ライフサイエンスコーパス: rat

1 IP) and regulated alternative translocation (RAT).

2 and female of another rat strain, the Dahl S rat.

3 a microdissected tubule RNA-seq dataset from rat.

4 ing protein 3-like 1 (CREB3L1) also involves RAT.

5 ble microbead occlusion model of glaucoma in rat.

6 activation in a slow release fashion in the rat.

7 parated from the digestive tract of a living rat.

8 ing anti-cancer mechanisms of the naked mole rat.

9 Rat AAA rupture was stimulated by the administration of

10 ion of whisking strategy consistent with the rat actively reallocating its remaining resources.

11 -X-C motif) receptor 4 (CXCR4) agonists in a rat acute respiratory distress syndrome (ARDS) model uti

12 ngs are relevant for interpreting results of rat adolescent THC exposure studies, and may lend new in

13 ats produce human-Abeta from a humanized-App rat allele because human-Abeta is more toxic than rodent

14 tity in AD, as compared to rodent Abeta, the rat Amyloid Precursor Protein (App) gene was mutated to

15 Histopathologic characterization of rat and human AAA tissues obtained from surgery revealed

16 st for canine erythrocytes, intermediate for rat and human cells and lowest for bovine cells.

17 meters with the observed data from published rat and human data following intravenous or oral silver

18 l in vitro studies were performed in primary rat and human hepatocytes and HepG2 cells.

19 o improved viability and function in primary rat and human islets under GLT.

20 In INS-1E cells and rat and human islets, proinflammatory cytokines reduced

21 yl-2-aminoquinoline and assayed them against rat and human nNOS, human eNOS, and murine and (in some

22 n described in various regions of the human, rat and mouse brain.

23 genetically manipulate cells in the neonatal rat and mouse brain.

24 gly protected from neurodegeneration in both rat and mouse models of glaucoma.

25 asome system (UPS), and protein synthesis in rat and mouse neurons.

26 outperformed the existing tools on both the rat and NHP ON datasets as judged by mean absolute error

27 reptozotocin-induced vascular leakage model (rat) and preliminary pharmacokinetic assessment of a fir

28 The mouse, rat, and human brain flatmap vector graphics files (Adob

29 in the pattern of labeling among the human, rat, and mouse in these brain regions as well as between

30 e typical laboratory animals, such as mouse, rat, and worm.

31 erived uracil DNA N-glycosylase (eUNG) and a rat APOBEC1 cytidine deaminase variant (R33A) previously

32 onoclonal line of conditionally immortalized rat atrial myocytes.

33 NFAT-DsRed rat basophil leukemia cell attachment and retention duri

34 shock, or nothing would be delivered to the rat being recorded from or a conspecific located in the

35 onfirm that Ade mediates the osteogenesis of rat BMSCs through the STAT3 signaling pathway and restra

36 hway and restrains the osteoclastogenesis of rat bone-marrow macrophages (BMMs).

37 ptic pathway by which principal cells in the rat (both sexes) OB excite GCs by evoking potent nondepr

38 medium, and large arteries and veins in the rat brain and revealed areas of lowest redistribution ov

39 MRP2 transport activities in male and female rat brain capillaries.

40 The adult mouse and rat brain flatmaps provide layered diagrammatic represen

41 otentials from labeled cortical neurons in a rat brain slice, without the need for trial averaging.

42 t blocking GABA transporters (GATs) in acute rat brain slices containing key parts of the thalamocort

43 In rat brain slices containing the intercalated cells, we f

44 dylcholine (PC) lipid cations generated from rat brain tissue via matrix-assisted laser desorption/io

45 in utero electroporation into the developing rat brain to interfere with Nesprin-2 function.

46 SMe has adequate NR2B-specific PET signal in rat brain to warrant further evaluation in higher specie

47 We isolated homogeneous rat brain V-ATPase through its interaction with SidK, a

48 tal weeks, it is also expressed in the adult rat brain.

49 nd expression was measured in Trem2(R47H) KI rat brains and microglia by qualitative and quantitative

50 global responses to rewarding stimulation in rat brains.

