ライフサイエンスコーパス: reproductive

1 We show that reproductive addiction of Rm to endobacteria extends to

2 and appear stable in the population, with no reproductive advantage.

3 hting block groups by the number of women of reproductive age (15-44 years).

4 Anemia in women of reproductive age (WRA) (age range: 15-49 y) remains a pu

5 dren (PSC) (age range: 6-59 mo) and women of reproductive age (WRA) (age range: 15-49 y).Cross-sectio

6 dren (PSC) (age range: 6-59 mo) and women of reproductive age (WRA) (age range: 15-49 y).Cross-sectio

7 and from 10 surveys for nonpregnant women of reproductive age (WRA) (n = 25,731) from the Biomarkers

8 Women of reproductive age and particularly pregnant women are the

9 Data on obesity status among men of reproductive age are scarce.

10 g (FP) use have been reported among women of reproductive age in union (WRAU) in Senegal.

11 Prevention of obesity in women of reproductive age is widely recognised to be important bo

12 level, Asia has seen the mCPR among women of reproductive age who are married or in a union grow from

13 dern methods of contraception among women of reproductive age who are married or in a union in the fo

14 In 2017, the mCPR among women of reproductive age who are married or in a union in the FP

15 ternal mortality rate (1.7 per 1000 women of reproductive age, 95% CI 1.3-2.1 in Ragh vs 0.2, 0.1-0.3

16 d reproductive potential among women of late reproductive age.

17 order affecting 6%-10% of all women in their reproductive age.

18 infection reported to the NNDSS; 2.1 million reproductive-aged women and 56 684 children who had HCV

19 s and Quest laboratory data regarding unique reproductive-aged women and children who were tested for

20 The vaginal microbiota of reproductive-aged women is largely made up of at least f

21 We analyzed a retrospective cohort of reproductive-aged women presenting to 5 West African ETU

22 suggest that, in Europe, the iron status of reproductive-aged women varies by region and worsens in

23 ong-individual processes contributing to the reproductive ageing patterns in three albatross species

24 , 8-month-old mice provide a useful model of reproductive ageing.

25 respiratory health often deteriorates during reproductive aging.

26 ividual life-history, morphometric, genetic, reproductive and disease data.

27 ilar groups of DEGs in the transcriptomes of reproductive and immune responses of the pistil makes it

28 ching financial losses caused by the porcine reproductive and respiratory syndrome (PRRS).

29 e dam at about 90 days of gestation, porcine reproductive and respiratory syndrome virus (PRRSV) cros

30 o infection with genotype 2 (type 2) porcine reproductive and respiratory syndrome virus (PRRSV).

31 plant-available Si, particularly during the reproductive and ripening phases.

32 of clonal offspring via seed and can provide reproductive assurance for isolated individuals.

33 Because of its inhibitory action on the reproductive axis in other vertebrates, we investigated

34 ancies per pairing was not different and the reproductive axis remained intact.

35 g lactotroph (LT) VEGFR2 expression, lifting reproductive axis repression in response to shorter day

36 In this paper, the modulation of the reproductive axis using existing agents that have such p

37 he integration of behavior with the hormonal reproductive axis.

38 use loud calls to deter challenges from non-reproductive "bachelor" males.

39 he earlier observation that post-pollination reproductive barriers develop between 5 and 10 million y

40 e not associated with weakened interspecific reproductive barriers or loss of known pistil SI factors

41 elegans, serotonin neurons that drive female reproductive behavior are directly modulated by inhibito

42 five distinct phenotypic groups by combining reproductive behavior with molecular data.

43 for maturation of the ovary and normal male reproductive behavior, but how JH distribution and activ

44 lesus) in the Baltic exhibit two contrasting reproductive behaviors: pelagic and demersal spawning.

45 penaers take on this task using an important reproductive behaviour in songbirds-dawn song.

46 e led us to hypothesize that it also confers reproductive benefits in Homo sapiens.

