ライフサイエンスコーパス: neonatally

1 hat express the receptor tyrosine kinase Ret neonatally.

2 develop in homozygotes and these animals die neonatally.

3 AKR and NFS strains when they are inoculated neonatally.

4 te loss of paternal gene expression and died neonatally.

5 -) pups develop severe hydrocephalus and die neonatally.

6 roup included all seven patients with a post-neonatally acquired or progressive brain lesion who coul

7 normal preoperative hand function and a post-neonatally acquired or progressive lesion predict a loss

8 e functional organization of this nucleus in neonatally amputated adult rats.

9 At the brainstem level, neonatally amputated rat cuneate neurons possessed the f

10 ignificantly smaller (P < 0.05) than that of neonatally amputated rats (4.3 +/- 1.3 mm(2) vs. 6.6 +/-

11 e to peripheral stimulation vs. neurons from neonatally amputated rats (48% vs. 16%, respectively).

12 functional reorganization observed in SI of neonatally amputated rats may reflect functional alterat

13 associated with the stump and hindlimb SI in neonatally amputated rats.

14 we show that mutant mice lacking miR-218 die neonatally and exhibit neuromuscular junction defects, m

15 sgenic lines were homozygote inviable, dying neonatally and exhibiting heart malformations involving

16 hat many human atopic diseases are initiated neonatally and herald more severe IgE-mediated disorders

17 ons is located exclusively in dendrites both neonatally and in adulthood.

18 were more robust in animals exposed to acid neonatally and rechallenged, acutely, at P60.

19 As adults, neonatally antisense-treated, androgenized females showe

20 lumbar levels does not enhance the growth of neonatally axotomized DC axons.

21 After rechallenge of adult rats, neonatally B-chain-tolerized animals showed diminished B

22 the mechanisms of activation of microglia in neonatally BDV-infected rat brain have not been investig

23 thick skin and a defective barrier; they die neonatally because of dehydration and restricted movemen

24 Given neonatally, BPZE1 also protected against RSV-induced wei

25 Homozygous Orai1(KI/KI) mice die neonatally, but Orai1(KI/KI) fetal liver chimeric mice a

26 (-)2(-)7(+) and CD3(-)2(+)7(+), were present neonatally, but were essentially absent at 1 year.

27 the hindlimb of normal, cardiomyopathic and neonatally capsaicin-treated (NNCAP) rats (rats that lac

28 nduced PR protein and mRNA in the female and neonatally castrated male MPN on PN 4, indicating that t

29 tosis in the developing MPNc was examined in neonatally castrated males following T or vehicle inject

30 Subsequently, we found that treating neonatally castrated males with testosterone propionate

31 arlier rise in CBT during the light phase in neonatally castrated males.

32 Thus, adult male rats neonatally castrated on the first day after birth displa

33 ver, mice with CHD invariably die prenatally/neonatally, causing CHD phenotypes to be missed.

34 arly lineage T cell populations were present neonatally: CD3(+)4(-)8(-) T cells were present at birth

35 se-2 (MKP-2) during adulthood in control and neonatally CLI-treated rats (CLI rats).

36 munocompetent cells in the brain, are active neonatally, contribute to normal brain development, and

37 ed a pronounced decrease in cell diameter in neonatally deafened cats studied about 1 year after deaf

38 tal day 0 (P0) to P90 in control hearing and neonatally deafened rats.

39 When the neonatally deprived D2 and D3 whiskers were paired at ma

40 planted into the cheek pouches of control or neonatally DES-exposed adult hosts, and both host groups

41 ost exclusively to the two that consisted of neonatally DES-exposed uteri.

42 tion was maintained in uterine tumors of the neonatally DES-treated mice.

43 is site, however, remained methylated in the neonatally DES-treated/ovariectomized mice, indicating t

44 Mice with FLVCR that is deleted neonatally develop a severe macrocytic anemia with proer

45 n the efficacy of prenatally transferred and neonatally developed viral immunity has yet to be addres

46 in the gene of its ligand (endothelin 1) die neonatally due to craniofacial and cardiac abnormalities

47 skin and a defective skin barrier; they die neonatally due to dehydration and restricted movements.

48 and a defective epidermal barrier; they die neonatally due to dehydration and restricted movements.

