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1 ty through exfoliated regions of the pleural mesothelium.
2 r smooth muscle cells arise from the surface mesothelium.
3 in spleen morphogenesis and expressed in the mesothelium.
4 gene expression to a specific region of the mesothelium.
5 ed in a coelomic cavity and are covered by a mesothelium.
6 uscle differentiation in the developing lung mesothelium.
7 ontransformed ovarian surface epithelium and mesothelium.
8 re cells in the early allantois and never in mesothelium.
9 hages, and the visceral and parietal pleural mesothelium.
10 and posterior tissues such as mesenchyme and mesothelium.
11 anced cell-cell adhesion to the lipid-loaded mesothelium.
12 ize by attaching to and invading through the mesothelium, a single layer of mesothelial cells lining
13 The developmentally regulated competency of mesothelium and a localized inductive signal might play
14 le gene expression program in the developing mesothelium and allow appropriate cell fate decisions to
15 of allantoic mesoderm into an outer layer of mesothelium and an inner vascular network begins in the
16 that specification of allantoic endothelium, mesothelium and chorio-adhesive cells does not occur by
17 signaling molecule that is expressed in lung mesothelium and epithelium and is required for lung deve
21 VEGF-A was immunolocalized to peritoneal mesothelium and TGF-beta1 increased VEGFA mRNA (P < 0.05
22 sitional (or junction) area between the OSE, mesothelium and tubal (oviductal) epithelium, as a previ
24 senting endogenous antigen in the peritoneal mesothelium and vessels led to the local recruitment of
25 ee cases, cells derived from lineage-labeled mesothelium are found inside the lung and as smooth musc
27 fic developmental stage, a large area of the mesothelium becomes competent to express proepicardial m
28 s show that the gut is initially devoid of a mesothelium but that serosal mesothelial cells expressin
30 , the inner endoderm and the outer jacket of mesothelium, coordinately regulate the proliferation and
31 ogene-driven fast growth of tumor nodules on mesothelium covered surfaces, causing ascites, bowel obs
32 Interaction of these MCAs with peritoneal mesothelium disrupts mesothelial integrity, exposing the
33 mechanism by which neutrophils adhere to the mesothelium during their transmigration into the inflame
34 -1 in monocyte transmigration across pleural mesothelium during tuberculous inflammation was investig
35 pression remained elevated in smooth muscle, mesothelium, endothelium, and fibroblasts in regions of
36 inflammatory cells, smooth muscle cells, and mesothelium exhibited increased TGF-beta1 expression and
37 whilst the distal outer layer of presumptive mesothelium gradually acquires vascular cell adhesion mo
39 ribute to the regeneration of the peritoneal mesothelium, indicating an inherent difference between p
41 dings further support a paradigm wherein the mesothelium is a source of progenitors for mesenchymal l
42 tochemistry, we demonstrate that the serosal mesothelium is the major source of vasculogenic cells in
45 s fluid phase and subsequent adhesion to the mesothelium lining covering abdominal organs to establis
47 uring heart development, epicardial cells (a mesothelium) move to and over the heart, undergo epithel
48 ranous VCAM-1 expression was observed on the mesothelium of 13 of 14 women with ovarian cancer compar
50 ar adhesion molecule (ICAM)-1 in the pleural mesothelium of patients with active pleural tuberculosis
51 ecules and is expressed predominantly in the mesothelium of the diaphragm during embryonic developmen
52 t interfacing of the beta1-fragment with the mesothelium of the peritoneal membrane via a biomaterial
53 vivo that macrophages adhere specifically to mesothelium overlying draining lymphatics and that their
55 introducing caHIF1alpha into the epicardial mesothelium prevented EPDCs from proper migration into t
56 impaired bacterial clearance, and defective mesothelium repair, suggesting a critical role of TNF to
57 Loss of Ezh2 specifically in the developing mesothelium reveals a mesothelial cell-autonomous role f
61 blast growth factor (FGF) 9 signals from the mesothelium (the future pleura) to sub-mesothelial mesen
62 rowth factor-sensitive events in the ovarian mesothelium, the tissue source of ovarian epithelial can
63 hat PDGF receptors cooperate in the yolk sac mesothelium to direct blood vessel maturation and sugges
64 ; rather, they migrate across the peritoneal mesothelium to the lymphatics, through which they furthe
65 lopment, cells of the superficial epicardial mesothelium undergo EMT to give rise to precursor cells
67 This tissue is a simple, poorly committed mesothelium which exhibits characteristics of epithelial
68 her VEGF isoforms and/or the outer sheath of mesothelium, whose maintenance did not appear to be depe
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