ライフサイエンスコーパス: rat

1 ssociated with hemorrhagic shock (HS) in the rat.

2 (proper) and to the extended amygdala in the rat.

3 ia coli K1 can be replicated in the neonatal rat.

4 neurons about paired whisker stimuli in male rat.

5 was completely absent in the liver of the KO rat.

6 t, immune activation is often explored using rat Abs in immunocompetent mouse models.

7 m injections of an anterograde tracer in the rat ACC and OFC.

8 sing transcranial current stimulation of the rat (all males) motor cortex consisting of a continuous

9 In a rat ALS model (SOD1(G93A) ) we previously demonstrated t

10 ated single-cell metabolomic profiling using rat alveolar macrophage cells incubated with different c

11 Golgi complex and synaptic-like vesicles in rat and human dopaminergic cells.

12 ith His342, benzonitriles conferred the best rat and human nNOS inhibition.

13 ompounds are especially potent and selective rat and human nNOS inhibitors.

14 We found that rat and human pancreatic islets release the intracellula

15 the Golgi and decreases surface delivery in rat and mice sensory neurons.

16 ogy in three rodent models of polyarthritis: rat and mouse collagen-induced arthritis, and mouse coll

17 ls of TAG, cholesteryl ester, and RE in both rat and mouse HSCs.

18 Y-27632, A-83-01, and CHIR99021, can convert rat and mouse MHs in vitro into proliferative bipotent c

19 xo after reperfusion reduces infarct size in rat and pig models of myocardial infarction.

20 Experiments done on the altricial rat and precocial guinea pig neonate demonstrated that t

21 ts obtained with hearts from a small mammal (rat) and a large mammal (human) with heart failure are s

22 Expression of hNTCP in mouse, rat, and dog hepatocytes permits HDV infection but does

23 enough to insert into a vein, which, for the rat animal model we employ, entails devices less than 20

24 Exposure of WKY rat aortas to IL-17F impaired endothelium-dependent vasc

25 RP-associated vasoconstriction in an ex vivo rat aortic ring bioassay.

26 METHODS AND Neonatal rat atrial cardiomyocyte monolayers expressing a depolar

27 he trace of the percept of stimulus 1 as the rat awaited stimulus 2.

28 On the example of rat barrel cortex (vS1), we illustrate that retrograde t

29 ACh tone on whisker-evoked NVC responses in rat barrel cortex, measured by cerebral blood flow (CBF)

30 sensitized mice were investigated by ELISA, rat basophil leukemia assay, T-cell proliferation experi

31 using human and mouse mast cells, as well as rat basophil leukemia cells, and in vivo in mice.

32 t, injecting mouse PSCs into Pdx-1-deficient rat blastocysts, we generated rat-sized pancreata compos

33 ll types have been previously defined in the rat BNSTALG based on differences in the voltage-response

34 Rat bone marrow stem cells were mingled with silk hydrog

35 response to mitral cell action potentials in rat (both sexes) brain slices.

36 We used intracellular recordings in rat (both sexes) neocortical brain slices to assess the

37 -EAs and EDP-EAs are endogenously present in rat brain and peripheral organs as determined via target

38 Rat brain and renal, hepatic, and splenic tissues were h

39 activity of several efflux pumps in isolated rat brain capillaries.

40 rved lncRNAs at different time points during rat brain growth.

41 eeding behavior and metabolic centers in ZDF rat brain or directly enhance glucose-stimulated insulin

42 3 cell clusters through 4.5 mm thick ex vivo rat brain tissue, we demonstrate photoacoustic tomograph

43 orthologous analysis of lncRNAs in human and rat brain tissues revealed a set of conserved lncRNAs.

44 d transgene expression throughout orthotopic rat brain tumors in vivo following administration by con

45 (11)C-Me-NB1 binding in rat brain was blocked in vitro and in vivo by the NTD mo

46 ogression of extrastriate areas that, in the rat brain, run laterally to primary visual cortex, encod

47 , here applied to noradrenaline receptors in rat brain.

48 Gene expression analysis of rat brains following neonatal infection showed increased

49 reas and melatonin-producing pineal gland in rat brains.

50 dropwise to a silk scaffold and applied to a rat calvarial defect.

