ライフサイエンスコーパス: rabbit

1 on during preimplantation development of the rabbit.

2 to the mammary pheromone produced by mother rabbits.

3 combinant form and antibodies were raised in rabbits.

4 st and during CBC activation in sham and CHF rabbits.

5 zed biodegradable thermogels in glaucomatous rabbits.

6 . 34 +/- 5% max) relative to scrambled-siRNA rabbits.

7 o the pericardium via subxiphoid puncture in rabbits.

8 evolution of myxoma virus (MYXV) in European rabbits.

9 ng a chimeric AAV capsid, were determined in rabbits.

10 ive antibodies against CR-Kp CPS in mice and rabbits.

11 th Sprague-Dawley rats and New Zealand White rabbits.

12 nstraints associated with its propagation in rabbits.

13 conformation-specific antibody responses in rabbits.

14 xvirus, which is highly virulent in European rabbits.

15 F in podocyte injury was studied in pregnant rabbits.

16 and developmental toxicity data for rats and rabbits.

17 A rabbit affinity purified antibody generated against a pe

18 rts corneal endothelial cell regeneration in rabbits after endothelial injury.

19 These rabbits also generated antibodies that recognized protei

20 Importantly, immunized rabbits also showed neutralizing activities against hete

21 f four placental mammals, mouse, guinea pig, rabbit and armadillo, and one marsupial, opossum.

22 Compound 25 showed robust effects in rabbit and canine pharmacodynamic models and an acceptab

23 veterinary disease that affects the European rabbit and has a significant economic and ecological neg

24 recombination in RHDV strains recovered from rabbit and Iberian hare samples collected in the mid-199

25 When administered to rabbit and monkey eyes, the half-life of the modified pr

26 croparticles released functional dual dAb in rabbit and primate eyes over 6months at sufficient level

27 n hemopexin, which was similarly nitrated in rabbit and rat hemopexins.

28 lateral carbachol in all preparations except rabbit and the H441 cell line.

29 V1V2-scaffold proteins for immunogenicity in rabbits and assessed the responses by enzyme-linked immu

30 /Cas9 system to generate Mstn knock-out (KO) rabbits and goats and then analyzed the changes in their

31 conclusion, we efficiently generated Mstn KO rabbits and goats using CRISPR/Cas9 technology.

32 ssum attachment reaction and implantation in rabbits and humans.

33 GMS drop was administered to 5 normotensive rabbits and intraocular pressure (IOP) was monitored for

34 h VX2 tumors implanted on both hind limbs of rabbits and investigated the feasibility to enhance tumo

35 otent isolate-specific antibody responses in rabbits and macaques, but so far failed to induce broadl

36 an papillomavirus (HPV) protection models in rabbits and mice, our study has identified a prophylacti

37 ion of the web of trophic interactions among rabbits and their dependent predators suggests that RHDV

38 assessments of PPC were performed in 20 live rabbits and were compared with manual continuous curvili

39 he new trimers, tested them as immunogens in rabbits, and found that the blocking glycans eliminated

40 ducers; untreated male monkeys, guinea pigs, rabbits, and hamsters; and female dogs.

41 Striatopallidal neurons were identified by rabbit anti-enkephalin antibody.In NT mice, PDE10A is eq

42 essed and purified and raising of polyclonal rabbit anti-OmpW was done.

43 ion was assessed in different brain areas by rabbit anti-PDE10A antibody immunohistochemistry and Wes

44 busulfan, cyclophosphamide, fludarabine, and rabbit anti-thymocyte globulin.

45 Rabbit antibodies generated against recombinant Pfs230 d

46 further corroborating the value of the naive rabbit antibody library as a rich and virtually unlimite

47 ing immunization, we generated a large naive rabbit antibody repertoire represented by a phage displa

48 ction categories: no-induction, alemtuzumab, rabbit antithymocyte globulin (r-ATG), and interleukin-2

49 ne were randomized for 3 different regimens: rabbit antithymocyte globulin (r-ATG)/EVR (N = 85); basi

50 stics, we generated 1:1 pairs of alemtuzumab-rabbit antithymocyte globulin (rATG) (5330 pairs) and ba

51 g using total lymphoid irradiation (TLI) and rabbit antithymocyte serum (ATS) (the murine preclinical

52 Here we develop a simple "parsimonious" rabbit AP model that is mathematically identifiable (i.e

53 IKs amplitude and kinetics during the normal rabbit AP.

54 Rabbits are highly resistant to naturally acquired TSEs,

55 tivities of MC neurons, recorded in behaving rabbits, are related to and preceded the initiation of c

56 XN1, RAG2, IL2RG, and PRKDC) immunodeficient rabbits, as well as multigenic mutant immunodeficient ra

57 of preterm rabbits at D3 compared with term rabbits at D0, but not in D7 preterm relative to D4 term

58 GEs of preterm pups at D3 compared with term rabbits at D0.

59 ls were more abundant in the MGEs of preterm rabbits at D3 compared with term rabbits at D0, but not

60 rm-born (born on E32; examined on D0 and D4) rabbits at equivalent postconceptional ages.

