ライフサイエンスコーパス: cat

1 lex fac,anti-(ONO(Cat))Re(O)(mu-O)2Re(O)(ONO(Cat)).

2 ant homology to carnitine O-acyltransferase (cAT).

3 cken) or quadrupedal mode (crawling-baby and cat).

4 accelerated with respect to the speed of the cat).

5 if an object is six feet tall, it isn't your cat).

6 much improved selectivity over cathepsin-D (CatD).

7 significantly higher than those for FAS and CAT.

8 e sensory deprivation, the congenitally deaf cat.

9 e and proceeds under mild conditions (CH3CN, cat.

10 as likewise decreased in children exposed to cat.

11 g group could be removed in good yield using cat.

12 ncrease in H2O2 when GLO is dissociated from CAT.

13 slow progressive pressure overload in adult cats.

14 (but not in primary auditory cortex) of deaf cats.

15 RI acquired at 7 T from eight adult domestic cats.

16 he nares and anal mucosa of healthy dogs and cats.

17 or cortex dynamics is comparable in rats and cats.

18 implants in adult hearing controls and deaf cats.

19 sting low or no bioavailability for DBDPE in cats.

20 from the posterior lobe hemisphere in awake cats.

21 e, miRNAs have not been carefully studied in cats.

22 cross-modal (visual) reorganization in deaf cats.

23 hat dust is a significant exposure route for cats.

24 nt-DNA studies have focused on saber-toothed cats [1-3], and they have been restricted to short fragm

25 novel mechanism whereby interactions between Cat-1 and its binding partner paxillin are necessary to

26 We further show that knocking down Cat-1 expression in HeLa cells leads to a reduction in A

27 growth capability of HeLa cells depleted of Cat-1 expression.

28 hese results suggest that the requirement of Cat-1 for this hallmark of cellular transformation is co

29 Although knocking down Cat-1 prevents HeLa cells from forming colonies in soft

30 tion, we recently showed that the ability of Cat-1 to bind paxillin, a major constituent of focal com

31 ssociated tyrosine-phosphorylated protein 1 (Cat-1) is a signaling scaffold as well as an ADP-ribosyl

32 when paxillin is knocked down together with Cat-1, the cells are again able to undergo anchorage-ind

33 1 from birch pollen (16.3%) and Fel d 1 from cat (14.4%).

34 ust mite (-4.3%; 95% CI, -6.0% to -2.6%) and cat (-2.1%; 95% CI, -3.6% to -0.7%) decreased more than

35 he overall study prevalence of Salmonella in cats (3 of 542) was <1%.

36 Tralokinumab (CAT-354) is an IL-13-neutralising human IgG4 monoclonal

37 Together, we used 9 cats (7 females, 2 males).

38 tracers into the medial rectus muscle of the cat, a highly visual nonprimate with frontally placed ey

39 )(O2 C(t) Bu)2x+2 ] rings is reported where Cat=a secondary or tertiary alkyl ammonium ion, x=7, 8 o

40 A mild and unique AcOH(cat.)/AcCl system was found to promote an autocatalytic-

41 al activity from ensembles of LGN neurons in cats across early development.

42 Physiological parameters, SOD, POD, PPO, CAT activity, free proline, soluble protein and MDA cont

43 e find that several BACE1 inhibitors blocked CatD activity in cells with much greater potency than th

44 e to different sizes of CeO2 while catalase (CAT) activity was not affected by either size of CeO2 th

45 dmill (LTM); (2) to assess the capability of cats after a unilateral spinal hemisection at T10 to cop

46 itization, especially to house dust mite and cat, after the age of 20 years.

47 roteins such as ovalbumin (OVA) or the major cat allergen Fel d 1.

48 d in 441 (99.5%) of 443 school dust samples, cat allergen in 420 samples (94.8%), and dog allergen in

49 Cat allergen levels were inversely associated with asthm

50 ave previously shown that Fel d 1, the major cat allergen, displayed in a repetitive fashion on virus

51 Exposure to dog and cat allergens in DCC often reached levels of households

52 dust concentrations of cockroach, mouse, and cat allergens in the first 3 years of life were associat

53 -IgE mAbs profoundly block human peanut- and cat-allergic IgE-mediated basophil CD63 induction indica

54 Cs significantly reduces AP alternans, while CaT alternans remains unaffected.

55 , II, and IV and >10-fold selectivity versus CatD, although varying the flap pocket substituent led t

56 y 36,000 to 10,000 years ago), saber-toothed cats, American lions, dire wolves, and coyotes competed

57 l (AP) morphology or cytosolic Ca transient (CaT) amplitude, is a high risk indicator for cardiac arr

58 ing non-tumoral parenchyma, had nuclear beta-Cat and Axin2 overexpression.

