ライフサイエンスコーパス: squirrel

1 ssible animal reservoirs (armadillos and red squirrels).

2 blue Off center ganglion cells in the ground squirrel.

3 subsequences were only found in primates and squirrel.

4 reas 17 and 18 compared with the terrestrial squirrel.

5 of a larger, highly visual rodent, the gray 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 n organization in euthermic or torpid ground squirrels.

12 st territorial invasions from non-kin ground squirrels.

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

14 13 types of cone bipolar cells in the ground squirrel, 11 of which contact contiguous cones, with the

15 logy, 2011;519(6):1071-1094) reported in the squirrel a feedback projection from the PulC to the SC.

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

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

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

19 luding the hibernation-capable Arctic ground squirrel (AGS).

20 Squirrels also emerged from their burrows earlier and re

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

37 rrels Tamiasciurus hudsonicus, hereafter red squirrels, and how the timing of this event mediated the

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

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

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

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

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

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

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

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

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

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

48 We found that red squirrels breed earlier and had higher lifetime fitness

49 nd in 5% from the habitat of lepromatous red squirrels (British Isles).

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 tional study and field experiments show that squirrels can anticipate increases in food availability

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

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

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

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

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

59 d ion channel CNGA3, and that mouse, but not squirrel, CNGA3 is potentiated by cold.

60 filing in quadriceps muscle of arctic ground squirrels, comparing hibernating (late in a torpor and d

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

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

63 elerometer recordings (489 deployments; 5066 squirrel-days).

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

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

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

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

68 t (Marmota marmota), a large ground-dwelling squirrel exquisitely adapted to the "ice-age" climate of

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

70 Ground squirrel eyecups were incubated in medium containing (14

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

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

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

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

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

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

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

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

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

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

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

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

83 by hoarding behaviour, as males and mid-aged squirrels had the largest hoards, and these effects pers

84 story plasticity, energetics research in red squirrels has overturned several standard pillars of kno

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

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

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

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

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

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

91 Thirteen-lined ground squirrels (Ictidomys tridecemlineatus) are obligatory hi

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

93 n mice and hibernating thirteen-lined ground squirrels (Ictidomys tridecemlineatus) to investigate th

94 13-lined ground squirrels, Ictidomys tridecemlineatus, are obligate hibe

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

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

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

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

99 Squirrels inhabited two different areas: an exposed floo

100 This suggests that the red squirrel is the reservoir host for human infection in Eu

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

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

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

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

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

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

107 We report that, in comparison to squirrels, mice have a larger proportion of cold-sensiti

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

109 le model of glaucoma, we elevated IOP in the squirrel monkey (Saimiri boliviensis) using intracameral

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

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

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

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

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

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

116 of glaucoma (microbead occlusion in rat and squirrel monkey and the genetic DBA/2 J mouse model) wit

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

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

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

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

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

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

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

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

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

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

127 Preliminary squirrel monkey imaging and human serum/liver microsome

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

129 ations increased hippocampal neurogenesis in squirrel monkey males.

130 nths in the chronic DBA/2 J model and in the squirrel monkey model reduced expression and activation

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

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

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

134 1R2 residue I67, which corresponds to S67 in squirrel monkey receptor, modulates the higher affinity

135 One squirrel monkey started to delay gratification in Phase

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

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

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

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

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

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

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

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

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

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

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

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

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

149 Squirrel monkeys (Saimiri sciureus) that had learned to

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

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

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

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

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

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

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

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

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

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

160 Squirrel monkeys and rats were trained to self-administe

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

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

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

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

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

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

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

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

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

170 The CWD-inoculated squirrel monkeys developed a progressive neurodegenerati

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

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

173 hite matter tracts within the spinal cord of squirrel monkeys following traumatic injuries, and their

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

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

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

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

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

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

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

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

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

183 Squirrel monkeys that previously self-administered anand

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

185 Juvenile squirrel monkeys underwent one of five treatment conditi

186 Male squirrel monkeys underwent quantitative PET studies of c

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

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

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

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

191 Twenty squirrel monkeys were randomized to intermittent stress

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

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

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

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

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

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

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

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

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

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

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

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

204 ntracortical microstimulation (ICMS) in male squirrel monkeys.

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

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

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

208 eurochemical effects of nicotine in rats and squirrel monkeys.

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

210 week after median nerve compression in adult squirrel monkeys.

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

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

213 gions of the ipsilateral hemisphere in adult squirrel monkeys.

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

215 vior when self-administered intravenously by squirrel monkeys.

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

217 during active and passive head movements in squirrel monkeys.

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

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

220 1,1'-biphenyl]-3-yl-cyclohexylcarbamate), in squirrel monkeys.

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

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

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

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

225 (R(2) = 0.83) expressed by free-ranging red squirrels over 4 years, as quantified through accelerome

226 ing of semi-arboreal and arboreal monkey and squirrel populations from ca. 45,000 years ago, in a tro

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

228 vival, whether the population density of red squirrel predators and mean temperature overwinter were

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

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

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

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

233 tion status during hibernation, we show that squirrels remain hydrated during torpor by depleting osm

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

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

236 In ground squirrel retina, whose triangular cone lattice resembles

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

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

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

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

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

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

243 Ground squirrel RTECs had significantly less apoptosis compared

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

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

246 A total of 39% (24/62) of red squirrel (S. vulgaris) samples from the Netherlands were

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

248 m a B. washoensis strain isolated from a red squirrel (Sciurus vulgaris orientis) from China.

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

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

251 2011 and 2013, three breeders of variegated squirrels (Sciurus variegatoides) had encephalitis with

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

253 Ground squirrel (Spermophilus beecheyi) retinas were detached f

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

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

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

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

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

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

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

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

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

266 Juvenile red squirrel survival was lower in the years of high predato

267 Ground squirrels tailor their defensive signals to the predator

268 dy of individually marked North American red squirrels Tamiasciurus hudsonicus Erxleben in the Yukon,

269 nter survival of juvenile North American red squirrels Tamiasciurus hudsonicus, hereafter red squirre

270 North American red squirrels (Tamiasciurus hudsonicus) guard food hoards, a

271 years of monitoring from North American red squirrels (Tamiasciurus hudsonicus) in Canada.

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

273 ut arousal, lasting up to 48 h, during which squirrels temporarily return to an active-like state and

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

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

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

277 t yet investigated the energetic response of squirrels to elevated density or its association with li

278 and life-history responses of individual red squirrels to fluctuations in food abundance and conspeci

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

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

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

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

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

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

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

292 data from a population of North American red squirrels, we assessed how kinship and familiarity with

293 survival of individually marked juvenile red squirrels, we tested how the timing of territory acquisi

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

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