61 ments were performed using New Zealand White rabbits at several times points after injections of AuNP

62 Rabbit ATG appears to achieve excellent cost-effectivene

63 coproteins are also strongly immunogenic and rabbit ATG induces serum sickness disease in almost all

64 signal in murine infarcts and both mouse and rabbit atherosclerotic plaques.

65 d intra-SR ([Ca(2+) ]SR ; fluo-5N) Ca(2+) in rabbit atrial myocytes revealed that Ca(2+) release from

66 ed mechanisms of cardiac alternans in single rabbit atrial myocytes.

67 0.736), however, 4/12 (33%) of the diabetic rabbits became bacteremic.

68 In this study, we characterized rabbit BM after the arrest of B lymphopoiesis and found

69 In contrast, Chol-fed rabbits, but not WHHL rabbits, exhibited pronounced infl

70 t the human and mouse orthologs of THSD7A in rabbits by coimmunization with the respective cDNAs.

71 o mice, we worked to develop immunodeficient rabbits by CRISPR/Cas9.

72 nistration of antisera generated in mice and rabbits by immunization with a hypoallergenic Cyp c 1 mu

73 Transgenic mice over-expressing rabbit calpastatin (CalpTG) are protected against vascul

74 bute to sustained ROS production in isolated rabbit cardiac mitochondria following inner membrane por

75 It is composed of rabbit conjunctival epithelium and lacrimal gland cell s

76 For all rabbits, conventional ultrasonography, two-dimensional s

77 In the current study, we performed in vivo rabbit corneal endothelial cell (CEC) injury via CEC scr

78 the concentration 0.5 ppm wt/vol, applied on rabbit corneas during UVB irradiation and healing (UVB d

79 We found rabbit corneas in the CEC scraping group healed with tra

80 roma during infection of ex vivo and in vivo rabbit corneas using multiphoton fluorescence and second

81 Ex vivo, rabbit corneas were subject to three partial thickness w

82 le to TSEs, others are apparently resistant (rabbits, dogs, and horses) to the same agent.

83 In a rabbit ear model, PUT induced a 68.5% reduction in blood

84 Although we observed that rabbit embryos have several features in common with mous

85 coli and found to potently inhibit lysis of rabbit erythrocytes in assays of the alternative pathway

86 ting rabbit Mstn, and found that the Mstn KO rabbits exhibited increased birthweight and a significan

87 In contrast, Chol-fed rabbits, but not WHHL rabbits, exhibited pronounced inflammatory responses and

88 Rabbit eye IOP was modulated through cannulation in ex v

89 anterior and posterior segment of mouse and rabbit eyes using implantable microsensors.

90 dentified in a 3-hour study using euthanized rabbit eyes whose IOP was controlled at 10 or 40mmHg by

91 actone intracameral drug delivery devices in rabbit eyes.

92 livery was not a significant effect in alive rabbit eyes; however, choroidal circulation seems to be

93 A co-crystal structure of the rabbit family 4 enzyme CYP4B1 with its substrate octane

94 peated for human alpha-cardiac myosin S1 and rabbit fast skeletal muscle S1.

95 Five noninjured rabbits fed a chow diet were used as controls.

96 ight carotid artery and abdominal aorta of 7 rabbits fed an atherogenic diet.

97 rmed by proteolysis of the fusion protein in rabbit following intravenous administration of lipidated

98 tion of MYXV and the increased resistance of rabbits following the release of MYXV in Australia is on

99 factured from the JDBM-2 were implanted into rabbits for long-term evaluation.

100 d to quickly and efficiently generate mutant rabbit founders.

101 at mixtures containing beef, chicken, camel, rabbit, goat and sheep with varying percentage of pork (

102 Recently, a new variant of the rabbit haemorrhagic disease virus (RHDV2 or RHDVb) argua

103 ed that corneal endothelial wound healing in rabbits has different outcomes depending upon the presen

104 as well as multigenic mutant immunodeficient rabbits have been produced.

