ライフサイエンスコーパス: ovarian follicle

1 triggered by luteinizing hormone (LH) in the ovarian follicle.

2 on of TAFII105 in the granulosa cells of the ovarian follicle.

3 by which a mature oocyte is released from an ovarian follicle.

4 ch changes rapidly with luteinization of the ovarian follicle.

5 e relies on the protected environment of the ovarian follicle.

6 ell-to-cell communication network within the ovarian follicle.

7 eceptors in the mural granulosa cells of the ovarian follicle.

8 al from the surrounding somatic cells in the ovarian follicle.

9 granulosa cell compartment of the mammalian ovarian follicle.

10 ractions with somatic granulosa cells of the ovarian follicle.

11 t human gene required for the maintenance of ovarian follicles.

12 genic female revealed eGFP expression in her ovarian follicles.

13 study the hormonal regulation of atresia in ovarian follicles.

14 s associated with major increases of cAMP in ovarian follicles.

15 rimordial germ cells, meiotic germ cells and ovarian follicles.

16 ween printed layers, affects the survival of ovarian follicles.

17 usive expression of R-spondin2 in oocytes of ovarian follicles.

18 d serum estrogen and higher numbers of large ovarian follicles.

19 lcyclohexene diepoxide (VCD, n=8) to deplete ovarian follicles.

20 he assembly, preservation, and maturation of ovarian follicles.

21 genes are expressed in developing mammalian ovarian follicles.

22 s, short-term in vitro activation of dormant ovarian follicles after stimulation of the PI3K-Akt path

23 between the somatic cells and oocyte of the ovarian follicle and is crucial for the regulation of me

24 quired to maintain meiotic arrest within the ovarian follicle and suggests that the follicle may keep

25 enotypes, including the overgrowth of excess ovarian follicles and anovulation.

26 N-cadherin expression was evaluated in ovarian follicles and corpora lutea utilizing immunohist

27 n (M105I mutation) causes early depletion of ovarian follicles and female subfertility.

28 ing effector Yes-associated protein (YAP) in ovarian follicles and follicle growth.

29 r the development of Drosophila melanogaster ovarian follicles and NE morphology of myonuclei.

30 and coordinate the development of mammalian ovarian follicles and that the rate of follicular develo

31 ceptors are required for the early growth of ovarian follicles and that they exert this function by p

32 The growth of oocytes within ovarian follicles and their development to mature eggs h

33 ongly expressed by granulosa cells in normal ovarian follicles, and by ovarian dysgerminomas and gran

34 els primarily in ova cytoplasm of developing ovarian follicles, and in the nucleus of spermatogonia a

35 oocyte death, early depletion of functional ovarian follicles, and secondary infertility.

36 pellucida in the functional and degenerative ovarian follicles, and the ovaries remained histological

37 In the ovarian follicle, anti-Mullerian hormone (Amh) mRNA is e

38 Cocaine-induced ovarian follicle apoptosis and adult lethality appear to

39 erial grafts for transplantation of isolated ovarian follicles as a means to preserve fertility.

40 bursa of Fabricius and comparatively low in ovarian follicles at all stages of development.

41 ties abrogated LH-induced steroidogenesis in ovarian follicles but not MA-10 cells, suggesting that L

42 and triggers the rupture of the preovulatory ovarian follicle by stimulating proteolysis and apoptosi

43 ion of luteinizing hormone (LH) on the mouse ovarian follicle causes meiotic resumption by inhibiting

44 cytokinesis failure, accumulate in Myb-null ovarian follicle cell and wing disc epithelia.

45 In the Drosophila ovarian follicle cell epithelium, apical membranes are s

46 DPP and EGF signals set the boundary for an ovarian follicle cell fate.

47 ATD, and enzymatic and manual removal of the ovarian follicle cell layers significantly increased spo

48 protein is initially expressed uniformly in ovarian follicle cell nuclei, and is subsequently downre

49 By studying Drosophila ovarian follicle cell progenitors, we identified lysine-

50 Furthermore, by measuring polyploid 16C ovarian follicle cell underreplication we estimated the

51 fly Drosophila melanogaster, where polyploid ovarian follicle cells amplify genomic regions containin

52 s of chorion (eggshell) proteins, Drosophila ovarian follicle cells amplify the chromosomal loci cont

53 f membrane skeletal components in Drosophila ovarian follicle cells and in somatic clones of mutant c

54 The fates of two small subgroups of the ovarian follicle cells appear to be linked: mutations in

55 velopmental gene amplification in Drosophila ovarian follicle cells as a model to investigate how chr

56 phological analyses of the roles of Notch in ovarian follicle cells during Drosophila oogenesis.

57 al for viability, although it is required in ovarian follicle cells for normal eggshell development.

