ライフサイエンスコーパス: rabbit

1 lian species (Wistar rats, New Zealand White rabbits).

2 elephant shrew, hyrax, capybara, beaver, and rabbit.

3 groups, though not in ectodomain-vaccinated rabbits.

4 tly to levels of myocytes from sham-operated rabbits.

5 to restore uterine structure and function in rabbits.

6 minished recurrent disease in HLA transgenic rabbits.

7 eted on BG505 and B41 SOSIP trimer-immunized rabbits.

8 after circumflex coronary artery ligation in rabbits.

9 arger APD dispersion in LQT2 but not in LQT1 rabbits.

10 diosis, a protozoal infection in poultry and rabbits.

11 ought in the geographic regions inhabited by rabbits.

12 s with copulation-induced ovulation, such as rabbits.

13 fer protection against syphilis in immunized rabbits.

14 d white rabbits and 3 Dutch Belted pigmented rabbits.

15 erable aortic plaques in vivo among all WHHL rabbits.

16 es of retinal vein occlusion (RVO) in living rabbits.

17 n vivo half-life following administration to rabbits.

18 ts undergoing heart surgery, as well as from rabbits.

19 l anesthetic, which was delivered to newborn rabbits.

20 ASYMP) individuals and HLA-A*0201 transgenic rabbits.

21 compared to standard DES in atherosclerotic rabbits.

22 d I(p) relative to that for 10 sham-operated rabbits.

23 reproductive capability of the injured male rabbits.

24 gB/MF59 vaccination was closely mimicked in rabbits.

25 In healthy rabbits, (18)F-LMI1195 was administered followed by the

26 antified with >= 2 unique peptides from >= 3 rabbits, a total of 673 differentially expressed (DE) pr

27 f vulnerable plaque structure and biology in rabbit abdominal aorta.

28 tibody responses in female New Zealand White rabbits after immunization with ICs made from BG505 SOSI

29 al LNs of two healthy male New Zealand white rabbits aged 6-8 weeks.

30 relation is further explored in vivo using a rabbit alkali burn model.

31 oreal membrane oxygenation (ECMO) setting in rabbits, all without increasing the bleeding risk.

32 n platelets were incubated with HDL from CKD rabbit and hemodialysis groups than with HDL from the co

33 I(CaL) and APs were recorded from rabbit and human atrial myocytes by whole-cell-patch cla

34 verage quantification method and the UniProt rabbit and human databases.

35 S) in fully innervated, Langendorff-perfused rabbit and mouse hearts.

36 Among the remaining species, ACE2s from rabbit and pangolin strongly bound to the S1 subunit of

37 ocyte were highly correlated in both healthy rabbit and pig myocytes, despite high overall cell-to-ce

38 Testing with acute rabbit and porcine models, the device is proven to have

39 to measure I(NaL) and I(Kr) during the AP in rabbit and porcine ventricular cardiomyocytes to test ou

40 tection of different host and foreign cells (rabbit and yeast), we uncovered a 2-fold discriminatory

41 20 Sprague-Dawley rats, 10 New Zealand White rabbits and 14 Hartley guinea pigs.

42 G), and administered to 13 New Zealand white rabbits and 3 Dutch Belted pigmented rabbits.

43 s were generated from four New Zealand white rabbits and confirmed to be myofibroblasts by immunocyto

44 We showed that invasive rabbits and extreme weather events reduce reproductive o

45 able of eliciting immobilizing antibodies in rabbits and fish suggesting that the antigen itself was

46 In both rabbits and humans, platelet aggregation and activation

47 Ab responses against the autologous virus in rabbits and macaques that are significantly enhanced whe

48 ate that neutralizing antibodies produced in rabbits and nonhuman primates injected with lipid nanopa

49 HDL from CKD rabbits and patients on hemodialysis exhibited an impair

50 HDL from CKD rabbits and patients on hemodialysis had HNE adducts.

51 travenous administration of (64)Cu-Macrin in rabbits and pigs, we detected heightened macrophage numb

52 osorbent assay (ELISA) using sera from naive rabbits and rabbits with S. aureus-mediated osteomyeliti

53 ic IgG response were performed on serum from rabbits and RM given identical modified vaccinia virus A

54 se, a thalamocortical connection in a female rabbit, and an auditory brainstem synapse in a female ge

55 s with HF relative to indices of 6 untreated rabbits, and it eliminated ascites.