51 evoked Ca(2+) responses in astrocytes of the rat brainstem were blocked by (1) antagonists of connexi

52 We simultaneously recorded from rat CA1 and caudodorsal lateral septum in rat during a r

53 osophila L(2)gl, Llgl1 depletion in cultured rat cardiomyocytes decreased Yap protein levels and blun

54 Fisetin enhances viability of rat cardiomyocytes following hypoxia/starvation - reoxyg

55 In rat cardiomyocytes, AKAP6 anchors centrosomal proteins t

56 mostly confined to the T-tubules of healthy rat cardiomyocytes.

57 We have previously reported a rat carrying a TUBB4A (A302T) mutation and sharing most

58 The RHV Sprague-Dawley rat challenge model enables comparative testing of vacci

59 ex vivo (IPAH-PAAF, IPAH-PASMC) and in vivo (rat chronic hypoxia-induced PH and zebrafish angiogenesi

60 of 1.6 mg/kg and dose-dependent efficacy in rat collagen-induced arthritis.

61 uced responses of goblet cells cultured from rat conjunctiva.

62 Previously, in a rat contusion model of severe SCI, we demonstrated extra

63 pus oocyte), tissues (Xenopus epithelium and rat cornea), organs (Xenopus gills and mouse skin) and a

64 tered neurotrophic factor levels in diabetic rat corneas, which were partially restored by fenofibrat

65 rface of cultured human astrocytic cells and rat cortical astrocytes.

66 Using primary rat cortical cells pooled from both sexes, we tested the

67 gated this phenomenon in primary cultures of rat cortical neurons using overexpression of dominant-ne

68 ed mouse hippocampal neurons and dissociated rat cortical neurons.

69 Rat dams were treated with Delta(9)-tetrahydrocannabinol

70 Treating rat dams with cannabinoids during early lactation retard

71 The average CT absorbed dose for mouse and rat decreased to 37 mGy and 24 mGy, respectively.

72 to assess the feasibility of decellularising rat dental pulp tissue and evaluate the ability of such

73 Desert in North America, Merriam's kangaroo rat Dipodomys merriami and the sidewinder rattlesnake Cr

74 for genetics and gene expression studies in rat disease and toxicity models.

75 the advanced domestication of the laboratory rat does suggest that resuming studies of wild rats coul

76 function in an in situ and ex situ model of rat donor liver transplantation.

77 ering RNA-mediated knockdown of Setd6 in the rat dorsal hippocampus during memory consolidation.

78 s losses of the removed BTS samples from the rat duodenum were 2.1, 6.8, 11.2, 19.4, 26.1, and 56.8%

79 om rat CA1 and caudodorsal lateral septum in rat during a rewarded navigation task and compared spati

80 We found that the p53 protein in naked mole-rat embryonic fibroblasts (NEFs) exhibits a half-life mo

81 ive control subjects, in primary cultures of rat enteric neurons and in nuclear factor erythroid 2-re

82 ntial panning of a phage library on cultured rat EpiSCs and then subtracted phage that nonspecificall

83 ty (increases aqueous outflow resistance) of rat eyes.

84 nt FAAH while PpFAAH6 to PpFAAH9 were to the rat FAAH, categorized based on the membrane binding cap,

85 not show improvements in new bone quality in rat femur model.

86 e whether dissociation and reconstitution of rat fetal testis tissue during the MPW can be used to mo

87 d with H. pylori (10(8-) 10(10) CFU/mL; 1 mL/rat.) for 3 consecutive days; and (3) HP + genistein gro

88 Rat forebrain grey matter extracts contain a similar act

89 eased expression of immediate early genes in rat GC of both sexes, and with reduced amplitude of BLA-

90 Analysis of the naked mole-rat genome revealed, uniquely among mammals, a histidine

91 f irinotecan chemotherapy to the brain and a rat glioma model.

92 srupt the steroid potentiating effect at the rat GluN1 (G638; I642) and GluN2B (W559; M562; Y823; M82

93 Once the rat has decided to initiate a trial, it remains engaged

94 The Norway rat has important impacts on our life.

95 MiR-30e-3p was downregulated in human and rat HCCs, and its downregulation associated with TP53 mu

96 nderlying molecular mechanisms in Long-Evans rat heart and in HL-1 cardiomyocyte cell line.

97 we investigated the interaction of neonatal rat heart cells with engineered spider silk protein (eAD

98 Utilizing a rat heart isogeneic transplant model, we identified infl

99 WT and MCU KO mice and the isolated working rat heart.

100 ethod to randomly occlude capillaries in the rat hindlimb to mimic the capillary rarefaction observed

101 We used rat hippocampal cultures and their acute cholesterol dep

102 ed miRNA-seq to study TBI-induced changes in rat hippocampal miRNAs up to one year post-injury.