58 lification at the chorion loci in Drosophila ovarian follicle cells is a model for the developmental

59 two clusters of chorion genes in Drosophila ovarian follicle cells is essential for rapid eggshell b

60 Gene clusters amplified in the ovarian follicle cells of Drosophila serve as powerful m

61 patterning by regulating pipe expression in ovarian follicle cells, before its previously described

62 In ovarian follicle cells, in contrast, Vps4 does not affec

63 In ovarian follicle cells, localization of Baz at the apica

64 lamenco locus, which is expressed in somatic ovarian follicle cells, suggesting a role for piRNAs bey

65 overexpression of sprouty in wing veins and ovarian follicle cells, two other tissues where EGF sign

66 Because the fusilli RNA is present in ovarian follicle cells, we propose that fusilli acts dow

67 nes all contribute to replication control in ovarian follicle cells, which become 16C polyploid and s

68 Here, we utilize the Drosophila ovarian follicle cells, which exhibit re-replication und

69 m requires the activity of the nudel gene in ovarian follicle cells, which provide dorsoventral posit

70 NA requires the action of fettucine (fet) in ovarian follicle cells.

71 recognition complex to specific sites in the ovarian follicle cells.

72 cturally modular protein that is secreted by ovarian follicle cells.

73 ically reduces chorion gene amplification in ovarian follicle cells.

74 s required for Hippo signaling in Drosophila ovarian follicle cells.

75 menco, are specifically expressed in OSS and ovarian follicle cells.

76 promote cellular growth and proliferation in ovarian follicle cells.

77 discs, as well as for gene amplification in ovarian follicle cells.

78 The mammalian ovarian follicle consists of a multilayered complex of s

79 Taken together, these results show that ovarian follicles contain membrane-associated beta-arres

80 ant BaP dose x Gclm genotype interactions on ovarian follicle counts and ovarian tumor multiplicity a

81 In the epithelium of Drosophila ovarian follicles, cytoplasm-filled intercellular bridge

82 Menopause as a result of ovarian follicle depletion is thought to contribute to h

83 e age of 40 and is associated with premature ovarian follicle depletion.

84 Activation of a limited pool of diminishing ovarian follicles determines women's reproductive lifesp

85 WNT5a is required for normal ovarian follicle development and antagonizes gonadotropi

86 beta) superfamily and is required for normal ovarian follicle development and female fertility.

87 The signals regulating ovarian follicle development and the mechanisms by which

88 many of the signaling pathways orchestrating ovarian follicle development are known, the downstream t

89 hormone receptors, known to be required for ovarian follicle development in vivo.

90 The classical view of ovarian follicle development is that it is regulated by

91 display reduced fertility due to defects in ovarian follicle development, decreased efficiency of ov

92 able, and the most marked defect is abnormal ovarian follicle development, resulting in impaired fert

93 terile and their ovaries exhibited defective ovarian follicle development.

94 processes ranging from muscle contraction to ovarian follicle development.

95 ne and that Ced-6 expression correlates with ovarian follicle development.

96 multiple functions of TAF4b during postnatal ovarian follicle development.

97 ds and is necessary for normal embryonic and ovarian follicle development.

98 tocrine/paracrine roles in the regulation of ovarian follicle development.

99 AMH is produced by ovarian follicles during their early growth stages and i

100 tissue and support continuous growth of the ovarian follicle epithelium.

101 mone/choriogonadotropin receptor (LH/CGR) in ovarian follicles exhibits desensitization of effector a

102 Ovarian follicle formation in Drosophila melanogaster re

103 enile hormone and/or serotonin in Drosophila ovarian follicle formation, but also a cocaine-sensitive

104 The severe oocyte loss observed and lack of ovarian follicle formation, together with the patterns o

105 Primordial and primary ovarian follicles from young female mice were extracted

106 ous tissues from the domestic hen, including ovarian follicle granulosa and theca layers.

107 Within the ovarian follicle, granulosa cells (GCs) surround and sup

108 (WNT) signaling pathway in the regulation of ovarian follicle growth and steroidogenesis are now esta

109 Gonadotropins induce ovarian follicle growth that is coincident with increase

110 Within the ovarian follicle, immature oocytes are surrounded and su

111 logically, lesions appear as areas devoid of ovarian follicles in all stages of development that have

112 Primordial ovarian follicles in mice form when somatic cells surrou

113 Ovarian follicles in native and transplanted ovaries wer

114 Mammalian oocytes grow within ovarian follicles in which the oocyte is coupled to surr

115 Maturation of secondary ovarian follicles into corpora lutea, which express high

116 yte and the somatic cell compartments of the ovarian follicle is highly coordinated; this coordinatio

117 The development of fetal ovarian follicles is a critical determinant of adult fem

118 mammalian ovary formation, the production of ovarian follicles is accompanied by an enormous loss of

119 Controlled maturation of ovarian follicles is necessary for fertility.

120 ablished dogma that the initial endowment of ovarian follicles is not supplemented by an appreciable

121 one/choriogonadotropin receptor (LH/CG R) in ovarian follicles is triggered by activation of ADP-ribo

122 ligand (KL), a product of granulosa cells in ovarian follicles, is a putative regulator of oocyte dev

123 m cells can be induced to differentiate into ovarian follicle-like cells (FLCs) in vitro.

