ライフサイエンスコーパス: hamster

1 feration in amoebic liver abscess induced in hamster.

2 mal species, namely, ferret, guinea pig, and hamster.

3 from three species: human, mouse, and Syrian hamster.

4 tion of CD in subordinate, but not dominant, hamsters.

5 aluation against A. ceylanicum infections in hamsters.

6 ard was determined in male and female Syrian hamsters.

7 e a highly lethal HPS-like disease in Syrian hamsters.

8 d cause highly lethal HPS in immunocompetent hamsters.

9 loped tests that measure long-term memory in hamsters.

10 e spleen and liver samples of SFTSV-infected hamsters.

11 the lack of genetic resources available for hamsters.

12 inhibition (HAI) titers than RD-Ad in Syrian hamsters.

13 high-titer AFIA-positive donations infected hamsters.

14 quality RSV-neutralizing serum antibodies in hamsters.

15 ng disruption of adaptive immunity in Syrian hamsters.

16 reduced CD response compared to subordinate hamsters.

17 vels of serum RSV-neutralizing antibodies in hamsters.

18 gainst lethal NiV challenge in Syrian golden hamsters.

19 hamsters and was uniformly lethal in RAG2 KO hamsters.

20 inoculating O. viverrini metacercariae into hamsters.

21 rginal reductions in replication in mice and hamsters.

22 in high-dose SARS-CoV-2 challenge in Syrian hamsters.

23 petitive fitness than the wild-type virus in hamsters.

24 d packaging was substantially attenuating in hamsters (10- to 100-fold) and rhesus monkeys (100- to 1

25 rome coronavirus 2 (SARS-CoV-2) infection in hamsters(5-7) and nonhuman primates(8-10) have generally

26 cy followed by estrogen withdrawal in Syrian hamsters, a first for this species.

27 l Syrian golden hamster model of MHF using a hamster-adapted MARV variant Angola.

28 ng antibodies (S2E12 and S2M11) that protect hamsters against SARS-CoV-2 challenge.

29 models, including the mouse, guinea pig, and hamster, also exist for Ebola, Marburg, and Ravn viruses

30 ders of magnitude in mammalian cell lines of hamster and human origin was confirmed by flow cytometry

31 a pig, dog, cat, rat, rabbit, ferret, mouse, hamster and macaque.

32 1) is the principal receptor for JUNV, while hamster and mouse orthologs fail to support viral entry/

33 ns on reconfiguration dynamics of the Syrian hamster and rabbit prion proteins.

34 (PrP) amyloids from human, mouse and Syrian hamster and show that their structural differences are m

35 iest skin prion-seeding activity at 3 wpi in hamsters and 20 wpi in Tg40h mice.

36 om 6 HeV-infected tissue samples from Syrian hamsters and 4 tissue samples from a NiV-infected Africa

37 s early as 2 weeks post inoculation (wpi) in hamsters and 4 wpi in Tg40h mice; RT-QuIC assay reveals

38 Hamsters and African green monkeys received a primary in

39 ted parasites colonized the biliary tract of hamsters and developed into adult flukes, but the infect

40 ersion (RT-QuIC) assays of skin samples from hamsters and humanized transgenic mice (Tg40h) at differ

41 iverrini and reacted with sera from infected hamsters and humans.

42 ansport was seen in experimental and control hamsters and mice, indicating that it was not species sp

43 nd quality of RSV-neutralizing antibodies in hamsters and nonhuman primates.

44 mmune responses than RD-Ad vectors in Syrian hamsters and rhesus macaques.

45 d infectivity by means of the inoculation of hamsters and the subsequent examination for parasitemia.

46 t will reduce the CD response in subordinate hamsters and thereby produce dominant-like behavior.

47 as prolonged in transiently immunosuppressed hamsters and was uniformly lethal in RAG2 KO hamsters.

48 ral DPP4 orthologs, including mouse, ferret, hamster, and guinea pig DPP4, do not.

49 as a determinant of permissivity for ferret, hamster, and guinea pig DPP4.

50 including humans, pigs, ferrets, dogs, cats, hamsters, and at least 2 genera of bats.

51 duction of Th1 type immune response in mice, hamsters, and dogs.

52 igher titers of pre-F specific antibodies in hamsters, and improved the quality of RSV-neutralizing s

53 Enrichment of LdHSP78 in infected humans, hamsters, and parasite amastigotes suggested its importa

54 ated male monkeys, guinea pigs, rabbits, and hamsters; and female dogs.

