ライフサイエンスコーパス: lateral plate

1 en's node can promote formation of IM in the lateral plate.

2 soderm that lies between the somites and the lateral plate.

3 ompartment comprising cells from somites and lateral plate.

4 ication has occurred in the node but not the lateral plate.

5 the prospective limb-forming regions of the lateral plate.

6 the prospective limb-forming regions of the lateral plate.

7 the prospective limb-forming regions of the lateral plate.

8 Subsequently, competing signals from the lateral plate and axial tissues modulate the number of c

9 ced by GSK3-beta inhibition did not generate lateral plate and cardiac mesoderm and favored instead s

10 te nonmyogenic cells to the limb: stage 9-12 lateral plate and distal portions of stage 25/26 limbs.

11 r that Pbx1 and Pbx2 are co-expressed in the lateral plate and early limb field mesoderm.

12 metric gene expression at the node or in the lateral plate and exhibit right isomerism of the lungs.

13 a transcription factors are expressed in the lateral plate and in vasculogenic regions of the avian s

14 ition to NMPs, generates progenitors for the lateral plate and intermediate mesoderm.

15 te mesoderm lies between the somites and the lateral plate and is the source of all kidney tissue in

16 eobox genes prx-1 and prx-2 are expressed in lateral plate and limb bud mesoderm, but targeted inacti

17 ed in conferring limb-forming ability to the lateral plate and may promote the initial outgrowth of l

18 Combining lateral plate and paraxial tissue in vivo or in vitro le

19 t apparently adopt the Hox expression of the lateral plate and participate in the morphology appropri

20 riginally specified as ventral type, such as lateral plate and primary blood islands.

21 riginate from several sources, including the lateral plate and somite mesoderm.

22 dermal protein expression was limited to the lateral plate and somitic mesoderm.

23 somite by inhibitory signals produced by the lateral plate and ventral neural tube.

24 ricted to the primitive streak and posterior lateral plate, and is absent from the anterior region wh

25 d the formation of all but the most anterior lateral plates, and another independently segregating fa

26 sis, ndr2 is expressed asymmetrically in the lateral plate as are nodal-related genes of other organi

27 tiation of human pluripotent stem cells into lateral plate, cardiac, and presomitic mesoderm.

28 esceinated dextran, confirms that, normally, lateral plate cells next to the notochord do not contrib

29 nt and explant experiments revealed that the lateral plate contains an activity that can repress IM f

30 Misexpression of Hoxd-12 in other lateral plate derivatives (sternum, pelvis) likewise phe

31 pression of mesoderm markers associated with lateral plate derivatives.

32 First, the majority of the avian scapula is lateral plate derived and the somitic contribution to th

33 We have identified a population of lateral plate-derived limb mesodermal cells in both chic

34 ns of somite-derived myogenic precursors and lateral plate-derived mesenchymal stroma to the establis

35 n the thoracic region, Hox genes pattern the lateral plate-derived sternum in a non-colinear manner,

36 e HSC lineage have been identified in dorsal lateral plate (DLP) mesoderm, and a transcriptional gene

37 putative adult haemangioblasts in the dorsal lateral plate (DLP) mesoderm.

38 ate embryo, the blood islands and the dorsal lateral plate (DLP), participate in early hematopoietic

39 The anterior lateral plate domain of GFP expression gives rise to pri

40 g. neural tube, axial and paraxial mesoderm, lateral plate, ectoderm, endoderm) to drive axis morphog

41 ey strongly support the hypothesis that left lateral plate expression of nodal-related genes is a cau

42 e absence of Shh, BMP administration induces lateral plate gene expression in cultured psm.

43 ediate mesoderm gene expression and activate lateral plate genes.

44 anism for information relay between node and lateral plate in a process that is critical for the esta

45 asymmetric information from the node to the lateral plate is mediated by Caronte (Car), a novel memb

46 erivatives, including pronephros, muscle and lateral plate is not disrupted.

