ライフサイエンスコーパス: coelomic

1 preventing the formation of a male-specific coelomic blood vessel and the production of steroids.

2 rom the mesonephros into the gonad to form a coelomic blood vessel.

3 cells that normally come to fill most of the coelomic cavities failed to develop.

4 n epithelial gut, and that excretory organs, coelomic cavities, and nerve cords evolved after xenacoe

5 of B cells that express CD5, are abundant in coelomic cavities, and often produce autoantibodies, has

6 , organized gonads, excretory structures and coelomic cavities.

7 Most internal organs are situated in a coelomic cavity and are covered by a mesothelium.

8 Suppression of TWIST1 function in the right coelomic cavity caused a severe disruption of the villou

9 demonstrate that homing of B1 cells into the coelomic cavity is not a requirement for generating prot

10 anting preganglionic quail hindguts into the coelomic cavity of chick embryos.

11 B1a and B1b cells are enriched in the coelomic cavity, contribute to T-cell-independent (TI) a

12 which, similar to the heart, is housed in a coelomic cavity.

13 In normal embryos, coelomic cells expressing Wt1, GATA-4, RALDH2 and RXRalp

14 However, coelomic cells lining the liver of Wt1-null embryos show

15 thelial cells migrate and reaggregate in the coelomic domain to form the major testicular artery.

16 64 glycoproteins isolated from the oocyte or coelomic egg envelopes exhibited sperm binding activity,

17 se proteins are part of the intact oocyte or coelomic egg envelopes, they are not accessible to eithe

18 ertilized oviposited eggs, not to oocytes or coelomic eggs.

19 phorectomy significantly reduced the risk of coelomic epithelial cancer (hazard ratio, 0.04; 95 perce

20 rophylactic oophorectomy reduces the risk of coelomic epithelial cancer and breast cancer in women wi

21 In XX gonads, coelomic epithelial cells also migrated into the gonad,

22 cted at the plasma membrane in proliferating coelomic epithelial cells and in the nucleus in Sertoli

23 In XY gonads, the migrating coelomic epithelial cells became Sertoli cells, as well

24 After the coelomic epithelial cells migrate into the gonad, there

25 stages, corresponding to 11.5-11.7 dpc, the coelomic epithelial cells no longer became Sertoli cells

26 stages, corresponding to 11.2-11.4 dpc, the coelomic epithelial cells of both sexes migrated into th

27 s surrounding the tube and, most externally, coelomic epithelial cells.

28 ly gonadogenesis, proliferating cells in the coelomic epithelium (CE) give rise to most of the somati

29 to Sertoli cells has its origins within the coelomic epithelium (CE) of the genital ridge, but from

30 procedure reduces the risk of cancers of the coelomic epithelium and breast in women who carry such m

31 erved in SF1-negative cells at and below the coelomic epithelium and did not give rise to Sertoli cel

32 ed to the Sertoli precursors and LHX9 to the coelomic epithelium and interstitium.

33 n was observed initially in the cells of the coelomic epithelium and occurred in two distinct stages.

34 titial/stromal compartment of the gonad: the coelomic epithelium and specialized cells along the gona

35 e endometrium and uterus also arise from the coelomic epithelium and the Mullerian ducts.

36 discontinuous, suggesting that cells in the coelomic epithelium at this stage might move inward.

37 in ovo, labelling at indifferent stages the coelomic epithelium by electroporation with a lacZ repor

38 were 3betaHSD-negative, indicating that the coelomic epithelium contributes only to non-steroidogeni

39 show that the posthepatic mesenchymal plate coelomic epithelium gives rise to a mesenchyme that popu

40 d the basement membrane layer underlying the coelomic epithelium had thickened to form the tunica alb

41 ll Mullerian duct components derive from the coelomic epithelium in both species.

42 ell as a reduction in genes expressed in the coelomic epithelium including the putative PGC chemo-att

43 duct and also the view of a tube forming by coelomic epithelium invagination along the mesonephros.

44 Taken together, our data show that the coelomic epithelium is a source of Sertoli cells as well

45 that the basement membrane barrier under the coelomic epithelium is discontinuous, suggesting that ce

46 t1 expression in cells delaminating from the coelomic epithelium is essential for the expansion of th

47 n increase in cell proliferation in the male coelomic epithelium is the earliest identified effect of

48 xpressing cells are initially present in the coelomic epithelium of both male and female urogenital r

49 ify a label-retaining cell population in the coelomic epithelium of the adult mouse ovary as candidat

50 utative somatic stem/progenitor cells of the coelomic epithelium of the mouse ovary.

