ライフサイエンスコーパス: ovary

1 een modeled extensively using the Drosophila ovary.

2 ling causes episodic LH secretion and cystic ovary.

3 ncies commonly originating in the kidney and ovary.

4 identity of ovarian-supporting cells and the ovary.

5 and follicle survival within the developing ovary.

6 vasculature is not recruited into the early ovary.

7 sposons in somatic and germline cells of the ovary.

8 epithelium (TE) before metastasizing to the ovary.

9 ic cancer samples from the breast, colon and ovary.

10 in migrating border cells of the Drosophila ovary.

11 broodstock might not be ready to develop its ovary.

12 ive organs showed atrophy of both testis and ovary.

13 rx3 and Irx5 transcription in the developing ovary.

14 esterone synthesized by luteal tissue in the ovary.

15 segments, as compared with benign and normal ovaries.

16 This reaction occurs mostly in the ovaries.

17 nd FOXL2 results in masculinization of fetal ovaries.

18 ng fish species retaining embryos within the ovaries.

19 evelop into the fallopian tubes, uterus, and ovaries.

20 GLI1 was significantly higher in testis than ovaries.

21 regulates PF formation in developing hamster ovaries.

22 h occurs from anterior to posterior in fetal ovaries.

23 ism in live-cell metabolic assays in exposed ovaries.

24 ment and embryogenesis were overexpressed in ovaries.

25 in the blood, brain, heart (ducklings), and ovaries.

26 tion from both in vitro- and in vivo-exposed ovaries.

27 th in vivo exposed mice and in vitro exposed ovaries.

28 ted from E12.5, E14.5, and E16.5 mouse fetal ovaries.

29 triple mutant gonads developed as atrophied ovaries.

30 bladder wall (2.41E-03 mSv/MBq), followed by ovaries (1.15E-03 mSv/MBq) and red marrow (8.49E-04 mSv/

31 bladder wall (2.41E-03 mSv/MBq), followed by ovaries (1.15E-03 mSv/MBq) and red marrow (8.49E-04mSv/M

32 excess, ovulatory dysfunction and polycystic ovaries(1), and is often accompanied by insulin resistan

33 lencing in liver (65%), adrenal gland (37%), ovary (35%), and kidney (78%).

34 that knockdown of cofilin in Chinese hamster ovary 7WD10 cells and primary neurons significantly redu

35 vations, we studied BAF contributions in the ovary, a tissue where Emerin/Otefin function is essentia

36 ession was also confirmed in the human fetal ovary across gestation.

37 ed sexual receptivity), physiological (e.g., ovary activation, ovulation, and modulation of pheromone

38 sured by likelihood to take mating flights), ovary activation, worker retinue response (which is infl

39 The development of female moth ovaries after three consecutive night flights appears to

40 interacts with germ plasm marker Vas in the ovaries and early embryo germ granules.

41 n the same subset of germ cells in perinatal ovaries and Figla ablation dramatically disrupts KIT, NO

42 Upon mating, 20HE titer in ovaries and hemolymph are increased and act on nearby mi

43 s-oocyte complexes derived from immature pig ovaries and provides a twofold increase in the efficienc

44 g a mouse model that segregates gonadal sex (ovaries and testes) from chromosomal sex (XX and XY), we

45 ors all involved in piRNA biogenesis in both ovaries and testes.

46 67 first trimester human embryonic and fetal ovaries and testis and confirmed by qPCR and immunohisto

47 teps occurring in the trichomes covering the ovaries and the last one occurring inside the ovary tiss

48 from benign and borderline precursors at the ovary and are not extra-ovarian metastases.

49 us, although ZIKV replicates in cells of the ovary and causes acute oophoritis, there is rapid resolu

50 scriptomic data set for the adult Drosophila ovary and connected tissues.

51 because BoHV-1 replicates efficiently in the ovary and corpus luteum.