47 MP signaling no longer induces expression of lateral plate markers but now induces robust chondrogene

48 at additional cell types within the anterior lateral plate mesoderm (ALPM) also underwent subduction,

49 1 and Cyp26c1, are expressed in the anterior lateral plate mesoderm (ALPM) and predominantly overlap

50 ring primitive neutropoiesis in the anterior lateral plate mesoderm (ALPM) but has little effect on e

51 scripts are conspicuously absent in anterior lateral plate mesoderm (ALPM), where SHF progenitors are

52 ification in the nkx2.5(+) field of anterior lateral plate mesoderm (ALPM).

53 ng activity) but negatively regulated by the lateral plate mesoderm (BMP4).

54 sient asymmetric Nodal signaling in the left lateral plate mesoderm (L LPM) during tailbud/early somi

55 t stem cells (HPSCs) through an intermediate lateral plate mesoderm (LM) stage.

56 In chicken, lateral plate mesoderm (LPM) adjacent to occipital somit

57 alities in asymmetric gene expression in the lateral plate mesoderm (LPM) and dorsal diencephalon of

58 is joined by dynamic expression in the left lateral plate mesoderm (LPM) and left dorsal endoderm.

59 mally is expressed predominantly in the left lateral plate mesoderm (LPM) and left side of the straig

60 elial to mesenchymal transition (EMT) in the lateral plate mesoderm (LPM) and myoblast migration into

61 l somatopleure, a tissue composed of somatic lateral plate mesoderm (LPM) and overlying ectoderm.

62 demonstrated loss of normal LR asymmetry in lateral plate mesoderm (LPM) antivin/lefty-1 and Pitx2 e

63 fish, asymmetric migration of the epithelial lateral plate mesoderm (LPM) displaces the gut leftward,

64 The lateral plate mesoderm (LPM) forms the progenitor cells

65 g in mouse embryonic stem cell (ESC)-derived lateral plate mesoderm (LPM) generates tracheal mesoderm

66 the primary heart field within the anterior lateral plate mesoderm (LPM) into a tubular heart involv

67 ulatory pathway specifically within the left lateral plate mesoderm (LPM) is critical for these event

68 os, the expression of Pitx2 gene in the left lateral plate mesoderm (LPM) is directly regulated by Xn

69 Nodal activity in the left lateral plate mesoderm (LPM) is required to activate lef

70 In VAD embryos nodal expression in left lateral plate mesoderm (LPM) is severely downregulated a

71 Disruption of lateral plate mesoderm (LPM) migration through knockdown

72 sion in the foregut endoderm and surrounding lateral plate mesoderm (lpm) prior to respiratory specif

73 These signals are then transferred to the lateral plate mesoderm (LPM) through cellular and molecu

74 the transmission of asymmetric cues from the lateral plate mesoderm (LPM) to the cardiac field but no

75 ide markers such as nodal bilaterally in the lateral plate mesoderm (LPM), indicating that loss of AC

76 restricted expression of Pitx2c in the left lateral plate mesoderm (LPM), left half of heart tube an

77 vements of the hepatic endoderm and adjacent lateral plate mesoderm (LPM), resulting in asymmetric po

78 es is thought to be derived exclusively from lateral plate mesoderm (LPM), which gives rise to a card

79 e node and Shh downstream genes in the right lateral plate mesoderm (LPM), while overexpression of ch

80 (hiPSCs) that were differentiated either to lateral plate mesoderm (LPM)-like cells, the development

81 to Nodal expression specifically in the left lateral plate mesoderm (LPM).

82 the asymmetric migration of the neighboring lateral plate mesoderm (LPM).

83 ch as Nodal and Lefty2 is absent in the left lateral plate mesoderm (LPM).

84 ling system are also present in the cavefish lateral plate mesoderm (LPM).

85 erse lineages including axial, paraxial, and lateral plate mesoderm (LPM).

86 nal response of Nodal expression in the left lateral plate mesoderm (LPM).