47 To better under its reproductive biology and to find a specific, effective,

48 An evolutionary perspective on reproductive biology could improve the efficacy of publi

49 nd demonstrate potential effects on the prey reproductive biology.

50 In this study, reproductive capacity was assessed in Japanese medaka (O

51 fixed pool causes an irreversible decline in reproductive capacity, known as the ovarian reserve, unt

52 ANT1) play a fundamental role in somatic and reproductive cell differentiation during early anther de

53 ether these neurons relay information to the reproductive circuit, we used AgRP-neuron ablation and o

54 oxymethylated and activated by TET2 for full reproductive competence.

55 r future studies aimed at understanding rare reproductive conditions.

56 suggests that the cost of inter-generational reproductive conflict between younger and older females

57 assical inclusive fitness calculations (the "reproductive conflict hypothesis" [6, 9]).

58 Our findings may inform the reproductive counseling of female AYA cancer survivors.

59 tions is differentially regulated during the reproductive cycle and by estradiol.

60 he interrogation of nearly every step in the reproductive cycle of vaccinia virus (VACV), a large DNA

61 fer between males and females and across the reproductive cycle.

62 hanges lead to tissue remodeling during each reproductive cycle.

63 he biological hypothesis proposes that human reproductive cycles are an adaptation to the seasonal (h

64 e primary environmental cue driving seasonal reproductive cycles is the change in day length (i.e., p

65 solation, health monitoring and detection of reproductive cycles, as well as monitoring physiological

66 ata to obtain estimates of the proportion of reproductive damage attributable to C. trachomatis Furth

67 t factors were identified as influencing the reproductive decision-making process in women living wit

68 ative and qualitative methods and addressing reproductive decisions in women living with HIV were inc

69 ctice when advising women with HIV in making reproductive decisions.

70 High temperatures during reproductive development are particularly detrimental to

71 dditional regulatory mechanism affecting the reproductive development in Arabidopsis that could be tr

72 ow a novel link between a TRAF-like gene and reproductive development in plants.

73 ng gene regulatory relationships during male reproductive development is essential for fundamental bi

74 In addition, the analyses indicate that reproductive development of females involves an insect-l

75 c interaction module associations with plant reproductive development, root architecture, and circadi

76 of fatty acids (FA) on sex determination and reproductive development, we examined and observed an im

77 hormone (GnIH)] in neuroendocrine control of reproductive development.

78 lopment, might also contribute to gymnosperm reproductive development.

79 ne, which encodes a GTPase central to fungal reproductive development.

80 quantitative representation variation across reproductive developmental stages.

81 the wild boar therefore probably lies on the reproductive, dietary and morphological characteristics

82 erus, and to overcome P4 resistance in human reproductive diseases, such as endometrial cancer.

83 utyl phthalate (DBP) to pregnant rats causes reproductive disorders in male offspring, resulting from

84 spectra, from craniofacial malformation and reproductive disorders to muscular dystrophy, which we s

85 duration of exposure period) contributing to reproductive disruption in fish.

86 tissues, including the kidneys, gonads, and reproductive ductal systems: the intermediate mesoderm.

87 ve births, age at first pregnancy, and total reproductive duration [time from menarche to menopause])

88 After adjusting for covariates, total reproductive duration in years was inversely associated

89 As such, PFOS-induced male reproductive dysfunction can possibly be managed through

90 ime, were found to have little potential for reproductive effects despite large variations in BOD5 an

91 o, we argue that our model mimics human male reproductive effects of smoking.

92 nsistent with POLS, individuals with greater reproductive effort changed more often between active an

93 sed adverse effects to the testis and to the reproductive endocrine system that persisted long-term.

94 a complex hormonal disorder characterized by reproductive, endocrine, and metabolic abnormalities.

95 Reproductive factors (number of live births, age at firs

96 Reproductive factors reflective of endogenous sex hormon

97 tivity, where helpers at the nest can buffer reproductive failure in harsh years.