52 nt leads to accelerated aging of the somatic ovary and decreased ovarian reserve in adulthood.

53 2019) use the simple model of the Drosophila ovary and elongation of each egg chamber to explore this

54 echnique is demonstrated using excised human ovary and fallopian tube specimens imaged immediately af

55 ppression of dmrt1 establishes a bipotential ovary and initiates female fate acquisition.

56 istinct expression patterns in the embryonic ovary and interact with each other and other oocyte-spec

57 itoes, it is essential for maturation of the ovary and normal male reproductive behavior, but how JH

58 ycopersicum pollen tubes to penetrate to the ovary and produce hybrids that, otherwise, would be diff

59 between breast, colorectal, head/neck, lung, ovary and prostate cancer, and between cancers and 38 ot

60 y unanticipated complexity of the developing ovary and provide a comprehensive resource for the syste

61 tissues (brain, heart, kidney, liver, lung, ovary and spleen) by tandem mass tag (TMT) labeling foll

62 FIID complex that is highly expressed in the ovary and testis and required for mouse fertility.

63 tingly, we found that synapsin expression in ovary and testis increased during sexual maturation in c

64 (cerebrum, cerebellum, heart, kidney, liver, ovary and testis) across developmental time points from

65 aring eyes with hexagonal and square facets, ovaries, and a unique association with epibiont thecideo

66 Kenya, localized to the mosquito midgut and ovaries, and is not associated with significant reductio

67 stably colonizes the mosquito midgut, female ovaries, and male accessory glands and spreads rapidly t

68 anscript abundance of PsACS and PsACO in the ovaries, and PsACO in the pedicels was correlated with h

69 piroplasma density was higher in testes than ovaries, and was significantly higher density in live ve

70 trium, decidua of embryos, placenta, uterus, ovary, and brain of foetuses by immunohistochemistry and

71 lay promotes mitochondrial biogenesis in the ovary, and thereby plays a role in limiting the transmis

72 In transfected Chinese hamster ovary AP-1 cells, the Leu515Phe mutant protein was corre

73 mammals; however, their roles in Drosophila ovaries are largely unknown.

74 follicle stem cells (FSCs) in the Drosophila ovary are an important experimental model for the study

75 ived innervation invades the interior of the ovary around E16.5.

76 ells protected against ZIKV infection in the ovary, as higher viral burden was measured in CD8-/- and

77 t and could be prevented with removal of the ovaries at 6 weeks of age but not at 12 weeks.

78 ional, evidenced by expression in testes and ovaries at the RNA and protein level.

79 These findings identify RUNX1, with an ovary-biased expression pattern conserved across species

80 for most of the organs, the testis/body and ovary/body ratio were dramatically decreased in 4.1N(-/-

81 erogeneous group of tumours that grow in the ovary but are not necessarily of ovarian origin.

82 ession begins after sex determination in the ovary but remains absent in the fetal testis.

83 C) progeny differentiation in the Drosophila ovary by directly regulating EGFR membrane trafficking a

84 ly, and associates with cysts throughout the ovary by E12.5.

85 e, we use egg-producing structures of insect ovaries, called ovarioles, to deduce systems-level gene

86 acute phase, ZIKV productively infected the ovary causing accumulation of CD4+ and virus-specific CD

87 mbrane protein antigens in a Chinese hamster ovary cell system.

88 We expressed human CTRP6 in Chinese hamster ovary cells and investigated the binding to different pu

89 sured in P2Y(14)R-expressing Chinese hamster ovary cells by flow cytometry.