59 SNP-genotyped 87%, 80% and 97% of the wolf, cat and bear samples, respectively.

60 l lung expression of the anti-oxidant marker CAT and decreased expression of the pro-oxidant marker N

61 ncluded cat and dog ownership from birth and cat and dog allergen levels in bedding at age 1 year.

62 High-titer IgE antibodies to cat and dog allergens were strongly associated with the

63 either cat or dog allergen molecules predict cat and dog allergy cross-sectionally and longitudinally

64 We investigated interactions between cat and dog exposure and single nucleotide polymorphism

65 P = .283), demonstrating interaction between cat and dog exposure and the rs7216389 genotype (adjuste

66 Exposures included cat and dog ownership from birth and cat and dog allerge

67 Cat and/or dog exposure from birth was associated with a

68 pared to a variant database from 51 domestic cats and a Pallas cat, revealed 50 candidate variants th

69 Early-life exposure to cats and dogs has shown diverging associations with chil

70 (including humans) and carnivores (including cats and dogs), which is inferred to be ancestral.

71 ses around individual parenchymal vessels in cats and established that the vascular and neural respon

72 ps (OPMs) are present in carnivores (such as cats and ferrets) and primates but are absent in rodents

73 cordings from humans and LFP recordings from cats and mice, we found that during NREM sleep the power

74 OD) in the primary visual cortex of ferrets, cats and monkeys can be individually changed by altered

75 but not necessarily identical to area V1 in cats and primates.

76 ince in China and spread to humans via civet cats and raccoon dogs in the wet markets before spreadin

77 In cats and rats, gadolinium has been used to investigate t

78 ra canis, T. cati, and T. vitulorum of dogs, cats and ruminants respectively, is recognized as an imp

79 Hearing cats and visual cortical areas served as a control.

80 D) activity, associated with lower catalase (CAT) and ascorbate peroxidase (APX) activities, leading

81 ies of superoxide dismutase (SOD), catalase (CAT) and peroxidase (POD) decreased at a later time peri

82 . grass and ragweed pollens, dust mites, and cat) and those that induce life-threatening anaphylaxis

83 Sentence Completion (SSC), category naming (CAT) and verbal fluency (FAS), in localizing the Wernick

84 different proteases, including cathepsin S (CatS) and the intramembrane protease signal peptide pept

85 Mite, mouse, cat, and dog allergens were mostly higher in DCC than in

86 year of life and as allergen levels of dog, cat, and house dust mite in bed dust samples at 1 year.

87 pathogens measured in seawater and in gull, cat, and raccoon feces.

88 eviously observed following protracted MD in cat, and they highlight a possibility for alternative th

89 cteristics of the disease in humans vs dogs, cats, and horses are most often caused by similar, but s

90 naphylactic degranulation; suppress peanut-, cat-, and dansyl-specific IgE-mediated passive cutaneous

91 h different CATs gives the compounds 1-4 for CAT=Anderson {FeMo6 } (1), Keggin {PMo12 } (2), Dawson {

92 ted cat studbook suggests additional captive cats are at risk.

93 Because cats are compared in various conditions (intact or hemis

94 CNS, locomotor abilities of animals (mainly cats) are often assessed on a simple flat treadmill (FTM

95 ed that while some species (sheep, mice, and cats) are readily susceptible to TSEs, others are appare

96 rded visual responses from single neurons in cat Area 18 using linear multielectrode arrays.

97 tant optogenetic stimulation of anesthetized cat area 21a produces gamma-band activity entailing a si

98 findings designate off-target inhibition of CatD as a principal driver of ocular toxicity for BACE1

99 ed to use chloramphenicol acetyltransferase (CAT), as chloroplasts are particularly vulnerable to chl

100 Pial surface arteries in cats, as well as surface arteries and penetrating arteri

101 Interestingly, beta-Cat, Axin2 and Dkk1 also increased during regeneration b

102 found that the block of CD74 degradation in CatS(-/-) B cells is incomplete, so that NTF levels are

103 could contribute to the milder phenotype of CatS(-/-) B cells.

104 erson with occupational exposure to infected cats became infected with the virus, representing the fi

105 data from published reports of the domestic cat brain.