51 ent in three typical forms of endocytosis at rat calyx of Held terminals by whole-cell membrane capac

52 en-type I hydrogel, a novel clonal strain of rat cancer-associated myofibroblasts (TDFSM) was co-cult

53 of NO generated from the normal and stressed rat cardiac cells as well as from the untreated and trea

54 drial calcium concentration were observed in rat cardiac myocytes.

55 We also used a neonatal rat cardiomyocyte culture system to elucidate the mechan

56 In addition, H9C2 rat cardiomyocytes were cultured in vitro and the phosph

57 dental caries by controlling S. mutans in a rat caries model without perturbing the oral microbiota.

58 In a rat carotid injury model, periadventitial delivery of re

59 Here we show that primary cells from the rat central nervous system respond differently to photo-

60 0) distinguishes several cell types from the rat central nervous system, largely based on the relativ

61 eton-related oligodendroglial protein in the rat central nervous system.

62 aureus biofilm infection when used in a CLS rat central venous catheter infection model.

63 ted through the analysis of sub regions of a rat cerebellum tissue section.

64 perforated patch clamp electrophysiology and rat cerebral arterial myocytes, we monitored STOCs in th

65 ant) in a preclinical RSV susceptible cotton rat challenge model compared to formaldehyde inactivated

66 acokinetics in rats and showed efficacy in a rat chemical model of osteoarthritis.

67 roblasts (TDFSM) was co-cultured with a pure rat cholangiocarcinoma cell strain (TDECC) derived from

68 xtended extracellular network in cultures of rat chondrosarcoma cells.

69 evious localization of the taiep mutation to rat chromosome 9, we tested whether the mutation resided

70 y comparable to dose of 10 mg/kg of 1 in the rat chronic constrictive injury model of neuropathic pai

71 r event sizes in bat claustrum compared with rat claustrum are consistent with events occurring in po

72 HES1 and NR3C1 bind to the CLDN1 promoter in rat colon crypts.

73 19 Wistar rats were implanted with 5 x 10(6) rat colorectal liver metastasis cell line cells.

74 t PgP can efficiently deliver pbeta-Gal in a rat compression SCI model.

75 nduced pluripotent stem cells, or in primary rat cortical neurons.

76 king itinerary for key synaptic molecules in rat cortical neurons.

77 teogenesis and bone formation with BMP2 in a rat critical size mandibular defect model.

78 without rMSC aggregates were implanted into rat critical-sized calvarial defects (CSD).

79 Compared with the wild-type (WT) rat, Cyp3a1/2 expression was completely absent in the li

80 Wistar rat dams were orally exposed to FM 550 during gestation

81 detailed pyramidal neuronal models based on rat data.

82 lthough they were functional and composed of rat-derived cells, the resulting pancreata were of mouse

83 ked insulin granules in human beta cells and rat-derived clonal insulin 1 (INS1) cells for which loca

84 exerted significant spasmolytic activity (on rat distal colon), with PhPeITC being almost 100 times m

85 In transfected small rat dorsal root ganglion neurons, expression of L1302F a

86 3 at the lysine 9 residue (H3K9me1), in the rat dorsomedial prefrontal cortex (dmPFC).

87 ther from E18 transgenic mouse model or from rat E18 embryos that were transiently transfected with A

88 o investigate integrin beta3 and paxillin in rat embryonic fibroblasts growing on two different extra

89 rated by in vivo imaging of a mouse colon, a rat esophagus, and small airways in sheep.

90 ed rats an HFM and showed that HFM increases rat fecal Gram-negative bacteria, elevates lipopolysacch

91 Here we examine how MIA dysregulates rat fetal brain gene expression (at a time point analogo

92 s show that the descending PFC fibers in the rat form WM fascicles embedded within the striatum.

93 first comprehensive characterization of the rat GI microbiota landscape for the research community,

94 uce tumor regression and improve survival in rat glioma.

95 despite having higher levels of ROS, the LEW rat had lower transcript levels for antioxidant enzymes

96 coordinated movements first observed in the rat half a century ago.

97 The laboratory rat has been used as a surrogate to study human biology

98 iterature based on whether normal or failing rat heart models were used.

99 Imaging in whole rat hearts indicated mitochondrial network formation and

100 iologically and pathologically hypertrophied rat hearts, and correlated these marks with their associ

101 livery of the progenitor cells into neonatal rat hearts, in vivo incubation and analysis.