87 asymmetric left-right gene expression in the lateral plate mesoderm (LPM).

88 limb connective tissue progenitors from the lateral plate mesoderm (LPM).

89 equently, Nodal expression is delayed in the lateral plate mesoderm (LPM).

90 quires asymmetric expression of nodal in the lateral plate mesoderm (LPM).

91 laterality and southpaw (spaw) expression in lateral plate mesoderm (LPM).

92 n begins during the convergence of posterior lateral plate mesoderm (PLM), well before aorta formatio

93 le effect on erythropoiesis or the posterior lateral plate mesoderm (PLPM) expression of neutrophil m

94 nct sites, the anterior (ALPM) and posterior lateral plate mesoderm (PLPM).

95 velopment of two structures derived from the lateral plate mesoderm - the heart and the pectoral fin.

96 phological boundaries between somites and in lateral plate mesoderm a wing- or non-wing-forming bound

97 age tracing in the living embryo, are in the lateral plate mesoderm adjacent to the notochord-prechor

98 Subsequently, Nodal signaling from the left lateral plate mesoderm alleviates this repression ipsila

99 are good candidates for encoding position in lateral plate mesoderm along the body axis and thus for

100 ating the transcription of VegfA in both the lateral plate mesoderm and also in the somites.

101 ric midline domains and unilaterally in left lateral plate mesoderm and anterior dorsal endoderm.

102 localized to the presumptive presomitic and lateral plate mesoderm and CYP26 mRNA to the presumptive

103 eage perturbed asymmetric gene expression in lateral plate mesoderm and disrupted organ LR asymmetrie

104 to initiate molecular asymmetry in the left lateral plate mesoderm and exhibit multiple left-right p

105 regulates the developmental potential of the lateral plate mesoderm and is required cell autonomously

106 nitially specified in the dorsal part of the lateral plate mesoderm and later become incorporated int

107 riginate in distinct regions of the anterior lateral plate mesoderm and migrate to the midline where

108 three intermediate lineages: neuroectoderm, lateral plate mesoderm and paraxial mesoderm.

109 to disrupt asymmetric gene expression in the lateral plate mesoderm and randomize the placement of in

110 tissues, a strong expression of RARbeta2 in lateral plate mesoderm and somites, and an anterior expr

111 ription factor expressed throughout the left lateral plate mesoderm and subsequently on the left side

112 known to be expressed asymmetrically in the lateral plate mesoderm and the brain during embryogenesi

113 The dermis originates from the somites, the lateral plate mesoderm and the cranial neural crest.

114 proliferation of hindlimb progenitors in the lateral plate mesoderm and the expression of a common fa

115 anscripts were enriched in cardiac mesoderm, lateral plate mesoderm and the neural plate.

116 The gene Pitx2 is expressed in the left lateral plate mesoderm and, subsequently, in the left he

117 Lateral plate mesoderm appears to pattern the endoderm i

118 symmetric patterns of gene expression in the lateral plate mesoderm are initiated by signals located

119 r-1 is re-expressed unilaterally in the left lateral plate mesoderm at neurula/tailbud stages.

120 e of a differential growth of cells from the lateral plate mesoderm at specific axial levels.

121 by reciprocal transplantation of somites or lateral plate mesoderm at stages prior to muscle formati

122 rafish development, cbfb is expressed in the lateral plate mesoderm at tail bud stage and in the inte

123 Here we show that T is expressed in lateral plate mesoderm at the onset of limb bud formatio

124 xperiments show that bmp2a, expressed in the lateral plate mesoderm at these stages, is essential for

125 The grl gene is expressed in lateral plate mesoderm before vessel formation, and ther

126 d with gata4 and nkx2.5 not only in anterior lateral plate mesoderm but also in noncardiac mesoderm a

127 ation, the cardiac progenitors reside in the lateral plate mesoderm but maintain close contact with t

