ライフサイエンスコーパス: fertility

1 ide thought to inhibit central regulation of fertility.

2 reproductive consequences, such as impaired fertility.

3 (NELL2-ROS1-OVCH2-ADAM3) signaling and male fertility.

4 rain asserting control of pubertal onset and fertility.

5 l for pollen tube elongation, and thus plant fertility.

6 le organs at adult age, normal histology and fertility.

7 the ovary and testis and required for mouse fertility.

8 inter-individual variability in measures of fertility.

9 rophase I and a concurrent reduction in male fertility.

10 clearance, cerebrospinal fluid movement, and fertility.

11 ntial for production of spermatozoa and male fertility.

12 bles the Gransden phenotype in terms of male fertility.

13 potent cells and have conserved functions in fertility.

14 ity, and is not obligatory for oogenesis nor fertility.

15 rm cells to support spermatogenesis and thus fertility.

16 eneic SSCT resulted in attainment of natural fertility.

17 is required for long-term Anopheles gambiae fertility.

18 so disrupt or dysregulate genes important in fertility.

19 ells, and exhibit temperature-sensitive male fertility.

20 g available soil moisture and impairing soil fertility.

21 of male secondary sexual characteristics and fertility.

22 lin-28 in somatic gonadal morphogenesis and fertility.

23 ctive expression in the spermatheca restores fertility.

24 r increases sharply after females reach peak fertility.

25 ationship between AM tree abundance and soil fertility.

26 utea had no effect on ovarian morphology and fertility.

27 e.g. biomass) relationships change with soil fertility.

28 osons in Drosophila ovaries, ensuring female fertility.

29 ere required for embryogenesis, viability or fertility.

30 diol feedback to central systems controlling fertility.

31 and show that Ddx5 is indispensable for male fertility.

32 Gy, both in terms of decreased mortality and fertility.

33 t the foundation of spermatogenesis and male fertility.

34 for observation of deformity, mortality, and fertility.

35 niature stature, retarded growth and reduced fertility.

36 is essential for germ plasm maintenance and fertility.

37 y transplantation, recipients usually regain fertility.

38 of spermatozoa, which is essential for male fertility.

39 te to intermediate gains of lateral spikelet fertility.

40 out the deleterious effects of drive on male fertility.

41 greatly diminished plant growth, and reduced fertility.

42 ve relationship between EM tree AGB and soil fertility.

43 with pleiotropic effects on plant height and fertility.

44 owth defects, leading to drastically reduced fertility.

45 thought to regulate genes required for male fertility.

46 critical role in sex determination and male fertility.

47 7L in human ovarian insufficiency and sub(in)fertility.

48 s for Maf1 and RNA pol III in mammalian male fertility.

49 en parental chromosomes and is essential for fertility.

50 e follicles developed normally and supported fertility.

51 lls is critical to maintaining cell fate and fertility.

52 and ablated mice exhibited apparently normal fertility.

53 AT3 are redundantly required for full pollen fertility.

54 age and genome alterations, which can impair fertility.

55 ation, migration to urban areas, and reduced fertility.

56 ut studies have shown that they support male fertility.

57 t be maintained outside the body for optimal fertility.

58 class of small non-coding RNAs essential for fertility.

59 uality and can accurately predict male mouse fertility.

60 hotspots is critical for synapsis, and hence fertility.

61 ously developed gene drives targeting female fertility.

62 autonomous role for MAFR-1 in nematode male fertility.

63 A-mutated breast cancer interested in future fertility.

64 hens with Guinea fowl male resulted in lower fertility, 0.14% viable offspring.

65 Restorer of fertility 4 (Rf4), the major fertility restorer gene of

66 ), and being married (11.7%), and have lower fertility (5.8%) and life-cycle earnings (8.6%).

67 al nutrition (14%), paternal education (6%), fertility (6%), maternal age (3%), and wealth accumulati

68 erature stress and, being a cause of reduced fertility, a trait of increasing importance.

69 vation of flagellar function related to male fertility across kingdoms.

70 focus on the role of birth season and female fertility adjusting for additional factors that modulate

71 on index (DFI) can predict sperm quality and fertility after cryopreservation.

72 , favorable safety profiles, rapid return to fertility after removal, and few contraindications, they

73 Fertility analyses were restricted to women whose age at

74 removed 131 non-mammalian species studies on fertility and 122 studies that were on non-human mammals

75 owland floodplains, in turn influencing soil fertility and biotic productivity downstream.

