ライフサイエンスコーパス: lactation

1 OSPW (OSPW-OF) in mice during pregnancy and lactation.

2 gut microbiota of sows during pregnancy and lactation.

3 genes in mammary tissue during pregnancy and lactation.

4 rity and secretion, resulting in sub-optimal lactation.

5 induce MO from weaning through pregnancy and lactation.

6 nd greater perirenal adiposity by the end of lactation.

7 riety of vegetables including carrot) during lactation.

8 hstand the metabolic demand of pregnancy and lactation.

9 miRNAs reflect mammary gland function during lactation.

10 communities from weaning (8 weeks) to first lactation.

11 rs that give birth but do not participate in lactation.

12 Body-composition changes are minimal during lactation.

13 eld and pup weights were recorded throughout lactation.

14 llected from eight sows during gestation and lactation.

15 ptations to low nutrient availability during lactation.

16 without 0.2% (w/w) RES during pregnancy and lactation.

17 diet (FASD) throughout mating, pregnancy and lactation.

18 of maternal vitamin D supplementation during lactation.

19 e requirements increase during pregnancy and lactation.

20 us anthracycline treatment, and pregnancy or lactation.

21 h natural mating and thrive through maternal lactation.

22 static regulator of the mammary gland during lactation.

23 ated with changes in body composition during lactation.

24 tribution of serotonin to the maintenance of lactation.

25 of MNCs to physiological challenge, such as lactation.

26 mice were fed either a control or HFD during lactation.

27 s associated with larger litters and shorter lactation.

28 diet before mating and during gestation and lactation.

29 to allow translation of targets crucial for lactation.

30 3 time points over the first three months of lactation.

31 in the offspring exposed to these drugs via lactation.

32 ancy on breast-milk VDA in the first 2 mo of lactation.

33 are probably not a phenomenon restricted to lactation.

34 h the transfer of maternal antibodies during lactation.

35 cell polarity and tissue homeostasis during lactation.

36 ned precipitously between late pregnancy and lactation.

37 glucose for maternal use in anticipation of lactation.

38 ty and terminate in secretory alveoli during lactation.

39 mother to the offspring during pregnancy and lactation.

40 clearance in involution following the first lactation.

41 scored each minute for 8 h d(-1) throughout lactation.

42 ial proliferation and differentiation during lactation.

43 nal sugar-sweetened beverage (SSB) intake in lactation.

44 umulate in preparation for the next round of lactation.

45 ls in human milk decrease over the course of lactation.

46 of pro-rFIX to rFIX while yielding a normal lactation.

47 easible or desirable for clinical studies of lactation.

48 accelerated metabolism during gestation and lactation.

49 ell proliferation and differentiation during lactation.

50 lishes a novel physiologic role for AFAP1 in lactation.

51 ted and tested from patients after the first lactation.

52 and composition change during pregnancy and lactation.

53 prior to breeding, throughout gestation, and lactation.

54 nactivated D pteronyssinus, or to PBS during lactation.

55 omes are also influenced by maternal SSBs in lactation.

56 and facilitate nutrient partitioning during lactation.

57 Sires were exposed during breeding and lactation.

58 etabolism for an optimal pregnancy and later lactation.

59 race, multiparity, and lifetime duration of lactation.

60 de-offs normally attributed to pregnancy and lactation.

61 s in the gut microbiome during pregnancy and lactation.

62 heir own reserves and prompting cessation of lactation.

63 orts from embryonic day 0.5 until the end of lactation.

64 ovided to the dam from preconception through lactation.

65 ring a 28 d skeletal restoration period post lactation.

66 eeks before mating, throughout pregnancy and lactation.

67 e to the high calcium demand associated with lactation.

68 ealth and milk production for the subsequent lactation.

69 ternal exposure from early gestation through lactation (0.05, 5 or 25 mg/kg/day PFHxS), alone or in c

70 ter pregnant women (n22) and repeated during lactation 12 weeks post-partum (n14) and twice in NPNL w

71 In lactation, 25(OH)D3 and 24,25(OH)2D3 were lower compared

72 then also during the gestation (3 weeks) and lactation (3 weeks) periods, with offspring always maint

73 s while undergoing prolonged fasting, making lactation a tremendously energy demanding period.

74 mption prior to and throughout pregnancy and lactation accelerates offspring metabolic ageing in a se

75 the mammary ducts and glands at the time of lactation adhere to a perfect fractal geometry - which i

76 interest in understanding the ways in which lactation affects maternal health.