128 ormed via repressing venous cell fate at the lateral plate mesoderm by Hh signaling during vasculogen

129 Left-side expression of XNR1 in the lateral plate mesoderm depends on XCR2, whereas posterio

130 ls, are generally described to come from the lateral plate mesoderm despite experimental evidence for

131 ential expression timing of Hox genes in the lateral plate mesoderm determines limb placement as well

132 essed in restricted bilateral domains in the lateral plate mesoderm directly adjacent to the liver-fo

133 repression of Xnr-1 expression in the right lateral plate mesoderm during closure of the neural tube

134 mmetric and topological within the fin-field lateral plate mesoderm during early fin bud initiation.

135 maintain the expression of Pitx2 in the left lateral plate mesoderm during the patterning of left-rig

136 Neural tube and lateral plate mesoderm enhancers can be separated, but i

137 ABD, or ACD; somite expression by ACDE; and lateral plate mesoderm expression by DE.

138 M) cells will adopt either a chondrogenic or lateral plate mesoderm fate.

139 oderm for hindbrain patterning, and rarab in lateral plate mesoderm for specification of the pectoral

140 lly in the perinodal region of the posterior lateral plate mesoderm for the establishment of laterali

141 In these fish, GFP-expressing cells in the lateral plate mesoderm form two tubes that migrate ventr

142 tein) signaling activity specifically during lateral plate mesoderm formation while reducing fibrobla

143 re, we find the pericardium forms within the lateral plate mesoderm from dedicated mesothelial progen

144 of the fetal limb and axial skeleton, and in lateral plate mesoderm giving rise to visceral muscle.

145 developing node and at later stages in left lateral plate mesoderm has been implicated as a key regu

146 l is generated at the node and transduced to lateral plate mesoderm in a linear signal transduction c

147 oD, Myf-5, and myogenin in both paraxial and lateral plate mesoderm in the absence of inducing tissue

148 pressed in the intermediate mesoderm and the lateral plate mesoderm in the presumptive chick forelimb

149 Subsequent nodal and Pitx2 expression in the lateral plate mesoderm in these mice is randomized, indi

150 quivalent embryological origin: the anterior lateral plate mesoderm in vertebrates and the dorsal-mos

151 Left-sided expression of Nodal in the lateral plate mesoderm is a conserved feature necessary

152 pendent regulation of Hox gene expression in lateral plate mesoderm may have been a key step in the e

153 in rargb morphants, suggesting Rargb affects lateral plate mesoderm migration.

154 Posterior lateral plate mesoderm normally forms blood, but cocultu

155 verely downregulated or abolished within the lateral plate mesoderm of Southpaw-deficient embryos.

156 COUP-TFII is expressed in lateral plate mesoderm of the early embryo prior to limb

157 gion produces the paraxial, intermediate and lateral plate mesoderm of the trunk.

158 abel single or small patches of cells in the lateral plate mesoderm of the zebrafish and to track the

159 ecursors of several organs reside within the lateral plate mesoderm of vertebrate embryos.

160 ere initially induced to form neuroectoderm, lateral plate mesoderm or paraxial mesoderm.

161 ntly in somites and unsegmented paraxial and lateral plate mesoderm overlapping atrial precursors in

162 Analysis of the cardiogenic potential of the lateral plate mesoderm posterior to nkx-2.5 and actR-IIa

163 ppropriate number of cardiomyocytes from the lateral plate mesoderm requires a careful balance of bot

164 r notochord in late neurulae, and finally in lateral plate mesoderm restricted to the left side of ta

165 s Islet1, a hindlimb-specific factor, in the lateral plate mesoderm results in a failure to induce hi

166 zyme in the gpi-biosynthetic pathway, in the lateral plate mesoderm results in normally patterned lim

167 ly identified, here we provide evidence that lateral plate mesoderm sends instructive signals to the

168 tion factor Hand2, which is expressed in the lateral plate mesoderm starting at the completion of gas

169 tion of zebrafish hrT expression in anterior lateral plate mesoderm suggest a very early role for hrT

170 tion as cardiac precursors converge from the lateral plate mesoderm territories toward the embryonic

171 ail2 function in a regulatory circuit within lateral plate mesoderm that directs normal vessel format

172 on of the expression domain corresponding to lateral plate mesoderm that is part of the early heart f

173 a7/lacZ reporter within neural, paraxial and lateral plate mesoderm tissues.