103 Here, we investigated, in rat hippocampal neuronal cultures derived from embryos o

104 on potentials in single trials from cultured rat hippocampal neurons and can be used in concert with

105 maging, we show that knocking down GluN3A in rat hippocampal neurons promotes the inducible transcrip

106 Knockdown of LASP1 in cultured rat hippocampal neurons results in a substantial reducti

107 and loss-of-function assays, we show that in rat hippocampal neurons the MPS is an actomyosin network

108 imaging and single nanoparticle tracking in rat hippocampal neurons to unveil the nanoscale topograp

109 Cultured rat hippocampal neurons were treated with cerebrospinal

110 tic spines and synaptic deficits in cultured rat hippocampal neurons.

111 ed with 40 nm spatial resolution, on primary rat hippocampal neurons.

112 excitatory postsynaptic currents (mEPSCs) in rat hippocampal slices.

113 We report that LASP1 is expressed in rat hippocampus early in development, and this expressio

114 ng glutamatergic mossy fiber synapses of the rat hippocampus express previously unrecognized electric

115 in anatomically defined subfields within the rat hippocampus.

116 Here the rat HPF flatmap was used as a starting point to construc

117 rofiling of human HSC microRNAs with that of rat HSC so as to identify those molecules that are conse

118 in expression during transdifferentiation of rat HSC, however only 17 underwent changes that were con

119 Therefore, normalization of rat:human organ sizes and correction for reconstruction

120 med cases were significantly associated with rat IgG positivity and RT-PCR positivity (P = .03 and P

121 tion, and among those with >=10 rats tested, rat IgG prevalence ranged 2%-70% and SEOV RT-PCR positiv

122 esent a detailed phenotyping of the TRPA1 KO rat in models of pain, itch, and asthma that have previo

123 entical to SEOV associated with previous pet rat infections in England, the Netherlands, and France.

124 selectively blocked GLT-induced apoptosis in rat insulinoma cells.

125 The brown rat is a cold-hardy global invasive that has reached mos

126 Furthermore, knockdown of HB-EGF in rat islets blocks beta-cell proliferation in response to

127 in vitro model of fibrosis in NRK-49F normal rat kidney fibroblasts.

128 Previously, we showed that rat kidney mesangial cells dividing during hyperglycemic

129 eins expressed in each of the 14 segments of rat kidney tubules and used the proteomic data that we o

130 NBCn1 and NBCn2 in the outer medulla (OM) of rat kidney.

131 osed of liver and gastric mucosa staining on rat kidney/liver/stomach sections.

132 ass 1b antiarrhythmic, mexiletine, using the rat Langendorff preparation.

133 as metabolically stable in rat plasma and in rat liver microsomes and efficacious in rats when given

134 -type oxygen electrode, we measured isolated rat liver mitochondrial respiration in the presence and

135 lls were released into perfusates from Lewis rat livers as a result of cold ischemia and machine perf

136 We previously showed that rat livers can be viably preserved three times longer by

137 analysis of gene regulation in regenerating rat livers temporally spaced at 24 h and 96 h after PH,

138 Angiostrongylus cantonensis (Ac), or the rat lungworm, is a major cause of eosinophilic meningiti

139 crophage phagocytosis allowing repression of rat macrophages by human CD47-positive cells.

140 whether BPA showed effects on the developing rat mammary gland using new quantitative and established

141 using ultra high field fMRI data to compare rat, marmoset, and human MFC functional connectivity.

142 -driven modularity-based parcellation of the rat medial prefrontal cortex (mPFC) combined with seed-b

143 ugh confocal fluorescence imaging of primary rat megakaryocytes.

144 recruited into the glomeruli and the damaged rat mesangial cells leads to diabetic nephropathy, fibro

145 n activating TRPC1-based SOCs in contractile rat mesenteric artery VSMCs.

146 m involved in activating TRPC1-based SOCs in rat mesenteric artery VSMCs.

147 Rat miRNA profiles identified TBI across all acute and c

148 One rat model carries the common human Phe508del (DeltaF508)

149 Using a rat model for exposure to an endocrine disrupting chemic

150 evelopment and application of an RHV outbred rat model for HCV vaccine development.

