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1  n = 11-12) and IUGR (n = 12) late gestation fetal sheep.
2  cardiovascular development or growth in the fetal sheep.
3 od flow and oxygen consumption rates in IUGR fetal sheep.
4 an hematopoiesis after transfer to preimmune fetal sheep.
5  acid uptake was significantly lower in IUGR fetal sheep.
6 ovascular adaptations in chronically anaemic fetal sheep.
7 evelopment of cerebral OXPHOS in hypothyroid fetal sheep.
8 e adipose tissue development of midgestation fetal sheep.
9 tic uptake following metformin infusion into fetal sheep.
10 ephalic vasculature of the intact, near term fetal sheep.
11  vasculature served by the carotid artery of fetal sheep.
12 factors reduces myofibre hypertrophy in IUGR fetal sheep.
13  we transplanted clonally derived BMSCs into fetal sheep.
14 hydrate metabolism and insulin signalling in fetal sheep.
15 or intrahepatic (n = 6) route into preimmune fetal sheep.
16 ion model in the instrumented 0.65 gestation fetal sheep.
17 -pseudotyped retroviruses for injection into fetal sheep.
18 nsplanted by intraperitoneal injections into fetal sheep.
19 anges of CBF in the chronically instrumented fetal sheep.
20  product of the gene c-fos in late-gestation fetal sheep.
21  resistance artery function of mid-gestation fetal sheep.
22 cortical vascular resistance by ~15 % in the fetal sheep.
23 lanted in the cerebral cortices of near-term fetal sheep.
24 rticotropic hormone (ACTH) in late-gestation fetal sheep.
25 mmunodeficiency (NOD-SCID) mice or preimmune fetal sheep.
26 s engrafted primary, secondary, and tertiary fetal sheep.
27 by improved fetal lung function after 4 d in fetal sheep.
28 ta reported in this study of unanaesthetised fetal sheep (1) show that minute-by-minute analyses of h
29                 During a 3-year period in 88 fetal sheep, 1) left-sided diaphragmatic hernias were cr
30                                     Fourteen fetal sheep (105-109 days gestational age) were instrume
31   In unanaesthetized chronically instumented fetal sheep (118-121 days gestation) we investigated the
32                                           In fetal sheep (123-129 days gestation) we investigated the
33 duced for 30 min in chronically catheterized fetal sheep (125 +/- 3 days), with or without ketamine (
34 tact and nine carotid sinus denervated (CSD) fetal sheep (125-128 days gestation) we measured heart r
35 ebral blood flow in chronically instrumented fetal sheep (127-135 days gestation, term approximately
36 was measured in cardiomyocytes isolated from fetal sheep (135 day gestational age) in response to 100
37 eration, and dendritic maturation in preterm fetal sheep 4 weeks after HI.
38                   We studied a total of nine fetal sheep (95 to 103 days of gestation; term = 145 to
39   VIP immunostaining was extremely robust in fetal sheep adrenal cortical neurofibers and cells while
40 eta-cell responsiveness in hypoglycaemic (H) fetal sheep and ascertain whether a 5 day euglycaemic re
41 sent throughout the adrenal cortices of both fetal sheep and baboons, were heavily innervated by VIP-
42 olypeptide (VIP) and tyrosine hydroxylase in fetal sheep and fetal baboon adrenal cortices and medull
43 t the liver is a site of metformin action in fetal sheep and macaques, given relatively abundant OCT1
44 mboxane mimetic stimulates ACTH secretion in fetal sheep, and that the endogenous production of throm
45                          Under anesthesia, 5 fetal sheep at 0.8 gestation were instrumented with vasc
46                        Under anaesthesia, 12 fetal sheep at 118 +/- 1 days of gestation (term ca 145
47 IL-6 mAbs and systemically infused mAbs into fetal sheep at 126 days of gestation after exposure to b
48 aortopulmonary anastomosis was created in 10 fetal sheep at 140 +/- 1.2 days of gestation.
49 med in cerebral cortical cell membranes from fetal sheep at 88, 120, and 136 d gestation (term = 150
50  (RV) ventricles from IUGR and control (CON) fetal sheep at 90% gestation were harvested.
51  the endogenous production of new glucose by fetal sheep at a time when the amount of glucose transfe
52 raperitoneal or intrahepatic route (IH) into fetal sheep at concentrations ranging from 1.1-2.6 x 10(
53 er with a fluorescent O2 probe, in near-term fetal sheep at low altitude (n = 8) and those acclimatiz
54  (~10 min) umbilical cord occlusion (UCO) in fetal sheep at ~0.88 gestation on fetal plasma cortisol
55  of measuring cerebral metabolic rate in the fetal sheep based on heat production in a local region o
56    In pancreatic islets isolated from intact fetal sheep, beta cell proliferation in vitro was reduce
57               Eight chronically catheterised fetal sheep between 122 and 134 days gestation were subj
58 del, and human cells harvested from chimeric fetal sheep bone marrow have been shown to successfully
59  androgen, estrogen, and progesterone in the fetal sheep brain during the critical period for sexual
60 ervated by VIP-immunoreactive neurofibers in fetal sheep, but not in fetal baboons.