174 red during somitogenesis within the anterior lateral plate mesoderm to induce myocardial differentiat

175 ine the relative contribution of somitic and lateral plate mesoderm to the avian scapula from quail-c

176 nt development, angioblasts migrate from the lateral plate mesoderm to the midline where they form a

177 regulation of the cell fate transition from lateral plate mesoderm to the specification of cardiomyo

178 ogenitor cells (HPCs) move from the anterior lateral plate mesoderm to the ventral midline, undergoin

179 that these cells migrate from the posterior lateral plate mesoderm to their site of differentiation

180 uilding on established methods, hPSC-derived lateral plate mesoderm treated with either retinoic acid

181 rmerly lefty-2), nodal and Pitx2 in the left lateral plate mesoderm was absent, suggesting that Gdf1

182 onephros induction, stage 7 or earlier chick lateral plate mesoderm was cocultured with caudal stage

183 ymmetric Nodal signaling cascade in the left lateral plate mesoderm was detected, and began to be unr

184 Snrk-1 control angioblast populations in the lateral plate mesoderm with Dusp-5 functioning downstrea

185 steps of this cascade (before it reaches the lateral plate mesoderm) results in random left-right asy

186 d shift of Nodal expression in the left LPM (lateral plate mesoderm), and speculate that the higher l

187 vascular zones are directly generated by the lateral plate mesoderm, a critical source of Sema3E.

188 ective angioblast migration in the posterior lateral plate mesoderm, a process known to depend on vas

189 rated and propagated from the KV to the left lateral plate mesoderm, activating a transcriptional res

190 skeleton and sternum arise from the somatic lateral plate mesoderm, and all of the muscles for both

191 The second population resides in the dorsal lateral plate mesoderm, and contains precursors of adult

192 tion to the neural groove, primitive streak, lateral plate mesoderm, and Hensen's node, while distinc

193 he nodal-related gene southpaw (spaw) in the lateral plate mesoderm, and its downstream targets pitx2

194 e of the genes specifically expressed in the lateral plate mesoderm, and later in its derivative, the

195 In the absence of FoxF1 function, the lateral plate mesoderm, and later the visceral mesoderm,

196 e, midbrain, spinal cord, paraxial mesoderm, lateral plate mesoderm, and limb bud.

197 superfamily, which is expressed in the left lateral plate mesoderm, and loss of nodal function produ

198 entral neural tube, notochord, ectoderm, and lateral plate mesoderm, and none was detected in the neu

199 soderm, the primitive streak at the level of lateral plate mesoderm, and the base of the allantois.

200 These somites induced ectopic pronephroi in lateral plate mesoderm, and the IM that received signals

201 llinear domains of expression in the forming lateral plate mesoderm, as demonstrated by functional pe

202 Hox gene expression is reprogrammed in lateral plate mesoderm, but is unaffected in paraxial me

203 silon is an adapter protein expressed in the lateral plate mesoderm, but its in vivo cardiac function

204 of Xc-Myc, XSlug/Snail2 or XTwist within the lateral plate mesoderm, but not the neural crest, provok

205 onveyed to the node, and subsequently to the lateral plate mesoderm, by a complex cascade of epigenet

206 mesenchyme with cranial mesenchyme, but not lateral plate mesoderm, could rescue expression of the R

207 tive signals emanating from the neighbouring lateral plate mesoderm, directing the endoderm towards s

208 eriments ruled out the need for signals from lateral plate mesoderm, ectoderm, or endoderm.