151 n vivo in an adjuvant-induced arthritis (AA) rat model in order to identify the ideal prodrug design

152 We used a novel rat model in which cholinergic stimulation of PFC produc

153 Our study, using a well-established rat model of alcohol dependence, ex vivo electrophysiolo

154 Conclusion: In a rat model of autoimmune myocarditis, (18)F-FOL shows spe

155 Using a rat model of cardiac hypertrophy induced by thoracic aor

156 on, and prevents pulmonary hypertension in a rat model of chorioamnionitis-induced BPD caused by ante

157 2) agonist, CYM-5478, reduces allodynia in a rat model of cisplatin-induced neuropathy and attenuates

158 We recently developed a rat model of drug relapse after palatable food choice-in

159 peptides in the hypothalamus in a postnatal rat model of fetal alcohol spectrum disorders.

160 rifampin, with and without vancomycin, in a rat model of foreign body osteomyelitis.

161 find no evidence for differences in PPI in a rat model of Fragile-X Syndrome (FXS) compared with wild

162 gus (LLTS) reduces cardiac inflammation in a rat model of heart failure with preserved ejection fract

163 We investigated this phenomenon using a rat model of hypertrophy induced by thoracic aortic band

164 Here, we developed a rat model of incubation of opioid craving after electric

165 d studied angiogenesis in a low protein diet rat model of IUGR.

166 d with amplified activity of PB neurons in a rat model of neuropathic pain.

167 We recently characterized a rat model of post-traumatic stress disorder with segrega

168 In a rat model of RA, the most promising derivative (5c) show

169 Similarly, in a rat model of renal ischemia/reperfusion injury, SAR24779

170 Using the MAM (methylazoxymethanol acetate) rat model of schizophrenia and saline-treated control an

171 Here we developed a rat model of sequential cocaine and alcohol self-adminis

172 rocomputed tomography (microCT) imaging in a rat model of subclinical orthopedic device-related infec

173 Using a rat model recapitulating fundamental features of the hum

174 Previous work using a rat model showed that the central amygdala (CeA) plays a

175 We previously demonstrated in the SOD1(G93A) rat model that misfolded SOD1 exists as distinct conform

176 y the onset of diabetes in the UC Davis T2DM rat model to a greater extent than moderate caloric rest

177 puromycin aminonucleoside (PAN) nephropathy rat model treated with amiloride, an inhibitor of plasmi

178 Using a rat model with streptozotocin-induced diabetes, we measu

179 In the classical incubation of drug craving rat model, drug seeking is assessed after homecage force

180 onality between humans and our severe injury rat model, highlighting significant metabolic dysfunctio

181 In a rat model, perinatal nicotine exposure results in an epi

182 Using a rat model, we investigated the possible association betw

183 A CRISPR/Cas9-generated rat model, with a 9-bp deletion within the hotspot analo

184 n synovial tissue in a preclinical arthritic rat model.

185 phenotypes following MC degranulation in the rat model.

186 distal, permanent MCA occlusion (pMCAo) in a rat model.

187 ine abnormalities and molecular changes in a rat model.

188 METx was also tested in vivo in a healthy rat model.

189 y targeting secondary degeneration in a pONT rat model.

190 y in the AD clinical spectrum and amyloid Tg rat model.

191 tings, as well as in the Dahl salt-sensitive rat model.

192 n IVD degeneration and pain using an in vivo rat model.

193 We report that antipsychotic efficacy in rat models declines in concert with extracellular striat

194 ivo biological tissue, and in vivo mouse and rat models of cancer with a thermal camera reveals mater

195 l and neurobehavioral abnormalities in three rat models of CKD, we induced CKD in rats by an adenine-

196 ic acid (NMDA) antagonist MK801-in mouse and rat models of focal cerebral ischaemia.

197 We used rat models of HFpEF and HFrEF to reveal distinct differe

198 We studied phenotypically verified rat models of HFrEF and HFpEF to compare excitation-cont

199 protective and neurorestorative in mouse and rat models of PD.

200 The CF rat models presented herein will prove useful for longit

201 Both rat models revealed a range of CF manifestations, includ

202 have utilized either non-littermate control rat models, or mouse models that lack significant C5b-9

203 In nephrotic rat models, TCF21 expression in podocytes increased alon

204 man and mouse cells, and ex vivo and in vivo rat models, we uncovered a function of 14-3-3zeta.

