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1 establishment of southpaw expression in the lateral plate mesoderm.
2 ion within a subset of cells in the anterior lateral plate mesoderm.
3 expression to the appropriate region of the lateral plate mesoderm.
4 ene expression around the node and/or in the lateral plate mesoderm.
5 to specifically alter gene expression in the lateral plate mesoderm.
6 itive streak derivatives such as somites and lateral plate mesoderm.
7 s as well as altered Pitx2 expression in the lateral plate mesoderm.
8 mesoderm precursors and then within the left lateral plate mesoderm.
9 res share an embryological origin within the lateral plate mesoderm.
10 arkers gata1 and gata2 in the most posterior lateral plate mesoderm.
11 enes in the paraxial mesoderm but not in the lateral plate mesoderm.
12 of the right-specific gene SnR in the right lateral plate mesoderm.
13 expansion at the expense of intermediate and lateral plate mesoderm.
14 ilateral primary heart fields located in the lateral plate mesoderm.
15 heart-specific gene expression in posterior lateral plate mesoderm.
16 nals derived from neural tube, notochord and lateral plate mesoderm.
17 diogenic and forelimb-forming regions of the lateral plate mesoderm.
18 asymmetrically in a large domain in the left lateral plate mesoderm.
19 e, ventral neural tube, and intermediate and lateral plate mesoderm.
20 sis of independent Hox codes in paraxial and lateral plate mesoderm.
21 naling pathway, is variably lost in the left lateral plate mesoderm.
22 dent induction of left-specific genes in the lateral plate mesoderm.
23 aintenance of high-level BMP-4 expression in lateral plate mesoderm.
24 sulting in asymmetric gene expression in the lateral plate mesoderm.
25 srupts asymmetric expression in the node and lateral plate mesoderm.
26 oderm, show expression in the right and left lateral plate mesoderm.
27 half of the Nkx2.5-expressing region in the lateral plate mesoderm.
28 ing to left-sided expression of nodal in the lateral plate mesoderm.
29 ons are derived from connective cells of the lateral plate mesoderm.
30 nd circumferentially in the intermediate and lateral plate mesoderm.
31 changes in expression of three Hox genes in lateral plate mesoderm.
32 ass of the trunk, a derivative of the dorsal lateral plate mesoderm.
33 Sonic hedgehog expression in the underlying lateral plate mesoderm.
34 progenitor specification within the anterior lateral plate mesoderm.
35 oposed domain in the splanchnic layer of the lateral plate mesoderm.
36 e first to identify a repulsive role for the lateral plate mesoderm.
37 fty/Pitx2 expression on the left side of the lateral plate mesoderm.
38 ignaling failed to be propagated to the left lateral plate mesoderm.
39 rmined by asymmetric Nodal signalling in the lateral plate mesoderm.
40 receded by abnormal Pitx2c expression in the lateral plate mesoderm.
41 ed with re-deployment of these mechanisms to lateral plate mesoderm.
42 derm, whereas paired appendages develop from lateral plate mesoderm.
43 phological boundaries between somites and in lateral plate mesoderm a wing- or non-wing-forming bound
44 vascular zones are directly generated by the lateral plate mesoderm, a critical source of Sema3E.
45 ective angioblast migration in the posterior lateral plate mesoderm, a process known to depend on vas
46 rated and propagated from the KV to the left lateral plate mesoderm, activating a transcriptional res
47 age tracing in the living embryo, are in the lateral plate mesoderm adjacent to the notochord-prechor
48 Subsequently, Nodal signaling from the left lateral plate mesoderm alleviates this repression ipsila
49 are good candidates for encoding position in lateral plate mesoderm along the body axis and thus for
50 at additional cell types within the anterior lateral plate mesoderm (ALPM) also underwent subduction,
51 1 and Cyp26c1, are expressed in the anterior lateral plate mesoderm (ALPM) and predominantly overlap
52 ring primitive neutropoiesis in the anterior lateral plate mesoderm (ALPM) but has little effect on e
53 scripts are conspicuously absent in anterior lateral plate mesoderm (ALPM), where SHF progenitors are
55 Ectopic expression of Pitx2 in the right lateral-plate mesoderm alters looping of the heart and g
57 ric midline domains and unilaterally in left lateral plate mesoderm and anterior dorsal endoderm.