55 contacts indicates that macaque, ferrets and hamster are the most suitable models for the study of in

56 tant biomedical research questions for which hamsters are an excellent model.

57 Hamsters are an ideal animal model for a variety of biom

58 us burdens in the livers of HAdV-C6-infected hamsters are higher than the virus burdens in HAdV-C5-in

59 tection from acute disease.IMPORTANCE Syrian hamsters are in use as a model of disease caused by SARS

60 Furthermore, when hamsters are infected intravenously with HAdV-C6, live,

61 Syrian hamsters are permissive for the replication of species C

62 Syrian hamsters are susceptible to infection with certain human

63 Here, we demonstrate that immunosuppressed hamsters are susceptible to low doses of virus and devel

64 Rodents (mice, rats, hamsters) are the most frequently used animal models in

65 re broadly, these experiments suggest Syrian hamsters as a novel organism in which to model the effec

66 icity (maximum tolerated dose = 150 mg/kg in hamster) as compared with niclosamide, supporting its fu

67 s more attractive than the odour of the same hamsters, before they were infected.

68 When inoculated into hamsters, both of these types of synthetic prions initia

69 HSI examples acquired from cryo-sections of hamster brain tissue using Fourier-transform infrared (F

70 ranscript expression in both female and male hamster brains and offers invaluable information to prom

71 r endothelial growth factor (VEGF) levels in hamster bronchoalveolar lavage (BAL) fluid early after i

72 cancer were made possible by the use of the hamster buccal pouch and mouse models.

73 amount of virus in the lung of ANDV-infected hamsters but altered neutrophil recruitment, MIP-1alpha

74 tes the efficacy of a novel FGF21 mimetic in hamsters, but reveals attenuated effects in the animal m

75 hich proved efficacious in murine sepsis and hamster C. difficile models of disease.

76 tantly, we also show that SFTSV infection in hamsters can be effectively treated with a broad-spectru

77 nd as well as the soft-shell clam and Syrian hamster, can advance studies of tumor biology.

78 ication of several OPXV species in a Chinese hamster cell line was caused by a species-specific diffe

79 n RVB mediates fusion of human cells but not hamster cells and, thus, may serve as a species tropism

80 e demonstrate that FANCJ deficient human and hamster cells exhibit reduction in the overall gene conv

81 irus mediates fusion of human cells, but not hamster cells, and enhances species A rotavirus replicat

82 ,12-Dimethylbenz[a]anthracene (DMBA)-induced hamster cheek pouch model of oral squamous cell carcinom

83 chemically-induced epithelial tumors in the hamster cheek pouch were treated.

84 donorleucine (Anl) to elongator tRNA(Met) in hamster (CHO), monkey (COS7), and human (HeLa) cell line

85 d from 1-, 2-, 3-, and 6-month post-infected hamsters compared to uninfected liver tissues.

86 In hamsters, CPO RSVs induced lower levels of serum RSV-neu

87 nd CHO DG44) and compared with seven Chinese hamster (Cricetulus griseus) tissues (brain, heart, kidn

88 These hamsters demonstrated a systemic and lethal disease in r

89 dependent escalation of aggression in female hamsters depends on activation of mGluR5 receptors.

90 rthermore, we demonstrate that RAG2 knockout hamsters develop severe/fatal disease when exposed to SA

91 Both the CyP-treated and RAG2 KO hamsters developed clinical signs of disease that were m

92 Here, we demonstrate that hamsters devoid of functional STAT2 are highly susceptib

93 ination with transcriptome sequencing of the hamster diencephalon under winter and summer conditions,

94 erformance liquid chromatography analyses of hamster ear extracts showed that OG treatment increased

95 ecyloxy)-2-furoic acid significantly reduced hamster ear sebaceous gland size, indicating that this p

96 sistently altered in abundance in serum from hamsters experimentally infected with scrapie.

97 xerts profound metabolic effects in Siberian hamsters exposed to long day (LD) photoperiods that incr

98 To date, mouse, hamster, ferret, guinea pig, and non-human primates have

99 icantly upregulated the percentage of PFs in hamster fetal ovaries in vitro compared with either of t

100 prophylactic dose of decoy protected Syrian hamsters from a subsequent lethal SARS-CoV-2 challenge.