205 d with hippocampal profiling from other bred rat models.

206 to glass-ionomer cement alone in vivo, in a rat molar pulpotomy model after six weeks.

207 The diabetic, hypertensive heart failure rat (mRen27/tetO-shIR) were treated with empagliflozin (

208 egulated aminopeptidase (EC 3.4.11.3) in the rat neocortex.

209 e bulk of GABA(A)Rs in oligodendrocytes from rat neonates.

210 ing electronics caused minimal damage to the rat nerve, which grows 2.4-fold in diameter, and allowed

211 fectively than shRNAs for Pten repression in rat neural crest-derived PC-12 cells, and enhanced neuri

212 s (PHD) inhibitors on PC12 cells and primary rat neurons following oxygen-glucose deprivation (OGD).

213 udies to date have been limited to mouse and rat neurons.

214 response to ozone was examined in Long-Evans rat offspring.

215 et CAs inhibition and to undergo cleavage in rat or human plasma depending on the NSAID portion.

216 ive to BDNF-TrkB-CREB signaling, whereas the rat ortholog is unresponsive.

217 mmune cell infiltration into the lung in the rat OVA model of asthma, on the other hand, appears to b

218 ditionally, we recorded from a freely moving rat over fourteen weeks, inserting fresh biosensors each

219 e to either polyclonal human (p < 0.0001) or rat (p = 0.0017) immunoglobulins.

220 We demonstrate that wild-type rat P2X2 expressed in Drosophila is fully functional (AT

221 hila taste neurons heterologously expressing rat P2X2 receptors as a screening platform.

222 -ATP, and to confirm its agonist activity on rat P2X2 receptors expressed in human cells.

223 agonist potency and specificity profiles for rat P2X2 receptors; triphosphate-bearing analogues displ

224 human p53, a larger proportion of naked mole-rat p53 protein is constitutively localized in the nucle

225 ed that the long half-life of the naked mole-rat p53 protein reflects protein-extrinsic regulation.

226 Islets in human and rat pancreases were analyzed by immunohistochemistry for

227 various doses of (67)Cu-CuSarTATE in AR42J (rat pancreatic exocrine) tumor-bearing mice was compared

228 In vivo, in the rat parietal cortex, these electrodes could detect brain

229 acious in rats when given orally to suppress rat paw inflammation, macrophage and mast cell activatio

230 human radiation doses were extrapolated from rat PET data.

231 ing an accurate transcriptional timeline for rat PGC development.

232 s study is to identify proton sensors in the rat pituitary gland.

233 JR14a was metabolically stable in rat plasma and in rat liver microsomes and efficacious i

234 iated from surrounding tissues in an in vivo rat prostate model.

235 nted that LB male, but not female preweaning rat pups display increased BLA neuron spine density para

236 iment 2, using an experimental BPD-PH model, rat pups exposed to room air or hyperoxia (85% O(2)) wer

237 latory pattern of the sham rat pups, injured rat pups had increased fR and predictability.

238 P23H rat pups were treated with 830 nm light (180 s; 25 mW/cm

239 red with the ventilatory pattern of the sham rat pups, injured rat pups had increased fR and predicta

240 In rat pups, we intratracheally injected either bleomycin t

241 We generated immunodeficient Rat Rag-/- Gamma chain-/- human signal regulatory protei

242 In the rat, recovery is accompanied by pronounced spontaneous p

243 or, given after ischemia, in the 5-week HFHF rat reduced ALT by 71% and reduced necrosis.

244 d context-induced reinstatement procedure, a rat relapse model.

245 However, specific microglial profiles in rat remain elusive due to tedious methodology and limite

246 Here, we used a syngeneic rat renal transplant and IRI model to evaluate the thera

247 he number of intact vibrissae available to a rat resulted in an alteration of whisking strategy consi

248 Overall, rat retina appeared slightly more sensitive to HG levels

249 Using rat retina RNA-seq data from ischemic and normal conditi

250 sic abnormality within CD8 T cells primed by rat RHV infection, an effect that is governed at least p

251 Using hair bundles from the rat's cochlea and the bullfrog's sacculus, we observed t

252 to continuously track the 3D kinematics of a rat's head, trunk, and limbs for week-long timescales in

253 p53 protein may contribute to the naked mole-rat's remarkable resistance to cancer.