58 localized to the presumptive presomitic and lateral plate mesoderm and CYP26 mRNA to the presumptive
59 eage perturbed asymmetric gene expression in lateral plate mesoderm and disrupted organ LR asymmetrie
60 to initiate molecular asymmetry in the left lateral plate mesoderm and exhibit multiple left-right p
61 regulates the developmental potential of the lateral plate mesoderm and is required cell autonomously
62 nitially specified in the dorsal part of the lateral plate mesoderm and later become incorporated int
63 riginate in distinct regions of the anterior lateral plate mesoderm and migrate to the midline where
65 to disrupt asymmetric gene expression in the lateral plate mesoderm and randomize the placement of in
66 tissues, a strong expression of RARbeta2 in lateral plate mesoderm and somites, and an anterior expr
67 ription factor expressed throughout the left lateral plate mesoderm and subsequently on the left side
68 known to be expressed asymmetrically in the lateral plate mesoderm and the brain during embryogenesi
70 proliferation of hindlimb progenitors in the lateral plate mesoderm and the expression of a common fa
73 d shift of Nodal expression in the left LPM (lateral plate mesoderm), and speculate that the higher l
74 skeleton and sternum arise from the somatic lateral plate mesoderm, and all of the muscles for both
75 The second population resides in the dorsal lateral plate mesoderm, and contains precursors of adult
76 tion to the neural groove, primitive streak, lateral plate mesoderm, and Hensen's node, while distinc
77 he nodal-related gene southpaw (spaw) in the lateral plate mesoderm, and its downstream targets pitx2
78 e of the genes specifically expressed in the lateral plate mesoderm, and later in its derivative, the
81 superfamily, which is expressed in the left lateral plate mesoderm, and loss of nodal function produ
82 entral neural tube, notochord, ectoderm, and lateral plate mesoderm, and none was detected in the neu
83 soderm, the primitive streak at the level of lateral plate mesoderm, and the base of the allantois.
84 These somites induced ectopic pronephroi in lateral plate mesoderm, and the IM that received signals
85 Expression reappears transiently in the left lateral-plate mesoderm, and in an unprecedented asymmetr
86 itx2 is asymmetrically expressed in the left lateral-plate mesoderm, and mutant mice with laterality
87 ess through the primitive streak and to form lateral plate mesoderm; and prospective mesoderm from on
89 symmetric patterns of gene expression in the lateral plate mesoderm are initiated by signals located
92 by reciprocal transplantation of somites or lateral plate mesoderm at stages prior to muscle formati
93 rafish development, cbfb is expressed in the lateral plate mesoderm at tail bud stage and in the inte
95 xperiments show that bmp2a, expressed in the lateral plate mesoderm at these stages, is essential for
98 d with gata4 and nkx2.5 not only in anterior lateral plate mesoderm but also in noncardiac mesoderm a
99 ation, the cardiac progenitors reside in the lateral plate mesoderm but maintain close contact with t
101 silon is an adapter protein expressed in the lateral plate mesoderm, but its in vivo cardiac function
102 of Xc-Myc, XSlug/Snail2 or XTwist within the lateral plate mesoderm, but not the neural crest, provok
103 ormed via repressing venous cell fate at the lateral plate mesoderm by Hh signaling during vasculogen
104 onveyed to the node, and subsequently to the lateral plate mesoderm, by a complex cascade of epigenet
105 mesenchyme with cranial mesenchyme, but not lateral plate mesoderm, could rescue expression of the R
107 mutant, the position of the hindlimb bud, a lateral plate mesoderm-derived structure, is posteriorly
108 es containing cells of all five of the major lateral plate mesoderm-derived tissues (cartilage, peric
109 tive signals emanating from the neighbouring lateral plate mesoderm, directing the endoderm towards s
110 essed in restricted bilateral domains in the lateral plate mesoderm directly adjacent to the liver-fo
111 repression of Xnr-1 expression in the right lateral plate mesoderm during closure of the neural tube
112 mmetric and topological within the fin-field lateral plate mesoderm during early fin bud initiation.