106 In particular, we show that CATS can model the viability of an antibody mutation kno

107 ATS and the surrounding tissues, mediated by CAT, can explain the complex auxin transport kinetics we

108 ; neop, neopentylglycolato; pin, pinacolato; cat, catecholato).

109 urces we considered chicken, pig, pet dog or cat, cattle, and poultry other than chicken.

110 areas in adult hearing and congenitally deaf cats (CDCs): the primary auditory field A1, two secondar

111 e introduce a three-dimensional atlas of the cat cerebral cortex based on established cytoarchitecton

112 detecting 68 animal manure pooled samples of cats, chickens, cows, dogs, ducks, pigs, and pigeons.

113 to fac,anti-(ONO(Cat))Re(O)(mu-O)2Re(O)(ONO(Cat)) cleaves the dimer into monomeric C1-symmetric fac-

114 We recovered mRNA from PBMCs from two cats, cloned and sequenced the variable and constant dom

115 re differences between transport of tENT and CAT compared to cENT through laboratory columns containi

116 Testing in additional affected cats confirmed that cats homozygous for a 2 base pair (b

117 The observation that plasma CatD correlated with NASH development and regression is

118 nation Survey identified several pollens and cat dander as among the most common allergens that induc

119 were intratracheally sensitized with OVA or cat dander extract (CDE) alone or together with SEA and

120 Here, twenty cat dander-sensitized patients were randomized to receiv

121 in photosynthesis, that is, LH, EnT, ET, and CAT, define the structure of this review with the only f

122 and full-sibling female African black-footed cat developed vision deficits and mydriasis as early as

123 oallergens, including rat, mouse, cockroach, cat, dog, and dust mites, measured in dust samples colle

124 Allergic sensitization to cat, dog, and house dust mites was diagnosed longitudina

125 931) from Trichoderma virens showed that the cAT domain is capable of esterifying the polyketide prod

126 Recapturing of the released product by cAT domain is suggested to facilitate complete gem-dimet

127 neuron somata within deprived layers of the cat dorsal lateral geniculate nucleus (dLGN).

128 o three nearby neurons in V1 of anesthetized cats during the presentation of drifting sinusoidal grat

129 d serum PBDE levels in California (CA) house cats during two time periods: 2008-2010 and 2012-2013 to

130 In banded cats, echocardiography at 4-months revealed concentric l

131 Taking human annotation of cAT EM data as ground truth, we show that our algorithm

132 metastasis, indicating that hypoxia-induced CAT enhances cell release rather than early organ coloni

133 survive Cm treatment when coinfected with a CAT-expressing strain.

134 tion, direction and retinal disparity in the cat (Felis catus) are all strongly related to the organi

135 African black-footed cats (Felis nigripes) are endangered wild felids.

136 ased on 29 different protein structures that CATS finds sequences and conformations that are signific

137 rickettsial infection, we characterized the cat flea (Ctenocephalides felis) innate immune response

138 homology to a Wolbachia strain isolated from cat fleas (Ctenocephalides).

139 ntly correlated with concentrations found in cat food for 6-OH-BDE47 (p < 0.002), 2,4,6-TBP (p < 0.03

140 ating families' pet cats were collected, and cat food was purchased matching the diet reported.

141 Paired samples of cat serum, house dust, and cat food were analyzed for brominated flame retardants/n

142 tion of OHCs (i) via house dust and (ii) via cat food.

143 g locomotor task; and (3) to regularly train cats for 6 weeks on the LTM to determine whether such re

144 f medical research on spontaneous disease in cats for applicability to both feline and human disease.

145 a role of early-life exposure, especially to cat, for attenuating the risk of childhood asthma, pneum

146 is space, we present an efficient algorithm, CATS, for computing atomic coordinates as a function of

147 ication of a codon-optimized sequence of the cat gene and a single colony selection yielded C. merola

148 CATS generalizes the iMinDEE and EPIC protein design alg

149 that {CAT} subset{Mo24 Fe12 } with different CATs gives the compounds 1-4 for CAT=Anderson {FeMo6 } (

150 parameters, such as antioxidant status (SOD, CAT, GPX and GSH) and lipid peroxidation was also studie

151 atory Health Survey 2, having information on cat/grass/D. pteronyssinus IgE levels and symptoms on ex

152 went skin prick testing for house dust mite, cat, grasses and moulds.