254 ree-air whisking carry information about the rat's upcoming exploratory direction, as demonstrated by

255 histone fold, as well as the C-terminal REM (rat sarcoma exchange motif), CDC25 (cell division cycle

256 etic and functional analyses implicating the rat sarcoma signaling protein, SOS1 (Son of sevenless ho

257 hreonine kinase (BRAF) mutation, and Kirsten rat sarcoma viral oncogene homolog gene (KRAS) mutation.

258 e reported the EF-directed migration of both rat Schwann cells (SCs) and oligodendrocyte precursor ce

259 ere, we used integrated optical imaging in a rat self-administration and a mouse noncontingent model,

260 (PE-LC-MS/MS), or animal-origin deconjugase (rat serum and chicken pancreas) (AE-LC-MS/MS) was used i

261 ic emissions and immunohistochemistry in the rat show that the peripheral hearing function and morpho

262 activation, we have found that the TRPA1 KO rat shows apparently normal behavioral responses in mult

263 e CB in vivo in a spontaneously hypertensive rat (SHR) model of hypertension.

264 gated by an in vitro digestion model using a Rat Small Intestine Extract (RSIE).

265 Functional connectivity architecture of the rat SN is supported by the mouse neuronal tracer data.

266 Finally, we demonstrated that the rat SN responds to conditioned cues and increases functi

267 Finally, we assessed the rat SN's response to conditioned cues in rats (n = 21) w

268 red prominent expression of alpha7 nAChRs in rat SOC, suggesting possible engagement of ACh-mediated

269 s in relaxed skeletal muscle sarcomeres from rat soleus.

270 nto the lesion site of completely transected rat spinal cord.

271 rasympathetic and sympathetic control of the rat stomach.

272 n aorta from both male and female of another rat strain, the Dahl S rat.

273 l WKY-hCD68-GFP monocyte/macrophage reporter rat strain.

274 but only WIS rats developed FGR despite both rat strains having equivalent microbial loads within the

275 We hypothesized that inbred rat strains possessing stress hyper-reactive-, depressiv

276 orted to induce SCZ-like phenotype in normal rat strains, increased NDEL1 enzyme activity in blood.

277 In this review we discuss mouse and rat studies on the development of threat response regula

278 The aim of this experimental rat study was to investigate the potential inflammatory

279 of opioid-induced MOR internalization in the rat substantia gelatinosa.

280 an wild-type alpha-syn unilaterally into the rat substantia nigra (SN).

281 ding reference atlases: Brain Maps 4.0 (BM4, rat) (Swanson, The Journal of Comparative Neurology, 201

282 Dissociated fetal rat testes were xenotransplanted subcutaneously into rec

283 Previously, we showed in rat that CO(2)/H(+)-vasoconstriction in the retrotrapezo

284 The laboratory rat thrives in captivity, and its domestication has prod

285 Rat tissue sections and myocardial autopsy samples from

286 gle units in behaving male mice exposed to a rat to investigate the encoding of predator fear in the

287 -implantation epiblast and all PGC stages in rat to reveal enrichment of distinct gene sets at each t

288 Our new rat transcriptome provides essential reference for genet

289 ize chimeras composed of capsaicin-sensitive rat TRPV1 (rTRPV1) and capsaicin-insensitive chicken TRP

290 trophysiology, and contractility of neonatal rat ventricular cardiomyocytes (NRVCMs) cultured on thes

291 upregulation of SK2 channels in hypertrophic rat ventricular cardiomyocytes is driven by protein kina

292 Neonatal rat ventricular cardiomyocytes were infected with adenov

293 yAB(WT) and CryAB(R120G)-expressing neonatal rat ventricular cardiomyocytes.

294 Adult rat ventricular myocytes expressing wild-type SERCA2b or

295 on ETV1 RNA sequencing dataset from neonatal rat ventricular myocytes transduced with Etv1 showed rec

296 Primary adult rat ventricular myocytes, adeno-associated virus (AAV)-m

297 In the rat ventromedial hypothalamus (VMH), leptin-induced acti

298 ant SK2 channels were overexpressed in adult rat VMs, revealing serine-465 as the site that elicits P

299 The average CT absorbed doses for mouse and rat were 72 mGy and 40 mGy, respectively.

300 Our hope is that the TRPA1 KO rat will become a useful tool in further studies of TRPA