76 We show that fertility and consumption behavior harbor a class of ext

77 ffective management practice to enhance soil fertility and crop production in the arid and semi-arid

78 ture and improper management may reduce soil fertility and deteriorate soil structure in Black soils

79 male germ line and a critical determinant of fertility and genetic integrity.

80 e engineered pigs exhibit normal physiology, fertility and germline transmission of the 13 genes and

81 children from the 2015-2016 Indian National Fertility and Health Survey with available data on hemog

82 sses whether asthma and/or hay fever predict fertility and impaired fecundity.

83 in-releasing hormone (GnRH) neurons controls fertility and is sculpted by sex-steroid feedback.

84 CH(4) in aquaculture, combined with the high fertility and low feed conversion ratios of finfish and

85 The repair is sufficient to support fertility and maintain health and genetic fidelity in of

86 As to control embryogenesis, stem cell fate, fertility and neurological functions in Drosophila.

87 Female fertility and offspring health are critically dependent

88 s explained by a combination of differential fertility and participation rates.

89 etylation leads to defects that disrupt male fertility and potentially early embryogenesis.

90 Despite its importance in human fertility and regenerative biology, our understanding of

91 ithin the ovarian reserve largely determines fertility and reproductive lifespan in mammals.

92 ess to contraception will hasten declines in fertility and slow population growth.

93 eir physiological roles in the regulation of fertility and stress responses.

94 This new link between falling fertility and the altered structure of the social networ

95 x ratio, the presence of own germ cells, the fertility and the phenotype of viable hybrids and the in

96 an essential role for the Tug1 locus in male fertility and uncover evidence for distinct molecular mo

97 anynana carries a high inbred load for male fertility and viability.

98 ranging from control of Golgi structure, fly fertility, and Akt signaling.

99 at multiple residues compromised viability, fertility, and DNA-damage responses.

100 pulation size and density fueled by elevated fertility, and increasing stresses due to heightened wor

101 hout trade-offs for subsequent adult growth, fertility, and life span.

102 Male development, fertility, and lifelong health are all androgen-dependen

103 for micro-sporogenesis that affected pollen fertility, and may determine the final grain number for

104 by abrupt decays in plant productivity, soil fertility, and plant cover and richness at aridity value

105 ing resulted in reduced panicle length, less fertility, and poor growth.

106 ER-1 in coordinating immunity, longevity and fertility, and reveal mechanisms that distinguish length

107 hthyosis, intellectual disability, decreased fertility, and short stature.

108 al activity led to changes in puberty onset, fertility, and stress responses, including stress and gl

109 s of cancer treatments on a patient's future fertility are a major concern affecting the quality of l

110 eveal that developmental masculinization and fertility are normal in mutant males.

111 importance of H2A.B for gene expression and fertility are unknown.

112 mates or requiring multiple mates to ensure fertility, are also likely to cause mate-finding Allee e

113 for additional factors that modulate female fertility as discussed in this comprehensive review.

114 The main outcome was change in female fertility as observed by maternal birth month and whethe

115 when coupled with the well-known decline in fertility as women age, maximizes reproductive success a

116 meric and more extensive cohesion loss limit fertility as women age.

117 novel and convenient method for non-invasive fertility assessment.

118 oped statistical models for completed cohort fertility at age 50 years (CCF50).

119 We show that all VRS genes repress fertility at carpel and awn emergence in developing late

120 rapid resolution and no long-term effects on fertility, at least in mice.

121 st birth (ALB) was >= 30 years, the age when fertility begins to decline.

122 enge for biodiversity, with reproduction and fertility being especially sensitive to heat.

123 ti-factorial mechanism underlying the female fertility - birth season relationship.

124 PubMed, we identified a set of 282 relevant fertility/birth season papers published between 1972 and

125 blood/immune system (e.g., CCDC88C) for male fertility, brain (e.g., TRIM46 and RAB6A) for milk produ

126 tellate (Su(Ste)) locus is required for male fertility, but both Su(Ste) piRNAs and their targets are

127 dies suggest that air pollution may decrease fertility, but prospective studies and examinations of w

128 While BCAs may reduce fertility by production of unbalanced gametes, a chromos

129 tigation of male pain-reliever use and human fertility carried out to date, Smarr et al. (Hum Reprod.

130 ctional study included 558 women attending a fertility center who provided one spot urine and one blo

131 roscopes that are available to virtually all fertility centers.

