戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 diated inflammation and is lethal during the perinatal period.
2 rm and somatic cell developmental during the perinatal period.
3 creased homeostatic proliferation during the perinatal period.
4 t the fast program of gene expression in the perinatal period.
5  is an important neurological problem of the perinatal period.
6  brain injury and white matter damage in the perinatal period.
7 mals exposed to nicotine in the prenatal and perinatal period.
8 ere neuronal migration continues through the perinatal period.
9 termined by mesenchymal induction during the perinatal period.
10 st coitum and die in either the fetal or the perinatal period.
11 fects of gonadal steroids during a sensitive perinatal period.
12 ce that survive to birth exsanguinate in the perinatal period.
13 tgrowth and terminal arborization during the perinatal period.
14 mice with an additional 30% lethality in the perinatal period.
15 ype was nearly completely fatal in the early perinatal period.
16 ognized requirement for ascorbic acid in the perinatal period.
17 infection are risk factors for stroke in the perinatal period.
18 ex compared with the occipital cortex in the perinatal period.
19  the majority of the SADDAN mice survive the perinatal period.
20 reas most of the SADDAN patients survive the perinatal period.
21 nction in infants exposed to the drug in the perinatal period.
22 f serologic testing during pregnancy and the perinatal period.
23 fter birth and the cdk5(-/-) mice die in the perinatal period.
24 uding respiratory diseases developing in the perinatal period.
25 erning of PEPCK-C gene expression during the perinatal period.
26 hyxia and other forms of acute injury in the perinatal period.
27 y important for brain development during the perinatal period.
28 d in foveal formation that occurs during the perinatal period.
29 satory increase in retinal blood flow in the perinatal period.
30 AATD) can manifest at any age, including the perinatal period.
31 associated with neuroanatomic changes in the perinatal period.
32 weeks of gestation, and 8720 died during the perinatal period.
33 n and metabolic maturation occur in the same perinatal period.
34 letion of mental health screening during the perinatal period.
35 nucleotide exchange factors (RhoGEFs) in the perinatal period.
36 on offspring's glucose metabolism during the perinatal period.
37 ive either high-dose rhEPO or placebo in the perinatal period.
38 s in health care use and outcomes during the perinatal period.
39 n maternal mental health problems during the perinatal period.
40 cy, childbirth, the puerperal period, or the perinatal period.
41  individuals who remained insured during the perinatal period.
42 ly tissue-resident cells that develop in the perinatal period.
43  and deviations from these models during the perinatal period.
44 igated by administration of rhEPO during the perinatal period.
45             Sleep problems are common in the perinatal period.
46 rm of psychosocial interventions) during the perinatal period.
47 ring blood glucose concentrations during the perinatal period.
48  partum, 12 months post partum, and the full perinatal period.
49 arefully weighed against the benefits in the perinatal period.
50 y capture these sexual identities during the perinatal period.
51 ntricular systolic dysfunction (LVSD) in the perinatal period.
52 nd major depressive disorders outside of the perinatal period.
53 ormations; and conditions originating in the perinatal period.
54 ird trimester and develop rapidly across the perinatal period.
55 ve higher risk of depressive symptoms in the perinatal period.
56  relatively mild outcome to death during the perinatal period.
57 ge into adulthood, long after the end of the perinatal period.
58  on depression symptoms among men during the perinatal period.
59 ion for neonates that is applicable from the perinatal period.
60 ential adverse effects manifesting after the perinatal period.
61 died by suicide, of whom 98 (2%) died in the perinatal period.
62  aged 20-35 years, 74 (4%) women died in the perinatal period.
63 ticular torsion may concern boys even in the perinatal period.
64 rocess of germline cyst breakdown during the perinatal period.
65 l switch to license thermogenesis during the perinatal period.
66 entricular cardiac myocytes in the immediate perinatal period.
67 omes ranging from very mild to lethal in the perinatal period.
68 pecially their expansion during the critical perinatal period.
69 nent of hypoxic-ischemic brain injury in the perinatal period.
70  cells in a stage-specific manner during the perinatal period.
71 , that vulnerability might be induced in the perinatal period.
72 stosterone secreted by the testes during the perinatal period.
73 diomyocyte proliferative capacity beyond the perinatal period.
74  infected with HIV type 1 (HIV-1) during the perinatal period.
75 eonates scanned cross-sectionally across the perinatal period.
76 ing data prospectively for pregnancy and the perinatal period.
77  fully developed from early childhood or the perinatal period.
78 yte proliferation during development and the perinatal period.
79 olyunsaturated fatty acids (LC-PUFAs) in the perinatal period.
80  outcomes for women and their infants in the perinatal period.
81 in is reduced during either the embryonic or perinatal period.
82  years who were infected with HIV during the perinatal period.
83  background mice results in death during the perinatal period.