209 In presumptive wing lateral plate mesoderm, ectopic Tbx18 expression leads t

210 first heart field differentiates earlier in lateral plate mesoderm, generates the linear heart tube

211 s show the requirement for Prt/Wnt2bb in the lateral plate mesoderm, in agreement with the inductive

212 The drl reporters initially delineate the lateral plate mesoderm, including heart progenitors.

213 embryos, tmem88a is expressed broadly in the lateral plate mesoderm, including the bilateral heart fi

214 absent, nodal signaling is randomized in the lateral plate mesoderm, leading to aberrant LR orientati

215 The chicken Tbx gene, Tbx18, is expressed in lateral plate mesoderm, limb, and developing somites.

216 is study, cux2, is expressed in the pre-limb lateral plate mesoderm, posterior limb bud and flank mes

217 n by altering the patterning of the anterior lateral plate mesoderm, potentially favoring formation o

218 1 disrupts asymmetric gene expression in the lateral plate mesoderm, resulting in aberrant looping of

219 that are normally expressed only in the left lateral plate mesoderm, show expression in the right and

220 n analyses show that Bmp2b, expressed in the lateral plate mesoderm, signals through Alk8 to induce e

221 In addition, we find that, in the lateral plate mesoderm, the domains of Hoxb-8 expression

222 tissues, as well as the surface ectoderm and lateral plate mesoderm, together act to pattern somitic

223 ne expression domains are established in the lateral plate mesoderm, ultimately determining the direc

224 odel with conditional deletion of WT1 in the lateral plate mesoderm, using the G2 enhancer of the Gat

225 m, and for the absence of Flk-1, a marker of lateral plate mesoderm, we derive a cell population from

226 different rostral and caudal domains of the lateral plate mesoderm, where limb induction occurs, mig

227 get genes Pitx2c, Nodal and Ebaf in the left lateral plate mesoderm, where they are required for esta

228 extra-embryonic mesoderm and intra-embryonic lateral plate mesoderm, which do not express Pax3.

229 orms the vertebral bodies and ribs, and from lateral plate mesoderm, which forms the sternum.

230 de dehydrogenase-2 (Raldh2) expressed in the lateral plate mesoderm, which generates a proximodistal

231 ular matrix degradation by SMCs derived from lateral plate mesoderm, which was confirmed using rat ao

232 Zebrafish gastrulae express agtrl1b in the lateral plate mesoderm, while apelin expression is confi

233 ty2/antivin, and Pitx2 does not occur in the lateral plate mesoderm, while in Cryptic mutants Lefty1

234 tissues from two different germ layers; the lateral plate mesoderm-derived mesenchyme and ectoderm-d

235 mutant, the position of the hindlimb bud, a lateral plate mesoderm-derived structure, is posteriorly

236 es containing cells of all five of the major lateral plate mesoderm-derived tissues (cartilage, peric

237 rmined by asymmetric Nodal signalling in the lateral plate mesoderm.

238 receded by abnormal Pitx2c expression in the lateral plate mesoderm.

239 ed with re-deployment of these mechanisms to lateral plate mesoderm.

240 derm, whereas paired appendages develop from lateral plate mesoderm.

241 ion within a subset of cells in the anterior lateral plate mesoderm.

242 expression to the appropriate region of the lateral plate mesoderm.

243 ene expression around the node and/or in the lateral plate mesoderm.

244 to specifically alter gene expression in the lateral plate mesoderm.

245 itive streak derivatives such as somites and lateral plate mesoderm.

246 establishment of southpaw expression in the lateral plate mesoderm.

247 s as well as altered Pitx2 expression in the lateral plate mesoderm.

248 mesoderm precursors and then within the left lateral plate mesoderm.

249 arkers gata1 and gata2 in the most posterior lateral plate mesoderm.

250 enes in the paraxial mesoderm but not in the lateral plate mesoderm.

251 of the right-specific gene SnR in the right lateral plate mesoderm.