132 6% vs. 67.35%, p<0.0001) from five different fertility centers.

133 ntrolled trial was undertaken in 21 academic fertility centres in China.

134 Dietary supplements marketed for male fertility commonly contain folic acid and zinc based on

135 ions where sex-reversed mice had measures of fertility comparable to those in control females.

136 d pathology of multiple organs, and improved fertility compared to kl/kl mice.

137 nd social determinants of health (adolescent fertility; completion of secondary education; not in edu

138 , higher education), gonadotoxic treatments, fertility concerns, previous unsuccessful attempts to co

139 ry analyses was used to investigate the male fertility control in Medicago truncatula.

140 Fertility critically depends on the gonadotropin-releasi

141 isms of ovarian aging and female age-related fertility decline remain unclear.

142 echnology of prenatal sex determination, and fertility decline.

143 lighting the benefits of family planning and fertility decline.

144 ts causal trigger is still seen in exogenous fertility decline.

145 onments, selection gradients on survival and fertility decrease with increasing age.

146 changes are causative for the observed male fertility defect.

147 s male, and rescue the sperm utilization and fertility defects of an SP-deficient first-male.

148 ed epithelial abnormality was accompanied by fertility defects, altered uterine growth and function,

149 sgenes in pollen fully rescued ala6/7 mutant fertility defects.

150 kout of ALA6/7 was shown to result in pollen fertility defects.

151 ologues of this gene coincide with a loss of fertility, demonstrating the evolutionary conservation o

152 Soil fertility deterioration, particularly phosphorus (P) def

153 Current male fertility diagnosis tests focus on assessing the quality

154 Here, we made use of a phenotypic male fertility difference between two moss (Physcomitrella pa

155 ng the index pregnancy, including the use of fertility drugs (clomiphene [n = 33 835], gonadotropins

156 ed Mendelian ratios, but show decreased male fertility due to reduced sperm numbers and sperm motilit

157 meiotic drive are expected to suffer reduced fertility due to the loss of sperm and associated harmfu

158 o unlink it from the negative effect on male fertility during breeding.

159 suggesting that systemic factors other than fertility (e.g. diet) do not easily explain Tsimane wome

160 is elegans Fam20C orthologue, contributes to fertility, embryogenesis, and development.

161 soil types, with declining lithological soil fertility EMF-hosting trees became more dominant.

162 morphology of stained human sperm cells for fertility evaluation, but, on the other hand, staining m

163 o that makes loss of mss adaptive after self-fertility evolves.

164 The suppressed pollen had increased fertility, fewer morphological defects and partially res

165 hypothesis that lithological drivers of soil fertility filter plant resource economic strategies in w

166 uld not test for long-term hybrid viability, fertility, fitness, or hybrid breakdown.

167 However, the developmental basis of reduced fertility following early-life starvation is unknown, an

168 le, and psychosocial factors might influence fertility for men and women, although evidence is mixed,

169 e AGB showed a negative trend along the soil fertility gradient driven mostly by a negative relations

170 rsity showed a positive trend along the soil fertility gradient driven mostly by a positive relations

171 riving forest community structure along soil fertility gradients and highlight the importance of tree

172 e alleles that had a negative impact on male fertility had the most positive substitution effects on

173 This pattern implies that differential fertility has increased and will continue to increase pu

174 g RNAs (phasiRNAs) contribute to robust male fertility; however, specific functions remain undefined.

175 e nervous system, the cardiovascular system, fertility, immunity, cancer and metabolism.

176 er, adverse cardiovascular risk and negative fertility impacts impel development of alternative appro

177 ntain genome integrity and are essential for fertility in a variety of organisms.

178 n livestock, causing abortions and decreased fertility in affected cows.

179 a novel function that is essential for male fertility in B. napus through neofunctionalization that

180 Ring canals and the fusome are required for fertility in Drosophila females, but little is known abo

181 opment and required for sperm maturation and fertility in Drosophila.

182 ated with seed size, flowering time and soil fertility in dune-adapted sunflowers.

183 ulating white blood cells is associated with fertility in heifers.

184 We found that rainfall only increases fertility in higher altitude locations (New Zealand, Rom

185 both been shown to contribute to declines in fertility in men.

186 K4) is essential for spermiogenesis and male fertility in mice.

187 tional hypoxia, with implications for future fertility in next-generation offspring of high-risk preg

188 or our understanding of infant mortality and fertility in past societies(1).

