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1 reduced in uninfected cells to allantoin and allantoic acid [1].
2 ally, tropical legumes utilize allantoin and allantoic acid as major nodule-to-shoot nitrogen transpo
3 entrations showed higher allantoin and lower allantoic acid contents.
4                   Transport of allantoin and allantoic acid out of nodules requires the function of u
5 d GmUPS1-2 (XP_003518768) - in allantoin and allantoic acid transport out of the nodule.
6                                  Addition of allantoic acid, a purine-degradative intermediate, to ni
7  metabolites in their sap, namely allantoin, allantoic acid, hydroxymethylglutamate, and methylene gl
8 d for synthesis of the ureides allantoin and allantoic acid, the major long-distance transport forms
9 oliage resulted in accumulation of xanthine, allantoic acid, ureidoglycolate, and citrulline, but tot
10 ts of fixation are the ureides allantoin and allantoic acid, which are also the dominant long-distanc
11 mosquitoes was shown by feeding allantoin or allantoic acid, which significantly increased unlabeled
12 N]-glutamine, [(15)N]-proline, allantoin, or allantoic acid.
13 ing of allantoin (5-ureidohydantoin) to form allantoic acid.
14 trogen transport molecule in plants, to form allantoic acid.
15     Glycome analysis of these cell lines and allantoic and amniotic egg membranes provide insights in
16  growth of bunyaviruses, was elevated in the allantoic and amniotic fluid in infected fetuses.
17 d formed (ie, those forming first--yolk sac, allantoic and endocardial vessels--were the first to dis
18 stocyst and subsequently give rise to chorio-allantoic and visceral yolk sac placentae, respectively.
19 uired for both survival and proliferation of allantoic angioblasts, it was not sufficient to induce a
20                                  LBP-1a(-/-) allantoic blood vessels fail to penetrate deeply and bra
21 allantoic dysmorphogenesis shortly after the allantoic bud formed.
22 all of which appear to be activated once the allantoic bud has formed.
23                                Diminution in allantoic cell number and proliferation was followed by
24                              How these three allantoic cell types are established is not known, altho
25 ned histologically for contribution of donor allantoic cells to the conceptus.
26 distally from the base; however, basal donor allantoic cells translocated typically only as far as th
27 e epiblast or through segregation within the allantoic core domain (ACD) through reduction of cell ad
28 idence, contains a pool of cells, called the Allantoic Core Domain (ACD), critical for allantoic elon
29  microsurgical perturbation of the wild-type allantoic core phenocopied the T(C)/T(C) vascularization
30 gs reveal that T is required to maintain the allantoic core, which is essential for allantoic elongat
31 d in the 6.5- to 9.5-day mouse embryo and in allantoic culture by analysis of spatial and temporal ex
32 ated cell proliferation in Flk-1(+) cells in allantoic cultures is decreased by pharmacological inhib
33 years since this discovery, the role of T in allantoic development has remained obscure.
34 as a new tool for shedding light not only on allantoic development, but for elucidating universal mec
35 ology, we have investigated the role of T in allantoic development.
36 idate cell and growth factor requirements in allantoic development.
37 ailed) (T(C)) mutation (T(C)/T(C)) exhibited allantoic dysmorphogenesis shortly after the allantoic b
38 n the allantoic core, which is essential for allantoic elongation and vascular patterning.
39 he Allantoic Core Domain (ACD), critical for allantoic elongation to the chorion.
40 y varying growth media demonstrated that the allantoic endothelial cell lineage, like that of other e
41 ervations, we conclude that specification of allantoic endothelium, mesothelium and chorio-adhesive c
42 e basis of these findings, we propose murine allantoic explants as a new tool for shedding light not
43                              Manipulation of allantoic explants by varying growth media demonstrated
44  preparations from cell culture supernatant, allantoic fluid and fecal matter.
45 er levels of VP1 protein in DF1 cells and in allantoic fluid of embryonated chicken eggs than did the
46 ciently isolating influenza virions from egg allantoic fluid with high purity.
47 pregnant ewes, cotyledonary chorioallantois, allantoic fluid, and caruncular endometrium contained hi
48  antigens in primary liquid standards, crude allantoic fluid, purified virus samples, and final vacci
49 pleen, intestine, and cloacal swabs, but not allantoic fluid, serum, or tracheal swabs The accuracy o
50 entome, ovary, and amniotic fluid but not in allantoic fluids harvested from CWD-infected Reeves' mun
51 y of ANUP was further confirmed in a chicken allantoic membrane (CAM) assay in which vascular endothe
52 ood vessels was tested in the chicken chorio-allantoic membrane (CAM).
53 he ENaC-alpha subunit is present in both the allantoic membrane and the trophoblast.
54 actor-enriched matrigel-plug assay and chick allantoic membrane assays to show that IGFBP-3 has poten
55  receptors, which are typical of chicken egg allantoic membrane.
56 isceral endoderm cells that migrate into the allantoic mesoderm before embryonic day 10.0.
57 resses formation of chorio-adhesive cells in allantoic mesoderm closest to it.
58 al analysis revealed that differentiation of allantoic mesoderm into an outer layer of mesothelium an
59 l-to-proximal gradient in differentiation of allantoic mesoderm into the endothelial cell lineage.
60        We demonstrate expression of Ptch1 in allantoic mesoderm of the placenta from wild-type mid-ge
61 d here suggest a model of differentiation of allantoic mesoderm that invokes intrinsic and extrinsic
62 lated with impaired Vegf-C expression in the allantoic mesoderm, suggesting that CYR61-regulated expr
63  the interface of chorionic trophoblasts and allantoic mesoderm.
64 t travels through it and is transformed into allantoic mesoderm.
65                  Moreover, no cells of donor allantoic origin were found in the fetus or yolk sac.
66 ine whether such erythroid cells could be of allantoic origin, host allantoises were made chimeric wi
67  (BMP4) did not contribute to restoration of allantoic outgrowth and differentiation during allantoic
68 LPP3 is essential to formation of the chorio-allantoic placenta and extra-embryonic vasculature.
69 yos deficient for LPP3 fail to form a chorio-allantoic placenta and yolk sac vasculature.
70                                   The chorio-allantoic placenta forms through the fusion of the allan
71 will become the umbilical cord of the chorio-allantoic placenta.
72                Unlike other in vitro assays, allantoic primordial vascular cells are situated on the
73 lantoic outgrowth and differentiation during allantoic regeneration.
74  Sgce, however, is strongly expressed in the allantoic region on day 9.5 but becomes more widely expr
75 g endothelium, whereas the base was the only allantoic region to exhibit relative pluripotency, colon
76 er time, endothelium spreads to the proximal allantoic region, whilst the distal outer layer of presu
77 AM1 domain does not extend into the proximal allantoic region.
78 the streak, normally VCAM1-negative proximal allantoic regions acquired VCAM1.
79                                  None of the allantoic regions contributed to paraxial mesoderm when
80 antois were further borne out when the three allantoic regions were placed into the base of the allan
81  far as the host's mid-region, whereas donor allantoic tip cells typically returned to the tip, often
82 dhesion molecule (VCAM1) and mediates chorio-allantoic union.
83 o-placental blood vessels (human), or chorio-allantoic vasculature (mouse), is crucial for embryonic
84                                      Whether allantoic vasculogenesis is associated with erythropoies