84 ernal stress, depression, and anxiety in the perinatal period.
85 onverted into iPS cells for treatment in the perinatal periods.
86 osed or unexposed to Zdv during prenatal and perinatal periods.
87 t frequently observed in the fetal and early perinatal periods.
88 07 per year [SD 0.96]; p=0.026), but not the perinatal period (-0.07 per year [0.37]; p=0.58).
89  number of women dying by suicide in the non-perinatal period (-2.07 per year [SD 0.96]; p=0.026), bu
90 ; (3) recruited samples prospectively in the perinatal period; (4) used masked assessment; and (5) di
91 p8(C362A/C362A)Mlkl(-/-) mice die during the perinatal period(5), whereas Casp8(-/-)Mlkl(-/-) mice ar
92 ms remained stable from pregnancy across the perinatal period, a finding that conflicts with a contin
93 er and how testosterone signaling during the perinatal period affects GABAergic transmission is uncle
94 eydig and peritubular myoid cells during the perinatal period, allowing us to identify candidate sign
95 hypothesis that exposure to a HFD during the perinatal period alters the electrophysiological, pharma
96 urons undergo marked changes during both the perinatal period and adolescence in the monkey PFC.
97 ferent types of changes occurring during the perinatal period and adolescence.
98  toward improving maternal health during the perinatal period and beyond.
99  of four papers about maternal health in the perinatal period and beyond.
100  link between maternal hypothyroidism in the perinatal period and childhood asthma risk.
101 on about onset of depressive symptoms in the perinatal period and complete prospective data for the t
102 ased in the liver and small intestine in the perinatal period and decreased in adult mice, whereas CE
103           cPGES/p23(-/-) pups die during the perinatal period and display retarded lung development r
104 ne biceps femoris skeletal muscle during the perinatal period and examined the role of thyroid hormon
105 more resources than a livebirth, both in the perinatal period and in additional surveillance during s
106 ing of A(H1N1)-vaccinated mothers beyond the perinatal period and into early childhood.
107 that mitochondrial function matures over the perinatal period and is dependent on thyroid hormones, w
108 ey mediator of pulmonary vasodilation in the perinatal period and its synthesis in the pulmonary vasc
109  and anxiety are highly prevalent during the perinatal period and linked to experiences of domestic v
110  TLR-mediated cytokine production during the perinatal period and may thereby modulate their innate a
111 of de novo DNA methyltransferases during the perinatal period and neurodevelopmental deficits associa
112 mall diameter primary sensory neurons in the perinatal period and the activity-dependent changes in d
113 opment of network controllability during the perinatal period and the effect of preterm birth in 521
114 ir increased susceptibility to stress in the perinatal period and their relatively poor perinatal out
115 ascular events that are diagnosed during the perinatal period and those diagnosed retrospectively, wh
116 k AMVP who developed malignant VA during the perinatal period and to assess if pregnancy and the post
117 atory network to respond to CO(2) during the perinatal period and under anesthesia.
118 cal models of risk and resilience during the perinatal period and used to design more effective early
119 ay a critical role in development during the perinatal period and, in particular, in enabling phenoty
120   Furthermore, Ncoa4(-/-) mice are anemic in perinatal periods and fail to respond to TH by enhanced
121 ess can have a devastating effect during the perinatal period, and has a profound impact on the care
122           However, liver LPL is found in the perinatal period, and in adults it can be induced by cyt
123 ay modulate pulmonary PGI2 production in the perinatal period, and it may also play a role in the eff
124 n the fetal ovary, follicle formation in the perinatal period, and oocyte growth and maturation in th
125 e-like B cell repertoire during neonatal and perinatal periods, and the prospect of targeting B cell
126 ternal physical and mental health beyond the perinatal period are lacking.
127 trongly suggest that events in the immediate perinatal period are most important in neonatal brain in
128 virus (HIV) epidemic and infected during the perinatal period are now young adults living with the vi
129 al principles of prescribing of drugs in the perinatal period are provided, but individual risk-benef
130                             The prenatal and perinatal periods are thought to be important times for
131                     This work highlights the perinatal period as a critical time window, especially r
132              Sall3-deficient mice die in the perinatal period because of dehydration and display alte
133 optimal women's mental health throughout the perinatal period, because maternal depressive symptoms a
134 influence of sex steroid hormones during the perinatal period, but how these hormones specify precise
135 l progenitors colonize the CNS widely in the perinatal period, but the pathways and mechanisms of mig
136            Thus, IFN-gamma expression in the perinatal period can induce SHH expression and medullobl
137 r novel therapeutic interventions during the perinatal period can influence the occurrence of neurolo
138 ychosocial stressors during the prenatal and perinatal periods can have major long-term mental health
139  environmental exposure, particularly during perinatal period, can have a life-long impact on organis
140 existence of an EGFR(+) cell enriched in the perinatal period capable of driving complex changes char
141                                   During the perinatal period, cardiomyocyte-specific PERK homogenous
142                                       In the perinatal period, cardiomyocytes still proliferate, and
143 rch on early adversity occurring across pre-/perinatal periods, childhood, and early adolescence, whi
144  disorder, or adjustment disorder during the perinatal period (conception to 12 months post partum) u
145               Thus, lack of tolerance in the perinatal period correlated with lack of activation of a
146                                          The perinatal period could impose increased risk of malignan
147  safety of pharmacological treatments in the perinatal period, despite quite high prescription rates.