189 We focus on fertility in sub-Saharan Africa and consumption in the r

190 (R = - 0.3) observed between male and female fertility in US Holsteins.

191 he ovary (cortex) has a key role in defining fertility in women as it harbors the ovarian reserve.

192 ts indicate that prokr1b is not required for fertility in zebrafish, although its loss determine chan

193 and cells work interdependently to optimize fertility, including modifying the female's physiology t

194 network typical during urbanisation, falling fertility, increased migration.

195 e General Social Survey indicate that higher-fertility individuals and their children are more conser

196 Climate and soil fertility influence seed yield, nutrient uptake, and nut

197 Soil fertility influences plant community structure, yet few

198 In the absence of EFCAB9, sperm motility and fertility is compromised, and the linear arrangement of

199 Completed cohort fertility is much more stable over time than the period

200 Globally, maternal birth season affects fertility later in life.

201 In contrast, heterozygotes had their fertility life table parameters significantly reduced on

202 Novel thermal fertility limits (TFLs) of species have been proposed al

203 tected organic matter inputs is key for soil fertility, long-term ecosystem carbon and nutrient seque

204 Elevating its levels ameliorates the fertility loss caused by infection, suggesting that TCER

205 o RNAs in plasma, are associated with female fertility, measured by pregnancy outcome.

206 e and alternative scenarios as a function of fertility, migration, and mortality rates.

207 ped novel methods for forecasting mortality, fertility, migration, and population.

208 t of this histone variant and its effects on fertility, nuclear organization, and gene expression.

209 measuring parasitism, development and adult fertility of C. cunea on T. molitor pupae of different a

210 on is an experimental method to preserve the fertility of prepubertal patients before they initiate g

211 Clothianidin is associated with an enhanced fertility of the parasitic mite Varroa destructor, as a

212 opolyploids is essential to maintain optimal fertility of the species.

213 surviving attack and the relative fecundity/fertility of the survivors, varied from a <4% positive e

214 Columbia-0 (Col-0), we partially rescued the fertility of this otherwise sterile ask1 allele in Lands

215 Among most human populations, changing mean fertility or survivorship alone requires unprecedented a

216 Of note, loss of the enhancer did not affect fertility or uterine growth responses.

217 is decrease arises primarily through reduced fertility, particularly at maternal ages corresponding t

218 Future fertility patterns are a key input to estimation of futu

219 tative fitness cues increase during the high-fertility phase of the menstrual cycle.

220 llele of exo70a2 also suppressed the hpat1/3 fertility phenotype, as did mutants of core exocyst comp

221 etic backgrounds, we observe a wide range of fertility phenotypes and ultimately demonstrate that PRD

222 d to growth, hormone levels affecting female fertility, physiological processes involved in female pr

223 nts (n = 780) that was phenotyped for tassel fertility, plants containing F187 were completely fertil

224 clinical discussions regarding the need for fertility preservation interventions in girls and young

225 acy and can improve oncological outcomes and fertility preservation of women treated surgically for c

226 g pretreatment patient counseling and use of fertility preservation services.

227 Although unmet needs include addressing fertility preservation, cardiovascular health, and survi

228 Pubertal blockade has implications for fertility preservation, transgender surgical care and ps

229 need for adjuvant chemoradiation and allows fertility preservation.

230 Conservative, fertility-preserving surgical procedures have become sta

231 VRS3 and VRS5 work through VRS1 to suppress fertility, probably by inducing VRS1 expression.

232 compared with defining it at the date of the fertility procedure (5.5/1,000 pregnancies).

233 tion estimate occurred within 14 days of the fertility procedure for 78.3% of pregnancies.

234 As of 2018, differential fertility raised the number of US adults opposed to same

235 er time than the period measure of the total fertility rate (TFR).

236 ore tissue alterations or lesions, and lower fertility rate associated with chlamydial infection.

237 000 livebirths to 23 per 1000, and the total fertility rate decreased from 5.61 to 2.11.

238 Chlamydia load, more pathology and decreased fertility rate following Chlamydia infection.

239 me per capita, years of education, and total fertility rate.

240 at it is possible for people to reduce their fertility rates and consumption demands without experien

241 Age-specific fertility rates were modelled as a function of CCF50 and

242 Based on fertility rates, number of embryos, and hydrosalpinx for

243 maternal and newborn care, and reductions in fertility/reduced interpregnancy intervals were strong c

244 oendocrine system and opens new horizons for fertility regulation.