77 rs originating from the maternal diet during lactation (alcohol, anise/caraway, carrot, eucalyptus, g

78 hts that exposure to maternal obesity during lactation alone can programme adiposity in a sex specifi

79 In contrast, exposure during lactation alone reduced offspring weight but increased a

80 mechanism by which the maternal diet during lactation alters milk HMO composition, which in turn sha

81 ion among maternal diet during pregnancy and lactation, amniotic fluid flavor, breast-milk flavor, an

82 During lactation, an improper glucose supply often threatens ma

83 iderable research into the neural control of lactation, an understanding of the signaling mechanisms

84 ressed genes (DEGs), we detected 157 at peak lactation and 497 in the non-lactating period with a hig

85 erican women, who have a lower prevalence of lactation and a higher prevalence of obesity than other

86 ernal iodine deficiency during gestation and lactation and abnormal hippocampal development in rat fe

87 ifferences in HMOs concentrations throughout lactation and among women with different Secretor and Le

88 ries, have examined the associations between lactation and cardio-metabolic outcomes.

89 rtance of maternal diet during pregnancy and lactation and caregiver feeding strategies and practices

90 een mothers' diet during either pregnancy or lactation and children's overall dietary intake.

91 econception and pregnancy may persist during lactation and compromise human milk composition.

92 nction in activated CD4(+) T cells from late lactation and dry cows compared to cells from early and

93 ysiological and pathological states, such as lactation and heart failure (HF).

94 remilk and hindmilk during the first 9 mo of lactation and identified indexes of importance to the co

95 complete information on female pregnancy and lactation and imperfect and biased recapture rates.

96 t TA on samples collected from cows in early lactation and in samples with high somatic cell count.

97 Among large-bodied mammals, prolonged lactation and infant dependence suggest particularly str

98 riod is important to the success of the next lactation and intramammary infections during the dry per

99 nal changes in response to a full pregnancy, lactation and involution.

100 ow (L, 8%) protein diet during gestation and lactation and maintained on the same diets (NN, LL) or s

101 triggers key maternal adaptations, including lactation and maternal care.

102 n involves the transition between periods of lactation and nonlactation (dry periods).

103 opmental stages; nulliparous, mid gestation, lactation and post involution.

104 cy obesity modifies the relationship between lactation and postpartum weight gain, makes an important

105 acunar remodeling in physiological states of lactation and provides genetic evidence that osteocyte-d

106 her Diptera by unique adaptations, including lactation and the birthing of live young (obligate vivip

107 information about the factors that influence lactation and/or HMC; 3) considerations for data quality

108 required for metabolic processes underlying lactation and/or progeny development.

109 st levels of cortisol during cycling (versus lactation), and this effect increased with age.

110 duced in the mammary gland upon the onset of lactation, and a C17orf99(-/-) mouse exhibits reduced le

111 mostly formula or mixed/inconsistent, mostly lactation, and exclusive lactation versus exclusive form

112 f these animals, particularly those in early lactation, and increase their susceptibility to infectio

113 lements (SQ-LNSs) provided during pregnancy, lactation, and infancy on attained size by 18 mo of age.

114 occur in the mammary gland during pregnancy, lactation, and involution.

115 or WSD prior to and during pregnancy through lactation, and offspring subsequently weaned to a contro

116 most expensive time of female reproduction, lactation, and that different male care behaviours incre

117 ofiles across different stages of gestation, lactation, and the empty (nonpregnancy) phase in 2 disti

118 aternal gut microbiota throughout pregnancy, lactation, and the empty phase, which could potentially

119 luenced by maternal fructose intake in early lactation, and this could be attributed to maternal SSB

120 amples collected from cows in early and late lactation, and was successively used to predict TA on sa

121 ur objective was to characterize dams with a lactation- and mammary-specific disruption of Lrp5 (WAP-

122 Pregnancy and lactation are associated with changes in vitamin D and c

123 In female mammals, gestation and lactation are expected to impose the major costs of repr

124 Researchers hypothesize that pregnancy and lactation are part of a continuum, with lactation meant

125 y of mass transfer from mother to pup during lactation as well as the weaning mass of pups.

126 ated with important components of pregnancy, lactation, as well as inflammation and disease.

127 crease in osteocyte lacunar area seen during lactation, as well as the effects of lactation to increa

128 Lactation-associated genes are conserved across all Glos

129 g maternal mice a high-fat diet (HFD) during lactation attenuated the activity of dopamine (DA) midbr

130 n serum Parathyroid Hormone (PTH) induced by lactation, but amplified the increase in serum 1,25(OH)2

131 e same rate as controls during gestation and lactation, but faster after weaning when direct maternal

132 typically exhibit energy compensation during lactation by downregulating their background metabolic r

133 high-sugar "junk foods" during pregnancy and lactation can alter the development of the central rewar

134 m 24-week-old offspring fed ezetimibe during lactation, compared with controls.