102 n of late gestation (embryonic day 19) fetal rat hepatocytes is mitogen-independent and that mechanis

103 show that chronic alcohol feeding sensitizes rat hepatocytes to Ca(2+) -mobilizing hormones resulting

104 d gene expression differ from those of adult rat hepatocytes.

105 receptor-expressing CHO-IR cells and primary rat hepatocytes.

106 A rat heroin self-administration model was used to obtain

107 ated FSS-induced collateral vessel growth in rat hind limbs.

108 have scrutinized cryo-electron tomograms of rat hippocampal neurons for the occurrence and spatial d

109 Short-term exposure of cultured rat hippocampal neurons or ex vivo human cortical slices

110 aptor protein complex, in the development of rat hippocampal neurons.

111 chanisms, we recorded neural activity in the rat hippocampus and prefrontal cortex, structures critic

112 Long-term potentiation (LTP) in the rat hippocampus is the most extensively studied cellular

113 2, Nav 1.6) in area CA1 and dentate gyrus of rat hippocampus.

114 eta; SMAD-2, -3, and -7; and SMURF-2) in the rat hippocampus.

115 mate and mouse may be similar to that of the rat in some aspects but perhaps significantly different

116 Our study in a diurnal rodent, the Grass rat, indicates that sleep deprivation in the early rest

117 oliferation of ovalbumin-specific T cells in rat insulin promoter-membrane-bound ovalbumin transgenic

118 ole of Ucp2 in cytokine-induced apoptosis of rat insulin-producing INS-1E cells.

119 ly, NMDAR-mediated signaling was observed in rat insulinoma 832/13 cells and in human beta-cells, ind

120 ZnT8A binding was detected on live rat insulinoma INS-1E cells, and the binding specificity

121 The inbred Fischer 344 rat is being evaluated for testing novel vaccines and th

122 iming, a model of pain chronification in the rat, is mediated by ryanodine receptor-dependent calcium

123 We exposed isolated rat islets for 1 h to increasing glucose concentrations

124 Rat islets were transplanted in the PDLLCL scaffold in a

125 Treatment of rat kidney epithelial cells (NRK-52E) with the mitochond

126 hypothesis, we employed an isolated perfused rat kidney model.

127 Similarly, in the postischemic rat kidney, sigma1-receptor activation by fluvoxamine tr

128 ced stages of FSGS, fawn-hooded hypertensive rat kidneys exhibited distinctly increased APA staining

129 nd cutaneous afferent synapses onto immature rat lamina I spino-parabrachial neurons, which serve as

130 accumulate in dendritic spines of the adult rat lateral amygdala (LA) during consolidation of aversi

131 opioid receptor (MOR) function in the female rat LC.

132 expression of the amylin receptor complex in rat LDTg tissue.

133 The rat limbic system contains head direction (HD) cells tha

134 her species, we developed a novel Bace1(-/-) rat line using zinc-finger nuclease technology and compa

135 ation dynamics around a beta-barrel protein, rat liver fatty acid-binding protein (rLFABP), to reveal

136 studies with hyperpolarized [(13)C]-Glyc in rat liver furnished metabolic products, [(13)C]-labeled

137 l, APAP) and (13)C6-APAP were incubated with rat liver microsomes, which are known to bioactivate APA

138 ignificantly improved metabolic stability to rat liver microsomes.

139 conserved human lncRNAs corresponding to 646 rat lncRNAs.

140 he pulmonary vasculature in a decellularized rat lung scaffold.

141 ebrafish, and chick retinal explants avoided rat M1-4 but freely crossed zebrafish M1-4 lanes-suggest

142 s growth permissive and less inhibitory than rat M1-4.

143 se) than the BN rat, suggesting that the LEW rat maintains cellular oxidative stress that it tolerate

144 Together, our results indicate that the LEW rat maintains inherent cellular oxidative stress that co

145 y of tissue-engineered cultures comprised of rat mesenchymal stem cells dynamically seeded on 85% por

146 Adult rat mesenteric tissues were harvested and cultured for t

147 y identify the pharmacological properties of rat mGlu heterodimers composed of mGlu2 and 4 subunits.

148 and reduced neural respiration in the intact rat, mimicking responses to glutamate excitation.

149 53T alpha-synuclein (aSyn)-overexpressing PD rat model (AAV1/2-A53T-aSyn).