105 ed using the lower-cost Langendorff-perfused rabbit heart model.

106 idated electrophysiology model for a healthy rabbit heart.

107 induced electrically in Langendorff-perfused rabbit hearts (n=22) and terminated with a defibrillator

108 mechanical stimuli were applied to isolated rabbit hearts during optical voltage mapping, combined w

109 ation and KATP activation in excised working rabbit hearts remains unknown.

110 ials from the surface of excised contracting rabbit hearts to assess when sarcolemmal KATP channels w

111 ly mapped action potentials (APs) in excised rabbit hearts to test the hypothesis that hypoxic change

112 simultaneous optical and electric mapping of rabbit hearts, and in vivo pig electrophysiology studies

113 m cardiac ventricular myocytes isolated from rabbit hearts.

114 Rabbit hemorrhagic disease (RHD) is a veterinary disease

115 In Portugal, rabbit hemorrhagic disease virus (RHDV) was reported in

116 ster prion (GHaPrP) and its less susceptible rabbit homolog (RaPrP).

117 0 billion independent antibodies in chimeric rabbit/human Fab format and validated it by next-generat

118 phage display to produce a panel of chimeric rabbit/human monoclonal antibody fragments (both Fab and

119 d hypertrophic scar formation in a validated rabbit hypertrophic scar model compared with saline cont

120 vated uptake of (64)Cu-ATSM was found in the rabbits' IF compared with the SF.

121 gated anti-mouse IgG and dye-conjugated anti-rabbit IgG (Alexa 647) detection.

122 hed a mouse model by the passive transfer of rabbit IgG against the murine homologs of two immunodomi

123 The lowest detectable concentrations of rabbit IgG and human PSA by the naked eye were down to 0

124 body injection, and immunohistochemistry for rabbit IgG and THSD7A as well as ultrastructural analyse

125 disease and to investigate whether mouse and rabbit IgG antibodies induced by immunization with a hyp

126 dies, 2 xenocarbohydrate epitopes present on rabbit IgG glycans and lacking in humans.

127 hemical detection was done based on the anti rabbit IgG HRP (Horseradish Peroxidase) which binds to t

128 obodies against all mouse IgG subclasses and rabbit IgG.

129 Polyclonal antihuman thymocyte rabbit IgGs (antithymocyte globulin [ATG]) are popular i

130 In rabbit immunizations with native-like trimers of the 327

131 We show here that rabbits immunized with a novel recombinant vaccinia viru

132 s of water-ethanol mixtures and detection of Rabbit immunoglobin G (IgG) whole molecule (H&L) respect

133 alytic tags in a competitive immunoassay for rabbit immunoglobulin G (IgG) detection.

134 ion of myxoma virus (MYXV) and wild European rabbits in Australia and Europe is a paradigm for the ev

135 n turn, suppressed abundances of rodents and rabbits in the absence of dingoes relaxed a recruitment

136 he patient, a hunter, recalled having killed rabbits in the days before the symptoms appeared.

137 and in liposomal formulations when tested in rabbits in vivo (sc and iv application).

138 cle and human artery samples in vitro and in rabbits in vivo.

139 Administration of HbF to pregnant rabbits increased the number of urinary EVs of podocyte

140 Both antigens were immunogenic in rabbits, inducing IgG that bound native Pfs25 and exhibi

141 In vivo, in mice and in rabbits, intravenous GM-CSF administration resulted in a

142 We investigated SERCA dimerization in rabbit left ventricular myocytes using a photoactivatabl

143 transarterial embolization (TAE) in the VX2 rabbit liver tumor model by using multimodality imaging,

144 To accelerate access to rabbit mAbs bypassing immunization, we generated a large

145 Moreover, ROR1- and ROR2-targeting rabbit mAbs demonstrated therapeutic utility as componen

146 Panels of rabbit mAbs selected from this library against two emerg

147 as a rich and virtually unlimited source of rabbit mAbs.

148 The lack of immunological reagents for rabbits makes such studies difficult.

149 Moreover, on immunization of mice and rabbits, MBC4 induced cross-reactive IgG antibodies, whi

150 x VX2 tumors (median diameter, 1.3 cm) in 20 rabbits (median weight, 2.8 kg) underwent successful DEB

151 rs in bulky normal muscle tissues based on a rabbit model and a preclinical HIFU system.

