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 ffer in their oncogenic potentials in Syrian golden hamsters.

6 e development of offensive behaviors in male golden hamsters.

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

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

9 in the regulation of offensive aggression in golden hamsters.

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

11 that suppresses the ethanol intake of Syrian golden hamsters.

12 he control of offensive aggression in Syrian golden hamsters.

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

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

15 everal differences when compared to wildtype golden hamsters.

16 ted with maintenance on short photoperiod in golden hamsters.

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

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

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

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

21 -8 has not been well characterized in Syrian Golden hamsters, an important model in the study of fat

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

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

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

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

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

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

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

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

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

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

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

33 Golden hamsters did not prefer their demonstrators' diet

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

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

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

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

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

39 Golden hamsters have at least 5 individually distinctive

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

55 Golden hamsters (Mesocricetus auratus) and dwarf hamster

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

57 Golden hamsters (Mesocricetus auratus) experimentally in

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

59 Female golden hamsters (Mesocricetus auratus) received aspirati

60 Female golden hamsters (Mesocricetus auratus) received electrol

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

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

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

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

65 In golden hamsters, microinjections of arginine-vasopressin

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

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

68 In golden hamsters, offensive aggression is facilitated by

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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