90 human receptors expressed in Chinese hamster ovary cells demonstrate that NDD-713 and -825 have nanom

91 gal (rhbeta-gal) produced in Chinese hamster ovary cells enabled direct and precise rhbeta-gal delive

92 Gal (rhBeta-Gal) produced in Chinese hamster ovary cells enabled direct and precise rhBeta-Gal delive

93 romote serotonin uptake into Chinese hamster ovary cells expressing either vesicular monoamine transp

94 Chinese hamster ovary cells expressing marmoset or human oxytocin recept

95 e human scFv library against Chinese hamster ovary cells expressing the oncogenic target epithelial c

96 dence of hERG kinetics using Chinese hamster ovary cells overexpressing hERG1a on the Nanion SyncroPa

97 single-channel recordings on Chinese hamster ovary cells overexpressing I(Ks) channels.

98 on assays using membranes of Chinese hamster ovary cells recombinantly expressing the human GPR84.

99 pression of p.T224M KCNQ1 in Chinese hamster ovary cells showed near complete loss of protein functio

100 platform, by applying it to Chinese hamster ovary cells stably expressing hERG1a.

101 e gene engineering screen in Chinese hamster ovary cells that enables production of lysosomal enzymes

102 We transfected Chinese hamster ovary cells with plasmids carrying wild type ACKR2 (ACKR

103 Conversely, transfection of Chinese hamster ovary cells with the core 2 GlcNAc transferase acting on

104 lls) and a cancer cell line (Chinese hamster ovary cells) were exposed to liquid and gas phase emissi

105 ilopodia and lamellipodia in Chinese hamster ovary cells, stimulate their motility, and enhance neuri

106 heterologously expressed in Chinese hamster ovary cells, supporting our findings in DRG neurons.

107 In Chinese hamster ovary cells, three classes of adhesion can be identified

108 g ficolin-2 and ficolin-3 in Chinese hamster ovary cells, we could detect ficolin-2/-3 heterocomplexe

109 uctions of human, mouse, and Chinese hamster ovary cells.

110 current was measured in nine Chinese hamster ovary cells.

111 esistance gene expression in Chinese Hamster Ovary cells.

112 res and human APP-expressing Chinese hamster ovary cells.

113 apsed, advanced, or metastatic cancer of the ovary, cervix, endometrium, bladder, prostate, oesophagu

114 n effort to create a "clean" Chinese hamster ovary (CHO) cell by disrupting multiple genes to elimina

115 etitive conditions (mAb in a Chinese Hamster Ovary (CHO) cell culture harvest).

116 Chinese hamster ovary (CHO) cell lines are widely used in industry for b

117 case of genetically unstable Chinese hamster ovary (CHO) cell lines with only draft genome assemblies

118 ange in mammalian cells, but Chinese hamster ovary (CHO) cells are nonpermissive for vaccinia virus (

119 Chinese hamster ovary (CHO) cells are the predominant production vehicle

120 al mouse cardiac myocytes or Chinese hamster ovary (CHO) cells expressing the mouse or human subunits

121 Single cell suspensions of Chinese hamster ovary (CHO) cells were plated on flasks and irradiated w

122 eated by stably transfecting Chinese Hamster Ovary (CHO) cells with plasmids encoding the rat angiote

123 monomeric GFP (mGFP-hDAT) in Chinese hamster ovary (CHO) cells.

124 brate B. mori and vertebrate Chinese hamster ovary (CHO) cells.

125 man heterohybridoma (HH) and Chinese hamster ovary (CHO) mAb-Ds blocked ADCC and clearance.

126 Chinese hamster ovary (CHO)- and human embryonic kidney (HEK)-derived WT

127 n WT or p.P888L SAP97 and in Chinese hamster ovary (CHO)-transfected cells.

