ライフサイエンスコーパス: squirrel

1 blue Off center ganglion cells in the ground squirrel.

2 subsequences were only found in primates and squirrel.

3 reas 17 and 18 compared with the terrestrial squirrel.

4 of a larger, highly visual rodent, the gray squirrel.

5 a cone-dominant mammal, the 13-lined ground squirrel.

6 igs are more efficient at molar chewing than squirrels.

7 cells described previously for chickens and squirrels.

8 rons in fixed slices from hibernating ground squirrels.

9 ctivity in hibernating thirteen-lined ground squirrels.

10 ation of genome structure between humans and squirrels.

11 st territorial invasions from non-kin ground squirrels.

12 n organization in euthermic or torpid ground squirrels.

13 the brains and livers of hibernating ground squirrels.

14 tectable in mRNA obtained from summer ground squirrels.

15 area (PM), as in previous investigations in squirrels.

16 hat this virus, tentatively named variegated squirrel 1 bornavirus (VSBV-1), forms a lineage separate

17 13 types of cone bipolar cells in the ground squirrel, 11 of which contact contiguous cones, with the

18 eden, one specimen each from an eastern gray squirrel, a chipmunk, and a deer mouse, and 4 water samp

19 al functional interactions in V1 of the gray squirrel, a highly visual rodent.

20 sonal hibernators, such as the arctic ground squirrel (AGS), display torpor only during the winter, h

21 ng the hibernation season from arctic ground squirrels (AGS; Spermophilus parryii) and 13-lined groun

22 Squirrels also emerged from their burrows earlier and re

23 enzymatic activities in cone-dominant ground-squirrel and chicken retinas: an all-trans-retinol isome

24 well as more versatile feeders than both the squirrel and guinea pig.

25 unknown bornavirus was detected in a contact squirrel and in brain samples from the three patients.

26 immunoreactive cells are also found in PH of squirrel and macaque monkeys.

27 Isolated hibernating ground squirrel and mouse RTECs were subjected to CS at 4 degre

28 eus of the optic tract were also observed in squirrel and owl monkeys.

29 product of glucose metabolism in both ground squirrel and rat retinas.

30 Scatter hoarding, as seen typically in squirrels and birds, involves placing small caches of fo

31 For example, ground squirrels and camels can tolerate temperatures more than

32 Our studies suggest that squirrels and camels co-opt a common molecular strategy

33 beetles, orthopterans, kangaroo rats, ground squirrels and lizards.

34 In ground-dwelling sciurid rodents (ground squirrels and marmots), for example, energy intake incre

35 otypic lineages: antelopes, fruit bats, tree squirrels and mongooses.

36 nts were created in the right eyes of ground squirrels and the animals immediately placed in normoxic

37 larger diurnal primates, including macaque, squirrel, and capuchin monkeys, and humans.

38 entromedial to dorsolateral sequence in owl, squirrel, and macaque monkeys, but an altered arrangemen

39 esenting the upper visual quadrant) of titi, squirrel, and owl monkeys.

40 cally distinct regions of temporal cortex of squirrels are also functionally distinct.

41 Results show that squirrels are more efficient at muscle-bite force transm

42 Red squirrels are thus a reservoir for leprosy in the Britis

43 However, models that emphasized red squirrel as the primary species had 7-24% lower southern

44 (WHcAg), ground squirrel (GScAg), and arctic squirrel (AScAg) viruses possess immunogen characteristi

45 cally implanted in striatum of Arctic ground squirrels before any of the animals began to hibernate.

46 f experience in the field were compared with squirrels born in a lab and with no experience in their

47 y ubiquitous neural plasticity in the ground squirrel brain during torpor.

48 found that mitochondria isolated from torpid squirrel brain show a high level of palmitate-induced un

49 P1 contributes to local thermogenesis in the squirrel brain, and thus supports nervous tissue functio

50 xcavated in northeastern Siberia from fossil squirrel burrows buried at a depth of 38 m in undisturbe

51 ntly eliminated in euthermic and torpid SCNx squirrels, but not in those with partial destruction of

52 el (Spermophilus tridecemlineatus) and using squirrel c-fos mRNA probe for in situ hybridization hist

53 echanisms that control hibernation in ground squirrels can guide efforts to develop improved treatmen

54 temporal cortex is functionally organized in squirrels can guide interpretations of temporal cortex o

55 Over two summers, squirrels captured from beacon-dense and beacon-thin are

56 ype of mammalian On bipolar cell, the ground squirrel cb5b, has a large tetrodotoxin (TTX)-sensitive

57 e identify important "dilution hosts" (e.g., squirrels), characterized by high tick burdens, low rese

58 the conclusion that the pulvinar complex of squirrels consists of four distinct nuclei.