56 are monoclonal antibodies derived from mice, rabbits, and other animals.

57 camels, cattle, horses, goats, sheep, cats, rabbits, and pangolins, were able to support cell entry

58 d FXII900, efficiently blocks FXIIa in mice, rabbits, and pigs.

59 rified recombinant protein was recognized by rabbit anti-C. irritans antiserum and was capable of eli

60 with Ab(ApoA1), and then mouse IgG (PMGO-1), rabbit anti-mouse IgG antibody (PMGO-2), and goat anti-r

61 nriched peptides after affinity selection on rabbit anti-NoV polyclonal antisera revealed five famili

62 be antigenic molecules that cross-react with rabbit anti-S. mansoni IgG antibodies in extracts of the

63 LMG-bovine serum albumin and rabbit anti-sheep IgG were immobilized on nitrocellulose

64 brogated most of the cross-reactivity of the rabbit anti-SmSEA antibodies, suggesting it was due to c

65 Cross-reactive rabbit anti-SmSEA IgG antibodies eluted from the three i

66 ese recommendations include a broader use of rabbit anti-T-cell globulin; lower steroid doses for the

67 ed upon the induction immunosuppression: (1) Rabbit anti-thymocyte globulin (rATG); (2) Alemtuzumab (

68 Rabbit antibodies against AMA1-RON2L, RH5, RIPR or CyRPA

69 identify the specificities of the protective rabbit antibodies and their respective targets.

70 Fc-independent and Fc-dependent functions of rabbit antibodies can be measured with commonly used in

71 homologous and heterologous challenges, the rabbit antibodies significantly ameliorate LD-induced ar

72 nonprotective (early) and protective (late) rabbit antibodies were identified and directly compared.

73 Rabbit antisera against this recombinant vaccine cross-r

74 were synthesized to raise selective anti-OTC rabbit antiserum and highly specific monoclonal antibody

75 Rabbit antithymocyte globulin (rATG) induction is associ

76 nt centers comparing a control group of with rabbit antithymocyte globulin (rATG) induction, rapid st

77 the prognostic influence of induction type: rabbit antithymocyte globulin (rATG; 2 mg/kg x 5)/rituxi

78 alemtuzumab (versus no induction, anti-CD25, rabbit antithymocyte globulin, or rabbit antithymocyte g

79 anti-CD25, rabbit antithymocyte globulin, or rabbit antithymocyte globulin/rituximab) induction (P =

80 DEB was demonstrated in an in vivo test in a rabbit aorta.

81 Rabbits are conventionally used to evaluate the ability

82 rom mice and rats, cells from spiny mice and rabbits are highly resistant to H(2)O(2).

83 feration, was seen in the liver of AAV2-LDLR rabbits associated with an increased expression of Cyr61

84 of anesthetized and mechanically ventilated rabbits, at baseline and following lung injury, using hi

85 Both arms included induction therapy with rabbit ATG, mycophenolate sodium, or mycophenolate mofet

86 equelae in MS patients undergoing AHSCT with rabbit ATG.

87 In 11 rabbit atrial myocytes in which EADs were generated eith

88 induced AP and CaT alternans were studied in rabbit atrial myocytes using combined Ca(2+) imaging and

89 edian split was used to create two groups of rabbits based on their performance.

90 -fMRI sessions were conducted on a cohort of rabbits before and after trace eyeblink conditioning.

91 In rabbits, BMS-529-complexed V3 glycan-targeting ch.SOSIP

92 st HIV-infected target cells was elicited in rabbits but not in RM, and we observed differences among

93 n shows that human mAb 1E6 is able to elicit rabbit, but not human, complement-mediated bactericidal

94 that is evolutionarily conserved in mice and rabbits, but not in primates.

95 and abolishes PVT in long QT syndrome type 2 rabbits by counterbalancing the reduced repolarization r

96 V and RVO models were created in New Zealand rabbits by Rose Bengal laser-induced RVO.

97 The structure of rabbit Ca(v) 1.1 bound to an achiral drug nifedipine rev

98 Computer simulations using a rabbit-cardiomyocyte model demonstrated that changes in

99 I (Na) and Nav1.5 surface protein levels in rabbit cardiomyocytes and in HEK cells stably expressing

100 Freshly isolated rat, guinea pig or rabbit cardiomyocytes were exposed to simulated ischaemi

101 essing decreases calcium transients in adult rabbit cardiomyocytes, which was associated with lower C

102 duration and decreased calcium transients in rabbit cardiomyocytes.