150 of the profound hypomyelination in the taiep rat model and determine its relevance to human white mat

151 This rat model characterizes the pattern of bone turnover and

152 CANCE STATEMENT: Relapse to cocaine use in a rat model is associated with transient increases in syna

153 ubcutaneous islet transplantation in a Lewis rat model is significantly improved by treating recipien

154 s are relevant to the validity of the cotton rat model itself and to safe development of nonlive RSV

155 KEY POINTS: In a rat model of ageing that is free of atherosclerosis or h

156 jections control extinction and relapse in a rat model of alcohol seeking.

157 We recently developed a rat model of incubation of methamphetamine craving after

158 Indeed, treatment of a rat model of inherited ALS (caused by a mutation in Sod1

159 or with potent memory-enhancing effects in a rat model of object recognition memory.

160 Here, using a rat model of osmotic demyelination, we showed that rapid

161 omparison with 3 by different paradigms in a rat model of oxaliplatin-induced neuropathic pain, showe

162 9 displayed oral efficacy in 6-OHDA lesioned rat model of Parkinson diseases.

163 ine whether this pathway is compromised in a rat model of Parkinsonism.

164 Using a rat model of PD, partial elimination of the functional i

165 n and characterization of a Shank3-deficient rat model of PMS, with a genetic alteration similar to a

166 a-articular injection in an adjuvant-induced rat model of RA induces apoptosis of FLS, leading to sig

167 re fluorescently labeled and injected into a rat model of radiation-induced lung injury via endotrach

168 locking antibody to inhibit alphavbeta5 in a rat model of renal IRI.

169 has opposite effects on choice behavior in a rat model of risky decision making, depending on the pha

170 rkers in a methylazoxymethanol acetate (MAM) rat model of schizophrenia and saline-treated control (S

171 A fluid-resuscitated, long-term (3 d) rat model of sepsis (fecal peritonitis) and recovery was

172 Interventional study in a rat model of septic shock (128 adult males) to assess th

173 d fast-spiking inhibitory interneurons, in a rat model of TBI as well as in brains of human epileptic

174 thy of prematurity, we developed a composite rat model of UPI and oxygen-fluctuations and removed pre

175 Using a rat model of upper extremity impairments after ischemic

176 rment and central nervous system injury in a rat model of vascular dementia.

177 stinal mycobiomes of patients with IBS and a rat model of visceral hypersensitivity.

178 cial shift in gut microbial communities in a rat model that mimics human menopause.

179 his study is to develop a novel peri-implant rat model using an established model of polymicrobial pe

180 The Cyp3a1/2 double KO rat model was successfully generated and characterized.

181 tation-induced microvascular leakage using a rat model with intravital microscopic imaging.

182 Using a rat model, we examined the effects of exposure to a bact

183 their progression over time in a transgenic rat model, which allows for a finer spatial resolution n

184 e osteotomies in a patient cohort and in the rat model.

185 ty with exogenous administration of ELA in a rat model.

186 rs of islets required to treat diabetes in a rat model.

187 rophores can identify intestinal injury in a rat model.

188 ouse model and a genetically engineered T2DM rat model.

189 uterine health, and body composition in this rat model.

190 planted in the PDLLCL scaffold in a diabetic rat model.

191 in reduction of neovascularization of a ROP rat model.

192 more accurately stage hepatic fibrosis in a rat model.

193 nutrition influence energy homeostasis in a rat model.

194 Our mechanistic findings in rat models and exploratory study in human cirrhosis sugg

195 However, the ictal characteristics of these rat models, including SWDs and associated immobility, ar

196 micromolar concentration range for human and rat monoamine oxidases with slight preference for monoam

197 or agonists that showed oral efficacy in the rat monocrotaline model of pulmonary arterial hypertensi

198 as then used in layers I-IV of slices of the rat motor cortex to determine the percent contribution o

199 In rat motor cortex, SMI32-postive pyramidal neurons expres

200 3.1b expression in sections from macaque and rat motor cortex, using two different antibodies (NeuroM

201 In this study, using rat motor cortex, we found that tACS effects are highly

202 that ER-localized THBS1 is cytoprotective to rat, mouse, and human beta-cells exposed to cytokines or

203 Indoor aeroallergens, including rat, mouse, cockroach, cat, dog, and dust mites, measure

204 and a switch toward type I and IIa fibers in rat muscle and myotubes in vitro.