98 rmatitis and nephropathy syndrome (PDNS) and reproductive failure.

99 vegetative changes occurred independently of reproductive fate.

100 Virgin gynes (reproductive females) produced this sex pheromone in the

101 heritable psychiatric disorders that reduce reproductive fitness is an evolutionary paradox.

102 ed L1 larvae that correlate with compromised reproductive fitness of the generation that experienced

103 , antitumor immunity, and cross-generational reproductive fitness, but its mode of action is unknown.

104 and longevity, and, at least in animals, on reproductive fitness.

105 utrient-sensing pathways in controlling both reproductive function and lifespan.

106 Mammalian reproductive function depends upon a neuroendocrine circ

107 herefore appears to cause early cessation of reproductive function, a condition that has been associa

108 ng hormone (LH) are pivotal events in female reproductive function.

109 rom two Populus species and assessing 96 non-reproductive functional traits.

110 between adiponectin levels and metabolic and reproductive functions in PCOS.

111 tabolic health but has only minor effects on reproductive functions in this PCOS-like mouse model.

112 mbiosis as a powerful system for identifying reproductive genes in Mucoromycotina.

113 did not affect transcript levels of the main reproductive genes.

114 in support of metabolism, and vegetative and reproductive growth are assessed.

115 We hypothesized that vegetative and reproductive growth of plants from ASP and SSP respond d

116 Early flowering time, a prolonged reproductive growth phase, and, thereby, increased seed

117 rmally at 22 degrees C, their vegetative and reproductive growth was severely compromised under chill

118 that cytokinin regulates various aspects of reproductive growth.

119 ed 211 women enrolled in the Environment And Reproductive Health (EARTH) prospective cohort study (20

120 , a survey designed by the WHO Department of Reproductive Health and Research was distributed to 41 c

121 We assessed progress in reproductive health services subnationally in India.

122 the Consortium on Safe Labor/Air Quality and Reproductive Health Study (United States, 2002-2008).

123 neonatal health, child health and nutrition, reproductive health, and prevention of violence against

124 f universal access and satisfying demand for reproductive health.

125 ed interaction is key to maintaining women's reproductive health.

126 iation with other disease states or impaired reproductive health.

127 um biomarkers involved in organ function and reproductive health.

128 WHR might indeed be a reliable cue to female reproductive history (with lower WHRs indicating lower n

129 mation on insecticide use, demographics, and reproductive history at enrollment in 1993-1997 and in 5

130 the effect of this genetic component on the reproductive history of 109,120 Icelanders and the conse

131 suggest that WHR is a reliable cue to female reproductive history, and we discuss our results in the

132 identify miR-7a2-regulated genes involved in reproductive hormone biosynthesis pathways and provide a

133 anding neuropsychiatric disorders related to reproductive hormones as well as illnesses with sex diff

134 gs establish a role for RFRP-3 in preserving reproductive immaturity, and challenge the view that sti

135 Male reproductive impairment might result from factors that a

136 Using reproductive information for a subset of turtles (n = 51

137 ion intensity, such as sexual dimorphism and reproductive investment.

138 (fixation index = 0.026), suggesting lack of reproductive isolation across the ocean.

139 nal variants involved in local adaptation or reproductive isolation and may therefore play an importa

140 Reproductive isolation and speciation are driven by the

141 ns is thought to be an important step toward reproductive isolation and speciation.

142 proteins, dMBD-R2 and dMBD2/3, contribute to reproductive isolation and survival behavioral strategie

143 Reproductive isolation defines species divergence and is

144 xpression, quantitative traits and intrinsic reproductive isolation in the yeast Schizosaccharomyces

145 wired neural mechanisms enforcing behavioral reproductive isolation include the interpretation of the

146 This example shows that reproductive isolation, which typically develops over hu

147 ectly documented example, from its origin to reproductive isolation.

