ライフサイエンスコーパス: New Zealand White rabbit

1 ion (55%) against virus challenge in outbred New Zealand White rabbits.

2 eal keratocytes isolated from the corneas of New Zealand White rabbits.

3 ) was performed on the left eyes of 20 adult New Zealand White rabbits.

4 induced by coronary artery ligation in adult New Zealand White rabbits.

5 ne (n = 5) were given in a volume of 2 ml to New Zealand white rabbits.

6 natured Oms66 (hOms66) were used to immunize New Zealand White rabbits.

7 li was deposited onto the abraded corneas of New Zealand White rabbits.

8 a major organ in catabolism of Lp B-70.5 in New Zealand white rabbits.

9 next to each other in both thighs in 10 male New Zealand white rabbits.

10 by using confocal microscopy in vivo in six New Zealand White rabbits.

11 Seventeen anesthetized adult male New Zealand White rabbits.

12 The coronary ligation model was used in New Zealand white rabbits.

13 nted them into carotid arteries of recipient New Zealand White rabbits.

14 tilated, pump-perfused lungs from euthanized New Zealand White rabbits.

15 ed on anaesthetized, artificially ventilated New Zealand White rabbits.

16 ging experimental atherosclerotic lesions in New Zealand White rabbits.

17 ained from the lacrimal glands of adult male New Zealand White rabbits.

18 ies treated with mitomycin-C were created in New Zealand White rabbits.

19 lly into the vitreous of the right eye of 10 New Zealand White rabbits.

20 DL)-mediated endothelial dysfunction in male New Zealand White rabbits.

21 ted into the vitreous of the right eye of 10 New Zealand White rabbits.

22 e tubercle bacilli in commercially available New Zealand white rabbits.

23 loon-damaged, flow-reduced iliac arteries of New Zealand White rabbits.

24 rmal or previously denuded iliac arteries of New Zealand White rabbits.

25 ameter) were performed using microneedles in New Zealand white rabbits.

26 twelve 3-month-old and ten 12-month-old male New Zealand White rabbits.

27 e created at the root of the right CCA in 16 New Zealand white rabbits.

28 hemia and hemorrhage in large clot embolized New Zealand white rabbits.

29 , obtained from both Sprague-Dawley rats and New Zealand White rabbits.

30 superficial femoral artery was induced in 14 New Zealand white rabbits.

31 Experiments were performed on New Zealand White rabbits.

32 -8 weeks) and aged (approximately 30 months) New Zealand White rabbits.

33 A) to detect atherosclerotic lesions in male New Zealand White rabbits.

34 r samples from normal and dry eyes of female New Zealand White rabbits.

35 ently available methods, of measuring IOP in New Zealand White rabbits.

36 es obtained from naive untreated and treated New Zealand White rabbits.

37 asuring IOP in the range of 0 to 50 mm Hg in New Zealand White rabbits.

38 g growth and invasion inhibitory antisera in New Zealand White rabbits.

39 artery angioplasty was performed in 25 male New Zealand White rabbits.

40 tracellularly in retinas isolated from adult New Zealand White rabbits.

41 al division of the medial geniculate body of New Zealand white rabbits.

42 Experiments were carried out on 36 male New Zealand White rabbits, 13 normal and 23 CHF.

43 New Zealand White rabbits (2 kg) 12 days after implantat

44 Fifteen New Zealand white rabbits (3.2+/-0.39 kg).

45 In New Zealand White rabbits, 3 days of treatment with NTG

46 ed by a 0.5% cholesterol diet for 16 wk in 7 New Zealand White rabbits; 5 unmanipulated rabbits, fed

47 noparticles-47 [MION-47]) in cholesterol-fed New Zealand White rabbits 6 months after balloon injury.

48 Two groups of 12 New Zealand White rabbits ((99m)Tc-MAG3 and (99m)Tc-DTPA

49 endrimer eye drop formulation was studied in New Zealand White rabbits after a single dose or multipl

50 distribution of carboplatin was examined in New Zealand White Rabbits after a single intravenous inf

51 It was implanted into six eyes of New Zealand White rabbits after extracapsular lens extra

52 rnal administration of aluminum maltolate to New Zealand white rabbits, an animal system relevant to

53 New Zealand White rabbits and A/J (H-2K) mice produced h

54 Corneas were obtained from New Zealand White rabbits and cultured ex vivo using sta

55 ed from gluteal biopsies from volunteers and New Zealand White rabbits and mounted on a wire myograph