205 s were obtained following ACSL6 knockdown in rat myotubes, which was associated with a decreased accu

206 f 1, Fel d 1, Der f 1, Der p 1, Mus m 1, and Rat n 1) in dust vacuumed from nearly 7000 bedrooms were

207 nges of the elastic stiffness of the injured rat neocortex and spinal cord at 1.5 and three weeks pos

208 hanisms can be induced in tandem in cultured rat neocortical pyramidal neurons by chronic manipulatio

209 the viability of mouse neural stem cells and rat neuroblastic cells was improved on NDandante and NDH

210 Understanding the rat neurochemical connectome is fundamental for explorin

211 Using CRISPR/Cas9, we generated HID-1 KO rat neuroendocrine cells, and we show that the absence o

212 le patch-clamp recordings from 6068 pairs of rat neurons with validation in additional mouse and huma

213 eous neurotransmission in cultured mouse and rat neurons.

214 cellent concordance between the preclinical (rat, NHP) and human studies with PF-04958242, and in sil

215 HK) was microinjected into the anaesthetized rat nTS or applied to rat nTS slices.

216 into the anaesthetized rat nTS or applied to rat nTS slices.

217 nsporter assays and in vivo microdialysis in rat nucleus accumbens.

218 We found, in acute rat OB slices from both sexes, that inhibitory synchrony

219 ive ultrastructural analyses of glomeruli in rat olfactory bulb under conditions in which specific ce

220 It was subsequently also found in the rat olfactory neuroepithelium, especially at the apical

221 R family-related protein agonistic Ab DTA-1 (rat or murinized IgG2a) can induce the development of an

222 P < .001) of rat orthotopic esophageal cancers.

223 the ovariectomized and dexamethasone treated rat osteoporosis model.

224 site, which described some effects of IVM on rat P2X4R.

225 ed fatty acid-induced apoptosis in human and rat pancreatic beta-cells, as well as in human and murin

226 To validate the approach, single rat pancreatic islet cells were rapidly analyzed with op

227 n of hDF-EpiSC-loaded native de-cellularized rat parotid gland scaffolds into the renal capsule of nu

228 ective PDE2a enzyme inhibitor with favorable rat pharmacokinetic properties.

229 uce a catheterization procedure that keeps a rat physiologically stable for 1.5 mo.

230 Applied to tissue sections of rat pituitary, the platform demonstrated improved spatia

231 e on inhibitory synaptic transmission in the rat PL were determined using whole-cell recordings in la

232 ition, quantitation with minimally processed rat plasma samples was demonstrated with three different

233 acyclic triterpenes from Olea europaea L. in rat plasma.

234 ow cytometry immunophenotyping revealed that rat podocytes express the protease-activated receptor fa

235 injured conditionally immortalized human and rat podocytes.

236 eptor 1 and protease-activated receptor 4 in rat podocytes.

237 In mouse and rat primary hippocampal cultures, synaptic activity caus

238 ariability in the spike-field coherence of a rat primary motor cortical neuron to the LFP theta rhyth

239 ACSL6 genic inhibition in rat primary myotubes decreased lipid accumulation, as we

240 rent study measured HCA1 and HCA2 entry into rat primary neurons and cultured Neuro2A cells.

241 ured proximal tubule cells and microperfused rat proximal tubules, with greater uptake from the apica

242 zygote genome editing and show enrichment of rat PSC-derivatives in several tissues of gene-edited or

243 The polymeric particles were safe to rat pulmonary arterial smooth muscle cell and to the lun

244 d PKA phosphorylation were demonstrated in a rat pup model of NEC.

245 del of status epilepticus in postnatal day 7 rat pups that results in widespread neuronal injury, we

246 ecordings from calyceal terminals in newborn rat pups.

247 Rat pyramidal cells typically lack these channels, while

248 In normal rats, the infusion of rat recombinant FGF23 enhanced phosphaturia and increase

249 ector in situ We now show that EV from adult rat renal tubular cells significantly improved renal fun

250 standardise the mechanical stimulation of a rat's hindpaw.

251 mal growth factor receptor (EGFR) or Kristen rat sarcoma viral (KRAS) mutations, respectively.