128 RNA-seq analysis of mutant mouse ovaries collected at 11 h post-hCG unveiled numerous CBF

129 maturation in fatty acid composition in the ovary consistently resembled those of the digestive glan

130 Multiple labs have reported that mammalian ovaries contain oogonial stem cells (OSCs), which can di

131 ell lines (OVCAR3 and A2780), normal hamster ovary control cells (CHOK1) and alphavbeta3-deficient or

132 The outer lining of the ovary (cortex) has a key role in defining fertility in w

133 ncing performed over a time series on murine ovaries, coupled with several bioinformatics analyses, t

134 ort interfering RNA knockdown in mouse fetal ovary cultures, allowing investigation of Dazl function

135 Using neonatal C57/Bl6 mouse ovaries densely populated with primordial follicles, CCN

136 iCre conditional knockout (Setd1b(Gdf9) cKO) ovaries develop through all stages; however, follicular

137 of environmental low dose radiation on fish ovaries development, a high-throughput transcriptomic ap

138 requent foraging fulfils the dual purpose of ovary development and dispersal prior to nest searching.

139 may be invented for non-lethal prediction of ovary development and sex because only a small amount of

140 resent work, we developed regression between ovary development and three ribosome RNA (rRNA) indexes,

141 nstrating species-specific quantification of ovary development can be established in species with eit

142 ine, we show that innervation is specific to ovary development, is not dependent on the genetic sex o

143 nd might also play a role in D. melanogaster ovary development.

144 stomach, colon, rectum, pancreas, lung, and ovary) diagnosed between 1995 and 2014, and followed up

145 Individual neural crest cells colonize the ovary, differentiate into neurons and glia, and form a d

146 In chickens, the embryonic ovary differentiates into two distinct domains before me

147 e plasma membrane of germ line stem cells in ovaries during the early stages of oogenesis in Drosophi

148 ovarioles, the egg-producing subunits of the ovary [e.g., 1].

149 are consistent with previous reports in the ovary, early embryo, and imaginal discs.

150 s (piRNAs) silence transposons in Drosophila ovaries, ensuring female fertility.

151 e trafficking, and lipid synthesis while the ovary exhibited enrichments in extracellular matrix and

152 B locus that promote beta-catenin-responsive ovary expression.

153 ically interact with and sequester a key pro-ovary factor beta-CATENIN, which may lead to up-regulati

154 (1988) stage IIB-IV epithelial cancer of the ovary, fallopian tube, or primary peritoneum.

155 ation of cells in the hypothalamus-pituitary-ovary feedback control loop.

156 In flam(KG) mutant ovaries, flam transcripts containing the first and, part

157 In older ovaries follicle growth was associated with nuclear excl

158 t a study of expression in (i) embryos; (ii) ovaries from partially and fully engorged females; (iii)

159 les were assessed in cultures of mouse fetal ovaries from the onset of meiotic differentiation of ger

160 global gene expression profiles in perinatal ovaries from wildtype, FiglaNull, Lhx8Null and Sohlh1Nul

161 the single-cell transcriptomic landscape of ovaries from young and aged non-human primates (NHPs) an

162 dge bases, and analysis of the covariance of ovary gene expression with surface water chemistry.

163 In ovaries, gene expression of RSPO1, LIN28, FOXL2, WNT2B,

164 Dazl hypomorph ovaries had a phenotype of impaired germ cell nest break

165 The Drosophila ovary has been a model to study how coordinated stem cel

166 Single-cell analysis of the adult ovary has identified four IGS subpopulations (IGS1-IGS4)

167 The mdr1a mutant ovaries have a dramatically different transcriptomic pro

168 Quantitative analysis shows that malignant ovaries have greater tumor vessel volume, length and num

169 these transcription factors, such as newborn ovary homeobox gene (NOBOX), are candidate genes for pri

170 Unique for the ovary, hormonally regulated folliculogenesis, ovulation,

171 Small cell carcinoma of the ovary, hypercalcemic type (SCCOHT) is a rare and aggress

172 Pase subunits in small cell carcinoma of the ovary, hypercalcemic type (SCCOHT)(2-5), SMARCA4-deficie

173 g gene, underlie small cell carcinoma of the ovary, hypercalcemic type (SCCOHT).

174 e expression analysis in mature and immature ovaries identified a number of differentially expressed

175 the majority of which are maintained in the ovaries in a unique state of meiotic prophase arrest.

