle mediolateral birthdate-gradients in S cells were still e

77 ervations suggest that at least two separate mediolateral boundary systems exist in the cerebellum, a

78 and higher Ezrb activation rescues defective mediolateral cell alignment and migration paths in vangl

79 After mediolateral cell division, N-cadherin is enriched in th

80 xtension with little convergence by allowing mediolateral cell elongation and dorsally biased interca

81 m of noncanonical Wnt11 signaling to mediate mediolateral cell elongation required for dorsal cell mo

82 12/13) function cell-autonomously to mediate mediolateral cell elongation underlying intercalation du

83 ll polarity (PCP) signaling is essential for mediolateral cell elongation underlying these movements,

84 quired for normal gastrulation including the mediolateral cell intercalation behaviors that drive con

85 arity gene, Ptk7, as essential regulators of mediolateral cell intercalation during mammalian CE.

86 highlighting an important difference in how mediolateral cell intercalation is controlled in the two

87 Mediolateral cell intercalation is proposed to drive mor

88 events--convergent extension (CE) driven by mediolateral cell intercalation, and bending of the neur

89 mouse embryos, that mesodermal CE occurs by mediolateral cell intercalation, driven by mediolaterall

90 alignment zone has formed, does not inhibit mediolateral cell intercalation, involution and converge

91 differ in degree of neighbor exchange during mediolateral cell intercalation.

92 ithout notoplate), all cells express bipolar mediolateral cell motility.

93 Moreover, how defective mediolateral cell polarity impacts CE is not understood.

94 planar cell polarity (PCP) pathway-dependent mediolateral cell polarity is important for notochord mo

95 nical Wnt signaling pathway in promoting the mediolateral cell polarization that underlies this morph

96 a planar cell polarity pathway and regulates mediolateral cell polarization underlying CE.

97 tension by preventing Rho/Rac activation and mediolateral cell polarization.

98 urface area drives a tendency to shorten the mediolateral (circumblastoporal) aspect of the IMZ, ther

99 he direction of cell division from AP to the mediolateral circumference (ML).

100 hat a density moves inferiorly (down) on the mediolateral compared with the mediolateral oblique view

101 gical remodeling that is consistent with the mediolateral component of convergent extension.

102 jections exhibit rostrocaudal elongation and mediolateral compression, compared with their cutaneous

103 ate consists of just 40 cells, which undergo mediolateral convergence (intercalation) to form a singl

104 ckening (CT) was originally described as the mediolateral convergence and radial thickening of the ex

105 his actomyosin network contracts to generate mediolateral convergence forces in the context of these

106 Newborn Egfr-/- mice have facial mediolateral defects including narrow, elongated snouts,

107 audal expansion occurs at a slower rate than mediolateral development.

108 ry cortex, information flows serially in the mediolateral dimension from core, to belt, to parabelt.

109 but not sucrose, were more widespread in the mediolateral dimension than neurons that responded to bo

110 The length (rostrocaudal dimension), width (mediolateral dimension), thickness (dorsoventral dimensi

111 in gastrulation, cells undergo increasingly mediolateral-directed elongation and autonomous converge

112 ropic with significant higher results in the mediolateral direction (all P = 0.002).

113 as observed in the lateral attachment in the mediolateral direction and the posterior superior attach

114 easing path radius caused slips with greater mediolateral direction components.

115 n the multivariable model, STD values in the mediolateral direction during translational stimulus wer

116 For the mediolateral direction, coefficients were negligible for

117 ere observed to spread preferentially in the mediolateral direction, crossing the boundaries of the p

118 us trended higher in the temporal region and mediolateral direction.

119 taneous values when shear was applied in the mediolateral direction.

120 lum behavior in both the anteroposterior and mediolateral directions and were derived from both kinem

121 ADC values in the cephalocaudal and mediolateral directions were higher than those in the an

122 s, especially PM shifts in the posterior and mediolateral directions, as well as with annular area (P

123 and condylar regions and anteroposterior and mediolateral directions.

124 oes a biphasic dispersion: an early phase of mediolateral dispersion and a late phase of anteroposter

125 re relatively small and spatially limited to mediolateral distances of approximately 50 mum, whereas

126 RP-IR labeling was prevalent in an extensive mediolateral distribution at the base of the dorsal horn

127 In both species, a prominent mediolateral distribution pattern was observed at rostra

128 ocot and eudicot leaves undergo expansion of mediolateral domains at different times in ontogeny, dir

129 oject their dendrites to largely stereotyped mediolateral domains in the dorsal region of the neuropi

130 ck diencephalon were widely dispersed in the mediolateral, dorsoventral and rostrocaudal planes.