61 l model, ASOs were delivered midgestation to fetal sheep by IA or intracranial injection.
62 episode of complete UCO late in gestation in fetal sheep can result in prolonged effects on fetal bra
63                                  We isolated fetal sheep cardiomyocytes and cultured them for 96 h, a
64 ized that suppression of MEIS1 expression in fetal sheep cardiomyocytes leads to a metabolic switch a
65 nsin II (Ang II) stimulates proliferation in fetal sheep cardiomyocytes when growth is dependent on t
66 exposure on later reactivity to adenosine in fetal sheep cerebral arterioles.
67 examethasone (n = 6) was infused for 48 h in fetal sheep commencing at 125 days of gestation.
68 drenal cortex and medulla is much greater in fetal sheep compared to fetal baboons.
69 normal sera from neonatal and adult, but not fetal, sheep contained IgM and IgG XNA reactive with rat
70 medulla were smaller in diameter compared to fetal sheep cortex (1.22+/-0.13 vs. 2.93+/-0.34 microm,
71                                This study in fetal sheep demonstrates that fetoscopic and open transu
72 and dyadic assembly proceed gradually during fetal sheep development, from 93 days of gestational age
73 y proceed gradually in cardiomyocytes during fetal sheep development, from 93 days of gestational age
74  distribution of ligand binding sites in the fetal sheep diencephalon indicated that the highest leve
75 distribution of adenosine A(2A) receptors in fetal sheep diencephalon, we have used a receptor autora
76 ysiological responses to acute hypoxaemia in fetal sheep during and following maternal treatment with
77 ic GHR mRNA has therefore been determined in fetal sheep during late gestation and after experimental
78 The results show that glucogenesis occurs in fetal sheep during late gestation in conditions in which
79                                           In fetal sheep during late gestation the aims of the presen
80  human mesenchymal stem cell population into fetal sheep early in gestation, before and after the exp
81        In a model of human chorioamnionitis, fetal sheep exposed to a single injection, but not repea
82 ing primary and to a lesser degree secondary fetal sheep, failed to engraft tertiary recipients.
83 erformed studies in primary hepatocytes from fetal sheep, fetal macaques, and juvenile macaques.
84 , transfer of CD34+/CD38+ cells to preimmune fetal sheep generated only short-term human hematopoiesi
85  We tested the hypothesis that high-altitude fetal sheep have evolved cardiovascular compensatory mec
86 tation intrauterine growth-restricted (IUGR) fetal sheep have fewer binucleated cardiomyocytes, refle
87 de that cardiac nerves in the late-gestation fetal sheep have minor influences on plasma renin activi
88 identification and pathway analysis of novel fetal sheep heart transcriptome splice variants is a fir
89               We have examined the expressed fetal sheep heart transcriptome using high-throughput se
90               A recent finding of persisting fetal sheep hypoxia beyond the duration of CO2 pneumoper
91 ateral ventricle of chronically instrumented fetal sheep in utero at 128 +/- 1 days gestation (term i
92 ultilineage human hematopoiesis in the human-fetal sheep in vivo model.
93 nd dexamethasone treatment of late-gestation fetal sheep, in doses similar to those employed clinical
94                            Hypothyroidism in fetal sheep induced by removal of the thyroid gland caus
95 , and that growth retardation in hypothyroid fetal sheep is associated with reductions in pancreatic
96                  One marker of this state in fetal sheep is neck nuchal muscle atonia (NA).
97 ronary conductance with adenosine in anaemic fetal sheep is twice that of non-anaemic fetuses.
98                                  In isolated fetal sheep islets studied in vitro, thyroid hormones in
99  While cortisol is known to reduce growth in fetal sheep, its effects on the uteroplacental handling
100 10 days of umbilicoplacental embolization in fetal sheep, IUGR fetuses had elevated circulating long-
101 10 days of umbilicoplacental embolization in fetal sheep, IUGR fetuses had elevated circulating long-
102 term rise in tri-iodo-l-thyronine (T(3) ) in fetal sheep leads to the inhibition of proliferation and
103 ndrial proteins driving ATP synthesis in the fetal sheep lung.
104  in cerebral vascular response to hypoxia in fetal sheep may not be attributed to changes in vascular
105                                VIP fibers in fetal sheep medulla were smaller in diameter compared to
106 PS), we validated this hypothesis in primary fetal sheep microglia cultures re-exposed to LPS in pres
107                        We employed a preterm fetal sheep model of global cerebral ischemia in which a
108                               Here we used a fetal sheep model of in utero transplantation to investi
109  during basal and insulin clamp periods in a fetal sheep model of placental insufficiency and IUGR.