135 ing, nursing staff education and experience, lactation consultant availability, and nurse-reported br

136 Mothers in the BLISS group received lactation consultant support (>/=5 contacts) to extend e

137 Maternal supplementation during lactation could increase milk B-vitamin concentrations,

138 igh-fat diet (HFD) rats during pregnancy and lactation could promote brown/beige adipogenesis and pro

139 ry cows compared to cells from early and mid-lactation cows.

140 taset from bovine mammary tissue over entire lactation cycle was used to further illustrate our strat

141 mmary epithelium during successive pregnancy/lactation cycles, eIF4E overexpression increased self-re

142 udy, the rumen microbial composition of late lactation dairy cows grazing perennial ryegrass only (PR

143 s (MECs) isolated on pregnancy day (P)14 and lactation day (L)2 revealed that the majority of differe

144 consistent with interspecific differences in lactation, diet, and immune function.

145 Conversely, offspring exposed to MHFD during lactation display the metabolic syndrome and schizophren

146 , pups receiving anti-BMP9/10 antibodies via lactation displayed consistent and robust vascular patho

147 as a part of normal pregnancy, and that when lactation does not occur, women maintain an elevated ris

148 Time-dependent lactation duration showed graded inverse associations wi

149 capital breeders that undergo short, intense lactations, during which they fast while transferring su

150 the lactation period are more likely to end lactation earlier than expected.

151 s we have examined the influence of stage of lactation (early lactation into the dry period) on cellu

152 Mechanistically, maternal HFD feeding during lactation elevated peripheral serotonin, which decreased

153 esorption, including cathepsin K (Ctsk), and lactation elevates their expression.

154 An adverse maternal in utero and lactation environment can program offspring for increase

155 l-to-mesenchymal transition, and resulted in lactation failure as a result of abnormal alveolar forma

156 accumulation, loss of secretory function and lactation failure.

157 cts and alveoli during pregnancy resulted in lactation failure.

158 iet showed extensive bone loss by the end of lactation, followed by full skeletal recovery in NN dams

159 t, with high MeHg intake in utero and during lactation, followed by increasing consumption of solid f

160 exposure to H pylori in utero and/or during lactation for susceptibility to viral and bacterial infe

161 Participants provided data on weight, lactation, gestational weight gain, education, diet, and

162 iry cows from 2 weeks to the middle of first lactation (>2 years) as well as rumen-associated communi

163 ified fish sauce through pregnancy and early lactation had higher eTDP and breast milk thiamine conce

164 Notably, lactation has been shown to be protective against breast

165 buttermilk glycosylation over the course of lactation have not been extensively investigated.

166 men metaproteome utilizing three mid to late-lactation Holsteins.

167 low milk protein percentage during the peak lactation (HP vs LP) and during the non-lactating period

168 Lactation improves glucose metabolism, but its role in p

169 lerance and related immune parameters during lactation in a mouse model.

170 he altered energetic demands associated with lactation in dairy cows impacts T cell metabolic reprogr

171 causes of high body temperature (Tb) during lactation in mice as a putative limit on energy intake.

172 maternal high-fat diet (HFD) feeding during lactation in mice elicits long-lasting changes in gene e

173 in omega-3 fatty acids during pregnancy and lactation in mice, which permanently reduces endocannabi

174 pression suppresses lobuloalveologenesis and lactation in mice.

175 rnal low protein diet (LPD) during pregnancy/lactation in mice.

176 analysis of LD growth and secretion at peak lactation in real time.

177 n the mammary gland was reduced during early lactation in the AFAP1-null mouse and the localization o

178 egnancy and/or meet the energetic demands of lactation in years of poorer prey availability rather th

179 micronutrient concentrations declined during lactation, independent of changes in human milk producti

180 ot interact with Avprs in vivo in a model of lactation-induced bone loss in which Oxt levels are high

181 Lactation-induced bone loss occurs due to high calcium r

182 Lactation induces bone loss to provide sufficient calciu

183 ase (XOR) modulates milk lipid secretion and lactation initiation.

