ライフサイエンスコーパス: postnatal age

1 poor responders" (<1000 g and > or = 10 days postnatal age).

2 ole-sensitive GABAA receptors increased with postnatal age.

3 t barrier function is attained within 2-4 wk postnatal age.

4 l immediately after birth and increases with postnatal age.

5 s not expressing this subunit, regardless of postnatal age.

6 nditional, with the relevant condition being postnatal age.

7 n subnuclei of this structure with advancing postnatal age.

8 infections occurred more often at a younger postnatal age.

9 rrespective of the extent of gland growth or postnatal age.

10 that are regulated by synaptic activity and postnatal age.

11 ne anesthesia exposure conducted at an early postnatal age.

12 it hypomyelination and gliosis at 2 weeks of postnatal age.

13 retinal homogenates increased with advancing postnatal age.

14 eaked at 1 day of age and then declined with postnatal age.

15 colocalization was observed with increasing postnatal age.

16 TH at P1, but colocalization increased with postnatal age.

17 glucocorticoid exposure persists to 5 months postnatal age.

18 ion were investigated in pigs at 3 months of postnatal age.

19 retinal capillaries is strongly dependent on postnatal age.

20 itioned responses increased as a function of postnatal age.

21 KD specimens obtained at different fetal and postnatal ages.

22 logy of single axons was examined at several postnatal ages.

23 rectifying K+-channel in the brain at later postnatal ages.

24 migration was predominantly radial at early postnatal ages.

25 tern was consistently maintained through all postnatal ages.

26 st common form of degeneration seen at early postnatal ages.

27 release by melanotrophs from fetal and early postnatal ages.

28 pplied to brains fixed at different pre- and postnatal ages.

29 ne in the inner ear at various embryonic and postnatal ages.

30 ence of distinct fear responses at different postnatal ages.

31 brainstem preparations of rats at different postnatal ages.

32 te gyrus in the rat hippocampus during early postnatal ages.

33 e and female offspring were analyzed at five postnatal ages.

34 d remained active in all lens cells, even at postnatal ages.

35 2/3 of the ferret visual cortex at different postnatal ages.

36 the hippocampus at late embryonic and early postnatal ages.

37 protect against fibrocalcific disease during postnatal aging.

38 One week later at postnatal age 0 (P0), the equivalent of a full-term preg

39 rterially perfused neonatal rat preparation (postnatal age 0-4 days) to assess the effects of blockin

40 and height, and cortical layer thickness at postnatal ages 0, 1, 3, 6, 15, 24, 48, and 72 months, fo

41 ssue samples at 14 to 39 weeks gestation and postnatal ages 0-83 years.

42 We found at relatively mature postnatal ages (15-17 d after birth) LES rat calyces sho

43 c response to hyperthermia in neonatal rats (postnatal age 2-4 days), pregnant dams were exposed to n

44 ession (LTD) in CA1 that is (1) sensitive to postnatal age, (2) saturable, (3) induced postsynaptical

45 ry cortex, where the maximum is reached near postnatal age 3 months.

46 l immune system, but rapidly diminished with postnatal age; 3) lacked IFN-gamma production capability

47 s ranging from gestational age 17 wk through postnatal age 4 wk.

48 hypoxic challenge (10% O2) were conducted at postnatal ages 5, 10, 15, and 30 days.

49 HT inside postnatal mouse LSO neurons, pups (postnatal ages 5-6) were treated with fluoxetine and LSO

50 ynaptic connections exists from the earliest postnatal ages, although it gives rise to responses that

51 filiform-like spines, each as a function of postnatal age and anterior/posterior location.

52 [(3)H]WIN 35,428 binding did not change with postnatal age and did not differ between cocaine and sal

53 lotting and revealed different patterns with postnatal age and location.

54 of CARTp-IR and nNOS or TH was dependent on postnatal age and showed an inverse relationship.

55 in the spinal gray matter in cats of varying postnatal ages and adults.

56 ker than mGluR1alpha immunoreactivity at all postnatal ages and showed a similar change in subcellula

57 licate room air control animals at different postnatal ages and triplicate oxygen-treated animals at

58 Corticogeniculate innervation occurred at postnatal ages and was delayed compared with the arrival

59 f 124 infants had acquired MRE by 2 weeks of postnatal age, and 69 (56%) infants had acquired MRE by

60 riety of factors, including gestational age, postnatal age, and birth weight, and may be influenced b

61 cy matched according to sex, gestational and postnatal age, and preimaging serum Cr levels with neona

62 r allowing for sex, ethnic group, body size, postnatal age, and socioeconomic status, TPTEF:TE remain

63 ndantly during fetal development than during postnatal ages, and their expression was higher in the h

64 losure rates with INDO for neonates >10 days postnatal age are the result of pharmacokinetic differen

65 Postnatal age at diagnosis ranged from 5 to 34 days.

66 s, gestational age at birth, infant sex, and postnatal age at magnetic resonance imaging scan.

67 analyses adjusted for sex, season of birth, postnatal age at neonatal sample collection, preterm bir

68 , there was a strong correlation between the postnatal age at which GABA(A)-R antagonists decreased a

69 three main CNS neural cell types at various postnatal ages between postnatal day 1 (P1) and P30.

70 developing hair cells continues until early postnatal ages, but the function of this late expression

71 edical OC projection to the cochlea at early postnatal ages, ChAT immunoreactivity was detected below

72 of the mouse PFC, and found that, from early postnatal age, ChCs and BCs differ in laminar location.

