ライフサイエンスコーパス: golden hamster

1 the autonomic innervation of the eye in the golden hamster.

2 nt, Arvicanthis niloticus, and the nocturnal golden hamster.

3 d on the floor of the third ventricle of the golden hamster.

4 uced in the buccal cheek pouch of the Syrian golden hamster.

5 ction against lethal NiV challenge in Syrian golden hamsters.

6 tudied over several time points using Syrian golden hamsters.

7 yndrome coronavirus 2 (SARS-CoV-2) in Syrian golden hamsters.

8 r regeneration in SARS-CoV-2 infected Syrian golden hamsters.

9 s in a model using highly susceptible Syrian golden hamsters.

10 ffer in their oncogenic potentials in Syrian golden hamsters.

11 e development of offensive behaviors in male golden hamsters.

12 C and was attenuated in the lungs of Syrian golden hamsters.

13 in the regulation of offensive aggression in golden hamsters.

14 rmic (control), cold control and hibernating golden hamsters.

15 that suppresses the ethanol intake of Syrian golden hamsters.

16 alin had no cross-reactivity with common and golden hamsters.

17 he control of offensive aggression in Syrian golden hamsters.

18 ol extract of RP assist uptake of daidzin in golden hamsters.

19 d mRNA levels in the hypothalamus of Lak.LVG golden hamsters.

20 everal differences when compared to wildtype golden hamsters.

21 ted with maintenance on short photoperiod in golden hamsters.

22 sgenic, C57BL/6J, and 129S2 mice, and Syrian golden hamsters.

23 Syrian golden hamsters (15:16 EHS:cr) given quartz by both rout

24 , which produce heat endogenously, or Syrian golden hamsters (8-day-olds), which do not produce heat

25 under physiological conditions in the Syrian golden hamster, a model with close similarity to humans

26 ort- and long-term systemic responses in the golden hamster after either SARS-CoV-2 or influenza A vi

27 ined the pattern of central infection in the golden hamster after intravitreal inoculation with a rec

28 s in C57BL/6J mice, nNOS-/- mice, and Syrian golden hamsters after intraduodenal and oral fat adminis

29 domestic dogs, white-tailed deer, mink, and golden hamsters, among others.

30 -8 has not been well characterized in Syrian Golden hamsters, an important model in the study of fat

31 ssible mink encephalopathy (TME) into Syrian golden hamsters and examined the selection of distinct s

32 so far undefined, controls ethanol intake of golden hamsters and mediates the antidipsotropic effect

33 nNOS inhibition in Syrian golden hamsters and protein kinase G (PKG) inhibition in

34 ale and female rodents including rats, mice, golden hamsters, and Arvicanthis niloticus.

35 Finally, we propose the use of the Syrian golden hamster as a model for photoreceptor development

36 By using in situ hybridization in the golden hamster brain, we have found that vgf mRNA levels

37 zin may, in fact, suppress ethanol intake of golden hamsters by inhibiting ALDH-2.

38 CTAs, established in golden hamsters by injection of lithium chloride, were q

39 cs in the aerosols, and new transmissions in golden hamsters challenged with SARS-CoV-2.

40 Following exposure to short daylengths, in golden hamsters, changes in basal adrenal glucocorticoid

41 in-vivo fusion of two Hodgkin lymphomas with golden hamster cheek pouch cells, resulting in serially-

42 y which daidzin suppresses ethanol intake in golden hamsters clearly differs from that proposed for t

43 nsfer from vaccinated volunteers into Syrian golden hamsters controlled replication of SARS-CoV-1 aft

44 f hACE2 mice and post-infection treatment of golden hamsters demonstrates the efficacy of the monospe

45 onstrators and observers revealed that adult golden hamsters did not investigate foods hoarded by the

46 Golden hamsters did not prefer their demonstrators' diet

47 Because week-old golden hamsters do not exhibit BAT thermogenesis, their

48 escribes the clinical laboratory findings in golden hamsters experimentally infected with yellow feve

49 Microvessels of Syrian Golden hamsters fitted with a dorsal window chamber were

50 increases the aggressiveness of male Syrian golden hamsters for about 30 min; the effect peaks 10-15

51 ncer, we studied six groups of female Syrian golden hamsters: groups 1 to 3 (n = 12 each) were given

52 Golden hamsters have at least 5 individually distinctive

53 iasmatic nucleus (SCN) in freely moving male golden hamsters housed in running-wheel cages under both

54 Syrian golden hamsters immunized with mtdVSV-S triggered SARS-C

55 of GAL can block VP-induced flank marking in golden hamsters in a dose dependent manner.

56 or serial passages of CWD isolates in Syrian golden hamsters, incubation periods rapidly stabilized,

57 (VP) into the anterior hypothalamus (AH) of golden hamsters induces a rapid bout of flank marking, a

58 vivo in K18-hACE2 transgenic mice and Syrian golden hamsters infected with six VOCs of SARS-CoV-2.