176 lly toxic metals from bone and muscle to the ovaries in gravid females, which may have direct deleter

177 is highly expressed in the trichomes of the ovaries in pyrethrum flowers, similar to TcJMH and other

178 quencing data from brain, heart, testis, and ovary in both stickleback and zebrafish identified suite

179 tudy, we assessed the effects of ZIKV on the ovary in nonpregnant mice.

180 iption factor RUNX1 is enriched in the fetal ovary in rainbow trout, turtle, mouse, goat, and human.

181 Side effects to the ovary include damage to the ovarian reserve, resulting i

182 al profiles for every major cell type in the ovary, including the germline stem cells and their niche

183 of fatty acids in the mantle muscle and the ovary increasing during maturation, indicating some ener

184 ipts accumulate at higher levels in flam(KG) ovaries indicating that piRNA biogenesis may occur witho

185 In the Drosophila ovary, inner germarial sheath (IGS) cells form a niche f

186 otein receptor kinase (GRK); pretreatment of ovary-intact female mice with the selective GRK2/3 inhib

187 31B interactome and compared it to the known ovary interactome.

188 llowing menopause or surgical removal of the ovaries is a widespread medical practice, yet little is

189 Sclerosing stromal tumor (SST) of the ovary is a rare type of sex cord-stromal tumor (SCST), w

190 The Drosophila ovary is a widely used model for germ cell and somatic t

191 ecessary surgery if the risk of the examined ovary is extremely low.

192 mechanism by which DRP1 is regulated in the ovary is largely unknown.

193 endothelial kidney 293-F or Chinese hamster ovary-K1 systems.

194 ythrocytes when expressed in Chinese hamster ovary-K1, but not in human endothelial kidney 293-F cell

195 uencing data from pancreas, small intestine, ovary, kidney, and heart with existing p53 chromatin imm

196 ut are lost during meiosis in the developing ovary, leading to adult female sterility.

197 e germ line nurse cells (GLKD) of Drosophila ovaries leads to activation of transposons.

198 gical tumours including those of the breast, ovary, lung, liver, gastrointestinal tract, pancreas, bo

199 tissues, we detect ERbeta protein in testis, ovary, lymphoid cells, granulosa cell tumours, and a sub

200 RAME expression is limited to the testes and ovaries, making it a highly attractive cancer target.

201 r-complete Wolbachia genomes from individual ovary metagenomes of four wild Culex pipiens mosquitoes

202 , the upper FRT (uterus, Fallopian tubes and ovaries) might be sterile in healthy individuals or cont

203 sive resource for the systematic analysis of ovary morphogenesis.

204 In Drosophila ovaries, most piRNAs originate from dual-strand clusters

205 en, DNA repair deficient cancers: breast and ovary (n = 755 samples total).

206 ich well-developed embryos were found in the ovaries of a three-spined stickleback (Gasterosteus acul

207 on in environmental water samples and in the ovaries of fruit flies.

208 process for developing functional oocytes in ovaries of many species.

209 However, the ovaries of PitERtgKO adult mice displayed a more overt c

210 he enzyme aromatase, highly expressed in the ovaries of reproductive-aged women and in the brains of

211 ZIP9 shows the highest expression in ovaries of teleosts, a tissue in which both androgen sig

212 The active ovaries of the fly produce the steroid hormone ecdysone,

213 mal tumours, and small cell carcinoma of the ovary of hypercalcaemic type.

214 me of the effects of surgical removal of the ovaries on the structure and function of brain cells in

215 rved for heart failure (0.40) and polycystic ovaries or ovarian cysts (0.27).

216 octopaminergic neurons (OPNs) and not in the ovaries or the insulin-producing cells (IPCs).

217 including whether it genuinely arises at the ovary or is metastatic disease from other organs.