131 The initial events in the onset of CE are mediolateral elongation, alignment and orientation of me

132 are coordinated with the anteroposterior and mediolateral embryonic axes.

133 performed for obstetric indications, use of mediolateral episiotomy should result in fewer anal sphi

134 s resulted in a number of defects, including mediolateral expansion of the cerebellar vermis, reduced

135 ic expression of Wnt-3a in vivo results in a mediolateral expansion of the dermomyotome and myotome.

136 ominence failed to undergo proximodistal and mediolateral expansion.

137 s, participants mapped temporal events along mediolateral (Experiment 1) and anterioposterior (Experi

138 Cs is associated with ZII stripes across the mediolateral extent of an entire folium.

139 l trigeminal nerve is represented in an 8-mm mediolateral extent of area 3b lateral to the representa

140 widespread distribution and fill the entire mediolateral extent of the arm area.

141 ally as a broad band that spanned the entire mediolateral extent of the fused dorsal horns (caudal S2

142 Expression was seen throughout the mediolateral extent of the Hcrt field.

143 This labeling covered the entire mediolateral extent of the SC, but, in keeping with the

144 eral intra-oral structures measuring 6 mm in mediolateral extent.

145 superficiale throughout the rostrocaudal and mediolateral extents of the SC.

146 Fetuses with VOGM and wide mediolateral falcine sinus diameters are at high risk fo

147 the APA exceeded 10-20% of the mean baseline mediolateral force.

148 t stresses: Since VM and VL produce opposing mediolateral forces on the patella, the high positive co

149 ibutes a unit of three pinnae to half of the mediolateral frond axis.

150 y is initially specified by rostrocaudal and mediolateral gene expression gradients in neuroepithelia

151 Finally, while MNs do appear to die in a mediolateral gradient during the period of MN PCD, this

152 ient of longitudinal strain that, unlike the mediolateral gradient for locomotion, occurs along the d

153 Striatal activity followed a mediolateral gradient in which behavioural correlates pr

154 We discovered a mediolateral gradient of connectivity, such that the med

155 Yet, axial locomotion produces a mediolateral gradient of muscle strain that should force

156 ith fiber architecture shown to counteract a mediolateral gradient suggests that bluegill sunfish sho

157 to the increased vertical moment arm of the mediolateral ground reaction force.

158 le contractile proteins confirms the myotome mediolateral growth directions, and shows that the myoto

159 lamic acid (NPA), highlighting their role in mediolateral gynoecium patterning.

160 This behavior is thought to drive the mediolateral intercalation and convergent extension of t

161 at stage 101/2 the first cells that undergo mediolateral intercalation and form the vegetal alignmen

162 ediated boundary formation and PCP-dependent mediolateral intercalation are each able to drive a rema

163 Mediolateral intercalation begins in a group of cells ca

164 ghly organized cellular intermixing known as mediolateral intercalation behavior (MIB).

165 Prickle, which has a severe defect in early mediolateral intercalation but forms a robust notochord

166 We propose that neural deep cells accomplish mediolateral intercalation by applying their protrusions

167 ential for neural CE, as shown by failure of mediolateral intercalation in embryos mutant for two pro

168 reas XTRPM7 is mainly involved in regulating mediolateral intercalation in the medial region of the n

169 second axis because it stimulates precocious mediolateral intercalation of caudal, dorsal mesoderm.

170 terize the neural deep cell motility driving mediolateral intercalation, also using time-lapse videor

171 homologue XTRPM7, whose loss interferes with mediolateral intercalation, depletion of XTRPM6 but not

172 In such embryos, mediolateral intercalation, involution and convergent ex

173 ecializations of the same basic mechanism of mediolateral intercalation, tailored to accommodate othe

174 cellular junctions predominantly between the mediolateral interfaces of neighboring cells.

175 iated from just two epidermal cells, and the mediolateral leaf axis is the first to be established.

176 d the coleoptile, while mutations disrupting mediolateral leaf development also disrupt scutellum and

177 njections placed at various rostrocaudal and mediolateral levels in these cortices revealed extensive

178 ortex mainly gave rise to projections to mid-mediolateral levels, although some fibers did enter eith

179 investigate how the ball position along the mediolateral (M-L) direction of a golfer causes a chain

180 g notochord cells show polarity first in the mediolateral (M/L) axis during C/E, and subsequently in

181 Engrailed-2 also affects the transient mediolateral (M/L) pattern of En-1 and Wnt-7b expression

182 canaliculi sensorial role in the context of mediolateral mandibular movements.

