ライフサイエンスコーパス: intoxicated

1 iders (91.3%) and 86 bicyclists (69.4%) were intoxicated.

2 milarly intoxicated than if tested while not intoxicated.

3 nly apparent if the animals are tested while intoxicated.

4 grade memory task of alcohol impairment when intoxicated.

5 lls are not able to take up TpeL and are not intoxicated.

6 tic brain-injured (TBI) patients are alcohol intoxicated.

7 e-Scooter riders were more often intoxicated (336 [39.5%] vs 180 [7.7%]) and had a lower

8 Finally, apoptosis was observed in CNF1-intoxicated 5637 cells.

9 .1% vs 7.1%) or conviction for driving while intoxicated (7.9% vs 1.2%).

10 Intoxicated AM remained fully capable of B. anthracis sp

11 nflammasome activation and apoptosis of LeTx-intoxicated and B. anthracis-infected macrophages.

12 For this, thioacetamide (TAA)-intoxicated and bile-duct-ligated (BDL) rats were used a

13 Fibroblasts that were intoxicated and later stimulated to proliferate failed t

14 e drinking, physical fighting, driving while intoxicated, and alcohol-related health problems and wer

15 or driver age, sex, history of driving while intoxicated, and survival status, implementation of the

16 fects and clinical presentation if abused or intoxicated, and to know what anesthetic options would b

17 clists, did not use helmets, were more often intoxicated, and were more often injured during nighttim

18 MPTP-intoxicated animals that received Cop-1 immune cells sho

19 f-function mutants resemble those of ethanol-intoxicated animals.

20 n intoxication allowed the rescue of 100% of intoxicated animals.

21 om agonist-treated mice administered to MPTP-intoxicated animals.

22 stry values from buffer-treated versus ricin-intoxicated animals.

23 ects on vulnerable neurons or mediated by GA-intoxicated astrocytes that fail to support neuron funct

24 unable to communicate clearly, and who were intoxicated at the time of screening.

25 However, intoxicated bees were as willing to engage in trophallax

26 0 adults who had blood alcohol measured were intoxicated (blood alcohol content >22 mmol/L [100 mg/dL

27 Intoxicated burned mice demonstrated a two-fold (p < 0.0

28 and sciatic nerves was reduced in galactose-intoxicated, but not streptozotocin-diabetic rats.

29 at the time of injury, and 516 (16.2%) were intoxicated by alcohol or other drugs.

30 ouse diaphragm neuromuscular junctions fully intoxicated by BoNT serotype A.

31 In contrast, synapses fully intoxicated by BoNT serotypes D or E were refractory to

32 ndplate potentials in mouse diaphragms fully intoxicated by BoNT/A.

33 tantial redistribution in human airway cells intoxicated by ExoS, -T, and -Y.

34 We find that DeltacpgA cells are intoxicated by glucose or other carbon sources that feed

35 in the evaluation of all patients who may be intoxicated by natural substances.

36 Senescence is transmitted to non-intoxicated bystander cells by an unidentified senescenc

37 Dermonecrotic lesions of supernatant intoxicated CD36(-/-) mice are significantly larger, wit

38 ating that BFT did not injure HT29/C1 cells, intoxicated cells exhibited regulatory volume decrease,

39 capacity of Stxs to alter gene expression in intoxicated cells have been limited to individual genes.

40 p1-induced mitochondrial fission within VacA-intoxicated cells inhibited the activation of the proapo

41 uction of lethal mitochondrial damage in TNF-intoxicated cells is discussed.

42 e the mammalian cell, ExoU rapidly lyses the intoxicated cells via its phospholipase A(2) (PLA(2)) ac

43 In Stx-intoxicated cells, the NLRP3 inflammasome triggered the

44 sing depolarisation of the inner membrane in intoxicated cells, together with increased outer membran

45 Within intoxicated cells, vacuolation precedes cytochrome c rel

46 ng distinct ion selectivities and impacts on intoxicated cells.

47 to quantify the cytosolic pool of PTS1 from intoxicated cells.