101 s glycoprotein protected up to 70% of Syrian hamsters from lethal NiV challenge, despite animals havi

102 herapeutic application of CV07-209 protected hamsters from SARS-CoV-2 infection, weight loss, and lun

103 Here, we describe a novel model of SFTS in hamsters genetically engineered to be deficient in a pro

104 changes in specific taxanomic groups in the hamster gut microbiome.

105 Similarly to mouse models, in hamsters, HAdV-C6 is sequestered by macrophages to a les

106 The hamster has been shown to share a variety of metabolic s

107 The use of hamsters has declined, however, most likely due to the d

108 Feeding hamsters HCHFD markedly reduced hepatic Acsl1 mRNA and p

109 stochemistry in liver of S. mansoni-infected hamsters, Huh7 cells, primary hepatocytes, and human liv

110 LTR-mediated gene remodeling also extends to hamster, human, and bovine oocytes.

111 th either the stimulatory mAb to LAIR-1 or a hamster IgG control.

112 We show that in hamsters immunized with Bacillus subtilis spores express

113 Syrian hamsters immunized with FiloRab1 PBV-processed vaccines

114 the attractiveness of the odour of the same hamster in a Y-tube olfactometer bioassay, at a late sta

115 ite, Ancylostoma ceylanicum, on cognition in hamsters in a controlled laboratory setting.

116 ne expression in entrained versus arrhythmic hamsters in the suprachiasmatic nucleus (SCN) that paral

117 h murine bone marrow-derived macrophages and hamsters, in association with enrichment of proinflammat

118 Here, we show that Syrian hamsters, in contrast to mice, are highly permissive to

119 attached to SMA lipid particles in mice and hamsters indicated that these amphipathic polymers offer

120 Sera from hamsters infected with D614 virus exhibit modestly highe

121 by negative effects on parasite fecundity in hamsters infected with hookworms.

122 xtraction from brain homogenates from Syrian hamsters infected with Hyper prions and WT mice infected

123 These results strongly indicate that hamsters infected with Le. infantum become significantly

124 Hamsters infected with SARS-CoV-2 expressing spike(D614G

125 this study was to determine if the odour of hamsters, infected with Le. infantum, was more attractiv

126 emonstrate that the nasal mucosa of mice and hamsters is not an absolute anatomical barrier to inhale

127 that SFTSV infection in STAT2 knockout (KO) hamsters is responsive to favipiravir treatment, which p

128 heir replication cycles was examined in baby hamster kidney (BHK) cells.

129 in native lipid nanodiscs derived from baby hamster kidney cells, that G12V-KRAS samples three confo

130 Similarly, administration in hamsters limits weight loss and decreases lung titers an

131 ve binding assay was performed using Chinese hamster lung (CHL) cells transfected with GLP-1R.

132 ve binding assay was performed using Chinese hamster lung (CHL) cells transfected with the GLP-1R.

133 Chinese hamster lung V79 cells and its mutant cell lines, V-C8 (

134 ons from postnatal day (P)0-P2 golden Syrian hamsters (Mesocricetus auratus) of either sex to study t

135 els of SARS-CoV-2 neutralizing antibodies in hamsters (Mesocricetus auratus), mice (Mus musculus) and

136 uld not be attributed to defects in infected hamster mobility or to lack of interest.

137 port the use of the newly described STAT2 KO hamster model for evaluation of promising antiviral ther

138 In a hamster model of acute C. difficile disease, the CmrRST

139 d robust virulence and 100% lethality in the hamster model of acute CDI.

140 Optimal efficacy in the hamster model of C. difficile was achieved with compound

141 The STAT2 knock-out hamster model of CCHFV infection may provide some furthe

142 n in vitro and in decreased virulence in the hamster model of CDI.

143 te to hantavirus disease pathogenesis in the hamster model of HPS.

144 bited increased toxin gene expression in the hamster model of infection.

145 eir ability to cause disease in the standard hamster model of leptospirosis.

146 t of a novel, uniformly lethal Syrian golden hamster model of MHF using a hamster-adapted MARV varian

147 de, allowing for prophylactic treatment in a hamster model of oral inflammatory lesions in vivo.

148 h prophylactic and therapeutic efficacy in a hamster model of SARS-CoV-2 infection, possibly enhanced

149 h prophylactic and therapeutic efficacy in a hamster model of SARS-CoV-2 infection.

150 Using the hamster model of visceral disease, we demonstrate that p

151 This MHF hamster model represents a powerful tool for further dis

152 ctivator of transcription 2 (STAT2) knockout hamster model to expand the repertoire of animal models

153 These findings from the hamster model were confirmed by analyses of human biopsi

154 In a hamster model(2) and in macaques, YF-S0 prevents infecti

155 (b.i.d., orally) in the Leishmania infantum hamster model.