49 ronal and muscle ion channels, but can occur neonatally due to placental transfer of maternal antibod

50 Neonatally engrafted hiPSC OPCs robustly myelinated the

51 D, we established human HD glial chimeras by neonatally engrafting immunodeficient mice with mutant h

52 anomalous, mirror-symmetric map observed in neonatally enucleated animals, are present by P6-7, just

53 ysis of susceptibility to viral infection in neonatally exposed mice revealed that CD28 deficiency di

54 tributes to the adult sexual deficit in rats neonatally exposed to citalopram.

55 However, offspring neonatally exposed to cocaine displayed a greater drug-i

56 In a 3-hr preference test, males neonatally exposed to exogenous OT exhibited a significa

57 not arise at increased frequency in animals neonatally exposed to ionizing radiation or the carcinog

58 l dose of the barbiturate, males and females neonatally exposed to phenobarbital exhibited a dramatic

59 aine was more pronounced in female offspring neonatally exposed to the drug.

60 sor exhibit two distinct clinical phenotypes-neonatally fatal and later-onset.

61 ransgene of an NMDAR1 splice variant rescues neonatally fatal NMDAR1 knockout (KO) mice, although the

62 Connexin43 knockout mice die neonatally from conotruncal heart malformation and outfl

63 males that were exposed to 160 microg/ml CSC neonatally had increased rates of pup resorption.

64 Adult male mice neonatally handled for 10 min/day exhibited a blunted co

65 Thus, neonatally implanted hGPCs outcompeted and ultimately re

66 Kittens were deafened neonatally, implanted at 4-5 weeks with intracochlear el

67 Neonatally induced microgyric lesions produce defects in

68 Thus, recovery from neonatally induced T cell anergy requires B7 molecules t

69 LPS challenge prevents memory impairment in neonatally infected (NI) rats.

70 in vulnerability were replicated in vivo in neonatally infected LEW and SD rats.

71 but, like the parent virus, it persisted in neonatally infected mice without clinical signs of disea

72 Furthermore, quinolinic acid was elevated in neonatally infected rat brains.

73 KMO protein levels were increased in neonatally infected rats and colocalized with neurons, t

74 After LPS, neonatally infected rats exhibited faster increases in i

75 in glial cell marker mRNA in hippocampus of neonatally infected rats, and this increase remained ele

76 y prevented LPS-induced memory impairment in neonatally infected rats.

77 a brain region- and time-dependent manner in neonatally infected rats; however, its expression was hi

78 s acute cerebral amyloid angiopathy (CAA) in neonatally-injected transgenic CRND8 mice.

79 ltured MSCs can restore normal compliance in neonatally injured lungs, possibly by paracrine modulati

80 duces clinical neurologic disease in 100% of neonatally inoculated mice, with an incubation period of

81 NIH/Swiss mice neonatally inoculated with MoFe2 developed T-cell lympho

82 ed from the spleen of a Mus spicilegus mouse neonatally inoculated with Moloney MLV.

83 Neonatally irradiated and control Ptch1(+/-) mice were c

84 th factor beta/Smad signaling pathway in the neonatally irradiated lens, and up-regulation of mesench

85 arlier in life in ARF-null animals that were neonatally irradiated or given dimethylbenzanthrene, and

86 g was measured in several brain regions from neonatally isolated (ISO) and nonhandled (NH) adult male

87 on (LTD) of BLA-DG synapses were recorded in neonatally isolated and non-handled freely behaving adul

88 Atelosteogenesis type II (AO II) is a neonatally lethal chondrodysplasia whose clinical and hi

89 ment of pulmonary veins (ACD/MPV) is a rare, neonatally lethal developmental disorder of the lung wit

90 s of human skeletal dysplasia, including the neonatally lethal dwarfism known as thanatophoric dyspla

91 inactivation of individual ENaC subunits is neonatally lethal in mice.

92 ndrome (MKS) is a genetically heterogeneous, neonatally lethal malformation and the most common form

93 nclude the most severe forms of MFS, such as neonatally lethal presentations.

94 des of FATP4 expression led to rescue of the neonatally lethal skin defects, and the resulting mice w

95 In mice, the complete lack of CBS is neonatally lethal.

96 nction affects all expressing tissues and is neonatally lethal; heterozygous null mutations cause ani

97 Neonatally, males received either an injection of OT, an

98 Recordings from VPL of neonatally manipulated rats revealed a small, but signif

99 etrograde tracers into the MGN of normal and neonatally operated adult ferrets, respectively.