48 xoS trafficking to the perinuclear region of intoxicated cells.

49 ading to cell cycle arrest and distension of intoxicated cells.

50 , which inhibits the accumulation of cAMP in intoxicated cultured cells, significantly decreases the

51 1-556) plus anthrax toxin protective antigen intoxicated cultured mammalian cells and caused actin re

52 re significantly reduced or abolished in Stx-intoxicated D-THP-1 cells in which the expression of NLR

53 involvement in risky driving, riding with an intoxicated driver and being taken advantage of sexually

54 to determine probable cause and to arrest an intoxicated driver at the scene, the results are prelimi

55 e validity of this test in the conviction of intoxicated drivers.

56 astrocytes in the hippocampus of 26 lethally intoxicated drug addicts and 35 matched controls are des

57 0,+)AT-rBAT transfectants became selectively intoxicated during exposure to Cys-S-Hg-S-Cys.

58 s, and improved locomotor activities in MPTP-intoxicated Gfaf(cre) mice, but not Gdnf( astro) mice la

59 ere were 65 abnormal CT scans (10.3%) in the intoxicated group.

60 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-intoxicated hemiparkinsonian monkeys.

61 Pet-intoxicated HEp-2 and HT29 cells stained with fluorescei

62 plasma membrane to the perinuclear region of intoxicated host cells.

63 Alcohol-intoxicated humans have high levels of fatty acid ethyl

64 ifetime ounces of alcohol consumed and times intoxicated in lifetime estimated at visits 1 week or mo

65 2 are activated in vivo in the colon of Stx2-intoxicated infant rabbits, a model in which Stx2 induce

66 SDL), information learned while an animal is intoxicated is recalled more effectively when the subjec

67 abrogates IL-1beta and IL-18 secretion by DT-intoxicated keratinocytes, while ZAKalpha deletion or in

68 CBD treatment significantly improved ethanol-intoxicated larval survival rate by 40% and also improve

69 ght percent of trespassers were killed while intoxicated (median alcohol level, 56 mmol/L [260 mg/dL]

70 ary bacterial burden was observed in alcohol-intoxicated mice at 16 and 24 h and was associated with

71 Orally intoxicated mice could be rescued by MAb 11E10 6 h but n

72 etected Stx2a in kidney sections from orally intoxicated mice in the same region as the epithelial ce

73 stration 4 h after MRSA infection in alcohol-intoxicated mice rescued USA300 clearance in vivo.

74 Furthermore, kidney sections from Stx2a-intoxicated mice revealed multifocal, acute tubular necr

75 l-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-intoxicated mice where it inhibits parkin through tyrosi

76 istopathology, and full protection of orally intoxicated mice with monoclonal antibody (MAb) 11E10 di

77 x with the enzyme, their protective index on intoxicated mice, and their pharmacokinetics.

78 s and protected dopaminergic neurons in MPTP-intoxicated mice, but at levels less than simvastatin.

79 rs and improved locomotor activities in MPTP-intoxicated mice.

80 locomotor activities in SARS-CoV-2 spike S1-intoxicated mice.

81 locomotor activities in SARS-CoV-2 spike S1-intoxicated mice.

82 istent and progressive disease in acute MPTP-intoxicated mice.

83 inuous impairment of motor functions in MPTP-intoxicated mice.

84 itters, and improved motor functions in MPTP-intoxicated mice.

85 t against nigrostriatal degeneration in MPTP-intoxicated mice.

86 l-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-intoxicated mice.

87 of neuronal cell bodies and termini in MPTP-intoxicated mice.

88 unced effects in VIPR2 agonist-treated, MPTP-intoxicated mice.

89 nd that ricin rapidly reaches the kidneys of intoxicated mice.

90 and GGTI also protected nigrostriata in MPTP-intoxicated mice.

91 n the substantia nigra pars compacta of MPTP-intoxicated mice.

92 to non-transplanted, X-irradiated cuprizone-intoxicated mice.

93 itters, and improved motor functions in MPTP-intoxicated mice.