148 to accumulation of rapid, strong interploid reproductive isolation.

149 rearrangements are strongly associated with reproductive isolation.

150 high probability of recruitment and extended reproductive life span.

151 growth rate, because it strongly influenced reproductive loss, and hence subsequent fecundity (92%),

152 The most common reproductive manipulation is cytoplasmic incompatibility

153 nts with improved cognition suggests present reproductive, maternal, neonatal, and child health progr

154 tes Foundation (collectively termed ODA+) to reproductive, maternal, newborn, and child health for 20

155 INTERPRETATION: The increase in reproductive, maternal, newborn, and child health fundin

156 child health for 2013 and complete trends in reproductive, maternal, newborn, and child health suppor

157 groups, as well as the American Society for Reproductive Medicine, Asia Pacific Society of Human Gen

158 s present different social organizations and reproductive modes, from near-random mating in protandry

159 ions by the public and other stakeholders to reproductive modification in forest plantations.

160 defined the fitness of AVR strains as their reproductive number relative to their co-circulating AVS

161 Basic reproductive number was smaller (2.1 vs 4.0) and hence v

162 Models have focused primarily on the reproductive numbers of the disease that represent the a

163 rkably, heat shock (HS)-induced RCD, but not reproductive or vascular development, was found to invol

164 We show enhanced impairment of male reproductive organ development and exacerbation of the C

165 In the other, reproductive organs develop on very short lateral branch

166 ng its possible habit of visiting gymnosperm reproductive organs for pollen feeding and/or pollinatio

167 In one, reproductive organs form apically, terminating growth of

168 riptional networks coordinate Cu delivery to reproductive organs is poorly understood.

169 tract (kidneys and ureters) or lower tract (reproductive organs) of the genitourinary (GU) system ar

170 duced microbial loads in both the midgut and reproductive organs.

171 Although the full spectrum of adverse reproductive outcomes caused by Zika virus infection is

172 rupting chemical, is associated with adverse reproductive outcomes in females.

173 targeted treatment of M. genitalium improve reproductive outcomes in women are necessary to guide pu

174 ity to infections and contribute to negative reproductive outcomes such as infertility and preterm bi

175 reat amount of variation in plant longevity, reproductive output and growth rate is fundamental to ef

176 ose a greater risk to C. dubia, with reduced reproductive output observed at concentrations within an

177 ienced by adult group members can modify the reproductive output of groups.

178 fort was positively associated with lifetime reproductive output up to a high level of annual effort.

179 ffering substantially in longevity, lifetime reproductive output, age at first reproduction and in th

180 osed offspring, and limited changes in other reproductive parameters were observed.

181 unctional analysis of nematode infective and reproductive parameters.

182 fine the complete molecular exchange between reproductive partners because parents contribute to a co

183 ins and their unique contributions to female reproductive pathologies with a focus on those mediated

184 Endometriosis, a major reproductive pathology affecting 8-10% of women is chara

185 Age-related variation in reproductive performance is ubiquitous in wild vertebrat

186 The age trajectory of reproductive performance of many iteroparous species fea

187 Reproductive performance of resident and migrant males,

188 The vegetative-to-reproductive phase change in tulip (Tulipa gesneriana) i

189 During the reproductive phase ERA promotes the establishment of the

190 formation during both the vegetative and the reproductive phase in snapdragon.

191 stress during the late vegetative and early reproductive phases of crop growth accounting for the ma

192 ns between biomarkers of ovarian reserve and reproductive potential among women of late reproductive

193 r in species with greater dispersal ability, reproductive potential, and ecological generalization.

194 e are being promoted as potential markers of reproductive potential.

195 at FGFR3 kinase activity may regulate the PV reproductive program through phosphorylation of the E2 p

196 tor, where adult workers can transition to a reproductive, queen-like state called gamergate.

197 offspring growth and possibly maturation and reproductive rate.