103 Serum bactericidal antibody titers (rabbit complement) were measured against NmA reference s

104 ha-SMA, desmin, and vinculin) generated from rabbit corneal fibroblasts treated with transforming gro

105 ation and contractility, we cultured primary rabbit corneal keratocytes on flexible substrata of vary

106 from paired WST-D/NIR treated and untreated rabbit corneas.

107 Recombinant fragments of a rabbit coronavirus (RbCoV-HKU14) were identified at the

108 Studies in infant rabbits demonstrated that VgpA is translocated into inte

109 ntly reduced IOP for 27 days in normotensive rabbits, demonstrating potential for clinical utility.

110 the combination of extreme rainfall and high rabbit density explained 33% of total trait variability

111 Temporal variability in rabbit density explained 33-76% of the variability in br

112 Patients received rabbit-derived intravenous anti-thymocyte globulin 0.5 m

113 burgdorferi antibodies of New Zealand White rabbits, despite the surface expression of VlsE.

114 Thus, this finding that NZW rabbits develop a unique repertoire of very potent antib

115 ibutes to intestinal fluid accumulation in a rabbit diarrhoeal model of V. parahaemolyticus infection

116 are morphologically distinct from mouse and rabbit direction-selective RGCs.

117 inly in large-animal models, including pigs, rabbits, dogs, and nonhuman primates.

118 tablished in the ventral skin of New Zealand rabbits' ears.

119 achieved robust antithrombotic efficacy in a rabbit efficacy model at doses which preserved hemostasi

120 es, small unilamellar vesicle liposomes, and rabbit erythrocytes.

121 puncture surgery of the annulus fibrosus in rabbits, ex vivo puncture experiments and electrospun na

122 m waves, we modified a mathematical model of rabbit excitation-contraction coupling coupled to a mode

123 gB nucleoside-modified mRNA-LNP-immunized rabbits exhibited an enhanced durability of vaccine-elic

124 However, all rabbits exhibited broken elastic fibers and collagen dep

125 All WHHL rabbits exhibited sparse to severe macrophages.

126 Scleral patches from rabbit eyes were cross-linked using paraformaldehyde, gl

127 demonstrated biocompatibility and patency in rabbit eyes.

128 imal models, i.e. guinea pig, dog, cat, rat, rabbit, ferret, mouse, hamster and macaque.

129 rotective efficacy was observed in immunized rabbits following intramedullary challenge with S. aureu

130 lly processed meat products to differentiate rabbit from other commonly-consumed animal species.

131 ortantly, at 12 weeks post-implantation in a rabbit full thickness osteochondral defect model, the qu

132 Addition of rabbit gastric lipase significantly increased the releas

133 Adding rabbit gastric lipase, lipase inhibitor (orlistat) and t

134 e output in albatrosses and that eliminating rabbits had a positive effect on albatross reproduction.

135 ganglia of non-protected SYMP HLA transgenic rabbits had higher frequencies of dysfunctional tissue-r

136 nt vaccine against an osteomyelitis model in rabbits has previously been developed and shown to be ef

137 It is unlikely that rabbits have 91 types of RGC, but is argued here that th

138 More than 30 years ago, I estimated that rabbits have about 40 types of RGC.

139 cal sympathetic innervation and perfusion in rabbit hearts.

140 Here, we used laboratory data from a rabbit-helminth system and developed a within-host model

141 d rabbit numbers, due to the introduction of rabbit hemorrhagic disease and prolonged drought in sout

142 mbers declined following the introduction of rabbit hemorrhagic disease virus and drought in the geog

143 Previous studies have shown that rabbit IgG antibodies against Schistosoma mansoni egg an

144 i-mouse IgG antibody (PMGO-2), and goat anti-rabbit IgG antibody (PMGO-3) were added together.

145 then detected using an immobilized goat anti-rabbit IgG polyclonal antibody on the SPR sensor chip.

146 ound to target-molecule-bound mouse IgG1 and rabbit IgG primary antibodies, whereas the bispecific rI

147 c-ABD, mutually bound to both mouse IgG1 and rabbit IgG primary antibodies.