184 Higher lactation intensity and longer duration were independent

185 There were graded inverse associations for lactation intensity at baseline with incident DM and adj

186 d the influence of stage of lactation (early lactation into the dry period) on cellular metabolism in

187 siological changes over the course of a full lactation into the dry period, which impacts their immun

188 increasingly delaying childbearing, and thus lactation, into their 30s and 40s, when mammography woul

189 Lactation is a unique period in which the maternal skele

190 io in the maternal diet during pregnancy and lactation is a useful early preventive strategy against

191 e mammary morphogenesis during pregnancy and lactation is accompanied by increased cap-binding capabi

192 in giant pandas, and possibly in all bears, lactation is adapted to provisioning a highly altricial

193 Lactation is necessary for both infant and fetal develop

194 mug/d) of mercury during gestation, although lactation is their main exposure route.

195 ts role in social behaviors, childbirth, and lactation, is a promising addiction pharmacotherapy.

196 HFD during pregnancy (intrauterine [IU]) and lactation (L).

197 and Drug Administration's new Pregnancy and Lactation Labeling Rule and the most up-to-date safety i

198 Although pregnancy and lactation lead to increased iodine needs, no UK recommen

199 their mothers, by enabling them to share the lactation load.

200 During lactation, mammary epithelial cells secrete huge amounts

201 Lactation may prevent DM after GDM delivery.

202 Maternal diet during pregnancy and lactation may provide the earliest opportunity to positi

203 and lactation are part of a continuum, with lactation meant to "reset" the adverse metabolic profile

204 models evaluated independent associations of lactation measures with incident DM adjusted for potenti

205 s that the decline in miR-150 is crucial for lactation, MEC-specific constitutive miR-150 was achieve

206 early-postpartum oocytes suggest that early lactation metabolic stress may affect imprint acquisitio

207 Colostrum and early lactation milk samples were collected from 285 mothers e

208 nancy and a further three to five years into lactation, nematode load did not vary with four differen

209 Here, we show that, during lactation, neuroendocrine dopamine neurons, the "TIDA" c

210 ggest that adaptive changes in pregnancy and lactation occur that prevent pronounced changes in vitam

211 During the uniquely short lactations of true seals, pups acquire a greater proport

212 of ovulation, fertilization, pregnancy, and lactation often interspersed with periods of anoestrus w

213 An effect for lactation on breast cancer outcome after diagnosis has n

214 tion beginning in gestation and continued in lactation on infant serum 25(OH)D and compared the preva

215 thers, but the impact of maternal HFD during lactation on offspring BAT function is unknown.

216 varied cafeteria diet, during pregnancy and lactation on these measures in rat offspring prior to we

217 roup members between mating and the onset of lactation) on these fitness measures.

218 ed to the ChS diet only during gestation and lactation; once weaned at postnatal day 21, Gen-1 mice w

219 the model on milk samples from cows in early lactation or with high somatic cell count, the root mean

220 2+) load, such as mammary gland cells during lactation, or in cells with a low ATP content, such as k

221 d potentially help improve the pregnancy and lactation outcomes for both animals and humans.

222 ght gain decreased with increasing months of lactation (P for trend<0.01), whereas among obese women

223 t gain increased with increasing duration of lactation (P for trend=0.04).

224 e race, lack of breastfeeding, and increased lactation peanut consumption.

225 o farmers combine specific information about lactation performance and testing results, which existin

226 ch as SLC30A2 has important implications for lactation performance in women, and that milk-derived mi

227 tion as a modifier of secretory capacity and lactation performance.

228 one individual to another according to their lactation period and secretor status.

229 ls that fail to energy compensate during the lactation period are more likely to end lactation earlie

230 without despite being supported by a shorter lactation period, implying that they grow faster.

231 neighbouring pen (socialisation) during the lactation period, while keeping 12 litters isolated in t

232 ing the involution process at the end of the lactation period.

233 rity of development occurring over a lengthy lactation period.

234 True seals have the shortest lactation periods of any group of placental mammal.

235 which males carry the offspring have shorter lactation periods, which leads to more frequent breeding

236 rs of preterm infants was monitored in three lactation phases and after storage of expressed milk by

237 ring, and low maternal energy balance during lactation predicted larger, not smaller, juvenile size.

238 n tributyltin (TBT) throughout pregnancy and lactation predisposes unexposed F4 male descendants to o

239 nclusion exposure to maternal obesity during lactation programmes offspring adiposity and insulin res

240 Following lactation, prolactin levels decline and mammary-specific

241 ntation of HFD-fed dams during pregnancy and lactation promoted white adipose browning and thermogene

242 with PQQ, particularly during pregnancy and lactation, protects offspring from WD-induced developmen

243 Lactation provides the singular source of nourishment to

244 djusted mean differences for >/=12 months of lactation relative to no lactation were -1.56 kg (95% co

245 l and metabolic changes during pregnancy and lactation remain elusive.