156 ), we visualized virus tropism in the Syrian hamster model.

157 the therapeutic and toxic effects in Syrian hamster models of pancreatic cancer (PaCa).

158 These immunosuppressed hamster models provide researchers with new tools for ev

159 ctiveness of odour collected from individual hamsters (n = 13), before they were infected, was compar

160 re more severe than those in immunocompetent hamsters, notably weight loss, viral loads, and fatality

161 er JUNV replication compared to infection of hamster or mouse macrophages.

162 Moreover, in YFV-infected hamsters, oral administration of BDAA protected 90% of t

163 polymerase I promoters of human and Chinese hamster origin performed equally well.

164 (E2) upregulates PF formation in developing hamster ovaries.

165 resent an effort to create a "clean" Chinese hamster ovary (CHO) cell by disrupting multiple genes to

166 and competitive conditions (mAb in a Chinese Hamster Ovary (CHO) cell culture harvest).

167 rfusion culture of an IgG1-producing Chinese hamster ovary (CHO) cell line for 18-25 days.

168 Chinese hamster ovary (CHO) cell lines are widely used in indust

169 in the case of genetically unstable Chinese hamster ovary (CHO) cell lines with only draft genome as

170 platform to image endogenous H2S in Chinese hamster ovary (CHO) cells and use the developed construc

171 d host range in mammalian cells, but Chinese hamster ovary (CHO) cells are nonpermissive for vaccinia

172 Chinese hamster ovary (CHO) cells are the predominant production

173 te any current when transfected into Chinese hamster ovary (CHO) cells but, surprisingly, exerted "ch

174 n neonatal mouse cardiac myocytes or Chinese hamster ovary (CHO) cells expressing the mouse or human

175 dy, we evaluated the genotoxicity to Chinese hamster ovary (CHO) cells induced by municipal secondary

176 We show that Chinese hamster ovary (CHO) cells used to express recombinant gp

177 Single cell suspensions of Chinese hamster ovary (CHO) cells were plated on flasks and irra

178 Treatment of fibroblasts or Chinese hamster ovary (CHO) cells with 25OH caused a 50-70% redu

179 were created by stably transfecting Chinese Hamster Ovary (CHO) cells with plasmids encoding the rat

180 ed as luciferase reporter fusions in Chinese hamster ovary (CHO) cells, where the putative cis elemen

181 used to monomeric GFP (mGFP-hDAT) in Chinese hamster ovary (CHO) cells.

182 invertebrate B. mori and vertebrate Chinese hamster ovary (CHO) cells.

183 stribution in the plasma membrane of Chinese hamster ovary (CHO) cells.

184 human embryonic kidney (HEK 293) and Chinese hamster ovary (CHO) cells.

185 cells used in bioreactors, including Chinese Hamster Ovary (CHO) cells.

186 mouse-human heterohybridoma (HH) and Chinese hamster ovary (CHO) mAb-Ds blocked ADCC and clearance.

187 as performed on mouse myeloma SP2/0, Chinese hamster ovary (CHO), and human embryonic kidney (HEK) ce

188 Chinese hamster ovary (CHO)- and human embryonic kidney (HEK)-de

189 ing human WT or p.P888L SAP97 and in Chinese hamster ovary (CHO)-transfected cells.

190 king the cytotoxicity of the HBQs in Chinese hamster ovary (CHO-K1) cells.

191 e found that knockdown of cofilin in Chinese hamster ovary 7WD10 cells and primary neurons significan

192 In transfected Chinese hamster ovary AP-1 cells, the Leu515Phe mutant protein w

193 icles isolated from AQP1-transfected Chinese hamster ovary cell cultures.

194 at its endogenous locus in isogenic Chinese hamster ovary cell lines.

195 ainst membrane protein antigens in a Chinese hamster ovary cell system.

196 (ILs) on zebrafish (Danio rerio) and Chinese hamster ovary cells (CHO) was investigated with specific

197 three homologs that are expressed in Chinese hamster ovary cells (DPY19L1, DPY19L3, and DPY19L4) and

198 We expressed human CTRP6 in Chinese hamster ovary cells and investigated the binding to diff

199 ecordings from channels expressed in Chinese Hamster Ovary Cells at different temperatures (32, 37, a

200 was measured in P2Y(14)R-expressing Chinese hamster ovary cells by flow cytometry.