198 showed high courtship levels, and low early reproductive rates, group growth rates, offspring mass a

199 ocin (whose effects are confined to romantic/reproductive relationships and often do not survive cont

200 The growth and reproductive responses of ASP and SSP of A. edgeworthii

201 re Act with a "better reform", his stance on reproductive rights, and his approaches to other areas,

202 as phylogenetic distance, as well as female reproductive schedules, sexual size dimorphism, and body

203 r were found during the peak of the seagrass reproductive season (September to December), with viabil

204 s review, we discuss the connections between reproductive senescence and somatic aging and give an ov

205 y vaginal opening, larger litters, and early reproductive senescence.

206 nongonococcal urethritis in men and adverse reproductive sequelae in women-for example, cervicitis,

207 th and development of the fetus, mediated by reproductive signals acting on metabolic organs.

208 y to expectation, male bonobos have a higher reproductive skew and a stronger relationship between do

209 reproductive success and the extent of male reproductive skew should be lower in bonobos than in chi

210 We found that FIS2 and MEA have reproductive-specific expression patterns that are corre

211 in the proportion of the life spent in each reproductive state.

212 es in pheromone detection that characterizes reproductive status and colony membership.

213 ved because low WHR provided a cue to female reproductive status and health, and therefore to her rep

214 than non-reproductive workers, the shift to reproductive status rather than age differences matched

215 in olfactory sensitivity after transition to reproductive status with significant reductions in elect

216 odour of a non-relative of the same sex and reproductive status.

217 can selfishly alter arthropod sex ratios and reproductive strategies to increase the proportion of th

218 This may represent a shift in reproductive strategy from queen flights, reported in th

219 ries provide early evidence of the peracarid reproductive strategy, as seen in modern Tanaidacea, and

220 How Cu affects fertility, which reproductive structures require Cu, and which transcript

221 d by frost through damage to flower buds and reproductive structures.

222 by factors derived from both male and female reproductive structures.

223 olecular approaches, we compared variance in reproductive success (V k*) and effective population siz

224 ntenance of sexual dimorphism, (4) influence reproductive success among females of at least one speci

225 ion has previously been shown to reduce both reproductive success and survival in several avian speci

226 that the influence of male dominance rank on reproductive success and the extent of male reproductive

227 Also reproductive success differed among foraging hotspots; f

228 turn, longer migration correlates with lower reproductive success in both populations.

229 is an important determinant of the lifetime reproductive success in leopards.

230 Animals often show reduced reproductive success in urban compared to adjacent natur

231 The reduced reproductive success of G. pallida at 22.5 degrees C rel

232 Olfaction is crucial for the reproductive success of parasitoid wasps.

233 colonisation also increased growth rate and reproductive success of S. avenae on these varieties.

234 al selection, we recorded mating success and reproductive success over time, using a simultaneous her

235 Storm-petrel reproductive success showed a quadratic response to risi

236 nger relationship between dominance rank and reproductive success than chimpanzees.

237 e faithful to a specific location had higher reproductive success than non-specialists, and between y

238 oss of pregnancy-induced protection, whereas reproductive success was unaffected.

239 cess seems to negatively affect its own male reproductive success, an effect that only becomes visibl

240 of Avpr1a and Oxtr RRAMs was associated with reproductive success, but population density and the sex

241 e preferred social partners and have greater reproductive success, providing a pathway by which group

242 COL4A5 variation was associated with reproductive success, which, combined with spatiotempora

243 evolutionary value in terms of survival and reproductive success.

244 should produce drones and swarms to maximize reproductive success.

245 idelity that is more clearly associated with reproductive success.

246 ces to attract animal pollinators and ensure reproductive success.

247 to prepare the oocyte for fertilization and reproductive success.

248 immunity, transplantation, autoimmunity, and reproductive success.

249 relies upon the detection of mate calls for reproductive success.

250 Arctic foxes may affect mating behavior and reproductive success.

251 rectly impacts paternity share and therefore reproductive success.