148 ration of Pru p 3, determined by ELISA using rabbit IgG, occurred when the protein was treated at 500

149 Rabbit immunization experiments identify key immunodomin

150 The sera from rabbits immunized with several CONE immunogens display E

151 Rabbits immunized with SOSIP-NVP elicited strong neutral

152 Monitoring meat species other than rabbit in the examined pates using pork-, lamb- and chic

153 volution of myxoma virus (MYXV) and European rabbits in Australia is one of the most important natura

154 ight cerebellum were also identified between rabbits in the top or bottom halves of the group as meas

155 en evolving in a novel host species-European rabbits-in Australia since 1950.

156 on of Aii signals to ON CBCs is conserved in rabbit, including one class entirely lacking direct Aii

157 different scenarios of immune regulation in rabbits infected with one or two helminth species.

158 Here, we show that similar to humans, infant rabbits infected with S. flexneri experience severe infl

159 sults that LD spirochetes lose lp28-1 during rabbit infection could potentially explain the failure o

160 Moreover, with the use of the rabbit infective endocarditis model, we demonstrate that

161 ency organized neuron ensembles in the awake rabbit inferior colliculus (IC).

162 lonal antibody were detected in the serum of rabbits injected with the LNP-formulated DNA.

163 Rabbit is a healthy meat, with low allergenicity and exc

164 dominant autologous neutralizing epitope in rabbits is located in an exposed region of the heavily g

165 and -3 increased the subsequent infection of rabbit kidney (RK13) cells, which was dependent on viral

166 d EHV1 particle aggregation and infection of rabbit kidney (RK13) cells.

167 d to spontaneous prion formation in the RK13 rabbit kidney cell model.

168 Conclusion MRI in a rabbit liver tumor model was used to visualize resistanc

169 radiopaque bead (VERB) chemoembolization of rabbit liver tumors.

170 bility of three-dimensional SR US imaging of rabbit LN microvascular structure and blood flow by usin

171 sults SR images revealed microvessels in the rabbit LN, with branches clearly resolved when separated

172 Co-crystallization of the parental rabbit mAb in complex with the human ROR2 kringle domain

173 he affinity maturation and humanization of a rabbit mAb that binds human and mouse ROR2 but not human

174 The affinity-matured rabbit mAb was then humanized by complementarity-determi

175 ices by analysing pates-type products with a rabbit meat content ranging from 5% to 85%.

176 The global popularity of rabbit meat makes it a target for food fraud.

177 heat-stable peptides detected in pure cooked rabbit meat, three were consistently detected in all inv

178 Application of bootstrapping to rabbit MI tissue revealed distal sections comprised 18.9

179 In the rabbit model for CDH, the combination of maternal silden

180 Functionality was also assessed within a rabbit model of bullous keratopathy.

181 In a rabbit model of CRS, TEMPS was maintained in rabbit sinu

182 r intraocular pressure-lowering effects in a rabbit model of glaucoma.

183 In an infant rabbit model of infection, the VbrK C86S mutant induces

184 ocker GS967 on PVT induction in a transgenic rabbit model of long QT syndrome type 2 using intact hea

185 curbed the progression of disease in a novel rabbit model of mild PVR developed using C-PVR cells.

186 toxoids could prevent lethal challenge in a rabbit model of necrotizing pneumonia caused by the USA3

187 Upon systemic administration in a rabbit model of pediatric TBI, D-Sino conjugates specifi

188 inical findings using the established HLA Tg rabbit model of recurrent herpes highlight that blocking

189 ms implicated in glaucoma were assessed in a rabbit model of the disease achieving an intraocular pre

190 calcium phosphate (beta -TCP) in an immature rabbit model through the time of facial maturity.

191 implanted into corpus cavernosa defects in a rabbit model to show good histocompatibility with no imm

192 A rabbit model was used to determine the pharmacokinetic p

193 ties of HDL, we used a CKD (5/6 nephrectomy) rabbit model.

194 current ocular herpes in HLA transgenic (Tg) rabbit model.

195 ty studies and a preliminary in vivo carotid rabbit model.

196 ir of a critical-sized calvarium defect in a rabbit model.

197 rimental groups and the highest to date in a rabbit model.

198 ole in preventing myocardial damage in OSAHS rabbit model.

199 NDEBs was evaluated using an atherosclerosis rabbit model.

200 s little to no reactivation in the mouse and rabbit models of induced reactivation.

201 In preclinical rodent and rabbit models, we show that this system enabled the dete

202 on in reactivation of HSV-1 in the mouse and rabbit models.