218 The human ovary orchestrates sex hormone production and undergoes

219 dder, kidney, liver, lung, lymphatic system, ovaries, pancreas, stomach, uterus, cervix, and endometr

220 s of the colorectum, esophagus, liver, lung, ovary, pancreas, breast, or stomach.

221 seven cancer types, including breast, lung, ovary, pancreas, melanoma, bone, and brain tumors.

222 -catenin signals paramount for promoting the ovary pathway.

223 time mature human oocytes are stored in the ovary prior to ovulation.

224 six major types of cancer-colorectal, lung, ovary, prostate, pancreas, and melanoma-by using transcr

225 dysfunctional ovulation, classic polycystic ovaries, reduced large antral follicle health, and sever

226 CEE and outcomes among women with conserved ovaries, regardless of age.

227 cover all known cell types of the developing ovary, reveal transcriptional signatures, and identify c

228 pment and sex because only a small amount of ovary sample (<50 mg) is needed for the approach establi

229 orrelated with higher ethylene evolution and ovary senescence and pedicel abscission in fruits that w

230 Histological examination of testes and ovaries showed impaired spermatogenesis and ovarian foll

231 nscript is detectable only in the testes and ovaries, showing a strong positive signal in oocytes and

232 piRNA)-targeted reporter assay in Drosophila ovary somatic sheet (OSS) cells [1].

233 my including resection of SNs related to the ovary, SPECT/CT was performed within 24 h.

234 ree swallow using six tissues (brain, blood, ovary, spleen, liver, and muscle) collected from breedin

235 partially with FOXL2 occupancy in the fetal ovary, suggesting that RUNX1 and FOXL2 target common set

236 Transcriptomic profiling of ovaries suggests that loss of oocyte Ube2i caused defect

237 ted in women with androgen excess polycystic ovary syndrome (AE-PCOS).

238 nterval (95% CI): 1.22-1.53)) and polycystic ovary syndrome (OR = 1.51 (95% CI: 1.33-1.72)) in women,

239 loci that are associated with the polycystic ovary syndrome (PCOS) affection status by screening 731,

240 1 (TIMP)-1 ratio in patients with polycystic ovary syndrome (PCOS) and systemically healthy controls

241 iffered in women with and without polycystic ovary syndrome (PCOS) between a Caucasian and Middle Eas

242 Women with polycystic ovary syndrome (PCOS) commonly suffer from miscarriage,

243 Women with polycystic ovary syndrome (PCOS) commonly suffer from miscarriage,

244 Polycystic ovary syndrome (PCOS) has been associated with diabetes

245 Women with polycystic ovary syndrome (PCOS) have been shown to be less insulin

246 Polycystic ovary syndrome (PCOS) is a common problem among Arab wom

247 Polycystic ovary syndrome (PCOS) is a common, complex genetic disor

248 Polycystic ovary syndrome (PCOS) is a complex hormonal disorder cha

249 Polycystic ovary syndrome (PCOS) is a complex syndrome with cardiov

250 Polycystic ovary syndrome (PCOS) is a hypothalamic-pituitary-gonada

251 Polycystic ovary syndrome (PCOS) is a major reproductive disorder t

252 Polycystic ovary syndrome (PCOS) is characterized by androgen exces

253 ssociated with conditions such as polycystic ovary syndrome (PCOS).

254 insulin resistance in women with polycystic ovary syndrome (PCOS).

255 women (n = 9), and in women with polycystic ovary syndrome (PCOS; n = 6) or hypothalamic amenorrhea

256 0.007); and genetic liability to polycystic ovary syndrome and endometrioid carcinoma (OR per 50% hi

257 ginal microbiota between cases of polycystic ovary syndrome and healthy controls.

258 In patients with polycystic ovary syndrome and insulin resistance, pioglitazone-indu

259 rplasia, premature adrenarche and polycystic ovary syndrome, as well as in androgen-dependent tumours

260 ciated with spontaneous abortion, polycystic ovary syndrome, myocardial infarction and melanoma.