201 hat use human receptors expressed in Chinese hamster ovary cells demonstrate that NDD-713 and -825 ha

202 an Beta-Gal (rhBeta-Gal) produced in Chinese hamster ovary cells enabled direct and precise rhBeta-Ga

203 an beta-gal (rhbeta-gal) produced in Chinese hamster ovary cells enabled direct and precise rhbeta-ga

204 s exon promote serotonin uptake into Chinese hamster ovary cells expressing either vesicular monoamin

205 Chinese hamster ovary cells expressing marmoset or human oxytoci

206 tic naive human scFv library against Chinese hamster ovary cells expressing the oncogenic target epit

207 re dependence of hERG kinetics using Chinese hamster ovary cells overexpressing hERG1a on the Nanion

208 well as single-channel recordings on Chinese hamster ovary cells overexpressing I(Ks) channels.

209 ompetition assays using membranes of Chinese hamster ovary cells recombinantly expressing the human G

210 Expression of p.T224M KCNQ1 in Chinese hamster ovary cells showed near complete loss of protein

211 ch-clamp platform, by applying it to Chinese hamster ovary cells stably expressing hERG1a.

212 rehensive gene engineering screen in Chinese hamster ovary cells that enables production of lysosomal

213 In Chinese hamster ovary cells that express the channels, Kir2.1 cu

214 Second, in Chinese hamster ovary cells that heterologously express the chan

215 Transport was measured in Chinese hamster ovary cells that stably expressed the human orth

216 We transfected Chinese hamster ovary cells with plasmids carrying wild type ACK

217 Conversely, transfection of Chinese hamster ovary cells with the core 2 GlcNAc transferase a

218 elial cells) and a cancer cell line (Chinese hamster ovary cells) were exposed to liquid and gas phas

219 ent of filopodia and lamellipodia in Chinese hamster ovary cells, stimulate their motility, and enhan

220 channel heterologously expressed in Chinese hamster ovary cells, supporting our findings in DRG neur

221 In Chinese hamster ovary cells, three classes of adhesion can be id

222 xpressing ficolin-2 and ficolin-3 in Chinese hamster ovary cells, we could detect ficolin-2/-3 hetero

223 hERG1a current was measured in nine Chinese hamster ovary cells.

224 omycin resistance gene expression in Chinese Hamster Ovary cells.

225 reconstructions of human, mouse, and Chinese hamster ovary cells.

226 al cultures and human APP-expressing Chinese hamster ovary cells.

227 cancer cell lines (OVCAR3 and A2780), normal hamster ovary control cells (CHOK1) and alphavbeta3-defi

228 upregulation; however, in HEK293T or Chinese hamster ovary-K1 cells overexpressing M3R, pilocarpine i

229 he human endothelial kidney 293-F or Chinese hamster ovary-K1 systems.

230 human erythrocytes when expressed in Chinese hamster ovary-K1, but not in human endothelial kidney 29

231 These findings indicate that in hamsters, pathology resulting from intravenous infection

232 riments sequenced and annotated the Siberian hamster (Phodopus sungorus) genome, a model organism for

233 Here, we show that, in the Siberian hamster (Phodopus sungorus), the programming effect of m

234 Circadian-arrhythmic Siberian hamsters (Phodopus sungorus) exhibit substantial deficit

235 mediated immune responses in adult Siberian hamsters (Phodopus sungorus).

236 eptibilities to aggregation: the susceptible hamster prion (GHaPrP) and its less susceptible rabbit h

237 We conclude that the hamster prion is prone to aggregation at pH 4.4 because

238 -infected transgenic mice overexpressing the hamster prion protein (Tg7 mice) suffer from mitochondri

239 linically ill transgenic mice overexpressing hamster prion protein (Tg7) infected with the hamster pr

240 Hamster prion replication required absence of mouse PrP,

241 amster prion protein (Tg7) infected with the hamster prion strain 263K suffer from a severe deficit i

242 Tg7 mice infected with the 263K hamster prion strain have little or no signs of mitochon

243 When exposed to the 263K, HY, or 139H hamster prion strains, these cells stably propagated hig

244 Here we show that hamster prion-infected transgenic mice overexpressing th

245 -/-) cells) can be chronically infected with hamster prions following stable expression of hamster Pr

246 Although hamster prions have been widely used to study prion repl

247 on were susceptible to mouse prions, but not hamster prions upon expression of cognate PrP, suggestin

248 plication required absence of mouse PrP, and hamster PrP inhibited the propagation of mouse prions.