152 Cs were evaluated in a normotensive glaucoma rabbit model for their intraocular pressure (IOP) loweri

153 yseal long bone radial defects in a diabetic rabbit model it was demonstrated that co-delivery of PEI

154 ing agent (64)Cu-ATSM to detect hypoxia in a rabbit model of atherosclerosis imaged on a simultaneous

155 ptability was demonstrated in a pre-clinical rabbit model of bullous keratopathy using a tissue-engin

156 ivo in a photorefractive keratectomy-treated rabbit model of corneal fibrosis.

157 We used a recently established rabbit model of dextran sodium sulphate (DSS) induced co

158 n this study, we establish a large cohort of rabbit model of experimental osteomyelitis and investiga

159 o test these hypotheses, we used the preterm rabbit model of glycerol-induced IVH and analyzed autops

160 03971 in a validated and clinically relevant rabbit model of scar tissue formation after glaucoma fil

161 be significantly higher in a Type I diabetic rabbit model of Streptococcus pneumoniae endophthalmitis

162 hanges of the healing tendon in a transected rabbit model of the Achilles tendon.

163 In vivo pharmacodynamic data in rabbit model showed sustained reduction in intra ocular

164 tumor permeability in bulky VX2 tumors in a rabbit model using pHIFU technique.

165 roteases, we show that cardiac ischemia in a rabbit model was associated with a reduction in mature E

166 large segmental radius defects (1.5 cm) in a rabbit model was evaluated by radiography and histology.

167 cells and their regenerative potential in a rabbit model with lacrimal gland main excretory duct lig

168 oves functional Achilles tendon healing in a rabbit model, resulting in increased vascularization, mo

169 e pharmacodynamics and pharmacokinetics in a rabbit model.

170 n atherosclerotic plaques of an experimental rabbit model.

171 exone microspheres were investigated using a rabbit model.

172 re in an anatomically accurate biventricular rabbit model.

173 of rupture-prone atherosclerotic plaque in a rabbit model.

174 y a poxvirus prime-gp120 boost strategy in a rabbit model.

175 e and efficient tumor tissue ablation in the rabbit model.

176 yte centre both in patients with AF and in a rabbit model.

177 und that gene expression profiles of the two rabbit models were essentially similar in the aorta, eve

178 ls of cholera pathogenesis (infant mouse and rabbit models).

179 00 mg/ml concentration) was also verified in rabbit models.

180 mation that is available was generated using rabbit models.

181 liorates colitis severity in immunocompetent rabbits, modulates LPMC immune responses and reduces fae

182 to their high affinities and specificities, rabbit monoclonal antibodies (mAbs) have demonstrated va

183 PD-L1 was measured using E1L3N and SP142, 2 rabbit monoclonal antibodies, in 49 NSCLC whole-tissue s

184 he development and technical validation of a rabbit monoclonal antibody-based sandwich immunoassay fo

185 r embryo injection with two sgRNAs targeting rabbit Mstn, and found that the Mstn KO rabbits exhibite

186 of AMF, namely phosphoglucose isomerase from rabbit muscle (RmPGI).

187 An X-ray crystallography study of the rabbit muscle GPb inhibitor complexes revealed structura

188 mined the feasibility of this approach using rabbit muscle pyruvate kinase (rM1-PK) which catalyzes t

189 r well-established mathematical model of the rabbit myocyte.

190 In hypertrophic rabbit myocytes, selectively enhanced beta2 adrenergic r

191 to the myofilaments in hypertrophic failing rabbit myocytes.

192 on of caveolin-3 in the hypertrophic failing rabbit myocytes.

193 METHODS AND Atherosclerosis was induced in rabbits (n=31) using aortic balloon injury and high-chol

194 ivated fibers of fast skeletal muscle of the rabbit occurs during transition from isometric contracti

195 e designed to focus the antibody response of rabbits on the V1V2 epitopes of HIV-1 gp120 since such a

196 its subtype antibodies in animals (mice and rabbits) or patients with schistosomiasis were measured

197 y in Mediterranean ecosystems - the European rabbit (Oryctolagus cuniculus).