113 maintain the expression of Pitx2 in the left lateral plate mesoderm during the patterning of left-rig
119 oderm for hindbrain patterning, and rarab in lateral plate mesoderm for specification of the pectoral
120 lly in the perinodal region of the posterior lateral plate mesoderm for the establishment of laterali
121 In these fish, GFP-expressing cells in the lateral plate mesoderm form two tubes that migrate ventr
122 first heart field differentiates earlier in lateral plate mesoderm, generates the linear heart tube
123 of the fetal limb and axial skeleton, and in lateral plate mesoderm giving rise to visceral muscle.
124 developing node and at later stages in left lateral plate mesoderm has been implicated as a key regu
125 l is generated at the node and transduced to lateral plate mesoderm in a linear signal transduction c
126 oD, Myf-5, and myogenin in both paraxial and lateral plate mesoderm in the absence of inducing tissue
127 pressed in the intermediate mesoderm and the lateral plate mesoderm in the presumptive chick forelimb
128 Subsequent nodal and Pitx2 expression in the lateral plate mesoderm in these mice is randomized, indi
129 quivalent embryological origin: the anterior lateral plate mesoderm in vertebrates and the dorsal-mos
130 s show the requirement for Prt/Wnt2bb in the lateral plate mesoderm, in agreement with the inductive
132 embryos, tmem88a is expressed broadly in the lateral plate mesoderm, including the bilateral heart fi
134 sient asymmetric Nodal signaling in the left lateral plate mesoderm (L LPM) during tailbud/early somi
135 absent, nodal signaling is randomized in the lateral plate mesoderm, leading to aberrant LR orientati
136 The chicken Tbx gene, Tbx18, is expressed in lateral plate mesoderm, limb, and developing somites.
139 alities in asymmetric gene expression in the lateral plate mesoderm (LPM) and dorsal diencephalon of
140 is joined by dynamic expression in the left lateral plate mesoderm (LPM) and left dorsal endoderm.
141 mally is expressed predominantly in the left lateral plate mesoderm (LPM) and left side of the straig
142 l somatopleure, a tissue composed of somatic lateral plate mesoderm (LPM) and overlying ectoderm.
143 demonstrated loss of normal LR asymmetry in lateral plate mesoderm (LPM) antivin/lefty-1 and Pitx2 e
144 fish, asymmetric migration of the epithelial lateral plate mesoderm (LPM) displaces the gut leftward,
145 the primary heart field within the anterior lateral plate mesoderm (LPM) into a tubular heart involv
146 ulatory pathway specifically within the left lateral plate mesoderm (LPM) is critical for these event
147 os, the expression of Pitx2 gene in the left lateral plate mesoderm (LPM) is directly regulated by Xn
149 In VAD embryos nodal expression in left lateral plate mesoderm (LPM) is severely downregulated a
151 sion in the foregut endoderm and surrounding lateral plate mesoderm (lpm) prior to respiratory specif
152 These signals are then transferred to the lateral plate mesoderm (LPM) through cellular and molecu
153 the transmission of asymmetric cues from the lateral plate mesoderm (LPM) to the cardiac field but no
154 ide markers such as nodal bilaterally in the lateral plate mesoderm (LPM), indicating that loss of AC
155 restricted expression of Pitx2c in the left lateral plate mesoderm (LPM), left half of heart tube an
156 vements of the hepatic endoderm and adjacent lateral plate mesoderm (LPM), resulting in asymmetric po
157 es is thought to be derived exclusively from lateral plate mesoderm (LPM), which gives rise to a card
158 e node and Shh downstream genes in the right lateral plate mesoderm (LPM), while overexpression of ch
167 pendent regulation of Hox gene expression in lateral plate mesoderm may have been a key step in the e
170 verely downregulated or abolished within the lateral plate mesoderm of Southpaw-deficient embryos.