59 ior parietal cortex of the California ground squirrel contains multiple representations of the sensor

60 The temporal cortex of grey squirrels contains three architectonically distinct regi

61 n compared with the woodland suggesting that squirrels dealt with increased environmental variability

62 Furthermore, torpid squirrels during the hibernation season keep their brain

63 Hibernators, such as the 13-lined ground squirrel, endure severe hypothermia during torpor follow

64 This is consistent with observations that squirrels entered their burrows during the day to 'offlo

65 Ground squirrel eyecups produced lactate at a high rate and exh

66 Ground squirrel eyecups were incubated in medium containing (14

67 The squirrel family (Sciuridae) is one of very few mammalian

68 Squirrels fattened at the same rate and to the same degr

69 In both years squirrels from beacon-dense populations reached criterio

70 ly in a task of spatial memory compared with squirrels from beacon-thin areas.

71 se populations reached criterion faster than squirrels from beacon-thin populations, and a weak reari

72 and, Ireland, and Scotland, and M. leprae in squirrels from Brownsea Island, England.

73 y, and serology, we found M. lepromatosis in squirrels from England, Ireland, and Scotland, and M. le

74 In brain extracts from active ground squirrels, GADD34 bound both I-1 and PP1 and eIF-2alpha

75 atches the known diet of nuts and seeds that squirrels gnaw, and of grasses that guinea pigs grind do

76 During hibernation, the 13-lined ground squirrel (GS) cycles through repeated CI during torpor,

77 s derived from the woodchuck (WHcAg), ground squirrel (GScAg), and arctic squirrel (AScAg) viruses po

78 plications of these three morphologies, in a squirrel, guinea pig and rat.

79 The arboreal squirrel had a larger mean percentage of dorsolateral co

80 These data indicate that Cape ground squirrels have a labile T(b) which is sensitive to a num

81 Our results demonstrate that squirrels have a larger mean percentage of dorsolateral

82 Park), and the southeast side of Pittsburgh (Squirrel Hill).

83 age of the complete sequencing of the ground squirrel Ictidomys tridecemlineatus genome.

84 te receptor and auxiliary subunits in ground squirrel (Ictidomys tridecimlineatus) cb1a/b, cb2, and c

85 Here, we show that thirteen-lined ground squirrels (Ictidomys tridecemlineatus) and Bactrian came

86 ses, that neurons from thirteen-lined ground squirrels (Ictidomys tridecemlineatus) express mitochond

87 13-lined ground squirrels, Ictidomys tridecemlineatus, are obligate hibe

88 we infer that arrival and diversification of squirrels in Africa, on Sunda Shelf islands, across Beri

89 les in a wild population of Columbian ground squirrels in Alberta, Canada.

90 Red squirrels in Great Britain (Sciurus vulgaris) have incre

91 mong forebrain extracts prepared from ground squirrels in two summer, four winter and fall transition

92 Squirrels inhabited two different areas: an exposed floo

93 t pre-hibernation fattening of arctic ground squirrels is robust to changes in diet and is accomplish

94 Tree shrews are small squirrel-like mammals that are the closest living relati

95 Co-breeding female kin ground squirrels maintain close nest burrows, likely providing

96 t can reach the retina of hibernating ground squirrels maintained in the laboratory and affect hibern

97 echanisms that control hibernation in ground squirrels may guide efforts to develop improved treatmen

98 ning and the gut microbiota, and suggest the squirrels may possess a gut microbial community structur

99 Experimental playbacks with a biorobotic squirrel model reveal this signal's communicative functi

100 o species of New World monkeys - the diurnal squirrel monkey (Saimiri sciureus) and the nocturnal owl

101 cells outnumber type II hair cells (HCs) in squirrel monkey (Saimiri sciureus) cristae by a nearly 3

102 d 1 hamadryas baboon (Papio hamadryas) and 1 squirrel monkey (Saimiri sciureus) to respond to stimuli

103 zed by two methods in three NWM species, the squirrel monkey (Saimiri sciureus), the tamarin (Saguinu

104 cretin-1 in a wake-consolidating animal, the squirrel monkey (Saimiri sciureus).