252 expansion at the expense of intermediate and lateral plate mesoderm.

253 ilateral primary heart fields located in the lateral plate mesoderm.

254 heart-specific gene expression in posterior lateral plate mesoderm.

255 fty/Pitx2 expression on the left side of the lateral plate mesoderm.

256 nals derived from neural tube, notochord and lateral plate mesoderm.

257 diogenic and forelimb-forming regions of the lateral plate mesoderm.

258 asymmetrically in a large domain in the left lateral plate mesoderm.

259 e, ventral neural tube, and intermediate and lateral plate mesoderm.

260 sis of independent Hox codes in paraxial and lateral plate mesoderm.

261 naling pathway, is variably lost in the left lateral plate mesoderm.

262 dent induction of left-specific genes in the lateral plate mesoderm.

263 aintenance of high-level BMP-4 expression in lateral plate mesoderm.

264 sulting in asymmetric gene expression in the lateral plate mesoderm.

265 srupts asymmetric expression in the node and lateral plate mesoderm.

266 oderm, show expression in the right and left lateral plate mesoderm.

267 half of the Nkx2.5-expressing region in the lateral plate mesoderm.

268 ing to left-sided expression of nodal in the lateral plate mesoderm.

269 ons are derived from connective cells of the lateral plate mesoderm.

270 nd circumferentially in the intermediate and lateral plate mesoderm.

271 changes in expression of three Hox genes in lateral plate mesoderm.

272 ass of the trunk, a derivative of the dorsal lateral plate mesoderm.

273 res share an embryological origin within the lateral plate mesoderm.

274 Sonic hedgehog expression in the underlying lateral plate mesoderm.

275 ging mesoderm and, from E7.5 onwards, in the lateral plate mesoderm.

276 progenitor specification within the anterior lateral plate mesoderm.

277 oposed domain in the splanchnic layer of the lateral plate mesoderm.

278 e first to identify a repulsive role for the lateral plate mesoderm.

279 ignaling failed to be propagated to the left lateral plate mesoderm.

280 ess through the primitive streak and to form lateral plate mesoderm; and prospective mesoderm from on

281 Ectopic expression of Pitx2 in the right lateral-plate mesoderm alters looping of the heart and g

282 Expression reappears transiently in the left lateral-plate mesoderm, and in an unprecedented asymmetr

283 itx2 is asymmetrically expressed in the left lateral-plate mesoderm, and mutant mice with laterality

284 me), head paraxial mesoderm or non-paraxial (lateral plate) mesoderm tested in this assay were each a

285 ad us to propose that Tbx5a confers anterior lateral plate mesodermal cells the competence to respond

286 with later deficits in axial, paraxial, and lateral plate mesodermal derivatives.

287 ly the early mesodermal marker Brachy-T, the lateral plate mesodermal marker FLK1, and the endothelia

288 involve the directed migration of individual lateral-plate mesodermal cells into the future limb-bud-

289 rom the non-limb-forming flank region of the lateral plate of stage 9-15 chick embryos.

290 b-forming ability by discrete regions of the lateral plate of the chick embryo is dependent on a medi

291 b-forming ability by discrete regions of the lateral plate of the chick embryo is thought to depend o

292 as a second region also associated with the lateral plate phenotype.

293 f the strong association between stickleback lateral plate phenotypes and Ectodysplasin A (Eda) genot

294 on of the cryptic border between somitic and lateral plate populations reveals the dynamics of muscul

295 mits from the node to the distantly situated lateral plate remains unclear.

296 metrically in the left diencephalon and left lateral plate respectively, suggesting an additional rol

297 lance between Nodal and BMP signaling in the lateral plate that is critical for L/R axis formation.

298 the somites followed by lower levels in the lateral plate; the posterior half of the limb bud genera

299 , the node, and involves signal relay to the lateral plate, where it results in asymmetric organ morp

300 h as stage 9-15 neural tubes and stage 9- 12 lateral plates, while these transcripts are found at ver