198 We efficiently generated 24 Mstn KO rabbits out of 32 newborn infants after embryo injection

199 To this end, the structure of rabbit P450 4B1 complexed with its substrate octane was

200 ure transfection assays, M156 only inhibited rabbit PKR but not PKR from other tested mammalian speci

201 The species-specific inhibition of rabbit PKR by M156 and the M156 loss-of-function in Aust

202 rabbit PKR, revealed that only human but not rabbit PKR was able to restrict MYXV infection, whereas

203 which were stably transfected with human or rabbit PKR, revealed that only human but not rabbit PKR

204 A rabbit polyclonal antibody against one of the same epito

205 eloped using sandwich assay by utilising the rabbit polyclonal antibody as the capture antibody and c

206 Treatment with rabbit polyclonal IgGs in the absence of additional immu

207 SDS-PAGE and immunoassay analysis with rabbit polyclonal sera and human IgE indicated only mino

208 tively assess the impact of RHDV2 on natural rabbit populations and in two endangered apex predator p

209 om the South American tapeti to the European rabbit populations of Australia and Europe is a canonica

210 We found 60-70% declines in rabbit populations, followed by decreases of 65.7% in Ib

211 iguration dynamics of the Syrian hamster and rabbit prion proteins.

212 1-infected neurons in both the mouse and the rabbit provides an opportunity to experimentally explore

213 This allowed amino acid substitutions in rabbit PrP and accurate analysis of misfolding propensit

214 Using recombinant rabbit PrP as a model, this study describes critical mol

215 se, protease-resistant misfolded recombinant rabbit PrP was generated.

216 s increased the misfolding susceptibility of rabbit PrP.IMPORTANCE Prion disorders are invariably fat

217 substitutions on the mechanical behavior of rabbit psoas skeletal myofibrils by replacing endogenous

218 fibrous tissue and increased bone density in rabbit radial defect models.

219 lation sites conserved in human, guinea pig, rabbit, rat, and mouse alpha1C subunits.

220 Rabbits received ultrasmall superparamagnetic iron oxide

221 Here we report that IOP reduction in rabbits receiving a single brimonidine GMS drop was comp

222 Cornea thickness of rabbits receiving TE-EK graft gradually reduced over the

223 imonidine GMS drop was comparable to that of rabbits receiving twice daily, standard brimonidine drop

224 Wild-type rabbit recombinant PrP could not be misfolded into a pro

225 e amino acid substitution that distinguishes rabbit recombinant PrP from mouse recombinant PrP.

226 Therefore, rabbit recombinant PrP mutants were designed to contain

227 idue substitutions were identified that make rabbit recombinant PrP susceptible to misfolding, and us

228 transplantation, whereas corneas of control rabbits remained significantly thicker over 1,000 microm

229 rs of shrub seeds and seedlings, rodents and rabbits respectively.

230 fection of KLF2 to the carotid bodies in CHF rabbits restored KLF2 expression, and reduced AHI (7 +/-

231 ubcutaneous injection of the same variant in rabbits resulted in a 14% fall in IGF-I over 7 days.

232 at HBc expressed in a mammalian cell lysate, rabbit reticulocyte lysate (RRL), was able to assemble i

233 ues were potent inhibitors of translation in rabbit reticulocyte lysate.

234 roscopic immunocytochemistry, we show in the rabbit retina that bright-light-induced activation of do

235 In studies of rabbit retina, we found SAP102 and Chapsyn110 selectivel

236 l types spanning the inner two layers of the rabbit retina.

237 f orientation-selective ganglion cell in the rabbit retina.

238 is in recordings from 62 ON-OFF DSGCs in the rabbit retina.

239 Using rabbit retinal connectome RC1, we show that all cone bip

240 the same epitopes combined with a goat anti-rabbit secondary antibody produced very strong purple co

241 bimolecular association occurs, whereas the rabbit sequence avoids aggregation by reconfiguring 10 t

242 repeating unit were used to screen human and rabbit sera and identify epitope hits.

243 Anti-hypoallergenic Cyp c 1 mutant mouse and rabbit sera were tested for their ability to inhibit IgE

244 were given anti-thrombocyte serum or normal rabbit serum (control) 4 days after surgery.

245 DS-PAGE-immunoblotting with patient sera and rabbit serum anti-Pru p 3.

246 Mice injected with purified IgG from rabbit serum that was taken before immunization failed t

247 Studies on mice and rabbits show that BENAQ is non-toxic at concentrations 1

248 nt mammalian prions, whereas others, such as rabbit, show robust resistance to cross-species prion co

249 reduced intraocular pressure in normotensive rabbits significantly for 23weeks.

