ライフサイエンスコーパス: allantoic

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 d for synthesis of the ureides allantoin and allantoic acid, the major long-distance transport forms

8 oliage resulted in accumulation of xanthine, allantoic acid, ureidoglycolate, and citrulline, but tot

9 ts of fixation are the ureides allantoin and allantoic acid, which are also the dominant long-distanc

10 mosquitoes was shown by feeding allantoin or allantoic acid, which significantly increased unlabeled

11 N]-glutamine, [(15)N]-proline, allantoin, or allantoic acid.

12 ing of allantoin (5-ureidohydantoin) to form allantoic acid.

13 trogen transport molecule in plants, to form allantoic acid.

14 growth of bunyaviruses, was elevated in the allantoic and amniotic fluid in infected fetuses.

15 d formed (ie, those forming first--yolk sac, allantoic and endocardial vessels--were the first to dis

16 stocyst and subsequently give rise to chorio-allantoic and visceral yolk sac placentae, respectively.

17 uired for both survival and proliferation of allantoic angioblasts, it was not sufficient to induce a

18 LBP-1a(-/-) allantoic blood vessels fail to penetrate deeply and bra

19 allantoic dysmorphogenesis shortly after the allantoic bud formed.

20 all of which appear to be activated once the allantoic bud has formed.

21 Diminution in allantoic cell number and proliferation was followed by

22 How these three allantoic cell types are established is not known, altho

23 ned histologically for contribution of donor allantoic cells to the conceptus.

24 distally from the base; however, basal donor allantoic cells translocated typically only as far as th

25 e epiblast or through segregation within the allantoic core domain (ACD) through reduction of cell ad

26 idence, contains a pool of cells, called the Allantoic Core Domain (ACD), critical for allantoic elon

27 microsurgical perturbation of the wild-type allantoic core phenocopied the T(C)/T(C) vascularization

28 gs reveal that T is required to maintain the allantoic core, which is essential for allantoic elongat

29 d in the 6.5- to 9.5-day mouse embryo and in allantoic culture by analysis of spatial and temporal ex

30 ated cell proliferation in Flk-1(+) cells in allantoic cultures is decreased by pharmacological inhib

31 years since this discovery, the role of T in allantoic development has remained obscure.

32 as a new tool for shedding light not only on allantoic development, but for elucidating universal mec

33 ology, we have investigated the role of T in allantoic development.

34 idate cell and growth factor requirements in allantoic development.

35 ailed) (T(C)) mutation (T(C)/T(C)) exhibited allantoic dysmorphogenesis shortly after the allantoic b

36 n the allantoic core, which is essential for allantoic elongation and vascular patterning.

37 he Allantoic Core Domain (ACD), critical for allantoic elongation to the chorion.

38 y varying growth media demonstrated that the allantoic endothelial cell lineage, like that of other e

39 ervations, we conclude that specification of allantoic endothelium, mesothelium and chorio-adhesive c

40 e basis of these findings, we propose murine allantoic explants as a new tool for shedding light not

41 Manipulation of allantoic explants by varying growth media demonstrated

42 preparations from cell culture supernatant, allantoic fluid and fecal matter.

43 er levels of VP1 protein in DF1 cells and in allantoic fluid of embryonated chicken eggs than did the

44 pregnant ewes, cotyledonary chorioallantois, allantoic fluid, and caruncular endometrium contained hi

45 antigens in primary liquid standards, crude allantoic fluid, purified virus samples, and final vacci

46 pleen, intestine, and cloacal swabs, but not allantoic fluid, serum, or tracheal swabs The accuracy o

47 entome, ovary, and amniotic fluid but not in allantoic fluids harvested from CWD-infected Reeves' mun

48 y of ANUP was further confirmed in a chicken allantoic membrane (CAM) assay in which vascular endothe

49 he ENaC-alpha subunit is present in both the allantoic membrane and the trophoblast.

50 actor-enriched matrigel-plug assay and chick allantoic membrane assays to show that IGFBP-3 has poten

51 receptors, which are typical of chicken egg allantoic membrane.

52 isceral endoderm cells that migrate into the allantoic mesoderm before embryonic day 10.0.

53 resses formation of chorio-adhesive cells in allantoic mesoderm closest to it.

54 al analysis revealed that differentiation of allantoic mesoderm into an outer layer of mesothelium an

55 l-to-proximal gradient in differentiation of allantoic mesoderm into the endothelial cell lineage.

56 We demonstrate expression of Ptch1 in allantoic mesoderm of the placenta from wild-type mid-ge

57 d here suggest a model of differentiation of allantoic mesoderm that invokes intrinsic and extrinsic

58 lated with impaired Vegf-C expression in the allantoic mesoderm, suggesting that CYR61-regulated expr

59 the interface of chorionic trophoblasts and allantoic mesoderm.

60 t travels through it and is transformed into allantoic mesoderm.

61 Moreover, no cells of donor allantoic origin were found in the fetus or yolk sac.

62 ine whether such erythroid cells could be of allantoic origin, host allantoises were made chimeric wi

63 (BMP4) did not contribute to restoration of allantoic outgrowth and differentiation during allantoic

64 LPP3 is essential to formation of the chorio-allantoic placenta and extra-embryonic vasculature.

65 yos deficient for LPP3 fail to form a chorio-allantoic placenta and yolk sac vasculature.

66 The chorio-allantoic placenta forms through the fusion of the allan

67 will become the umbilical cord of the chorio-allantoic placenta.

68 Unlike other in vitro assays, allantoic primordial vascular cells are situated on the

69 lantoic outgrowth and differentiation during allantoic regeneration.

70 Sgce, however, is strongly expressed in the allantoic region on day 9.5 but becomes more widely expr

71 g endothelium, whereas the base was the only allantoic region to exhibit relative pluripotency, colon

72 er time, endothelium spreads to the proximal allantoic region, whilst the distal outer layer of presu

73 AM1 domain does not extend into the proximal allantoic region.

74 the streak, normally VCAM1-negative proximal allantoic regions acquired VCAM1.

75 None of the allantoic regions contributed to paraxial mesoderm when

76 antois were further borne out when the three allantoic regions were placed into the base of the allan

77 far as the host's mid-region, whereas donor allantoic tip cells typically returned to the tip, often

78 dhesion molecule (VCAM1) and mediates chorio-allantoic union.

79 Whether allantoic vasculogenesis is associated with erythropoies