203 clotting in catheter and arteriovenous shunt rabbit models.

204 SOSIP.664 trimers (BG505 trimers) and three rabbit monoclonal antibodies (MAbs) with different neutr

205 arge panel of novel APOL1-specific mouse and rabbit monoclonal antibodies.

206 Kinetic studies with rabbit muscle and human liver glycogen phosphorylases sh

207 e dependence of the allosteric regulation of rabbit muscle pyruvate kinase by Ala to demonstrate that

208 Rabbit myocardial slices cultured at SL = 2.2 mum remain

209 um cylinders were fixed onto the calvaria of rabbits (n = 20) that received (n = 10) or not (n = 10)

210 eointimal foam cell formation was induced in rabbits (n = 7).

211 y reflect a change in selection pressures as rabbit numbers declined following the introduction of ra

212 996 to 2012 saw significant declines in wild rabbit numbers, due to the introduction of rabbit hemorr

213 bserved after a lag period following highest rabbit numbers.

214 d in epinephrine-induced reactivation in the rabbit ocular model.

215 e inferior colliculus (IC) of unanesthetized rabbits of both sexes.

216 ), on HCO(3) absorption in isolated perfused rabbit OMCDi.

217 thood for human, rhesus macaque, mouse, rat, rabbit, opossum and chicken.

218 uantified the influence of invasive European rabbits Oryctolagus cuniculus and extreme weather patter

219 ve phenotype in the presence of HDL from CKD rabbits, patients on hemodialysis and peritoneal dialysi

220 rent species, including mice, rats, ferrets, rabbits, pigs, sheep, zebrafish, and fruit flies, have a

221 ids and during pharmacokinetic evaluation in rabbit plasma.

222 Guinea pig samples were extremely low, while rabbit plasmas showed variable PG curves demonstrating o

223 nti-CPS IgGs was examined using well-defined rabbit pneumococcal antisera.

224 For this, rabbit polyclonal antibody with specificity to C. jejuni

225 ion indicated that most of the blood flow in rabbit popliteal LN was at velocities lower than 5 mm/se

226 Myofibrils isolated from rabbit psoas were activated and relaxed using a perfusio

227 In a New Zealand White Rabbit radius defect model, the scaffolds degrade gradua

228 opathology in naive male rats and naive male rabbits receiving twice daily treatment of two drops for

229 an stimulate PRF to levels as high as 58% in rabbit reticulocyte cell-free translations and 81% durin

230 in vitro assay combining a ribosome-depleted rabbit reticulocyte lysate and ribosomes prepared from H

231 prepared from budding yeast, wheat germ, and rabbit reticulocyte lysates.

232 but powerful method of Golgi-impregnation to rabbit retina, studying the range of component neurons i

233 tion connectomics dataset of an adult female rabbit retina.

234 initive in fixing the number of RGC types in rabbit retina.

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

236 Repeated topical application in rabbits reveals a proteoform turnover time of 7 to 33 h

237 e resistance to enzymatic degradation of the rabbit sclera.

238 methods reduced the enzymatic degradation of rabbit scleral tissue by MMP1.

239 -linking methods increased the resistance of rabbit scleral tissue to MMP1-degradation.

240 In conclusion, the electrofusion of rabbit SCNT embryos induced oxidative stress, disturbed

241 e epitopes that are unique to the protective rabbit sera were mapped.

242 mers could deplete the NAb activity from the rabbit sera.

243 against pneumonia, while passive transfer of rabbit serum from MAV-vaccinated rabbits significantly p

244 th a KLH conjugate of this glycopeptide into rabbits showed high titer antibodies by ELISA assays, an

245 Control rabbits showed normal wall thickness with no presence of

246 transfer of rabbit serum from MAV-vaccinated rabbits significantly protected against sepsis caused by

247 Coronary ligation caused ascites in most rabbits, significantly increased lung-, heart-, and live

248 rabbit model of CRS, TEMPS was maintained in rabbit sinuses and effectively reduced sinonasal inflamm

249 Of those 15 rabbits, six underwent conventional transarterial chemoe

250 >99% of prothrombinase activity supported by rabbit skeletal and by bovine cardiac myosin.

251 igh levels of CD80 both in vitro in cultured rabbit skin cells and in vivo in infected mouse corneas.