59 Offensive aggression in golden hamsters is inhibited by 5-hydroxytryptamine (5-H

60 human cases of YF, which indicates that the golden hamster may be an excellent alternative animal mo

61 study indicate that MAP virus in the Syrian golden hamster (Mesocricetus auratus) can cause a diseas

62 Cultured neural retinas of the golden hamster (Mesocricetus auratus) exhibited circadia

63 The Syrian Golden hamster (Mesocricetus auratus) has been used to m

64 Chemically-induced tumors in the Syrian Golden hamster (Mesocricetus auratus) have been shown to

65 The golden hamster (Mesocricetus auratus) is a susceptible m

66 The Syrian golden hamster (Mesocricetus auratus) is an important mo

67 The Syrian golden hamster (Mesocricetus auratus) is uniquely suscep

68 vity of the medial vestibular nucleus of the golden hamster (Mesocricetus auratus) was evaluated usin

69 ixtures of taste stimuli were studied in the golden hamster (Mesocricetus auratus).

70 Golden hamsters (Mesocricetus auratus) and dwarf hamster

71 Infant Syrian golden hamsters (Mesocricetus auratus) do not exhibit en

72 Golden hamsters (Mesocricetus auratus) experimentally in

73 n-discrimination techniques, we exposed male golden hamsters (Mesocricetus auratus) on 3 to 4 trials

74 Female golden hamsters (Mesocricetus auratus) received aspirati

75 Female golden hamsters (Mesocricetus auratus) received electrol

76 In Experiment 2, male Turkish and golden hamsters (Mesocricetus auratus) treated the flank

77 igm, the authors investigated what cues male golden hamsters (Mesocricetus auratus) use to determine

78 gy milder, and weight loss reduced in Syrian golden hamsters (Mesocricetus auratus) vaccinated intran

79 drochloride in mixtures were investigated in golden hamsters (Mesocricetus auratus) with a conditione

80 In male golden hamsters (Mesocricetus auratus), attack frequency

81 In golden hamsters, microinjections of arginine-vasopressin

82 ng pathogenesis of HCPS is the lethal Syrian golden hamster model of ANDV infection.

83 Leveraging the golden hamster model of COVID-19, we sought to understan

84 ther define vascular pathologies in a Syrian golden hamster model of human COVID-19.

85 elopment of a novel, uniformly lethal Syrian golden hamster model of MHF using a hamster-adapted MARV

86 of these sensory abnormalities, we used the golden hamster model to characterize and compare the eff

87 In a pre-exposure Syrian golden hamster model, JNJ-9676 (25 mg per kg twice per d

88 I/-III responsive, in addition to an in vivo golden hamster model.

89 ccination and SARS-CoV-2 challenge of Syrian golden hamsters, mRNA-LPNs induced high spike-specific I

90 toma ceylanicum hookworm infection in Syrian golden hamsters of the outbred LVG strain.

91 In golden hamsters, offensive aggression is facilitated by

92 transmission, with most investigators using golden hamsters or ferrets.

93 The water permeability coefficient of the golden hamster pancreatic islet cells was determined to

94 ell as the water permeability coefficient of golden hamster pancreatic islet cells were determined.

95 In the SCN of the golden hamster, PKCalpha cells were most heavily concent

96 sters, transgenic mice expressing the Syrian golden hamster prion protein, and RML Swiss and C57BL10

97 The Syrian golden hamster provides a useful model for studying lipi

98 cultured cell contributions to chimaeras in golden hamster, rat and pig, definitive ES cell lines wh

99 Syrian golden hamsters recapitulate histopathologic pulmonary v

100 Female golden hamsters received aspiration lesions of ORB/AI or

101 Cloning of Fxr from Syrian golden hamster revealed four hamster Fxr splice variants

102 d in transgenic mice that express the Syrian golden hamster (SGH) Prnp.

103 ty and luteinizing hormone (LH) secretion in golden hamsters share a common circadian pacemaker in th

104 Vaccination of both mice and Syrian Golden hamsters showed that vaccination induced potent n

105 n both male hACE2-transgenic mice and Syrian golden hamsters that both multimerized and biparatopic B

106 In Syrian golden hamsters, the serum levels of SARS-CoV-2-specific

107 We describe use of the golden hamster to study EEEV-induced acute vasculitis an

108 the suppression of ethanol intake in Syrian golden hamsters was compared with that of crude daidzin

109 The odour of six of the golden hamsters was significantly more attractive to 50%

110 efore infection and the odour of four of the golden hamsters was significantly more attractive to 75%

111 ome time after the light pulse is presented, golden hamsters were treated with the protein synthesis

112 Male golden hamsters were weaned at postnatal day 25 (P25), e

113 macaques, which may model mild disease, and golden hamsters, which may model more severe disease.

114 Treatment of Syrian Golden hamsters with PF-332 (250 mg/kg, twice daily) com

115 Vaccination of Syrian Golden hamsters with RALA-SME derivatives produced funct

116 d their antidipsotropic activities in Syrian golden hamsters with their effects on monoamine metaboli