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1 by coordinating the production of neural and mesodermal tissue.
2 t have been one of the earliest functions of mesodermal tissue.
3 ences the development of adjacent neural and mesodermal tissue.
4 sterior identity in the epiblast and induces mesodermal tissue.
5 signaling can occur without inducing ectopic mesodermal tissues.
6 trulation and is unlikely to operate through mesodermal tissues.
7 migration phase and aberrantly contribute to mesodermal tissues.
8 the axial midline, which patterns neural and mesodermal tissues.
9 it has a role in the development of specific mesodermal tissues.
10  genotypic and phenotypic characteristics of mesodermal tissues.
11 ession of an H19 reporter gene in a range of mesodermal tissues.
12 ene expression of H19 and Igf2 in a range of mesodermal tissues.
13  the development and homeostasis of multiple mesodermal tissues.
14 tion and differentiation in early Drosophila mesodermal tissues.
15 -catenin and the formation of endodermal and mesodermal tissues.
16 e segmented trunk in both the ectodermal and mesodermal tissues.
17 t the progenitor zone to integrate neural or mesodermal tissues.
18 ures with a notochord and ventral neural and mesodermal tissues.
19 lier origin of NC, independent of neural and mesodermal tissues.
20         Mutant limbs possess a broad band of mesodermal tissue along the distal periphery that is abs
21 ic downregulation of Igf2 transcripts in all mesodermal tissues and the placenta.
22  prox1 expression in adjacent endodermal and mesodermal tissues appeared unaffected by these manipula
23                                              Mesodermal tissues arise from diverse cell lineages and
24 VegT is required for the formation of 90% of mesodermal tissue, as measured by the expression of meso
25 ere, we show that coordination of neural and mesodermal tissue at the zebrafish head-trunk transition
26                         Changes in neural or mesodermal tissue configuration arising from defects in
27 ion factor Tinman (Tin) to induce all dorsal mesodermal tissue derivatives, which include dorsal soma
28 here appears to be expression of yps mRNA in mesodermal tissue during embryogenesis.
29 omologues are widely expressed in neural and mesodermal tissues during early embryogenesis.
30 differ in their abilities to activate dpp in mesodermal tissues during embryogenesis.
31 s of Xenopus Dishevelled (Xdsh) to neural or mesodermal tissues elicited different defects that were
32  is secreted extracellularly, and it induced mesodermal tissue formation in animal cap assays.
33 he axial skeleton with origins from distinct mesodermal tissues have repatterned over the course of e
34 idgestation with severe defects in posterior mesodermal tissues; heterozygous mice are viable but hav
35 perfamily member, activin, is able to induce mesodermal tissues in animal cap explants from Xenopus l
36 ole in the proper development of a subset of mesodermal tissues in C. elegans.
37 production is distributed between neural and mesodermal tissues in the dorsal isolate, and the notoch
38 d the developmental relationship between two mesodermal tissues in the Drosophila embryo, the gonadal
39 ired for the differentiation of a variety of mesodermal tissues in the Drosophila embryo, yet its lig
40 mportant role in growth control in embryonic mesodermal tissues in which it is selectively expressed.
41                           A new fate map for mesodermal tissues in Xenopus laevis predicted that the
42 ly inhibited the formation of endodermal and mesodermal tissues including micromere-derived skeletoge
43 vents leading to the development of specific mesodermal tissues, including skeletal muscle; however,
44 TACC1 and TACC2, which are also expressed in mesodermal tissues, including somites.
45 ex (Tin-C) controls the patterning of dorsal mesodermal tissues, including the dorsal vessel or heart
46  mutants exhibit expanded neural and reduced mesodermal tissues, indicating a role of Sall4 in NMP di
47                                       During mesodermal tissue induction in Drosophila, various combi
48 austion, and the latter leads to breaches of mesodermal tissue integrity.
49                     Our understanding of how mesodermal tissue is formed has been limited by the abse
50                                  Prospective mesodermal tissue is, however, induced and we present ev
51  inducing and patterning adjacent neural and mesodermal tissues is well established.
52 ral mesendoderm, which give rise to nonaxial mesodermal tissues; its expression is extinguished as ti
53 DiI labelling, we show that the neural crest-mesodermal tissue juxtaposition that later forms the cor
54                         BMP-11 induced axial mesodermal tissue (muscle and notochord) in a dose-depen
55  pathway - being robustly established within mesodermal tissue on the left side only.
56                     The results suggest that mesodermal tissues originally evolved from endoderm tiss
57 During vertebrate embryogenesis, most of the mesodermal tissue posterior to the head forms from a pro
58 n, yet their lineage relationship with other mesodermal tissues remains unclear.
59 hancers identified by eFS as being active in mesodermal tissues revealed enriched DNA binding site mo
60 e mesoderm and allocate cells into different mesodermal tissues such as body muscle or heart is commo
61 t the functions of RA in aligning neural and mesodermal tissues temporally precede the specification
62 tion, patterning and alignment of neural and mesodermal tissues that are essential for the organizati
63 lyzed the effects of embryonic expression in mesodermal tissues that include the cardioblasts of the
64 e that, in addition to patterning neural and mesodermal tissues, the notochord plays an important rol
65  vivo for expression of both H19 and Igf2 in mesodermal tissues to sequences downstream of the H19 ge
66 ing cues specify germ layer contribution and mesodermal tissue type specification of multipotent stem
67 embryonic tissue from somitic and presomitic mesodermal tissue, we identified new genes enriched in t
68 ificant levels were consistently detected in mesodermal tissues which contribute nonmyogenic cells to
69  necessary to create many different types of mesodermal tissues while causing a dramatic expansion of
70                                              Mesodermal tissue with heart forming potential (cardioge