94 nigra pars compacta of PD patients and MPTP-intoxicated mice.

95 e nigrostriatal dopaminergic pathway in MPTP-intoxicated mice.

96 l-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-intoxicated mice.

97 is downregulated in PD patients and in MPTP-intoxicated mice.

98 We used the progressively MPTP-intoxicated monkey model that expresses recovery from mo

99 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-intoxicated monkey model to further elucidate the nature

100 l-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-intoxicated monkeys (when motor symptoms are less appare

101 rior olive neurons obtained from chronically intoxicated monkeys revealed a significant up-regulation

102 only used antimalarial agent, endows anthrax-intoxicated murine peritoneal macrophages with a 50% and

103 medication inhibiting cytochrome 450 3A, or intoxicated on the day of surgery were excluded.

104 vents by increasing risk-taking behaviors in intoxicated or impaired persons.

105 SH and GSSG in rat urine and plasma samples, intoxicated or not by lead.

106 enzimidazoles, those who were acutely ill or intoxicated, or those reporting treatment within the pre

107 chemical and histological parameters in mice intoxicated orally versus intraperitoneally with Stx2a.

108 We also propose that mice intoxicated orally with ricin likely die from distributi

109 Specifically, intoxicated participants showed higher false recognition

110 In a misinformation task, intoxicated participants were more susceptible to false-

111 vidence for enhanced false-memory effects in intoxicated participants.

112 ne clearance based on a normal CT scan among intoxicated patients with no gross motor deficits appear

113 en; mean age, 40.3 years), 13 age-matched CO-intoxicated patients without parkinsonism, and 13 age-ma

114 the cervical spine should not be cleared in intoxicated patients, resulting in prolonged immobilizat

115 mal CT scans are sufficient to clear CSIs in intoxicated patients.

116 on reduces GCS, thus limiting its utility in intoxicated patients.

117 e" outbreak because of the appearance of the intoxicated persons.

118 ompare the unadjusted mortality of the total intoxicated population and for specific intoxication sub

119 ared to both control (P<0.001) and galactose-intoxicated rats (P<0.05).

120 e-mediated function in LED-treated, methanol-intoxicated rats.

121 onses were profoundly attenuated in methanol-intoxicated rats.

122 ith unchanged metallothionein-I in manganese-intoxicated rats.

123 n bile duct-ligated and carbon tetrachloride intoxicated rats.

124 3-beta-glucanase mRNA was up-regulated in Al-intoxicated roots, with highest expression after 12 h.

125 ists that rescue neurotransmission in BoNT/A-intoxicated synapses provides compelling evidence for po

126 y when the subject is tested while similarly intoxicated than if tested while not intoxicated.

127 gans undergoes olfactory learning (OL) while intoxicated, the learning becomes state dependent such t

128 ocations of the individual subunits in cells intoxicated, under various conditions, with hybrid heter

129 ith toxins) and endogeneous (serum from mice intoxicated via oral, intranasal, and intravenous routes

130 mates of lifetime ounces of alcohol or times intoxicated were observed.

131 In addition, many trauma patients are also intoxicated, which generally worsens outcomes.

132 nfers significant survival benefits for mice intoxicated with alpha-toxin or wSP in both therapeutic

133 estrain violent subjects, who are frequently intoxicated with cocaine and other drugs of abuse.

134 odulate enterotoxin expression because cells intoxicated with heat-labile toxin overproduce and relea

135 Rats were intoxicated with methanol, and retinal function was asse

136 We observed similar results in aged monkeys intoxicated with MPTP: they developed severe DOPA-respon

137 We observed that Vero cells intoxicated with Stx1a behave differently than those int

138 ted with Stx1a behave differently than those intoxicated with Stx2 subtypes: cells challenged with St

139 bunit delayed the mean time to death of mice intoxicated with Stx2a and reduced the cytotoxic effect

140 WldS and wild-type mice were intoxicated with the cancer chemotherapeutic agent pacli

141 akim Hospital ED and GI clinic who were lead-intoxicated, with or without opiate use disorder.