105 ll, 65% of the photocoagulation sites in the squirrel monkey and 37% of sites in macaque monkey elici

106 In one squirrel monkey and one galago we demonstrated that thes

107 In squirrel monkey and owl monkey, receptive fields of magn

108 described in the macaque monkey hold for the squirrel monkey and owl monkey.

109 g results for the duct system of humans, the squirrel monkey and the rhesus macaque, making compariso

110 Preliminary PET/MRI of squirrel monkey brain was conducted along with HPLC asse

111 Like the macaque, the squirrel monkey can be considered a useful primate model

112 HIV-1 did not detectably bind or utilize squirrel monkey CD4 for entry, and marmoset CD4 was also

113 Using human/squirrel monkey chimeras, mutagenesis, and molecular mod

114 enomes of two cytomegalovirus (CMV) species, squirrel monkey CMV (SMCMV) and owl monkey CMV (OMCMV),

115 actile adaptation on the optical response of squirrel monkey contralateral SI cortex to vibrotactile

116 rel monkeys independently of DBP1 binding to Squirrel monkey erythrocytes.

117 Unexpectedly, 76% of the FVT sites in squirrel monkey eyes and 27% of the sites in macaque eye

118 ay structures of human FKBP51, to 2.7 A, and squirrel monkey FKBP51, to 2.8 A, by using multiwaveleng

119 Preliminary squirrel monkey imaging and human serum/liver microsome

120 Here we test this hypothesis in adult squirrel monkey males exposed to intermittent social sep

121 ations increased hippocampal neurogenesis in squirrel monkey males.

122 eptors, in the present study we used rat and squirrel monkey models of reward and relapse to examine

123 acchus herpesvirus is frequently detected in squirrel monkey peripheral blood lymphocytes, indicating

124 ded the optical intrinsic signal response of squirrel monkey primary somatosensory cortex (SI) to 25

125 1R2 residue I67, which corresponds to S67 in squirrel monkey receptor, modulates the higher affinity

126 One squirrel monkey started to delay gratification in Phase

127 h correspond to residues T40 and E142 in the squirrel monkey Tas1R2, were found to be the critical re

128 olgi cells and recorded these neurons in the squirrel monkey ventral paraflocculus during oculomotor

129 of hypocretin-1 in the cisternal CSF of the squirrel monkey, a New World primate with a pattern of w

130 ns being more numerous in chinchilla than in squirrel monkey, afferent discharge properties are simil

131 a local area resembled those present in the squirrel monkey, and no evidence was found for column/pa

132 In the squirrel monkey, hypocretin-1 works in opposition to the

133 monkey were significantly slower than in the squirrel monkey, in both species magnocellular neurones

134 f the nucleus tractus solitarii (NTS) in the squirrel monkey, Saimuri sciureus, was investigated by n

135 ylogenetically with those of the opossum and squirrel monkey, two of its preferred mammalian hosts in

136 to NPNFP in the brainstems of 5 cats and one squirrel monkey.

137 ribed in the laboratory rat, owl monkey, and squirrel monkey.

138 els are represented in striate cortex of the squirrel monkey.

139 ns of angioscotomas in striate cortex of the squirrel monkey.

140 p representations of Brodmann area 3b in the squirrel monkey.

141 Here, we report that infection of squirrel monkeys (Saimiri sciureus) fulfills these requi

142 Three squirrel monkeys (Saimiri sciureus) learned to reach tow

143 Squirrel monkeys (Saimiri sciureus) that had learned to

144 our capuchin monkeys (Cebus apella) and four squirrel monkeys (Saimiri sciureus) were given demonstra

145 s been extensively characterised (humans and squirrel monkeys (Saimiri sciureus)), the aVOR response

146 (MT(C)) in owl monkeys (Aotus trivirgatus), squirrel monkeys (Saimiri sciureus), and macaque monkeys

147 To investigate if squirrel monkeys (Saimiri sciureus), which are reported

148 cellular electrophysiological study employed squirrel monkeys (Saimiri sciureus), which moved freely

149 st established experimental WNV infection of squirrel monkeys (Saimiri sciureus).

150 isual area (DL(C)) were investigated in four squirrel monkeys (Saimiri) following extracellular injec

151 ay and compared results from owl monkeys and squirrel monkeys 5-10 weeks after lesions with controls.

152 as seeded in the dominant male of a group of squirrel monkeys and an alternative technique in the dom

153 Indeed, previous experiments on squirrel monkeys and macaque monkeys showed that social

154 ual digit representations of area 3b in four squirrel monkeys and one prosimian galago.