252 We additionally compared Kirsten rat sarcoma viral oncogene homolog (KRAS) mutations in p

253 derived sensory neurons can be cultured with rat Schwann cells, and have produced for the first time

254 njection of 6 mul of 150 mum ATP into female rat sciatic nerve quadrupled the number of axons growing

255 lope glycoprotein gp120 application onto the rat sciatic nerve to test the role of phosphorylated C/E

256 MDA was injected directly into crush-injured rat sciatic nerves, ERK1/2 phosphorylation was observed

257 Stimulation of rat segmental dorsal cutaneous nerves (DCNs) evokes the

258 Knockdown of Shrm4 in rat severely impairs GABABR activity causing increased a

259 exually dimorphic effects of morphine in the rat.SIGNIFICANCE STATEMENT We demonstrate that periaqued

260 dx-1-deficient rat blastocysts, we generated rat-sized pancreata composed of mouse-PSC-derived cells.

261 rimary aim of this study was to determine in rat skeletal muscle the influence of a brief (two weeks)

262 etase 6 (ACSL6) mRNA is present in human and rat skeletal muscle, and is modulated by nutritional sta

263 fat diet (HFD) caused insulin resistance in rat skeletal muscle.

264 ificant adhesion strength ( 1.6Ncm(-2)) with rat skin.

265 immunohistochemical approach in normal adult rat small intestinal and ascending colonic tissue.

266 d the mechanisms of mPFC deactivation in the rat spared nerve injury (SNI) model of neuropathic pain.

267 ticity and neuropathic pain behaviors in the rat spinal nerve ligation (SNL) model.

268 We also review results from rat studies in which PAMs or NAMs of mGluRs were injecte

269 antly expressed isoform of T-channels in the rat subiculum.

270 a 1, and glutathione peroxidase) than the BN rat, suggesting that the LEW rat maintains cellular oxid

271 Intact and pressurized rat superior cerebellar arteries were labelled for confo

272 bstitutions at their equivalent positions in rat SUR2A (D207E, Y981S, G985E, M1056I, and R1150Q/R1150

273 0.05) improved function and recipient Lewis rat survival compared to UW solution alone.

274 Also, in rat T9-T10 hemisection spinal cord injury (SCI), we demo

275 -photon targeted patch-clamp recordings from rat TC and TRN neuron dendrites to measure bAPs directly

276 olol glucuronide phase II metabolites from a rat thin tissue section was also illustrated.

277 erent from that previously described for the rat, thus, elucidating potential neuronal pathways invol

278 d upon iodination of TG secreted from PCCL3 (rat thyrocyte) cells was augmented from cells previously

279 In rat tissues, which could be collected at multiple time p

280 flect a further adaptation of the naked mole-rat to living in an environment with high-carbon dioxide

281 ht in intact ventricular trabeculae from the rat to measure the axial movement of the myosin motors d

282 Each rat underwent catheterization of the right femoral arter

283 sed for the determination of GSH and GSSG in rat urine and plasma samples, intoxicated or not by lead

284 In a rat venous patch angioplasty model, control patches deve

285 pression using Tag-seq and RNA-seq in female rat Ventral Mesenchymal Pad (VMP) as well as adjacent ur

286 ould then be identified in situ in slices of rat ventral tegmental area (VTA) with MAPK activation an

287 nd electrophysiological property of neonatal rat ventricular myocyte (NRVM) cultures.

288 ced hypertrophy in H9c2 cardiac cells, adult rat ventricular myocytes, and human induced pluripotent

289 re performed using Fluo-3 in voltage clamped rat ventricular myocytes.

290 Patch-clamp recordings of cultured neonatal rat ventricular myofibroblasts revealed that TGF-beta1,

291 sex differences in decision making using the rat version of the Iowa gambling task.

292 We applied the SDC criterion to data from rat visual and somatosensory cortex and discovered that

293 uli in a way that depended on which room the rat was in; nearly all neurons were tonically selective

294 l activity levels or body weight gain in the rat, whereas it depleted muscle carnitine content (all m

295 od suitable for visualization of one or more rat whiskers.

296 tocin in the central amygdala makes a mother rat willing to put her life in danger in order to protec

297 n generator (SEG) has been identified in the rat with lumbar galaninergic interneurons playing a pivo

298 We reevaluated this technique in the rat with the aim to transfer it to the mouse because com

299 and when viral Env was receptor triggered on rat XC cells.

300 ting proliferation in tumor cell lines and a rat xenograft model.