148 d claims documentation of Z codes during the perinatal period, driven by increases in the prenatal pe
149 eptor is experimentally inhibited during the perinatal period, either by pharmacological intervention
150 portance of proper choline intake during the perinatal period, especially when the fetus is known to
151  mutant mice survive to birth but die in the perinatal period exhibiting multiple vascular pathologie
152 he mother and infant dyad may present in the perinatal period from 20 weeks of gestation to 28 days o
153 the mammalian forebrain are generated in the perinatal period from progenitors in the subventricular
154    Consequently, mutant mice died during the perinatal period from severe skeletal muscle hypoplasia.
155 eatment (10 ppm propylthiouracil) during the perinatal period (GD19-PN2) induces a periventricular he
156        In this study, we report that, during perinatal period, germline mutation of FoxP3 in scurfy m
157 s of maternal depressive symptoms across the perinatal period had smaller gray and white matter volum
158 utritionally-induced growth faltering in the perinatal period has been associated with reduced adult
159 eased burden of invasive NTHi disease in the perinatal period has been reported by a number of studie
160 ts born extremely or very preterm during the perinatal period has no measurable effects on retinal fu
161 isk factors (eg, food insecurity) during the perinatal period has the potential to improve pregnancy-
162      Maternal depressive symptoms during the perinatal period have been associated with offspring neu
163      bFGF effects were not restricted to the perinatal period; hippocampal DNA synthesis was stimulat
164 eased risk of mortality and morbidity in the perinatal period; however, there is a gap in co-produced
165      First lifetime episodes occurred in the perinatal period in 7.6% of cases.
166 induces the peristaltic machinery during the perinatal period in a timely fashion to accommodate the
167 l vector (AAV)-mediated gene transfer in the perinatal period in animal models of severe congenital f
168 sue (BAT) depots disappear shortly after the perinatal period in humans, PET imaging using the glucos
169 ze levels of mast cells and microglia in the perinatal period in male and female offspring, as well a
170 ulogenesis) are processes not limited to the perinatal period in mammals.
171 ants and testicular somatic cells during the perinatal period in mice.
172  who are most (and least) at risk during the perinatal period in order to target resources and assist
173 nmt3L) is expressed in testes during a brief perinatal period in the non-dividing precursors of sperm
174 ity at lower exposure levels during critical perinatal periods in mammals.
175 l long-term effects when administered during perinatal periods, increasing the risk to develop anxiet
176 and neurobehavioral differences later in the perinatal period, independent of their androgen profiles
177 that early-life adversity, especially in the perinatal period, influences the maturation of brain cir
178 overlap with autoimmune disease (AD) and the perinatal period involve immune system adaptations and A
179                                          The perinatal period is a critical time window in establishi
180                                          The perinatal period is a critical window for distribution o
181         Hypoxic-ischemic brain injury in the perinatal period is a major cause of morbidity and morta
182                                          The perinatal period is a time of high risk for onset of dep
183  autophagy in the mammalian heart during the perinatal period is an essential adaptation required to
184                     Domestic violence in the perinatal period is associated with adverse obstetric ou
185                         Infection during the perinatal period is associated with an increased risk of
186                                          The perinatal period is associated with an increased risk of
187         In short, Aire expression during the perinatal period is both necessary and sufficient to ind
188                                          The perinatal period is critically important to the developm
189                                          The perinatal period is known to be critically important in
190                                          The perinatal period is particularly critical for neurodevel
191 lescence, albeit to a lesser degree than the perinatal period, is a critical window of susceptibility
192 upting chemicals during pregnancy and/or the perinatal period leads to the failure of normal follicle
193                                   During the perinatal period, many SP neurons die.
194                             During fetal and perinatal periods, many nutrients, such as long-chain po
195 ion efforts in response to challenges in the perinatal period may persist into adulthood.
196 gic factors associated with the prenatal and perinatal periods may be specific to age at neuroblastom
197 outinely delivered care for women during the perinatal period might be economically viable.