245 Thus, repeated fertility-related communication throughout survivorship

246 underlie human infertility and research into fertility-related molecules.

247 ALE STERILITY 5 (MS5) in Brassica napus is a fertility-related new gene, which has two wild-type alle

248 vely investigate the birth season and female fertility relationship.

249 logical factors on the birth season - female fertility relationship.

250 its clinical importance for preventing male fertility remain to be determined.

251 trial heterotrophic biomass, metabolism, and fertility respectively.

252 ing F187 were completely fertile, indicating fertility restoration, and plants containing Y187 were s

253 aining Y187 were sterile, indicating lack of fertility restoration.

254 ation of tissue engineering approach for the fertility restoration.

255 Restorer of fertility 4 (Rf4), the major fertility restorer gene of CMS-C, is located on chromoso

256 recombinants and then phenotyped for tassel fertility, resulting in a final map-based cloning interv

257 scence across species with diverse aging and fertility schedule phenotypes.

258 05) negative substitution effects on US sire fertility (SCR).

259 ell bovine embryos derived from high and low fertility sires.

260 involved in treating this group of patients, fertility sparing surgery and decrease of acute and long

261 or postremission counseling and referrals to fertility specialists.

262 ys for 18 African countries with and without fertility stalls, thus creating a pooled dataset of more

263 ause treatment-indicated risk does not equal fertility status after treatment.

264 f this study was to investigate whether male fertility status is associated with the RNAs present in

265 wide cross section of 30 men varying in age, fertility status, methylenetetrahydrofolate reductase (M

266 ns as well as concordance of perceptions and fertility status.

267 veland Clinic and divided according to their fertility status: proven fertile (n = 39); primary infer

268 of Diet, Exercise, and Lifestyle (IDEAL) on Fertility Study is a prospective cohort with contemporan

269 showed low pollen production and overall low fertility, suggesting a monoecy-paradioecy pathway at fu

270 iciency of UUG-rich transcripts and impaired fertility, suggesting a role of m(5) C tRNA wobble methy

271 ) offspring displayed normal development and fertility, suggesting that the expression of the paterna

272 al lineage F3 DEHP males exhibited decreased fertility, testicular steroidogenic capacity, and sperma

273 soil has still a lower chemical and physical fertility than the undisturbed sites, the plant species

274 ess and could aid in the development of male fertility therapies.

275 the direct effects of education on lowering fertility, these less-educated female cohorts were also

276 The brain regulates fertility through gonadotropin-releasing hormone (GnRH)

277 e explained <10% of variance in the ratio of fertility to age at first reproduction (F/alpha) and lif

278 These findings link fertility to nutritive environment and point to Sax sign

279 c, chemical and topographic environment of a fertility tract.

280 most positive substitution effects on female fertility traits (DPR, CCR and HCR).

281 (QTL) distribution) underlying 25 floral and fertility traits.

282 Maternal fertility treatment during the index pregnancy, includin

283 was not found for the use of other types of fertility treatment examined.

284 children worldwide are born after the use of fertility treatment, although it remains unclear whether

285 5 years, attempting pregnancy, and not using fertility treatment.

286 n of inherited genetic disorders and improve fertility treatments for couples with disease-causing mu

287 at DCL5 and 24-nt phasiRNAs are critical for fertility under growth regimes for optimal yield.

288 is, had no effect on spermatogenesis or male fertility under normal conditions.

289 ficient; and (3) societies that face falling fertility, urbanisation, and migration, are likely go th

290 mice were examined histopathologically, and fertility was determined by embryo enumeration after mat

291 in sensing plays a role in the regulation of fertility, we generated mice lacking IRs in astrocytes (

292 so critical to human reproductive health and fertility, we used small interfering to suppress NELF-B

293 s or spermatids, neither spermatogenesis nor fertility were affected.

294 Woody productivity increases with soil fertility, whereas residence time decreases, and biomass

295 Many health conditions can affect male fertility, which underscores the need for a thorough eva

296 variant is associated with favorable female fertility, which would explain its survival and the gene

297 Policy options to adapt to continued low fertility, while sustaining and enhancing female reprodu

298 for multiple chromosomes and showed improved fertility with both parents.

299 enescence-a decline in offspring survival or fertility with maternal age-has been demonstrated in man

300 Hsf2bp(S167L/S167L) females show reduced fertility with smaller litter sizes.