51 ls from a cell population originating in the coelomic epithelium overlying the nascent gonad that als

52 elial-to-mesenchymal transition (EMT) of the coelomic epithelium specifically within the presumptive

53 that ovarian epithelial tumours arise in the coelomic epithelium that covers the ovarian surface, it

54 This ability of the coelomic epithelium to give rise to Sertoli cells was de

55 the transition of MISRII expression from the coelomic epithelium to the mesenchyme and Mullerian duct

56 test this possibility directly, cells of the coelomic epithelium were labeled using the fluorescent l

57 duct is known to form by invagination of the coelomic epithelium, but the mechanism for its elongatio

58 Vegetal plate descendents comprise the coelomic epithelium, circumesophageal muscle, basal cell

59 f the ovarian and cervical epithelium is the coelomic epithelium, the same tissue that regresses unde

60 ese cells support correct development of the coelomic epithelium, the target of PGC migration.

61 s earlier and increases predominantly in the coelomic epithelium, whereas Alk3 expression appears lat

62 pture and regenerative repair of the ovarian coelomic epithelium.

63 mal cells derived from local delamination of coelomic epithelium.

64 tubules, the mesonephric mesenchyme, or the coelomic epithelium.

65 g both (59)Fe overlay assays of MYP enriched coelomic fluid and immunoprecipitation of native iron-bo

66 Chelation experiments on R. pachyptila whole-coelomic fluid and purified hemoglobins reveal a role fo

67 human RNA-seq data to proteomic data for the coelomic fluid bathing the yolk sac.

68 The lectin was purified from the coelomic fluid by affinity chromatography on a GlcNAc-de

69 ht to be a defense mechanism against loss of coelomic fluid if the body wall is punctured, and it may

70 We conclude that AML-1 purified from coelomic fluid is encoded by AML-1b and represents a nov

71 Within minutes after coelomic fluid is removed from the body cavity, a massiv

72 Lysenin from the coelomic fluid of the earthworm Eisenia fetida belongs t

73 ns, resulting in approximately 10% increased coelomic fluid serotonin, a pharmacological effect.

74 he vascular blood, V1 and V2, and one in the coelomic fluid, C1.

75 oprecipitation of native iron-bound MYP from coelomic fluid, support this classification.

76 d micronutrients, many of which are found in coelomic fluid.

77 was examined in muscleless limbs produced by coelomic grafting of early limb buds and (2) muscle deve

78 Using rat-chick coelomic grafts, neural tube cultures, and gut explants,

79 ted from the ectoderm and sequestered to the coelomic linings during myotome extension.

80 the archenteron (which includes presumptive coelomic mesoderm as well as presumptive endoderm) from

81 dult skeleton) fail to form, indicating that coelomic mesoderm, endoderm, or both are required for in

82 n intrinsic origin of mesothelial cells to a coelomic organ and provide a novel mechanism for the gen

83 Mesothelium is the surface layer of all coelomic organs and is crucial for the generation of the

84 erved mechanism in blood vessel formation to coelomic organs, and have major implications for our und

85 fic to the heart or applies broadly to other coelomic organs.

86 s to the development of blood vessels in all coelomic organs.

87 elomocyte adhesion is mediated by amassin, a coelomic plasma protein with a relative molecular mass (

88 the major contributor to the adult, but how coelomic pouch cells (CPCs) are specified during embryog

89 A third signal, Hedgehog, is required for coelomic pouch morphogenesis and institution of laterali

90 strulation and are then enriched in the left coelomic pouch of larvae.

91 scription factors asymmetrically in the left coelomic pouch only, which launch the pathway that event

92 micromeres, and later only expressed in that coelomic pouch which gives rise to the mesoderm of the v

93 These include cells in the left coelomic pouch, which forms the adult rudiment in the em

94 those left-sided structures, called the left coelomic pouch.

95 ockdown of foxY results in a failure to form coelomic pouches and disrupts the expression of virtuall

96 the creation of two sets of fully functional coelomic pouches and imaginal rudiments, and sex determi

97 In sea urchins, the coelomic pouches are the major contributor to the adult,

98 The migration of the small micromeres to the coelomic pouches in the sea urchin embryo provides an ex

99 n of late mesodermal derivatives such as the coelomic pouches to which the small micromeres contribut

100 ar cells, randomized left-right asymmetry of coelomic pouches, and disorganized circumesophageal musc

101 on of small micromeres to the left and right coelomic pouches.

102 a division and are not incorporated into the coelomic pouches.

103 the earthworm Eisenia fetida using E. fetida coelomic proteins (EfCP) as a native repertoire and feta

104 embryos, but contribute significantly to the coelomic sacs of the larvae, from which the major tissue

105 the sea urchin embryo contribute only to the coelomic sacs, which produce major components of the adu

106 ttachment structure with a long pedicle with coelomic space.

107 surface of the gonad, are restricted to the coelomic surface of Dax1-deficient testis.

108 in the peritubular space and extend from the coelomic surface to the dorsal surface of the gonad, are

109 During the conversion from the coelomic to the vitelline envelope, the gp69/64 sperm re

110 Wnt4 in the embryonic testis did not inhibit coelomic vessel formation but vascular pattern was affec

111 enin, including formation of testis-specific coelomic vessel, appearance of androgen-producing adrena

112 e, which includes the development of a large coelomic vessel, develops coincident with expression of