173 abel single or small patches of cells in the lateral plate mesoderm of the zebrafish and to track the
176 ntly in somites and unsegmented paraxial and lateral plate mesoderm overlapping atrial precursors in
177 n begins during the convergence of posterior lateral plate mesoderm (PLM), well before aorta formatio
178 le effect on erythropoiesis or the posterior lateral plate mesoderm (PLPM) expression of neutrophil m
180 Analysis of the cardiogenic potential of the lateral plate mesoderm posterior to nkx-2.5 and actR-IIa
181 is study, cux2, is expressed in the pre-limb lateral plate mesoderm, posterior limb bud and flank mes
182 n by altering the patterning of the anterior lateral plate mesoderm, potentially favoring formation o
183 ppropriate number of cardiomyocytes from the lateral plate mesoderm requires a careful balance of bot
184 r notochord in late neurulae, and finally in lateral plate mesoderm restricted to the left side of ta
185 1 disrupts asymmetric gene expression in the lateral plate mesoderm, resulting in aberrant looping of
186 s Islet1, a hindlimb-specific factor, in the lateral plate mesoderm results in a failure to induce hi
187 zyme in the gpi-biosynthetic pathway, in the lateral plate mesoderm results in normally patterned lim
188 steps of this cascade (before it reaches the lateral plate mesoderm) results in random left-right asy
189 ly identified, here we provide evidence that lateral plate mesoderm sends instructive signals to the
190 that are normally expressed only in the left lateral plate mesoderm, show expression in the right and
191 n analyses show that Bmp2b, expressed in the lateral plate mesoderm, signals through Alk8 to induce e
192 tion factor Hand2, which is expressed in the lateral plate mesoderm starting at the completion of gas
193 tion of zebrafish hrT expression in anterior lateral plate mesoderm suggest a very early role for hrT
194 tion as cardiac precursors converge from the lateral plate mesoderm territories toward the embryonic
195 me), head paraxial mesoderm or non-paraxial (lateral plate) mesoderm tested in this assay were each a
196 ail2 function in a regulatory circuit within lateral plate mesoderm that directs normal vessel format
197 on of the expression domain corresponding to lateral plate mesoderm that is part of the early heart f
198 velopment of two structures derived from the lateral plate mesoderm - the heart and the pectoral fin.
201 red during somitogenesis within the anterior lateral plate mesoderm to induce myocardial differentiat
202 ine the relative contribution of somitic and lateral plate mesoderm to the avian scapula from quail-c
203 nt development, angioblasts migrate from the lateral plate mesoderm to the midline where they form a
204 regulation of the cell fate transition from lateral plate mesoderm to the specification of cardiomyo
205 ogenitor cells (HPCs) move from the anterior lateral plate mesoderm to the ventral midline, undergoin
206 that these cells migrate from the posterior lateral plate mesoderm to their site of differentiation
207 tissues, as well as the surface ectoderm and lateral plate mesoderm, together act to pattern somitic
208 ne expression domains are established in the lateral plate mesoderm, ultimately determining the direc
209 odel with conditional deletion of WT1 in the lateral plate mesoderm, using the G2 enhancer of the Gat
210 rmerly lefty-2), nodal and Pitx2 in the left lateral plate mesoderm was absent, suggesting that Gdf1
211 onephros induction, stage 7 or earlier chick lateral plate mesoderm was cocultured with caudal stage
212 ymmetric Nodal signaling cascade in the left lateral plate mesoderm was detected, and began to be unr
213 m, and for the absence of Flk-1, a marker of lateral plate mesoderm, we derive a cell population from
214 different rostral and caudal domains of the lateral plate mesoderm, where limb induction occurs, mig
215 get genes Pitx2c, Nodal and Ebaf in the left lateral plate mesoderm, where they are required for esta
217 de dehydrogenase-2 (Raldh2) expressed in the lateral plate mesoderm, which generates a proximodistal
218 ular matrix degradation by SMCs derived from lateral plate mesoderm, which was confirmed using rat ao
219 Zebrafish gastrulae express agtrl1b in the lateral plate mesoderm, while apelin expression is confi
220 ty2/antivin, and Pitx2 does not occur in the lateral plate mesoderm, while in Cryptic mutants Lefty1
221 Snrk-1 control angioblast populations in the lateral plate mesoderm with Dusp-5 functioning downstrea
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