100 it cognitive changes in trisomic mice either neonatally or in adulthood.

101 n d3tx female mice, d3tx male mice, and d3tx neonatally ovariectomized (OX) females.

102 pare this to the development in rats treated neonatally (postnatal days 2-14) with anti-NGF.

103 A combination of 4 factors available neonatally predicted 78% of severe and 49% of attenuated

104 However, Prdm16 germline knockout mice died neonatally, preventing us from testing whether Prdm16 is

105 The enhanced neuroimmune response seen in neonatally primed animals could also be demonstrated in

106 amines were examined in adult rats which had neonatally received bilateral intracerebroventricular in

107 long lasting; rats trained at PND 60, after neonatally receiving the original high dose of MK-801, d

108 s administered 6-OHDA soon after weaning, or neonatally, respectively model Parkinson's disease (PD)

109 We hypothesized that increased GABA neonatally results in masculinization.

110 Neonatally screened carriers also had neuroblastoma (n =

111 osed in 11 of these carriers but in only two neonatally screened noncarriers (P < .001); six patient

112 mice undergoing primary infection as adults, neonatally sensitized mice showed enhanced airway fluid

113 Lungs of neonatally sensitized mice showed increased 5-lipoxygena

114 of orexin and orexin receptors in adult rats neonatally subjected to either ten days of MD or a contr

115 hat the development of autoimmune disease in neonatally thymectomized mice is caused by the escape of

116 in which retinal projections are redirected neonatally to the auditory thalamus have visually respon

117 ly reported that prolonged graft survival in neonatally tolerant mice was associated with enhanced Th

118 Similarly, LEW rats neonatally tolerized against either Rhsp65 or Bhsp65 wer

119 Neonatally tolerized animals were unable to mount antibo

120 nsgenic mouse model in which CD8 T cells are neonatally tolerized following interaction with a parenc

121 ing induction of EAE in adult mice that were neonatally tolerized with Ig-PLP1 restores and exacerbat

122 Neonatally transplanted human glial progenitor cells (hG

123 ly in adult transplanted mice but not in the neonatally transplanted mice.

124 , the adult splenic T cell response of these neonatally treated mice lacked the usual Vbeta8.2Jbeta1.

125 Animals neonatally treated with kainate, (+/-)-1-amino-1,3-cyclo

126 o sham-operated males, and adult female rats neonatally treated with testosterone propionate on the f

127 Neonatally undernourished females display attenuated pos

128 Neonatally vaccinated infants, infants born to vaccinate

129 ralizing antibody titers sufficed to protect neonatally vaccinated mice against a subsequent challeng

130 s neutralizing Ab titers sufficed to protect neonatally vaccinated mice against a subsequent challeng

131 We find that Atf5(-/-) pups die neonatally, which, as explained below, is consistent wit

132 in a transfer system, whereas those treated neonatally with anti-TNF show no alteration in ability t

133 Animals treated neonatally with capsaicin, to eliminate C-fiber input, d

134 and mature (21- and 30-day-old) mice treated neonatally with DES.

135 Adult rats treated neonatally with E. coli also had decreased hippocampal a

136 In experiment 2, rats treated neonatally with E. coli or PBS received as adults either

137 Next, rats treated neonatally with E. coli or PBS were injected in adulthoo

138 morphine analgesia than female rats treated neonatally with either vehicle (1-5 mg/kg) or testostero

139 rian hamsters retain-->of both sexes treated neonatally with monosodium glutamate (MSG) that destroys

140 Females treated neonatally with NBQX (2,3-dihydroxy-6-nitro-7-sulfonyl-b

141 ons die in utero with a phenocopy of DGS, or neonatally with neural tube defects.

142 In rats infected neonatally with the Borna disease virus that lack blood-

143 Surprisingly, mice treated neonatally with these antibiotics develop exacerbated ps

144 iii) CD4+CD25+ T cells from NOD mice treated neonatally with TNF show compromised effector function i

145 In adulthood, rats infused neonatally with TTX displayed motor hyperactivity after

146 nged the potency (20-30%) in females treated neonatally with vehicle.