246 n of milk by mammary epithelial cells during lactation remains largely unknown.

247 elated to maternal diet during pregnancy and lactation, respectively.

248 treatment/treated (MAT) during pregnancy and lactation resulted in profound alterations in the compos

249 ting rat dams with cannabinoids during early lactation retards transcriptional upregulation and expre

250 dicator of subclinical ketosis) in the first lactation (SCK1) and second and later lactations (SCK2)

251 first lactation (SCK1) and second and later lactations (SCK2) in Holstein dairy cows.

252 TCC exposure during gestation and lactation significantly reduced phylogenetic diversity (

253 The lactation stage is a manageable period for improving the

254 Lactation stage, season, study site, and maternal educat

255 es is elevated in the transgenic mice at the lactation stage, suggesting inhibition of mammary cell d

256 ithelial cells in the transgenic mice at the lactation stage.

257 od lasted for 2 months and ewes were at late lactation stage.

258 Upon termination of lactation STAT5 binding to a subset of mammary enhancers

259 During lactation, STAT5 occupies mammary-specific and universal

260 can and should be confidently used in future lactation studies to further elucidate the contribution

261 d be an early postpartum strategy to enhance lactation success in women at risk for delayed onset of

262 een current reproduction (both pregnancy and lactation), survival and future reproduction, including

263 fically, these animals displayed a defect in lactation that resulted in an inability to nurse efficie

264 ) or maternal control dietin uteroand during lactation, then weaned onto either obesogenic or control

265 OPs to their offspring through gestation and lactation; therefore, young cubs present higher POPs con

266 In dairy cows, the period from the end of lactation through the dry period and into the transition

267 In the high-prolactin state of lactation, TIDA neurons shift to faster membrane potenti

268 AD levels were significantly affected by the lactation time.

269 samples from individual donors at different lactation times, which may provide insight into the micr

270 ofile in dry secretions from the last day of lactation to 3, 10, and 21 days post dry-off.

271 These oligosaccharides decreased from early lactation to almost undetectable levels by weaning.

272 dated pharmacokinetic model of pregnancy and lactation to estimate concentrations of PFOS and PFOA in

273 specific XOR knockout (MGKO) mice, expecting lactation to fail.

274 during lactation, as well as the effects of lactation to increase osteoclast numbers and decrease tr

275 We assessed the relationship of lactation to long-term maternal weight gain among Africa

276 subchronic exposure throughout gestation and lactation to OSPW-OF (containing naturally occurring lev

277 a key mechanism linking maternal HFD during lactation to persisted metabolic disorder in the offspri

278 e involved in several functions ranging from lactation to social attachment.

279 Cannabis use by mothers during lactation transfers active cannabinoids to the developin

280 evated energy intake before birth and during lactation (up to 1.7-fold), through increased sugar, tot

281 debate on medication safety in pregnancy and lactation using the US Food and Drug Administration's ne

282 nconsistent, mostly lactation, and exclusive lactation versus exclusive formula feeding, respectively

283 ) that are induced during late pregnancy and lactation via use of the whey acidic protein (WAP)-Cre c

284 Exposure to maternal obesity during lactation was a driver for reduced offspring weight post

285 Relative to empty and gestation, lactation was associated with an increase in SCFA produc

286 Tb throughout lactation was correlated with daily increases in energy

287 bilization of endogenous lipid stores during lactation was highest for first-borns with diminished tr

288 Overall, lactation was not associated with mean weight gain.

289 Chronic hyperthermia during lactation was not caused by increased heat retention due

290 l surface of luminal epithelial cells during lactation was selectively lost in the absence of AFAP1.

291 transcriptional changes during pregnancy and lactation, we demonstrate a functional switch in activit

292 for >/=12 months of lactation relative to no lactation were -1.56 kg (95% confidence interval: -2.50,

293 up size between pre-pregnancy and postpartum lactation were associated with expression of genes contr

294 o tributyltin (TBT) throughout pregnancy and lactation were predisposed to obesity due to altered chr

295 ilk-specific protein production characterize lactation, which terminates at the birth of the progeny

296 the control ad libitum diet in pregnancy and lactation, which were growth restricted at birth.

297 evidence exists regarding an association of lactation with maternal postpartum weight status and dys

298 ty and, then, fed a HFD during pregnancy and lactation with or without MFGM-PL.

299 circulating serotonin concentrations during lactation, with no effect on milk yield or alveolar morp

300 id transition from colostrum to mature phase lactation yet observed.