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1 or tendon arise from either neural crest or somitic mesoderm.
2 rtilage and tendon lineages arising from the somitic mesoderm.
3 rives dynamic gene expression within the pre-somitic mesoderm.
4 r role in patterning the dermomyotome of the somitic mesoderm.
5 gene expression patterns observed in the pre-somitic mesoderm.
6 is by derepressing the expression of Sox9 in somitic mesoderm.
7 repressed by such signals and accelerated by somitic mesoderm.
8 ploys SFRP2 to reduce WNT1/4 activity in the somitic mesoderm.
9 and notochord promote chondrogenesis of the somitic mesoderm.
10 ions and that this effect is mediated by the somitic mesoderm.
11 or condensation and/or epithelization of the somitic mesoderm.
12 ression was limited to the lateral plate and somitic mesoderm.
13 m formation including absence of most of the somitic mesoderm.
14 de and appears to pre-configure the emerging somitic mesoderm.
15 eganglionic projections is influenced by the somitic mesoderm.
16 nes involved in specification of ventral and somitic mesoderm.
17 quires guidance cues located in the adjacent somitic mesoderm.
18 tissues, like the neural crest (NC) and pre-somitic mesoderm.
19 mary and secondary myotubes are derived from somitic mesoderm, a presumption, which up until now, has
21 which direct translation of pattern from the somitic mesoderm and de novo cell and tissue interaction
23 ctivation and inhibition of apoptosis in the somitic mesoderm and in repression of Pax7 during neural
24 ntisense oligonucleotides that entirely lack somitic mesoderm and in somite segmentation mutants that
26 een widely separated germ layers, namely the somitic mesoderm and the endoderm, in quail embryos.
27 nstrating that Wnt-1 likely acts directly on somitic mesoderm, and not through adjacent tissues via a
28 ans; instead, their basal ends adhere to the somitic mesoderm as a coherent layer, taking on somitic
29 cked somitic subtypes, CDX2 was required for somitic mesoderm but blocked cardiac differentiation.
30 es expression of cartilage-specific genes in somitic mesoderm, but also promotes the proliferation an
31 ting of the deep neural plate and underlying somitic mesoderm, but lacking a midline, show bipolar, m
32 ral fate, then further patterned to generate somitic mesoderm by signals from the gastrula organizer.
33 orm normally in tor mutant embryos, although somitic mesoderm defects are apparent later, when cells
35 continues, and the anterior notochordal and somitic mesoderm differentiate in the pre-involution mar
37 Pax3 is a transcription factor expressed in somitic mesoderm, dorsal neural tube and pre-migratory n
38 he hatching gland, head mesoderm, notochord, somitic mesoderm, endoderm and ventral aspect of the neu
40 ere loss of sclerotomal gene expression, and somitic mesoderm from these embryos cannot activate scle
41 In order to test whether segmental plate or somitic mesoderm has the ability to migrate in a cranial
42 e the chondrocyte differentiation program in somitic mesoderm in a bone morphogenetic protein (BMP)-d
43 in spadetail mutants that have very reduced somitic mesoderm, in no tail mutants injected with spade
44 e the chondrocyte differentiation program in somitic mesoderm, indicating that DNA binding by Nkx3.2
45 vertebrates, the dorsoventral patterning of somitic mesoderm is controlled by factors expressed in a
46 al alternating rostral-caudal pattern of the somitic mesoderm is disrupted, suggesting that intersomi
48 issues from these explants, we find paraxial somitic mesoderm is nearly twice as stiff as either the
50 hesis in the embryo, particularly within the somitic mesoderm, lateral mesoderm, kidney, heart, and s
51 very of an activated form of beta-catenin to somitic mesoderm mimics the effects of Wnt-1, demonstrat
52 mechanisms for fin development originated in somitic mesoderm of early vertebrates, and that the orig
53 of molecular clocks and gradients in the pre-somitic mesoderm of numerous vertebrate species has adde
54 e axial skeleton, which develops solely from somitic mesoderm, patterning of the rib cage is complica
55 an, in turn, induce robust chondrogenesis in somitic mesoderm, provided that BMP signals are present.
56 sis as a product of morphogenesis of the pre-somitic mesoderm (PSM) and the periodicity of a molecula
58 vefronts have now been identified in the pre-somitic mesoderm (PSM), there is not yet conclusive evid
60 ntrolateral lip of wing-level somites or pre-somitic mesoderm (segmental plate), myotome development
61 flanked laterally by superficial presumptive somitic mesoderm, the anterior tip of which also appears
62 tially from the area of Hensen's node to the somitic mesoderm, the intermediate mesoderm, and then to
63 tially from the area of Hensen's node to the somitic mesoderm, the intermediate mesoderm, and then to
64 gnized by mammalian angioblasts derived from somitic mesoderm through analysis of mouse-avian chimera
67 at key to this interaction is the ability of somitic mesoderm to repress Fgf8 transcription in the pr
68 rder in axolotl is congruent between LPM and somitic mesoderm, unlike in chicken and possibly other a
69 abeled cells from the prospective notochord, somitic mesoderm, ventrolateral mesoderm, neural ectoder
70 mesoderm, but not older Cerr1-nonexpressing somitic mesoderm, was able to mimic the anterior neurali
71 The thoracic skeleton is derived from both somitic mesoderm, which forms the vertebral bodies and r