249 cofactors, the P102L mutation in recombinant hamster PrP promoted prion formation when seeded by minu

250 und that in transgenic mice that overexpress hamster PrP(C), PrP(C) overexpression accelerated recomb

251 nd were infectious to naive cells expressing hamster PrP.

252 amster prions following stable expression of hamster PrP.

253 ng assay using the GeneBridge4 human/Chinese hamster radiation hybrid panel and found to be the MPZL1

254 Here, phenotypic screening of a human/hamster radiation hybrid panel identified SLC19A1, a fel

255 hat repeated aggressive experience in female hamsters resulted in an escalated response to future agg

256 high-dose intranasal SARS-CoV-2 infection in hamsters results in severe clinical disease, including h

257 significantly lower, while vaccinated Syrian hamsters revealed protection in a harsh challenge setup

258 ue inhibitor capable of antagonizing Chinese hamster SAMD9L (chSAMD9L).

259 While the Chinese hamster SAMD9L could not be inhibited by two previously

260 on by reconfiguring 10 times faster than the hamster sequence.

261 44 of human (Hu), bank vole (BV), and Syrian hamster (SHa) prion protein, from disordered monomers to

262 Syrian hamsters show reliable territorial aggression, but after

263 Here, we present a cryo-EM structure of a hamster SUR1/rat Kir6.2 channel bound to a high-affinity

264 Hamsters that achieve social dominance prior to social d

265 In hamsters that received a primary infection with RSV, a b

266 es in blood chemistry in NiV-infected Syrian hamsters that survived or succumbed to disease.

267 In hamsters, the presence of the RSV F gene, and in particu

268 In hamsters, the rB/HPIV3 expressing wt G conferred better

269 In hamsters, these viruses replicated to similar titers.

270 is similar to those of wild-type isolates in hamsters; they also transmitted efficiently between ferr

271 mass spectrometry, providing a comprehensive hamster tissue and cell line proteomics atlas.

272 e detailed comparisons of CHO cell lines and hamster tissues will enhance understanding of the relati

273 We established an infection model in Syrian hamsters to evaluate the efficacy of small molecules on

274 The transmission of L. donovani from sick hamsters to flies was surprisingly low (mean, 24% of fed

275 rain transcriptome of male and female Syrian hamsters to generate the necessary resources to continue

276 Our laboratory uses hamsters to study acute social stress, and we are beginn

277 L. donovani-infected hamsters underwent xenodiagnoses with Lutzomyia longipal

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

279 nfection and the odour of four of the golden hamsters was significantly more attractive to 75% of the

280 To replicate human acute pancreatitis with hamsters, we comparatively studied the efficacy of commo

281 ra from O. viverrini-infected and uninfected hamsters were analyzed using multivariate analysis, incl

282 Adult male and female Siberian hamsters were exposed to either dark nights (DARK) or dL

283 (CyP) immunosuppressed or RAG2 knockout (KO) hamsters were exposed to severe acute respiratory syndro

284 These hamsters were found to be susceptible to SFTSV and share

285 We find that hookworm-infected hamsters were fully capable of detecting a novel object.

286 Female hamsters were given five daily aggression tests with or

287 However, hookworm-infected hamsters were impaired in detecting a displaced object.

288 Syrian hamsters were inoculated intraperitoneally with brain-de

289 tion, whereas at higher levels of infection, hamsters were statistically unable to distinguish betwee

290 ed for at least 3 weeks after the arrhythmic hamsters were switched back to ad libitum feeding.

291 These hamsters were tested for behavioral assays of anxiety an

292 Syrian hamsters were treated, intratracheally, with clodronate-

293 A radiation hybrid panel of chicken-hamster Wg3hCl2 cells was used to map the genome locatio

294 ed by investigating effects of FGF21 in aged hamsters, which is associated with reduced adiposity.

295 es, which may model mild disease, and golden hamsters, which may model more severe disease.

296 Treatment of SARS-CoV-2-infected hamsters with a low dose of favipiravir or hydroxychloro

297 g enzyme 2 (ACE2) transgenic mice and Syrian hamsters with both viruses resulted in similar viral tit

298 In LD hamsters with increased adiposity, FGF21 lowered body we

299 We immunized Syrian hamsters with the best long-term stable FiloRab1 PBV vac

300 from lung disease in most of the vaccinated hamsters within as little as 10 days.