56 llow microneedle was performed in the eye of New Zealand White rabbits and was found to reduce IOP in

57 In vivo experiments were performed using New Zealand White rabbits at several times points after

58 Atherosclerosis was produced in 34 New Zealand White rabbits by balloon de-endotheliazation

59 Atherosclerosis was induced in New Zealand white rabbits by cholesterol diet and endoth

60 CHF was induced in male New Zealand White rabbits by chronic ventricular tachyca

61 A single retinal detachment was produced in New Zealand White rabbits by injecting approximately 50

62 Osteomyelitis was induced in 12 New Zealand white rabbits by injecting staphylococcus au

63 wing large clot embolism-induced ischemia in New Zealand white rabbits by intracisternally administer

64 Atherosclerosis was induced in 14 New Zealand White rabbits by means of a 1% cholesterol d

65 Saccular aneurysms were created in New Zealand White rabbits by using vessel ligation with

66 of detrusor myocytes following PBOO in male New Zealand White rabbits compared to that of controls.

67 Series I: Adult New Zealand White rabbit corneas were mounted in perfusi

68 Adult New Zealand White rabbit corneas were treated with 2 mM

69 onocclusive periarterial carotid collar into New Zealand White rabbits decreased collar-induced endot

70 eated 40 calvarial defects in 20 12-week-old New Zealand White rabbits, divided into four groups: (1)

71 s were taken from the hippocampi of 10 male, New Zealand white rabbits during classical discriminatio

72 ere topically administered to eyes of normal New Zealand White rabbits either as a single dose or thr

73 ts of simvastatin on measures of behavior in New Zealand white rabbits embolized using a suspension o

74 Sixteen freshly enucleated, New Zealand White rabbit eyes were investigated either i

75 Seventy albino (New Zealand white) rabbit eyes were exposed to UVB radia

76 aced into experimental saccular aneurysms in New Zealand White rabbits failed to elicit a fibrotic re

77 Atherosclerosis was induced in New Zealand White rabbits fed 1% cholesterol for approxi

78 d alternative, via sterol 27-hydroxylase) in New Zealand white rabbits fed 3 g cholesterol/per day fo

79 New Zealand White rabbits fed a Western diet for 4-6 wk

80 cular injection (2 microg/kg body weight) to New Zealand White rabbits fed with a 0.25% cholesterol d

81 ramagnetic nanoparticles were compared in 30 New Zealand White rabbits (four to six rabbits per group

82 Scintigraphic images obtained in New Zealand White rabbits having acute intramuscular E.

83 Using the New Zealand white rabbit iliac model of stenting, we exa

84 IgG polyclonal antiserum was generated in New Zealand White rabbits immunized with a 16-mer peptid

85 New Zealand White rabbits immunized with AS(44-331) were

86 New Zealand White rabbits immunosuppressed with cyclospo

87 Twenty-three New Zealand White rabbits implanted intrahepatically wit

88 density, 10 mA/cm(2)) was performed on three New Zealand White rabbits in vivo.

89 ribe here a comparison of inbred and outbred New Zealand White rabbits infected by aerosol with eithe

90 HTLV-I infection and further establishes the New Zealand White rabbit inoculated with the RH/K34 cell

91 ere performed on 22 human, 29 monkey, and 34 New Zealand White rabbit intact postmortem lenses in sit

92 of radiolabeled arterial LDL was measured in New Zealand White rabbits killed at several different ti

93 Ad.nNOS in atherosclerotic arteries, 10 male New Zealand White rabbits maintained on a 1% cholesterol

94 toradiographic technique, frozen sections of New Zealand white rabbit medulla were incubated with rad

95 30 mug/mL was measured for up to 26 hrs in a New Zealand white rabbit model.

96 Mature New Zealand white rabbits (n = 17).

97 Adult male New Zealand white rabbits (n = 20), weighing 1.4-4.2 kg.

98 New Zealand white rabbits (n = 23), weighing 2 to 3 kg.

99 New Zealand White rabbits (n = 27) received a 1% cholest

100 New Zealand White rabbits (n = 33) were given TGF-beta(2

101 Advanced aortic lesions were induced in New Zealand White rabbits (n = 40).

102 lerotic plaques were induced in the aorta of New Zealand White rabbits (n = 7) by a repeated balloon

103 ere-loaded stents were deployed in aortas of New Zealand white rabbits (n = 8).