155 Squirrel monkeys and rats were trained to self-administe

156 nd the synthetic cannabinoid WIN 55,212-2 in squirrel monkeys and rats, respectively, and it also pre

157 uR2, on abuse-related effects of nicotine in squirrel monkeys and rats.

158 the primary somatosensory cortices of adult squirrel monkeys at four postnerve injury survival durat

159 vity within the spinal cords of anesthetized squirrel monkeys at rest and show that the strength of c

160 d by magnetic resonance imaging in 31 female squirrel monkeys between the ages of 5 and 17 years.

161 s (FVT) were elicited in 12 maculae of seven squirrel monkeys by laser photocoagulation using optimiz

162 e and THC reinforcement and reinstatement in squirrel monkeys by the CB1-receptor inverse agonist rim

163 Inferior temporal cortex of squirrel monkeys consists of caudal (ITC), intermediate

164 Brain tissue from the CWD-infected squirrel monkeys contained the abnormal isoform of the p

165 The CWD-inoculated squirrel monkeys developed a progressive neurodegenerati

166 cicularis) infected with the same virus, the squirrel monkeys developed more-severe immunosuppression

167 thesis by recording from IN neurons in alert squirrel monkeys during vestibular and proprioceptive st

168 In addition, squirrel monkeys given ICV injections of adenoviral BDNF

169 expressing TRIM5alpha from either tamarin or squirrel monkeys in permissive cell lines resulted in a

170 show that Salvador (Sal) I P. vivax infects Squirrel monkeys independently of DBP1 binding to Squirr

171 The use of two tracers in squirrel monkeys indicated that terminations from adjace

172 ly follows median nerve transection in adult squirrel monkeys is dependent on normally functioning N-

173 ptor subunits in the area 3b cortex of adult squirrel monkeys one and five months after median nerve

174 n was found in PI(M) of macaques, whereas in squirrel monkeys PI(M) was light.

175 Self-administration of 2-AG by squirrel monkeys provides a valuable procedure for study

176 nance imaging (fMRI) studies on anesthetized squirrel monkeys revealed dynamic reorganizations of dig

177 mary cells derived from common marmosets and squirrel monkeys support every phase of HIV-1 replicatio

178 The CXCR4 molecules of both marmosets and squirrel monkeys supported HIV-1 infection, but the CCR5

179 Squirrel monkeys that previously self-administered anand

180 hydro-1H-purine-2,6-dione], respectively, in squirrel monkeys trained to intravenously self-administe

181 Male squirrel monkeys underwent quantitative PET studies of c

182 Results indicate that squirrel monkeys vaccinated with SEL-068 failed to acqui

183 ps from four hemispheres of two normal adult squirrel monkeys were created and used to derive express

184 avior and vocalizations of four group-housed squirrel monkeys were examined following administration

185 ceptibility of nonhuman primates to CWD, two squirrel monkeys were inoculated with brain tissue from

186 Twenty squirrel monkeys were randomized to intermittent stress

187 he present study compared visual learning in squirrel monkeys with ablations of ITC; ITI and ITR (gro

188 aural frequency map changes is chronicled in squirrel monkeys with asymmetric hearing loss induced by

189 of two diurnal primates (macaque monkeys and squirrel monkeys) and one nocturnal primate (owl monkey)

190 only been established in New World primates (squirrel monkeys).

191 of Goodpasture autoantibodies in the GBM of squirrel monkeys, a species susceptible to Goodpasture a

192 In cats, squirrel monkeys, and macaque monkeys, we found neuroche

193 om two macaque monkeys, two owl monkeys, two squirrel monkeys, and three galagos that were processed

194 We show here that in squirrel monkeys, focal deprivation by blood vessels lea

195 ) from common marmosets, spider monkeys, and squirrel monkeys, New World monkey (NWM) species that sh

196 In squirrel monkeys, there was a tendency for caudal DL to

197 y anterograde tracers injected in area MT of squirrel monkeys, to characterize these connections furt

198 In three other squirrel monkeys, unilateral dorsal column lesions were

199 (SAM) tones in the auditory cortex of awake squirrel monkeys, we show that the prior presentation of

200 week after median nerve compression in adult squirrel monkeys.

201 in the cervical spinal cord (C4-C6) in adult squirrel monkeys.