250 100 nm of the outer cell surface membrane in rabbit single-ventricular cardiomyocytes over 8 h post-i

251 Myxoma virus (MYXV) is a rabbit-specific poxvirus, which is highly virulent in Eu

252 In rabbits subject to pharmacological triggering, plaques t

253 B lymphopoiesis arrests precipitously in rabbits such that by 2-4 mo of age, before sexual maturi

254 rm memory and protective immune responses in rabbits superior to those elicited by the ST-5 CPS compo

255 ependent nicotine, and the native cottontail rabbit Sylvilagus nuttallii avoids jasmonate-producing N

256 al trauma-induced tremor, tardive tremor and rabbit syndrome, paroxysmal tremors (hereditary chin tre

257 In vivo pharmacokinetic studies in rabbit tear fluid showed significant increase in mean re

258 hen we tested these trimers as immunogens in rabbits, the induction of V3 non-NAbs was significantly

259 When transplanted to the ocular surfaces of rabbits, the tissue survived for up to 2 weeks.

260 de (SPIO) nanoparticles (SPIO-DOX), in a VX2 rabbit tibial tumor model.

261 The rabbit tissue also appeared to exhibit stronger viscous

262 were performed on mice and New Zealand White rabbits to assess the effect of GM-CSF on (18)F-FDG upta

263 bility to TSEs of certain species, the mouse-rabbit transmission barrier was used as a model.

264 into hepatic arteries of a VX2 tumor-bearing rabbit under fluoroscopy, followed by subsequent CT imag

265 in Australia has continued to evolve in wild rabbits under intense selection for genetic resistance t

266 Twenty New Zealand white rabbits underwent stenting of the nondiseased aortoiliac

267 llergen-specific antibodies were produced in rabbits using eight different allergens, extracts, and a

268 nt, BG505 SOSIP.664-E64K.M1M7, was tested in rabbits, V3 immunogenicity was eliminated while the auto

269 Four anesthetized rabbits, ventilated in pressure controlled mode.

270 We conducted experiments in rabbit ventricular myocytes at body temperature and foun

271 Isolated patch-clamped rabbit ventricular myocytes loaded with Fluo-4 to image

272 IKs was recorded from freshly isolated rabbit ventricular myocytes using whole-cell patch clamp

273 thromycin suppressed L-type Ca(++) currents (rabbit ventricular myocytes, IC50=66.5+/-4 mumol/L) and

274 both computer simulations and experiments of rabbit ventricular myocytes.

275 Rabbit ventricular rapidly activating delayed rectifier

276 KEY POINTS: [Ca(2+) ]i enhanced rabbit ventricular slowly activating delayed rectifier K

277 Twelve rabbit VX2 tibial tumors were treated, three with IRE, t

278 IO-DOX, and six with SPIO-DOX plus IRE; five rabbit VX2 tibial tumors were untreated (control group).

279 (lung, liver, kidney, heart, and brain) from rabbit was spiked to the same concentration with the dru

280 In awake female Dutch-Belted rabbits, we found 58% of CG neurons to be visually respo

281 the corticogeniculate visual system of awake rabbits, we investigate the functional significance of t

282 g antibodies (NAbs) efficiently in immunized rabbits, we sought to improve the efficiency with which

283 Thirty-six New Zealand white rabbits were classified into two groups: a control group

284 Hearts from New Zealand white rabbits were either chemically fixed by coronary perfusi

285 Liver pathologies in mice and rabbits were evaluated by gross pathology and histopatho

286 In vivo, New Zealand white rabbits were fit with P. aeruginosa laden contact lenses

287 Rabbits were imaged on a PET/MR system after injection o

288 New Zealand White female rabbits were subjected to surgical EAS myotomy and admin

289 Rabbits were then either euthanized (n=9) or underwent a

290 (CMR) T1 mapping were performed; all of the rabbits were then sacrificed for Masson's staining.

291 Rabbits were treated with alloxan to destroy pancreatic

292 e effect of TSO was lost in immunosuppressed rabbits, where TSO exacerbated colitis.

293 selectively destroy photoreceptors in adult rabbits while preserving the inner retina.

294 ktail approach by simultaneously vaccinating rabbits with a combination of plasmids encoding glycopro

295 elination and neurologic recovery in preterm rabbits with IVH.

296 ced myelination and neurological recovery in rabbits with IVH.

297 res myelination and neurological function in rabbits with IVH.

298 s from the 1950s and the 1990s in laboratory rabbits with no resistance.

299 eutralizing antibodies by DNA vaccination of rabbits with plasmids encoding the full-length glycoprot

300 studies were performed in 2 atherosclerotic rabbits with preinjection of the CXCR4 inhibitor AMD3100