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1 erlapping subsets of trophectoderm and extra-embryonic mesoderm.
2 al decidua, the trophectoderm, and the extra-embryonic mesoderm.
3 lls ("hemangioblasts") within the Drosophila embryonic mesoderm.
4  FoxQ1, are involved in patterning the early embryonic mesoderm.
5 ems derived from two distinct populations of embryonic mesoderm.
6 , the decapentaplegic (dpp) gene, within the embryonic mesoderm.
7 riving Bmp4 expression in extraembryonic and embryonic mesoderm.
8 al system of vertebrates is derived from the embryonic mesoderm.
9 ft LPM, but is present in the head and extra-embryonic mesoderm.
10 ls, in the maintenance and patterning of the embryonic mesoderm.
11 sed in the primitive streak and newly formed embryonic mesoderm.
12   Somatic muscle is derived from a subset of embryonic mesoderm.
13 he yolk sac, and are surrounded by the extra-embryonic mesoderm.
14 rare malignancies predominantly derived from embryonic mesoderm.
15 ouse placenta and for generating signals for embryonic mesoderm and axis formation.
16 os gastrulate generating embryonic and extra-embryonic mesoderm and definitive endoderm.
17 criptome and genome-wide binding profiles in embryonic mesoderm and Drosophila cells indicate that Ub
18 enic potential is well established for extra-embryonic mesoderm and intra-embryonic lateral plate mes
19 data support a hypoblast origin of the extra-embryonic mesoderm and primitive blood in humans.
20 vironment may alter differentiation of extra-embryonic mesoderm and result in an increased number of
21  lacZ expression in transgenic mice to extra-embryonic mesoderm and subsequently to both endothelial
22 roDpp is cleaved at the S1 site alone in the embryonic mesoderm and this generates sufficient ligand
23 development, Scl is first expressed in extra-embryonic mesoderm, and is required for the generation o
24                      These cells derive from embryonic mesoderm, but how they are specified is unknow
25 ite happens: Xwnt-8 functions to pattern the embryonic mesoderm by promoting ventral and lateral meso
26        Overexpression of MBC and ELMO in the embryonic mesoderm causes defects in myoblast fusion rem
27 GF signal, medicated by PI3K, can facilitate embryonic mesoderm cell spreading on fibronectin.
28  were meandrous but directional, while extra-embryonic mesoderm cells showed little net displacement.
29 t effect of PDGF AA on aggregates of Xenopus embryonic mesoderm cells.
30 gastrulating embryos, FOXF1 marks most extra-embryonic mesoderm derivatives including the chorion, th
31 1 marks all posterior primitive streak extra-embryonic mesoderm derivatives with the remarkable excep
32  co-expressed during Drosophila melanogaster embryonic mesoderm development or neural development sco
33  are not functionally interchangeable during embryonic mesoderm development.
34                             Most of the post-embryonic mesoderm develops from a single lineage.
35 e Eomesodermin (Eomes) is required for early embryonic mesoderm differentiation in mouse, frog (Xenop
36                                        Extra-embryonic mesoderm (ExM)-composed of the earliest cells
37 ablishing that Brat plays a critical role in embryonic mesoderm formation and body patterning.
38                                              Embryonic mesoderm in C. elegans derives from a number o
39  connection between initial formation of the embryonic mesoderm in Drosophila and subsequent cell-fat
40 cification of human hematopoietic cells from embryonic mesoderm in vivo.
41           Mutant embryos form abundant extra-embryonic mesoderm, including allantois, a rudimentary h
42 RLR immunoreactivity in tissues derived from embryonic mesoderm, including the periadrenal and perine
43    The 175-bp enhancer is also active in the embryonic mesoderm, indicating that this enhancer functi
44 function because misexpression of shd in the embryonic mesoderm instead of the epidermis, the normal
45 ast to absence of anterior structures, extra-embryonic mesoderm is abundant.
46                Development of the Drosophila embryonic mesoderm is controlled through both internal a
47                         Establishment of the embryonic mesoderm is dependent on integration of multip
48                                  Very little embryonic mesoderm is produced; in contrast, extraembryo
49  mesoderm inhibited embryonic, but not extra-embryonic mesoderm migration.
50                                       In the embryonic mesoderm, Notch is involved in the process by
51 ior primitive streak, from which much of the embryonic mesoderm of the wild-type embryo is derived.
52 egion gives rise to germ cells and the extra-embryonic mesoderm of the yolk sac; the distal region ge
53 actin showed abundance of actin filaments in embryonic mesoderm only.
54                         As a consequence, no embryonic mesoderm- or endoderm-derived tissues develop,
55 esponse elements from genes expressed during embryonic mesoderm patterning and midgut morphogenesis p
56           misshapen is also expressed in the embryonic mesoderm, pole plasm and other sites of cell s
57 e head and trunk muscles arise from distinct embryonic mesoderm populations, the origins of neck musc
58              These observations suggest that embryonic mesoderm regulatory protein may mimic physiolo
59                 Patterning of the Drosophila embryonic mesoderm requires the regulation of cell type-
60           Inhibition of Smurf1 expression in embryonic mesoderm results in loss of ephrinB1-mediated
61 h during lateral inhibition processes in the embryonic mesoderm, sensory organ specification in imagi
62                             In addition, the embryonic mesoderm that is produced does not become orga
63 rsoventral patterning of the C. elegans post-embryonic mesoderm, the M lineage.
64 usters of equivalent cells in the Drosophila embryonic mesoderm, the Ras/MAPK pathway--activated by b
65 mitment and differentiation from PSC-derived embryonic mesoderm through hematopoietic specification a
66 tte (ABC) transporter Mdr49 functions in the embryonic mesoderm to facilitate the transmission of the
67                          Embryonic and extra-embryonic mesoderm transcriptomes highlighted distinct g
68 experiments, exclusively targeting the intra-embryonic mesoderm were combined with QH1 immunostaining
69 al for early migration and patterning of the embryonic mesoderm, while BREATHLESS is required for pro
70 rovide the first demonstration that in mouse embryonic mesoderm, while Dicer is dispensable for somit
71 tn2 expression was also present in posterior embryonic mesoderm, while GATA-1 and GATA-2 expression w
72 ate filaments were highly expressed in extra-embryonic mesoderm, while live imaging for F-actin showe