124 In the preovulatory ovarian follicle, mammalian oocytes are maintained in pr

125 ion may have physiologic implications during ovarian follicle maturation given that both receptors ma

126 present pharmacological data that Drosophila ovarian follicle maturation requires COX-like activity a

127 h much has been learned about the process of ovarian follicle maturation through studies of oogenesis

128 regulation of chorion gene expression during ovarian follicle maturation.

129 ic oophorectomies, suggest that depletion of ovarian follicles might underlie the epidemiological fin

130 eroids promoted oocyte maturation in several ovarian follicle models, doing so by signaling through c

131 lso greatest on high P:C diets (1:1) whereas ovarian follicle number was greatest on P:C 3:1 associat

132 In rodents, the formation of ovarian follicles occurs after birth.

133 lly expressed between lines in the ovary and ovarian follicles of different size classes, respectivel

134 In preovulatory ovarian follicles of mice, meiotic prophase arrest in th

135 In ovarian follicles of Oncopeltus fasciatus, and of Xyloco

136 The Drosophila ovariole tip produces new ovarian follicles on a 12-hour cycle by controlling nich

137 ls is critical for the normal development of ovarian follicles, perturbations in oocyte-GC communicat

138 Thus, although the somatic compartment of ovarian follicles plays an essential role in the mainten

139 ood from germ-line stem cells to sustain the ovarian follicle pool has recently generated controversy

140 izing the role of Foxo3 as a guardian of the ovarian follicle pool in mammals and a potential determi

141 rgely results from the depletion of a finite ovarian follicle pool that is produced during embryonic

142 ritical for LH-induced steroid production in ovarian follicles, probably through matrix metalloprotei

143 oidogenesis, breast and prostate growth, and ovarian follicle recruitment, all of which are processes

144 Rupture of the ovarian follicle releases the oocyte at ovulation, a tim

145 stem cells in vitro, but generating a human ovarian follicle remains a challenge.

146 During female reproductive life, ovarian follicle reserve is reduced by maturation and at

147 one acetate (DMPA) inhibits proliferation of ovarian follicles, resulting in anovulation and a decrea

148 VCD is shown to selectively destroy small ovarian follicles, resulting in early depletion of funct

149 sts have long realized the importance of the ovarian follicle's somatic cells in nurturing oogenesis

150 /UAS transgene programming during Drosophila ovarian follicle stem cell differentiation and used them

151 og (Hh) signaling in Drosophila melanogaster ovarian follicle stem cells (FSCs) induces the activity

152 We have used Drosophila ovarian follicle stem cells (FSCs) to study how stem cel

153 an unbiased genetic screen using Drosophila ovarian follicle stem cells to probe essential functions

154 ces apoptotic death in cultured cells and in ovarian follicles, suggesting apoptosis as a mechanism o

155 osa cell gene expression required for normal ovarian follicle survival and proliferation in response

156 Interestingly, the rerouted FSH enhanced ovarian follicle survival, caused a dramatic increase in

157 In developing ovarian follicles, the regulation of cell proliferation

158 ic dorsal-ventral polarity originates in the ovarian follicle through the restriction of pipe gene ex

159 y low levels of caspase-1 mRNA expression in ovarian follicle tissues plus the inability of IL-1beta

160 e coordination of multiple events within the ovarian follicle to ensure ovulation of a fertilizable e

161 w that a microfluidic system supports murine ovarian follicles to produce the human 28-day menstrual

162 Luteinizing hormone (LH) acts on ovarian follicles to reinitiate meiosis in prophase-arre

163 (LH) acts on the somatic cells of vertebrate ovarian follicles to stimulate meiotic resumption in the

164 esponse of LH/CG R-stimulated AC activity of ovarian follicles to the preovulatory surge of LH can be

165 The majority of ovarian follicles undergo atresia, a hormonally controll

166 Ovarian follicles undergo exponential growth in response

167 r brn and weak grk or Egfr mutations produce ovarian follicles with multiple sets of nurse cell-oocyt

168 arian inflammation to the growing and mature ovarian follicles, with destruction of the ovarian funct