202 PMv) distal forelimb representation (DFL) in squirrel monkeys.

203 gions of the ipsilateral hemisphere in adult squirrel monkeys.

204 l optical imaging of areas 3b and 1 in awake squirrel monkeys.

205 vior when self-administered intravenously by squirrel monkeys.

206 ll number between young, middle-aged and old squirrel monkeys.

207 during active and passive head movements in squirrel monkeys.

208 ons in New World marmosets, owl monkeys, and squirrel monkeys.

209 duces dyskinesias in normal (ie, unlesioned) squirrel monkeys.

210 ired median and ulnar nerve section in adult squirrel monkeys.

211 ortical area 3b of New World owl monkeys and squirrel monkeys.

212 into localized regions of the caudal GPi in squirrel monkeys.

213 ed hand and normally activated face in adult squirrel monkeys.

214 1,1'-biphenyl]-3-yl-cyclohexylcarbamate), in squirrel monkeys.

215 -tetrahydrocannabinol (THC) or anandamide in squirrel monkeys.

216 a unilateral lesion of the dorsal column in squirrel monkeys.

217 sory cortex (areas 3b and 1) in anesthetized squirrel monkeys.

218 noise carriers in the auditory core of awake squirrel monkeys.

219 eurochemical effects of nicotine in rats and squirrel monkeys.

220 cending afferents from digit 1 to survive in squirrel monkeys.

221 rectly predicted the SCN lesion phenotype in squirrel monkeys: loss of circadian rhythmicity and emer

222 In free-ranging red squirrels, natural selection on offspring postnatal grow

223 Results suggest that squirrels need both local and global landmarks of the en

224 tic mixing of Scottish and Cumbrian genes in squirrel populations up to 100 kilometers from the site

225 ved inputs from the large visual pulvinar of squirrels, possibly accounting for the sensory architect

226 rodents with a well-developed visual system, squirrels provide a useful comparison of visual system o

227 dies showing that the caudal pulvinar of the squirrel receives a massive bilateral projection origina

228 econd major clade of the Rodentia order, the squirrel-related clade, taking advantage of the complete

229 Here, in the squirrel-related rodent clade, we identified the envelop

230 rding from adjacent cone pairs in the ground squirrel retina, and instead found that the glutamate re

231 pairs in slices from the dichromatic ground-squirrel retina, that green-green cone pairs are routine

232 In ground squirrel retina, whose triangular cone lattice resembles

233 ct detected in the medium bathing the ground squirrel retinas.

234 usly described in primate, mouse, and ground squirrel retinas.

235 cone synapses in mouse, macaque, and ground squirrel retinas.

236 rom several cell types in hibernating ground squirrels retract on entry into torpor, change little ov

237 Our findings suggest that ground squirrel RTECs are protected against apoptosis during pr

238 The XIAP expression was maintained in ground squirrel RTECs but was significantly decreased in mouse

239 Ground squirrel RTECs had significantly less apoptosis compared

240 Ground squirrel RTECs in which gene expression of Akt1 and XIAP

241 la isolate obtained from a California ground squirrel (S. beecheyi) were completely identical to homo

242 ail lengths of liver mRNA from arctic ground squirrels sacrificed during four hibernation states (ear

243 arousal from torpor) and from active ground squirrels sacrificed in the summer.

244 In cynomolgus (Macaca fascicularis) and squirrel (Saimiri sciureus) monkey eyes (n = 20), matrix

245 , gecko (Gekko gekko), mouse (Mus musculus), squirrel (Sciurus carolinensis), and human.

246 us, CA3, and CA1) of wild adult eastern gray squirrels (Sciurus carolinensis) throughout the year.

247 We reanalyze data for Gray Squirrels (Sciurus carolinensis), native to North Americ

248 ilus beecheyi), and wild-caught Eastern gray squirrels (Sciurus carolinensis).

249 2011 and 2013, three breeders of variegated squirrels (Sciurus variegatoides) had encephalitis with

250 ciations of human chromosomes present in the squirrel, six are well-known ancestral eutherian associa

251 Ground squirrel (Spermophilus beecheyi) retinas were detached f

252 omatosensory cortex of the California ground squirrel (Spermophilus beecheyii).