261 lity to 3 factors (endometriosis, polycystic ovary syndrome, type 2 diabetes) scaled to reflect a 50%

262 e-dependent cancers and diseases (polycystic ovary syndrome, uterine fibroids, endometriosis) as well

263 human MR are expressed in the brain, heart, ovary, testis, and other nonepithelial tissues, suggesti

264 was detected in mouse reproductive tissues (ovary, testis, and prostate) and lung and colon tissues

265 ia propagate much more vigorously in the fly ovary than mitochondria carrying fitness-impairing mutat

266 e anovulatory and develop cystic hemorrhagic ovaries that are thought to be due to persistently high

267 cterium strain (AS1) isolated from Anopheles ovaries that stably colonizes the mosquito midgut, femal

268 rehensive cell atlas of the adult Drosophila ovary that contains transcriptional profiles for every m

269 tion involves establishment of a bipotential ovary that undergoes sex-specific differentiation and ma

270 tion, we found that in the follicle cells of ovaries the 5'-ends of flam transcripts are usually loca

271 Similarly, in the ovary there is a lack of follicular development and lack

272 stence of germline stem cells in adult human ovaries, thereby reinforcing the dogma of a limited ovar

273 the composition of the matrisome of porcine ovaries through the cortical compartment, where quiescen

274 varies and the last one occurring inside the ovary tissues.

275 Brief (2 H) exposure of neonatal ovaries to TGFbeta1 (10 ng/ml) in vitro led to immediate

276 at steroid signalling in Drosophila from the ovaries to the gut promotes growth of the intestine spec

277 Exposure of ovaries to vinclozolin-at in vitro dosages ranging from

278 ion within the somatic follicle cells of the ovary to regulate folliculogenesis and ovulation in mamm

279 We compared the fatty acid profiles of the ovary to those of the mantle muscle (slow turnover rate

280 la oocytes are not extensively stored in the ovary under laboratory conditions like they are in the w

281 Testes and ovaries undergo sex-specific morphogenetic changes and a

282 To do this we sliced the ovaries, uniformly in two anatomical planes, enriched fo

283 RNA was detected in lymph nodes but not the ovaries, uterus, cervix, or vagina in FP isolate-infecte

284 rom 150 families with cancers of the breast, ovary, uterus, or colon, in >600 informative genotyped r

285 l and 3,915 postmenopausal women with intact ovaries/uterus from the Nurses' Health studies (Nurses'

286 l and 3,915 postmenopausal women with intact ovaries/uterus from the Nurses' Health Studies, and esti

287 cyte meiotic maturation and release from the ovary vary greatly between animal species.

288 tually antagonistic molecular signals ensure ovary versus testis differentiation with canonical Wnt/b

289 Inhibition of mTORC1 or mTORC1/2 within ovaries was achieved during chemotherapy cotreatment, co

290 Higher Spiroplasma density in testes than in ovaries was also detected by fluorescent in situ hybridi

291 ed cell death and tissue inflammation in the ovary was observed during the acute phase of infection,

292 ddress the role of Rspo1 expression in adult ovaries, we generated an Rspo1 gain-of-function mouse mo

293 While SMAD2/3 have important roles in the ovary, we do not fully understand the roles of SMAD2/3 i

294 mal findings in 11 (7.5%) women; one or both ovaries were not visualized in 41 (27.9%) women.

295 size, persistence, and separability from the ovary were most helpful for identification of nonphysiol

296 elevant hormones were largely limited to the ovary, whereas steroid binding genes were found in nearl

297 matic cells to form xenogeneic reconstituted ovaries, which are cultured under an air-liquid interfac

298 live vaccines, readily infects the fetus and ovaries, which can lead to reproductive failure.

299 upon oocyte determination in the Drosophila ovary, which necessitates active mitochondrial respirati

300 the mon1 mutant females have extremely small ovaries with complete absence of late stage egg chambers