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1 al alterations in the mucosa, submucosa, and serosa.
2 cable at the boundary between the amnion and serosa.
3 ve extra-embryonic membranes, the amnion and serosa.
4 nsed at the posterior pole in the absence of serosa.
5 tudinal muscles and within the submucosa and serosa.
6 mina propria (LP) and lacked the DSM and the serosa.
7           Another part forms extra-embryonic serosa.
8 istinct extraembryonic membranes, amnion and serosa.
9 cell shape transitions in the extraembryonic serosa.
10 inct extra-embryonic tissues, the amnion and serosa.
11 ce of the human and mouse lung from lumen to serosa.
12 cted to mesenchymal cells subadjacent to the serosa.
13 nterlayer junctional path, followed by PE-to-serosa active Na+ transport.
14 extraembryonic (EE) tissues - the amnion and serosa - actively rupture and withdraw in late embryogen
15  Thus, the role of zen in the interaction of serosa, amnion, and embryo may differ between species.
16 s of the beetle Tribolium are protected by a serosa, an extraembryonic epithelium that is present in
17 d Episyrphus balteatus (Syrphidae) develop a serosa and a dorsal amnion, suggesting that a dorsal amn
18 ity profile and function of BMP signaling in serosa and amnion patterning of the scuttle fly Megaseli
19  sog) by RNA interference revealed that both serosa and amnion specification of M. abdita are depende
20 ng specifies two extraembryonic tissues, the serosa and amnion, in basal-branching flies such as Mega
21  other insects two extraembryonic epithelia, serosa and amnion, line the inner eggshell and the ventr
22           Because of the esophagus's lack of serosa and its peculiar lymphatic drainage, esophageal c
23 onize not only systemic tissues but also the serosa and lamina propria region of the large intestine.
24  Medium-sized and large-sized vessels of the serosa and mesentery preferentially demonstrated histolo
25 rs of T cells and eosinophils infiltrate the serosa and mucosa of the inflamed intestines.
26 d during GS stage due to increased mucosa-to-serosa and serosa-to-mucosa flux, respectively.
27 on the bowel mesentery, located on the bowel serosa, and disease located within the adjacent pelvis p
28 primarily involves vessels of the submucosa, serosa, and mesentery, some mucosal alterations have bee
29 proteins were localized to the wasp embryo's serosa, and their expression increased following parasit
30            Moreover, the expanded amnion and serosa anlage correlates with a broader domain of Dpp si
31 f orthodenticle is sufficient to confine the serosa anlage of Episyrphus to dorsal blastoderm.
32                     Size and position of the serosa anlage vary between species, and previous work ra
33 on differentiation laterally adjacent to the serosa anlage.
34  specification that features an anterodorsal serosa anlage.
35 amnion as 'initiator' to coordinate with the serosa as 'driver' to achieve withdrawal.
36 amples were obtained by puncturing the bowel serosa at the identified ROIs and lactates were measured
37 t Tribolium castaneum, the non-proliferative serosa becomes regionalized into a solid-like dorsal reg
38 ) controls the fusion of the amnion with the serosa before dorsal closure.
39 n-regulated at the developmental stage, when serosa cells in lower Cyclorrhapha begin to expand.
40         RNAi phenotypes demonstrate that the serosa contracts autonomously.
41 ss of postgastrular zen expression abrogates serosa development but allows amnion development.
42 ons and the conserved requirement of zen for serosa development suggest that the origin of an amniose
43 e we show that during extraembryonic tissue (serosa) epiboly in the insect Tribolium castaneum, the n
44 npigmented (NPE; aqueous) and pigmented (PE; serosa) epithelial side hemichambers, respectively.
45 ced in mice by surgical abrasion of adjacent serosa followed by close apposition.
46 f u-shaped group genes are not essential for serosa formation but mediate germband retraction and dor
47 ion of zen in early Megaselia embryos allows serosa formation but perturbs amnion development.
48 criptome assays were performed with isolated serosa from Anopheles gambiae embryos.
49 how that bacteria propagate twice as fast in serosa-less eggs.
50 robial peptides in wild-type eggs but not in serosa-less eggs.
51 ra-embryonic domain into separate amnion and serosa lineages in A. gambiae correlates with novel patt
52 ereby mosquitoes contain separate amnion and serosa lineages while higher flies such as Drosophila me
53 ercalation of individual cells away from the serosa margin.
54 29 vs 632 mum; P = .013) muscularis propria, serosa (median, 245 vs 64 mum; P = .019), and muscularis
55 ermal cells, the ordered colonization of the serosa-mucosa axis by clonal descendants, and gut expans
56 t/mucosa was more densely populated than the serosa/muscularis layer, indicating preferential tempora
57 submucosa, n = 4; muscularis propria, n = 3; serosa, n = 1).
58 uring A. gambiae embryogenesis, first in the serosa of early embryos and then again during late stage
59     Benzalkonium chloride was applied to the serosa of the antrum in anaesthetized rats.
60 f cardiac pacing wires were implanted on the serosa of the stomach.
61 afluoroethylene (PTFE) ring placed under the serosa of the stomach.
62 urrence seems to correlate with a mid-dorsal serosa or amnioserosa anlage.
63 ored continuously; RBC velocity of the ileal serosa or mucosa was recorded by intravital videomicrosc
64  a redistribution of flow between mucosa and serosa, or an adjustment in the heterogeneity of perfusi
65 ion of these pathways, we compared mucosa-to-serosa permeability of small and large permeability mark
66 or 10 micro M digitonin led to an aqueous-to-serosa-positive ISC.
67                         We conclude that the serosa provides insect eggs with a full-range innate imm
68 rointestinal patterning events involving the serosa, pylorus, and villus smooth muscle.
69                                    Increased serosa-to-mucosa flux of both Na+ and Cl- characterized
70  stage due to increased mucosa-to-serosa and serosa-to-mucosa flux, respectively.
71 lude the following: mesothelial cells of the serosa transduce Hedgehog signals in fetal life; the hin
72 microcirculatory flows at jejunal mucosa and serosa were significantly higher in i-NE group at 4 and
73 lanted with 4 pairs of electrodes on gastric serosa were used in a 5-session study.