198                   A number of factors in the perinatal period, notably immigration from rural low-inc
199 showed that insurance transitions during the perinatal period occurred for more than 1 in 3 birthing
200 e odds of experiencing depression during the perinatal period (odds ratio, 1.85; 95% confidence inter
201 y acid docosahexaenoic acid (DHA) during the perinatal period of "brain growth spurt." Experimental d
202          Blocking Notch signaling during the perinatal period of plasticity rapidly eliminates epigen
203                                    Thus, the perinatal period offers a suitable time window for disea
204 on because of the transitional nature of the perinatal period, particularly high levels of anxiety ha
205 to which an individual is exposed during the perinatal period plays a crucial role in determining his
206           Over the course of a lifetime, the perinatal period plays an outsized role in the function
207 ratios (HRs) of psychiatric emergency in the perinatal period (pregnancy and 6 months postpartum) usi
208                                          The perinatal period presents a critical time in offspring d
209 e; thyroid hormone deficiency during a brief perinatal period produces severe neurological defects in
210 s in the cardiac metabolic milieu during the perinatal period redirect mitochondrial substrate prefer
211 mental trajectories of the connectome in the perinatal period remains incomplete.
212 the course of depressive symptoms across the perinatal period remains unclear, thus complicating scre
213                                          The perinatal period represents a critical window for cognit
214 disseminated intravascular thrombosis in the perinatal period, resulting in significant mortality sho
215                 Cannabis exposure during the perinatal period results in varied and significant conse
216 ous for the allele lacking exon 2 die in the perinatal period, so we generated mice with liver-specif
217 ining several metabolic processes during the perinatal period, the consequences of total ablation of
218                                   During the perinatal period, the independent expression of alpha3 m
219 ions during pregnancy, the timing within the perinatal period, the sex of the foetus, and exposure to
220 excess of adverse events during the pre- and perinatal periods, the presence of cognitive and behavio
221  of malignant VA in non-pregnant periods and perinatal period; the latter defined as occurring during
222  contact with midwives and nurses during the perinatal period, there is a lack of evidence which hamp
223 s of environmental factors acting during the perinatal period, therefore little is known about the im
224 ically, about 25% of these mice survived the perinatal period; these survivors appeared to develop no
225  was approximately 30-50% decreased from the perinatal period through adulthood, and the number of pa
226 er that ranges in severity from death in the perinatal period to an increased lifetime risk of fractu
227 cts of these changes range from death in the perinatal period to barely increased fracture frequency
228 iting is the prospect of treating TSC in the perinatal period to block the progression of brain patho
229 insurance continuity is important during the perinatal period to improve birth outcomes and reduce ma
230 anner, we find that Aire is essential in the perinatal period to prevent the multiorgan autoimmunity
231  in phenotypes that range from lethal in the perinatal period to severe deforming osteogenesis imperf
232  controllability develops rapidly during the perinatal period to support cognitive demands but could
233 he remaining women have episodes outside the perinatal period, usually within the bipolar spectrum.
234                    A single treatment in the perinatal period was sufficient to confer robust and sta
235 concern about men's mental health during the perinatal period, we still do not know whether men are m
236 ho died by suicide within versus outside the perinatal period were also more likely to be younger (cr
237 atal women, women who died by suicide in the perinatal period were more likely to have a diagnosis of
238 ith UK psychiatric services, suicides in the perinatal period were more likely to occur in those with
239 ed to the pregnancy, the puerperium, and the perinatal period were the most common serious adverse ev
240 GF(lo/+) formed fewer collaterals during the perinatal period when adult density was established, and
241 lly shapes immunity, particularly during the perinatal period when the immune system is underdevelope
242    However, these embryos survived until the perinatal period when they died from a spectrum of cardi
243  testosterone and its metabolites during the perinatal period, when many aspects of brain development
244 ay 9.5, mice lacking HDAC2 survive until the perinatal period, when they succumb to a spectrum of car
245 management of hematologic cancers during the perinatal period, which were developed by a multidiscipl
246 of mammalian kidneys is completed during the perinatal period with a dramatic increase in urine produ
247 ssociation of an insurance transition in the perinatal period with insurance type in the delivery mon
248 of the mouse Pkd1 gene leads to death in the perinatal period with massive cystic expansion in homozy
249 henotype, whereas homozygotes die during the perinatal period with massively enlarged cystic kidneys,
250 -out mice develop cardiac failure during the perinatal period with mutant hearts exhibiting several c
251 s identify the rapid remodeling of CL in the perinatal period with resultant alterations in the physi
252 srupted corticospinal projections during the perinatal period with the double benefit of restoring co
253 border-associated macrophages [BAMs]) by the perinatal period, with limited recombination in peripher
254 y lethality in Mig-6(-/-) mice occurs in the perinatal period, with mice displaying abnormal lung dev
255 is organization emerges gradually during the perinatal period, with neuronal stripe formation in the
256 centration rapidly increased normally in the perinatal period, with the highest concentrations found

 
Page Top