183 rostrocaudal plane; however, a preferential mediolateral mitotic spindle orientation could not be de

184 ditional anatomical anteroposterior (AP) and mediolateral (ML) axes.

185 eurons are topographically organized along a mediolateral (ML) axis.

186 and mechanical instability mainly along the mediolateral (ML) axis.

187 r (AP) embryonic axis is driven by polarized mediolateral (ML) cell intercalations and is influenced

188 oe clearance, across both age groups, though mediolateral (ML) CM-CP divergence in elderly subjects w

189 sure (COP), and its anteroposterior (AP) and mediolateral (ML) displacements.

190 xes: anteroposterior (AP), vertical (V), and mediolateral (ML) while participants walked an eight-met

191 ng human walking, step width is predicted by mediolateral motion of the pelvis, a relationship that c

192 ion boundaries along the anteroposterior and mediolateral neural axes that are important for proper p

193 This led to the self-organization of mediolateral neural patterns.

194 containing cells in the DRN rostrocaudal and mediolateral neuraxis by using a capsaicin challenge par

195 xcitatory transmission in the lateral septum mediolateral nucleus (LSMLN) after chronic cocaine admin

196 of the amygdala (CeA) and the lateral septum mediolateral nucleus (LSMLN).

197 ists who independently visually assessed 760 mediolateral oblique (MLO) images in 380 women (mean age

198 (91%) of 58 lesions on craniocaudal (CC) and mediolateral oblique (MLO) views of screening mammograms

199 mammographic view, craniocaudal (CC) versus mediolateral oblique (MLO).

200 Mediolateral oblique and craniocaudal digital mammograph

201 observer in 13.6% and 6.4% of the synthetic mediolateral oblique and craniocaudal images, respective

202 raphy unit, the facility submitted bilateral mediolateral oblique and craniocaudal mammograms obtaine

203 mammographic views; both modes included the mediolateral oblique and craniocaudal views in a fully c

204 For initial screening examinations, mediolateral oblique and craniocaudal views were obtaine

205 observer study was performed with bilateral mediolateral oblique examinations and corresponding synt

206 spective study, dual-energy craniocaudal and mediolateral oblique mammograms were obtained immediatel

207 q technetium 99m sestamibi, craniocaudal and mediolateral oblique MBI (2-minute acquisition per view)

208 estamibi and were imaged in craniocaudal and mediolateral oblique projections.

209 st-specific gamma camera in craniocaudal and mediolateral oblique projections.

210 (down) on the mediolateral compared with the mediolateral oblique view if it is lateral (out) to the

211 nipple to the pectoralis major muscle on the mediolateral oblique view of the diagnostic mammogram an

212 In subsequent examinations, the mediolateral oblique view was standard.

213 late radiomic features from craniocaudal and mediolateral oblique views in all study patients, matche

214 stimated by three experienced readers on the mediolateral oblique views of the contralateral breasts

215 ing a possible malignancy on craniocaudal or mediolateral oblique views or both.

216 Conventional craniocaudal and mediolateral oblique views were obtained in each patient

217 Each set of mammograms (craniocaudal and mediolateral oblique views) was digitized and analyzed b

218 compression in both the craniocaudal and the mediolateral oblique views.

219 ws], 0.64 mGy +/- 0.23 vs 1.79 mGy +/- 0.53 [mediolateral oblique views], both P = .0001).

220 ic examinations (n = 175; cranial caudal and mediolateral oblique) were randomly selected from a prev

221 raphic projection (craniocaudal, lateral, or mediolateral oblique).

222 h the other regions of the disc under either mediolateral or anteroposterior tension.

223 from adjacent tissues, whereas the nonrandom mediolateral orientation of cell division in the epiderm

224 nce movements with impaired cell elongation, mediolateral orientation, and consequently failure to mi

225 Clone geometry is further refined by mediolateral oriented migration and passive dispersion o

226 n zebrafish does not affect dorsoventral and mediolateral otic patterning, we now show that a gain of

227 nes in Arabidopsis, reveal that NS1 controls mediolateral outgrowth by repression of a growth inhibit

228 and leads to adaxial/abaxial patterning and mediolateral outgrowth of the leaf.

229 rgins of leaf primordia, and is required for mediolateral outgrowth.

230 t and slower anteroposterior (P < 0.001) and mediolateral (P = 0.002) CM velocities during initiation

231 n between their activation minimizes the net mediolateral patellar force.