104 New Zealand White rabbits (n = 85) underwent unilateral

105 New Zealand white rabbits (n=10) were rendered atheroscl

106 New Zealand White rabbits (n=48) were studied: group 1 (

107 New Zealand White rabbits (n=56) underwent unilateral fe

108 New Zealand White rabbits (n=56) were fed a 1% cholester

109 New Zealand White rabbits (n=60) underwent jugular-carot

110 Cholesterol-fed New Zealand White rabbits (n=8, 1% cholesterol diet) and

111 erol diet) and NEP-I-treated cholesterol-fed New Zealand White rabbits (n=8; candoxatril, 30 mg/kg pe

112 tion of subepithelial infiltrates in the Ad5/New Zealand White rabbit ocular model.

113 (Ad5) and their ability to replicate in the New Zealand White rabbit ocular model.

114 e compared to existing experimental data for New Zealand white rabbit patellar tendons.

115 New Zealand White rabbits received chow or chow suppleme

116 Forty-one adult New Zealand White rabbits received either a single IV in

117 Twenty-eight New Zealand White rabbits received either normal rabbit

118 lbumin nanoparticles (nPXL) was tested in 38 New Zealand White rabbits receiving bilateral iliac arte

119 mics, and morphology was investigated in the New Zealand White rabbit renal autograft model using nea

120 ree virus from the J94356(PBMC) cell line in New Zealand White rabbits results in seroconversion to t

121 Testing was performed on 22 adult New Zealand white rabbits that received the experimental

122 This study was performed in New Zealand White rabbits that underwent balloon angiopl

123 was performed on the iliac arteries of male New Zealand White rabbits that were fed an atherogenic d

124 ed from other locations were fed on dogs and New Zealand White rabbits to assess the competency of th

125 In vivo studies were performed on mice and New Zealand White rabbits to assess the effect of GM-CSF

126 intraarticularly to the knee joints of five New Zealand white rabbits to determine the in vivo diffu

127 Transcorneal freezing was performed in New Zealand White rabbits to induce an injury-mediated i

128 s and lactate concentration were measured in New Zealand White rabbits treated with the topical CA in

129 Surgical preparation on twelve New Zealand white rabbits under ketamine-propofol anesth

130 scribe the early response (< or =days) in 52 New Zealand White rabbits undergoing gene transfer (beta

131 Twenty-eight New Zealand White rabbits underwent aortic balloon injur

132 Thirty-nine New Zealand White rabbits underwent cryoinjury of the le

133 a after varying forms of arterial injury, 57 New Zealand White rabbits underwent iliac artery balloon

134 New Zealand white rabbits underwent laparotomy and expos

135 Pregnant New Zealand White rabbits underwent laparotomy and were

136 ized, prospective, masked-observer study, 21 New Zealand White rabbits underwent modified GFS.

137 ized, prospective, masked-observer study, 40 New Zealand White rabbits underwent modified glaucoma fi

138 New Zealand White rabbits underwent simultaneous balloon

139 Twenty New Zealand white rabbits underwent stenting of the nond

140 New Zealand White rabbits underwent transaortic catheter

141 hted imaging were performed on 79% gestation New Zealand white rabbits using a 3-Tesla magnetic reson

142 Periodontitis was initiated in 18 New Zealand White rabbits using ligatures around mandibu

143 Experimental periodontitis was induced in 21 New Zealand White rabbits using Porphyromonas gingivalis

144 n this animal care committee-approved study, New Zealand white rabbit VX2 liver tumors were treated t

145 One randomly chosen eye of 40 New Zealand White rabbits was assigned to silicone hydro

146 During pregnancy, 1 group of New Zealand White rabbits was fed control chow and 8 gro

147 One eye of six New Zealand white rabbits was given a subconjunctival in

148 PTCA of both iliac arteries of 23 New Zealand White rabbits was performed.

149 ligation of distal external iliac artery in New Zealand White rabbits, we directly injected 500 micr