110 y demonstrated in a chronically catheterized fetal sheep model that experimentally elevated glucagon
111                            We used a preterm fetal sheep model that reproduces key features of brain
112                            We used a preterm fetal sheep model using both sexes in twin 0.65 gestatio
113                            We used a preterm fetal sheep model using both sexes that reproduces the s
114                                           In fetal sheep (n = 8) with laser Doppler flowmeter, fluore
115                         We conclude that, in fetal sheep, neither adrenaline nor cGMP stimulate lung
116 ration induced by intraamniotic endotoxin in fetal sheep occurred without an increase in fetal plasma
117                                         In 5 fetal sheep of 109 to 111 days of gestation (term, 147 d
118                                      Sixteen fetal sheep of known gestational ages (124-128 days' ges
119                       We hypothesize that in fetal sheep of this age, medullary neurofibers derive pr
120                                              Fetal sheep of ~131 days gestation (n = 8) were chronica
121 tic hernias were created surgically in seven fetal sheep on gestational day 100 (term = 145 days).
122                           Experiments in the fetal sheep or neonatal rat, mouse, or pig reveal dramat
123                                       In the fetal sheep, parturition is triggered by an increase in
124                                              Fetal sheep physiology has been extensively studied sinc
125 have since used the chronically instrumented fetal sheep preparation to investigate the fetal compens
126 harvested from the brains of third trimester fetal sheep previously exposed in the second trimester t
127                     Late gestation singleton fetal sheep received a direct intravenous infusion of gl
128      Chronically catheterized late gestation fetal sheep received an intravenous infusion of glucagon
129 s were injected into a total of 14 preimmune fetal sheep recipients using the amniotic bubble techniq
130 Prenatal glucocorticoid plus T4 treatment of fetal sheep results in improvements in oxygenation, gas
131 days in media containing 10% control or IUGR fetal sheep serum (FSS).
132    The present study utilized late gestation fetal sheep, stereotaxic methodology and retrograde axon
133 rs occurred in greater (P<0.05) frequency in fetal sheep than in fetal baboons (14.82+/-3.10 vs. 0.84
134 3 mmHg) steady-state conditions in near-term fetal sheep that had undergone either surgical sham or b
135 al cortex (FCTX) and olfactory bulbs (OB) of fetal sheep that were delivered on day 64 of gestation.
136                                           In fetal sheep, the rates of growth and umbilical glucose u
137                                Therefore, in fetal sheep, thyroid hormones are important for the prep
138 eriments were carried out in unanaesthetized fetal sheep to evaluate the significance of non-N-methyl
139                              Exposure of the fetal sheep to moderate to severe hypoxic stress results
140 133-selected cells engraft successfully in a fetal sheep transplantation model, and human cells harve
141  conclusion, rodent grafts transplanted into fetal sheep undergo HAR, likely through direct activatio
142                                    Near-term fetal sheep underwent surgical instrumentation and were
143                                 Instrumented fetal sheep underwent UPE for either 10 or 20 days.
144             Experimental manipulation of the fetal sheep urinary tract has proved informative in unde
145 high-titer retroviral vectors into preimmune fetal sheep was previously demonstrated.
146                 The purpose of this study in fetal sheep was to assess the feasibility of fetoscopic
147          Using in utero transplantation into fetal sheep, we examined the capability of human bone ma
148 tion control (CON) (n = 8) and IUGR (n = 13) fetal sheep were catheterized with aortic and femoral ca
149                               Late gestation fetal sheep were chronically catheterised in utero to al
150                                      Sixteen fetal sheep were chronically instrumented at 118+/-2 day
151                                      Fifteen fetal sheep were chronically instrumented between 117 an
152                                              Fetal sheep were given intra-amniotic (IA) injections of
153                                              Fetal sheep were given intra-amniotic injections of sali
154 latory responses to acute hypoxia, near-term fetal sheep were instrumented with laser Doppler probes
155                        Under anaesthesia, 18 fetal sheep were instrumented with vascular and amniotic
156     Chronically instrumented, late-gestation fetal sheep were prepared to: (1) characterize cardiovas
157 effects on fetal brain functions are unknown Fetal sheep were subjected to umbilical cord occlusion (
158                                              Fetal sheep were surgically instrumented with catheters.
159 rticoids correct the pulmonary immaturity of fetal sheep with CDH by physiologic, biochemical, and hi
160                                  In summary, fetal sheep with IUGR have increased hepatic glucose pro
161  of systems approaches uniquely available in fetal sheep with the power of genomic studies.
162 otoxin would induce early lung maturation in fetal sheep without increasing fetal cortisol.

 
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