252 t respond to the pistil and are required for reproductive success; moreover, we find that these genes

253 we investigated the role of RFRP-3 in social reproductive suppression in NMRs.

254 The reproductive system complications of genital chlamydial

255 ung genes have a preferential impact on male reproductive system function.

256 BPA may have toxic effects on the female reproductive system in humans, as it does in animal mode

257 The persistence of Zika virus in the male reproductive system poses a risk of sexual transmission.

258 for GA in the genetic regulation of the male reproductive system, we additionally show that DELLA dow

259 of the life history and its role in shaping reproductive systems has remained undocumented.

260 o the liver, the immune, endocrine, and male reproductive systems, and the developing fetus and neona

261 astrointestinal, metabolic, respiratory, and reproductive systems.

262 xtant species, with spectacular diversity in reproductive systems.

263 f children born since the origin of Assisted Reproductive Technologies (ART) exceeds 5 million.

264 remains a significant challenge for assisted reproductive technology, with implantation failure occur

265 Assisted reproductive therapies (ART) have become increasingly co

266 el system for examining how trade-offs shape reproductive timing in organisms with seasonal environme

267 ssion of mERbeta2 mRNA was detected in mouse reproductive tissues (ovary, testis, and prostate) and l

268 ested and demonstrate invasion of the insect reproductive tissues during fungal infection.

269 vents between the pollen tube and the female reproductive tissues, which are controlled by extracellu

270 and amplify genes specifically expressed in reproductive tissues.

271 ss both acute toxicity and developmental and reproductive toxicity (DART).

272 nic bacteria ascending from the lower female reproductive tract (FRT) is associated with many gynecol

273 Disruption of the epithelium in the female reproductive tract (FRT) is hypothesized to increase HIV

274 The female reproductive tract (FRT) is one of the major mucosal inv

275 hormone profile, which controls human female reproductive tract and peripheral tissue dynamics in sin

276 n mixtures are separately stored in the male reproductive tract and sequentially transferred to the f

277 talium is an underappreciated cause of human reproductive tract disease, characterized by persistent,

278 t and sequentially transferred to the female reproductive tract during spermatophore assembly.

279 sed IFN has suggested a function for IFNs in reproductive tract homeostasis and protection from infec

280 dua and placenta by ascending from the lower reproductive tract or via hematogenous transmission.

281 odeling of tenofovir (TFV) in plasma, female reproductive tract tissue, cervicovaginal lavage fluid a

282 Ascension to upper reproductive tract tissues was not detected, even among

283 was limited to hemolymphatic tissues, female reproductive tract tissues, kidney, and liver, potential

284 ese stallions, EAV is detectable only in the reproductive tract, and viral persistence occurs despite

285 means to reduce ZIKV persistence in the male reproductive tract.

286 determine its pathogenic role in the female reproductive tract.

287 responses to Chlamydia muridarum within the reproductive tract.

288 l to study RNA virus persistence in the male reproductive tract.

289 ame intersex-possessing both female and male reproductive tracts.

290 Reproductive traits in both sexes evolved sensitivity to

291 s likely diminishes sexual selection of post-reproductive traits related to sperm competition among m

292 rindividual and interpopulation variation in reproductive traits, the dominant source of variability

293 stem niche at the bract axis but, after the reproductive transition, it is antagonized by the MADS b

294 expression occurred during the vegetative-to-reproductive transition, suggesting that is most active

295 he soluble form of MerTK (myeloid-epithelial-reproductive tyrosine kinase; ie, soluble MER), a critic

296 Here, we use the reproductive value method and detailed demographic data

297 hod of estimating Ne /N, which uses Fisher's reproductive value to account for dynamic age-structure,

298 tive status and health, and therefore to her reproductive value.

299 ntiation between targets in specification of reproductive versus perianth organs in the flower.

300 lived on average five times longer than non-reproductive workers, the shift to reproductive status r