150 Using the "in vivo bioreactor" in New Zealand White rabbits, we have engineered bone that

151 New Zealand White rabbits weighing 1.5-2.5 kg.

152 Corneas from New Zealand white rabbits (weight range, 2 to 3 kg) and

153 Fifteen male New Zealand White rabbits (weight, approximately 3.5 kg)

154 New Zealand White rabbits were actively immunized with F

155 Mature New Zealand White rabbits were anesthetized and instrume

156 New Zealand White rabbits were anesthetized with ketamin

157 Sixteen healthy 8-wk-old male New Zealand White rabbits were assigned to 1 of 2 groups

158 Twenty-five pairs of male New Zealand White rabbits were challenged intraperitonea

159 New Zealand White rabbits were challenged with the wild-

160 Thirty-six New Zealand white rabbits were classified into two group

161 Male and female Sprague-Dawley rats and New Zealand White rabbits were divided into equal groups

162 The renal pelves of 6 New Zealand White rabbits were drained by use of bilater

163 Hearts from New Zealand white rabbits were either chemically fixed b

164 Male New Zealand White rabbits were fed a 0.5% cholesterol di

165 New Zealand White rabbits were fed either a normal diet,

166 dysregulation of DDAH also occurred in vivo, New Zealand White rabbits were fed normal chow or a high

167 enous NO in the regulation of MCP-1 in vivo, New Zealand White rabbits were fed normal chow, normal c

168 New Zealand White rabbits were fed regular chow (Group A

169 Twenty male New Zealand white rabbits were fed regular chow with and

170 Forty New Zealand White rabbits were fed with cholesterol.

171 In vivo, New Zealand white rabbits were fit with P. aeruginosa la

172 Twenty-three New Zealand White rabbits were fitted unilaterally with

173 New Zealand White rabbits were given a periocular inject

174 Thirty New Zealand White rabbits were given three separate intr

175 Eight-week-old New Zealand White rabbits were injected intravenously wi

176 New Zealand White rabbits were injected intravitreously

177 Anesthetized, tracheotomized, and ventilated New Zealand White rabbits were injected with freshly pre

178 New Zealand White rabbits were inoculated intranasally a

179 Twenty-four New Zealand White rabbits were instrumented with cardiac

180 New Zealand White rabbits were intrastromally injected w

181 New Zealand White rabbits were intrastromally injected w

182 New Zealand White rabbits were killed, and the bulbar co

183 Thirty male New Zealand White rabbits were maintained on a 1% choles

184 Age- and sex-matched New Zealand White rabbits were maintained on a diet cons

185 The IOPs of 11 healthy New Zealand White rabbits were measured with a fluid-fil

186 an globes or eyes obtained from euthanatized New Zealand White rabbits were mounted in a perfusion ch

187 Groups of sexually mature female New Zealand White rabbits were ovariectomized and killed

188 New Zealand white rabbits were passively immunized with

189 Dutch-belted and New Zealand White rabbits were passively immunized with

190 New Zealand white rabbits were randomized to everolimus

191 Male New Zealand White rabbits were randomized to receive a n

192 New Zealand White rabbits were randomized to receive eit

193 Fifty New Zealand white rabbits were randomly assigned to one

194 e corneal epithelia in one eye of 8-week-old New Zealand White rabbits were scraped at weekly interva

195 Twenty-four New Zealand white rabbits were split into 4 groups.

196 Femoral arteries of 7 adult male New Zealand White rabbits were stenosed bilaterally to a

197 Twenty New Zealand White rabbits were studied before and after

198 Healthy New Zealand White rabbits were studied with (18)F-LMI119

199 ing sutural mineralization fronts in 8 young New Zealand White rabbits were subjected to nano-indenta

200 Near-term, 29 d gestation, pregnant New Zealand White rabbits were subjected to repetitive u

201 rtery from adult male and nonpregnant female New Zealand White rabbits were suspended in organ baths

202 Ten male New Zealand White rabbits were transplanted with cardiac

203 New Zealand White rabbits were treated topically in one

204 Isolated hearts harvested from New Zealand White rabbits were treated with either cardi

205 New Zealand White rabbits were used as cell donors and W

206 s (HSFs) were used for in vitro studies, and New Zealand White rabbits were used for in vivo studies.

207 CSG) were deployed in the iliac arteries of New Zealand White rabbits, which were killed 28 days aft

208 We injected the footpads of New Zealand White rabbits with 1.7 or 8.4 nmol of tilman

209 yclonal antibodies were raised by immunizing New Zealand White rabbits with a mixture of the gel frag

210 Experimental periodontitis was induced in New Zealand white rabbits with silk sutures tied around

211 In 15 New Zealand White rabbits with systemic hypoxemia, AO wa

212 Oral immunization of outbred New Zealand White rabbits with the recombinant Salmonell