253 cloning c-fos cDNA from the 13-lined ground squirrel (Spermophilus tridecemlineatus) and using squir

254 ods and Off cone bipolar cells in the ground squirrel (Spermophilus tridecemlineatus), we measured th

255 California ground squirrels (Spermophilus beecheyi) add an infrared compon

256 main reservoir species appears to be ground squirrels (Spermophilus beecheyi) in the western United

257 ld and laboratory study of California ground squirrels (Spermophilus beecheyi) provides evidence for

258 iates of rattlesnakes: (a) California ground squirrels (Spermophilus beecheyi) use incidental acousti

259 s norvegicus), wild-caught California ground squirrels (Spermophilus beecheyi), and wild-caught Easte

260 the ability of free-ranging Columbian ground squirrels (Spermophilus columbianus) to locate escape bu

261 Laboratory housed, wild caught Arctic ground squirrels (Spermophilus parryii) were implanted intraper

262 lerance in hibernating thirteen-lined ground squirrels (Spermophilus tridecemlineatus).

263 The antisnake behavior of rock squirrels (Spermophilus variegatus) was examined to dete

264 se activity (P=0.023) in the 13-lined ground squirrel, Spermophilus tridecemlineatus, during hibernat

265 arousal in two species of hibernating ground squirrels suggest that it could play a protective role d

266 on to recent observations in tree shrews and squirrels, suggest that parts of the organizational sche

267 , we describe the projection pattern of gray squirrel superior colliculus (SC) with the large and wel

268 filling in slice preparations of the ground squirrel superior colliculus.

269 34.7-38.9 degrees C) and hibernating ground squirrels (T(b) range 2.9-3.9 degrees C) using extrapola

270 ined in unrestrained, non-hibernating ground squirrels (T(b) range 34.7-38.9 degrees C) and hibernati

271 Ground squirrels tailor their defensive signals to the predator

272 Lepus americanus) to an alternate prey (red squirrel; Tamiasciurus hudsonicus) mitigates range restr

273 a flaviventris) is a social, ground-dwelling squirrel that lives either individually or in kin groups

274 ecemlineatus) during prolonged torpor and in squirrels that did not hibernate or had not been hiberna

275 er 2.5 years in female golden-mantled ground squirrels that sustained complete ablation of the suprac

276 n "Off" cone bipolar cell type in the ground squirrel, the cb2, whose transient postsynaptic response

277 S; Spermophilus parryii) and 13-lined ground squirrels (TLS; S. tridecemlineatus) during prolonged to

278 ed in the microdialysate of an arctic ground squirrel to illustrate the application to biological sam

279 e skull and masticatory muscles have allowed squirrels to specialise as gnawers and guinea pigs as ch

280 e have previously shown that 13-lined ground squirrel tubular cells are protected from apoptotic cell

281 ctional and pharmacologic analyses show that squirrel UCP1 acts as the typical thermogenic protein in

282 on was to determine whether Belding's ground squirrels (Urocitellus beldingi) from areas rich in beac

283 and somatic allocations in Columbian ground squirrels (Urocitellus columbianus), we tested the effec

284 the gut microbiota of captive arctic ground squirrels (Urocitellus parryii).

285 British red squirrels use "stepping stone" patches of habitat to mov

286 Most vertebrate gliders, such as flying squirrels, use symmetrically paired 'wings' to generate

287 lvinar projections in the Californian ground squirrel using cholera toxin B (CTb).

288 Long-range intrinsic connections in squirrel V1 extended 1-2 mm but were not patchy or perio

289 increased pAkt and pBAD expression in ground squirrel versus mouse RTECs subjected to CS/REW.

290 Unlike cold-torpid fall ground squirrels, warm-torpid individuals strongly resembled th

291 Using long term data on North American red squirrels we show that the environmental conditions indi

292 polar cell pairs in the retina of the ground squirrel, we show that the bipolar cell types sample con

293 In mRNA isolated from torpid ground squirrels, we observed a pattern of 12 poly(A) residues

294 Both SCNx and control squirrels were more likely to enter torpor at night and

295 al cortex ablations and sham-surgery control squirrels were presented with a caged rattlesnake pre- a

296 at mlEPSCs from cones of hibernating ground squirrels, which exhibit dramatically smaller ribbons th

297 Rock squirrels with orbital frontal cortex ablations and sham

298 ntal experience in spatial memory, wild-born squirrels with several days of experience in the field w

299 Ground squirrels withstand up to 90% reductions in cerebral blo

300 lls (RTECs) isolated from hibernating ground squirrels would be protected against apoptosis during CS

301 perature (T(b)) daily rhythms of Cape ground squirrels Xerus inauris inhabiting an area of Kalahari g