73 sed on statistically defined gestational and postnatal age-dependent normative blood pressure values

74 At 245 +/- 1 days postnatal age (DPNA), offspring were instrumented for bl

75 This overlap is largest at early postnatal ages followed by a significant refinement and

76 Somatic I(h) current density increased with postnatal age from 5 to 16 days old, suggesting that I(h

77 ial cells, but mean latencies decreased with postnatal age, from 33.1 +/- 2.78 ms at P3 to 7.3 +/- 0.

78 : GABA-evoked maximal current increased with postnatal age; GABAA receptors changed from BZ type 3 in

79 Somal growth occurs between all postnatal age groups tested for OV, LV, and DD nuclei, a

80 high glucose than adult SCG neurons whereas postnatal age had no influence on the response of CG/SMG

81 Ret phosphorylation markedly increased with postnatal age in SCG neurons in vitro and in vivo.

82 icate that K+ current density increases with postnatal age in the rat.

83 ates of cell death were seen at the earliest postnatal ages in most regions.

84 migration was predominantly radial at early postnatal ages in the gyrencephalic ferret cortex.

85 fic cortical region of conscious mice of any postnatal age, including perinatal and neonatal stages,

86 diversity of neuronal cell types present at postnatal ages, including chandelier cells.

87 ups were inoculated with LCMV at a series of postnatal ages, including postnatal days 1, 4, 6, 10, 21

88 tion of an alternative serotype at 12 months postnatal age increased hFVII levels to 165% +/- 6.2% of

89 These results suggest that postnatal age influences the regional vulnerability to h

90 the relationship between iron retention and postnatal age, iron nutritional status, iron intake (or

91 At all postnatal ages, layer I neurons were capable of repetiti

92 were noted between neonates categorized for postnatal age <10 days vs. > or = 10 days in total days

93 D curves were also similar for neonates with postnatal age <10 days vs. > or = 10 days.

94 At early postnatal ages (<P12), optic tract evoked responses were

95 At testing, SGA infants were of similar postnatal age (mean [SD]: SGA 6.8 [2.4] wk, AGA 5.9 [2.3

96 /wk) from 45-50 d gestational age to 72-77 d postnatal age (n = 4/group).

97 Newborn rabbits at 3 days postnatal age (n = 96) received room air or oxygen (80%-

98 al age; n = 5) or 3 to 4 wk old (matched for postnatal age; n = 5).

99 Sox2, specifically in SCs at three different postnatal ages (neonatal, juvenile and adult) in mice.

100 With advancing postnatal age, NR1 expression increased in the nucleus t

101 toplethysmographically at a median corrected postnatal age of 11 months (range, 1 week to 66 months).

102 or a higher-protein group at a median (IQR) postnatal age of 7 (6-8) days.

103 nit NR1 and c-fos after exposing rat pups at postnatal ages of 2 d, 5 d, 10 d, and 20 d and adult rat

104 at postsynaptic sites at both early and late postnatal ages on Renshaw cells.

105 sm in kittens, starting at birth and through postnatal age (P) 180 days as well as in adult cats.

106 ts and hypoxic ventilatory depression at all postnatal ages (p < 0.01).

107 ta-Gal/beta-Gal)) HCs, we examined neonatal (postnatal ages P0-P4.5) Math1-null chimeric mice in whic

108 f BDNF mRNA in granule cells was observed at postnatal age (P15), coincident with the onset of ataxia

109 scopy, and immunoelectron microscopy at four postnatal ages: P15, P25, P35, and adult.

110 ve similar innervation patterns at different postnatal ages (P18-P90), with only relatively small lat

111 postsynaptic membranes of synapses at early postnatal ages (P2 and P5) and was higher in climbing fi

112 Between postnatal ages P60 to P90, mice underwent a series of te

113 Since the anomalous current declines with postnatal age, PIEZO2 may contribute to hair cell develo

114 Gestational and postnatal ages played an equal role in absolute FFM accr

115 monkeys (Macaca mulatta) who, at 2 weeks of postnatal age, received selective bilateral ibotenic aci

116 ic architecture, we found that even at early postnatal ages relay cells could be readily classified a

117 cal microstimulation of the RVM at different postnatal ages revealed a robust shift in the balance of

118 RPE cell lysates from rat retinas of various postnatal ages revealed increasing levels of EBP50 and S

119 the telencephalon at different embryonic and postnatal ages showed that serotonin stimulates prolifer

120 effect on ventilation abates with increasing postnatal age suggesting that the neural substrate media

121 At later postnatal ages, these synaptic complexes stop maturing a

122 expression at all spinal levels across eight postnatal ages to detect regional and developmental diff

123 e Mecp2 gene in ~80% of brain cells at three postnatal ages to determine whether the need for MeCP2 v

124 nhibition of the miR-15 family from an early postnatal age until adulthood increases myocyte prolifer

125 neurons in mouse visual cortex at different postnatal ages, using two-photon calcium imaging in vivo

126 At all postnatal ages, vzg-1 expression was concentrated in and

127 Rabbits 1 day to 42 days of postnatal age were evaluated by in vivo confocal microsc

128 response rates based on treatment weight or postnatal age were observed.

129 rons in fetal nigral transplants occurs at a postnatal age when endogenous dopamine and BDNF show the

130 hesis of 5-HT, brainstem sections of mice at postnatal ages when 5-HT staining is the most robust wer

131 n by exposure to ionizing radiation in early postnatal age, when lens epithelial cells undergo rapid

132 c-to-hypertrophic growth transition at early postnatal age, which is important in establishing normal

133 lation of NG2-positive cells from very early postnatal ages, which migrates toward the pial surface a

134 s with gram-negative bacteria increased with postnatal age, while the percentage of sterile samples d

135 y cortex of developing rat pups at different postnatal ages with a high temporal resolution.

136 increased c-fos expression in the nTS at all postnatal ages, with a marked increase occurring in >/=