252 e to examine the effects of electrofusion on rabbit somatic cell nuclear transfer (SCNT) embryos, and

253 MS/MS approach for detecting and identifying rabbit-specific peptide-markers from thermally processed

254 Mouse-specific rILSA, MG1Nb-Nluc, and rabbit-specific rILSA, Nluc-ABD, selectively bound to ta

255 similar inflammatory response to a wild-type rabbit strain and, therefore, validated this model for c

256 The rabbit subjects used in this work are an ideal model sys

257 After intravitreous injection in rabbits, sunitinib microparticles self-aggregate into a

258 Our study included 10 Dutch Belted Rabbits that underwent TCP in their right eyes (n = 5, M

259 When tested as immunogens in rabbits, the AMC009 trimers did not induce autologous ne

260 rferi is mediated by humoral immunity in NZW rabbits, the previously reported results that LD spiroch

261 Compared to protected ASYMP HLA transgenic rabbits, the trigeminal ganglia of non-protected SYMP HL

262 s and displayed antithrombotic efficacy in a rabbit thrombosis model.

263 attern increased APD dispersion only in LQT2 rabbits through heterogeneous APD restitution and the sh

264 in eggs, poultry, bovine, ovine, porcine and rabbit tissue and exceptionally low LODs were achieved,

265 gel was injected into the soft palate of the rabbits to induce OSAHS.

266 ility of immunogenicity studies performed in rabbits to predict responses in RM will vary depending o

267 analysis of rs-fMRI conducted on a cohort of rabbits undergoing eyeblink conditioning can reveal func

268 The cohort of rabbits undergoing eyeblink conditioning exhibited incre

269 These six rabbits underwent 3-T MRI, including T1- and T2-weighted

270 Rabbits underwent a subtotal uterine excision and were r

271 knockdown of FXIII-B with siRNA in mice and rabbits using lipid nanoparticles resulted in a sustaine

272 Rabbits vaccinated with Hla toxoid alone or PVL componen

273 of antibody-cell interactions indicated that rabbit vaccine-induced antibodies effectively recruited

274 Using an in-silico subcellular model of rabbit ventricular myocyte, we show that the high dimens

275 ore the 3-dimensional nanostructure of TT in rabbit ventricular myocytes, preserved at different stag

276 -spike inhibitory interneurons in layer 4 of rabbit visual cortex.

277 lates the physiological redox environment of rabbit vitreous and maintains a steady-state redox poten

278 ific CD8(+) T(RM) cells in latently infected rabbits was associated with protection against recurrent

279 the retinal and choroidal vessels in living rabbits was enhanced by up to 82% for PAM and up to 45%

280 In mechanically ventilated rabbits, we found that both xenon gas transport and tran

281 BM-derived myofibroblast specimens from each rabbit were analyzed by LC MS/MS iTRAQ technology using

282 Groups of juvenile New Zealand White rabbits were administered 3 sequential doses of the full

283 Rabbits were divided into three groups.

284 The rabbits were euthanised at 4 weeks, and their dissected

285 Thirty New Zealand rabbits were randomized into three groups: the control g

286 Rabbits were treated with the beta3 AR agonists CL316,24

287 21 VX2 liver tumor-bearing New Zealand white rabbits were used between October 2018 and February 2020

288 ing units) intradermal model of infection in rabbits, which reproduces the characteristic staphylococ

289 tocols for infecting New Zealand White (NZW) rabbits with aerosols containing F. tularensis We evalua

290 on glycan hole can be achieved, we immunized rabbits with B41 SOSIP (gp120-gp41 disulfide [SOS] with

291 Immunization of rabbits with bivalent Ebola VLPs produced antibodies tha

292 e reactions identified in single infections, rabbits with both helminths also activate new pathways t

293 tulated by PET-CT in experimentally infected rabbits with cavitary TB and confirmed using postmortem

294 ues vascular abnormalities in lungs of fetal rabbits with CDH, it only partially improves airway morp

295 Only rabbits with cell-seeded constructs had normal pregnanci

296 weight ratios and prevalence of ascites in 8 rabbits with HF relative to indices for 13 untreated rab

297 tly reduced indices of organ congestion in 6 rabbits with HF relative to indices of 6 untreated rabbi

298 with HF relative to indices for 13 untreated rabbits with HF.

299 sk immunodominant glycan holes by immunizing rabbits with ICs consisting of the BG505 SOSIP.664 gp140

300 ay (ELISA) using sera from naive rabbits and rabbits with S. aureus-mediated osteomyelitis, and then