232 produce identical knee torques but opposing mediolateral patellar forces.

233 between VL and VM activation to minimize net mediolateral patellar forces.

234 lineates three clusters of the amygdala in a mediolateral pattern based on its connectivity with brai

235 2 is required to coordinate dorsiventral and mediolateral patterning in maize leaves.

236 In contrast, mediolateral patterning is generally only subtly affecte

237 h signalling is also required for the normal mediolateral patterning of myogenic cells within the som

238 HEL-LIKE HOMEOBOX3 (WOX3) genes, involved in mediolateral patterning of plant lateral organs, inform

239 cle progenitor cells and in dorsoventral and mediolateral patterning of the somite.

240 lex interplay between anterior-posterior and mediolateral patterning systems.

241 odistal, dorsoventral (adaxial-abaxial), and mediolateral patterns following initiation.

242 nted preferentially in both rostrocaudal and mediolateral planes, suggesting a role for nonrandomly o

243 other factors are responsible for setting up mediolateral polarity which becomes the dorsoventral (D-

244 This mediolateral polarization was under the control of plana

245 ermis or hemispheres form in the appropriate mediolateral position.

246 with previous studies reporting topographic mediolateral positional biases in flexor and extensor pr

247 s between motor neurons do not influence the mediolateral positioning of dendritic fields.

248 inly in accordance to their rostrocaudal and mediolateral positions.

249 e postcrossing commissural axons to distinct mediolateral positions.

250 l has long been thought to accumulate in the mediolateral protrusions in Xenopus chordamesoderm cells

251 singly, accumulations previously observed at mediolateral protrusions of chordamesodermal cells are n

252 e mesodermal cells because the neural cells' mediolateral protrusive activity is episodic, whereas th

253 holinos blocks both convergent extension and mediolateral protrusive behaviors in explant preparation

254 rovement than young people in two variables, mediolateral range (p=0.008), and critical mean square d

255 eural tube, which exhibits rostro-caudal and mediolateral regionalization.

256 Injections made into mid-mediolateral regions of the entorhinal cortex mainly gav

257 evelopment, although the anteroposterior and mediolateral relationships between cortical fields appea

258 teric, and inferior mesenteric arteries) and mediolateral (renal arteries) branch vessels in a cryoge

259 ersegmental boundaries with a 250 micrometer mediolateral resolution and a 200 micrometer dorsoventra

260 sual rotation was pseudo-randomly varied and mediolateral responses were measured from displacements

261 ctional signalling molecules in dorsoventral-mediolateral retinocollicular mapping.

262 approximately 24 barrels, arranged in eight mediolateral rows and a barrel-free zone capping the ant

263 al roles during neural development including mediolateral segmentation of the neural plate, neural cr

264 These defects are independent of mediolateral segmentation of the neurectoderm and of dor

265 al thalamus (MD), lateral hypothalamus (LH), mediolateral septum, dorsolateral periaqueductal gray, d

266 ve groups of cells represent digits 1-5 in a mediolateral sequence by injecting tracers into the cort

267 ot, lower leg, and upper leg terminated in a mediolateral sequence within the gracile nucleus.

268 ontralateral body from hindlimb to face in a mediolateral sequence, with individual movements such as

269 the hindlimb, trunk, forelimb, and face in a mediolateral sequence.

270 olated cell groups represent digits 1-5 in a mediolateral sequence.

271 motor neuron topography by coordinating the mediolateral settling position of motor neurons within t

272 We found no mediolateral spatial segregation between adductor and ab

273 d the response to A-77636 and eliminated the mediolateral staining gradient seen after A-77636 alone.

274 Whereas for all other comparisons, mediolateral sway amplitude was identified as the strong

275 ypothesized that the intermediate zone under mediolateral tension would exhibit lower dynamic moduli

276 cies, such as a weak intermediate zone under mediolateral tension.

277 nd length and multifidus anteroposterior and mediolateral thickness measured.

278 The mediolateral topography was less precise and the shift f

279 ion, describing inferior-superior as well as mediolateral trends in microstructural differentiation t

280 VII, in segments consistent with the coarse mediolateral VL topography; few or no cells were labeled

281 na V (in spinal segments consistent with the mediolateral VPL topography); few cells were labeled in

282 arget on postbiopsy images (craniocaudal and mediolateral), while in 18 (16%), the clip was within 6-

283 In contrast, excess SHH leads to a mediolateral widening of the FNP and a widening between

284 ed, extended (anteroposterior) and narrower (mediolateral), with the largest regional deviations bein