153 cortical circuit in the visual system of the cat have been central to our understanding of sensory en

154 The CAT-HF (Cardiovascular Improvements With MV-ASV Therapy

155 Ancient DNA from the saber-toothed cat Homotherium reveals that the late Pleistocene specie

156 g in additional affected cats confirmed that cats homozygous for a 2 base pair (bp) deletion within I

157 in the COPSAC2000 birth cohort data: (1) dog/cat/horse, (2) timothy grass/birch, (3) molds, (4) house

158 highest status areas lost 0.13% yr(-1) (IUCN Cat I).

159 her forest losses (e.g. 0.39% yr(-1) in IUCN cat III), yet even highest status areas lost 0.13% yr(-1

160 Allergen exposure was defined as dog or cat in the home during the 3rd trimester of pregnancy or

161 NASH, we observed increased levels of plasma CatD in patients with NASH compared to adults without he

162 er 2016, an H7N2 virus caused an outbreak in cats in multiple animal shelters in New York State.

163 irus, that occurred during an outbreak among cats in New York City animal shelters.

164 ce of Salmonella in a population of dogs and cats in the United States visiting veterinary clinics.

165 that GLO physically interacts with catalase (CAT) in rice leaves, and that the interaction can be der

166 in the plasma lysosomal enzyme, cathepsin D (CatD), in children with NASH compared to children withou

167 CatS inhibition by a cell-permeable inhibitor abrogated

168 CatS inhibitors currently in clinical trials are expecte

169 The domestic cat is an important human companion animal that can also

170 plication of antibody-based immunotherapy in cats is limited by the lack of species-specific complete

171 orientation suppression, are stronger within cat iso-orientation domains than at pinwheel centres.

172 The cat isocortex (Felis domesticus) shows a similar structu

173 cat /K m = 0.56 microM(-1)s(-1)) than NPP (k cat /K m = 0.044 microM(-1)s(-1)).

174 3-carene was over ten fold higher for GPP (k cat /K m = 0.56 microM(-1)s(-1)) than NPP (k cat /K m =

175 d increases, respectively, in activity and k cat/K m values toward 2-hydroxyacetophenone compared wit

176 The catalytic efficiencies (k cat/K m) indicated that cellotetraose and cellopentaose

177 dherin activity, higher Snail, vimentin, and Cat L activity, and a p110/p90 active CUX1 form, compare

178 Treatment of mesenchymal cells with the Cat L inhibitor Z-FY-CHO led to nuclear-to-cytoplasmic r

179 We hypothesized that nuclear Cat L may promote EMT via CUX1 and that this could be an

180 Cathepsin L (Cat L) is a cysteine protease that can proteolytically a

181 to nuclear-to-cytoplasmic relocalization of Cat L, decreased binding of CUX1 to Snail and the E-cadh

182 positive feedback loop between Snail-nuclear Cat L-CUX1 drives EMT, which can be antagonized by Z-FY-

183 and that this could be antagonized with the Cat L-specific inhibitor Z-FY-CHO.

184 njected tracer into the orbital layer of the cat lateral rectus muscle.

185 esence/absence data of seven species (golden cat, leopard, forest elephant, forest buffalo, western g

186 gated the prevalence of sensitization to the cat lipocalin Fel d 7 among 140 cat-sensitized Swedish p

187 Saber-toothed cats (Machairodontinae) are among the most widely recogn

188 Pet cats may be used as a biomarker for assessing exposures

189 from the lower Yellow Cat Member (Early Cretaceous) of Utah (USA), is the firs

190 Moabosaurus utahensis from the lower Yellow Cat Member of Utah (USA) is also a member of this clade.

191 Like rats and cats, mice have an ovoid core of medium-sized Bar neuron

192 as undertaken to define and characterize the cat miRNAome in normal feline tissues.

193 tations, and increased lifespan in mouse and cat models of NPC1.

194 in the claustrum, and anatomical studies in cats, monkeys, and rats have demonstrated topographic or

195 Male domestic short hair cats (n = 20), underwent either sham procedures (n = 8)

196 occupational exposure to H7N2 virus-infected cats, necessitating the evaluation of this virus for its

197 -carene as the major product, with K m and k cat of 3.69 +/- 1.17 microM and 2.01 s(-1) respectively.

198 The K m and k cat of AnCDA for the first deacetylation of penta-N-acet

199 have observed, however, that Ve patterns in cats of both sexes appear more monopole-like for lower-f

200 r results show that reticular neurons in the cat operate over discrete spatial scales, at once suppor

201 dog symptoms than results of IgE tests with cat or dog allergen extract, respectively.

202 in childhood and polysensitization to either cat or dog allergen molecules predict cat and dog allerg

203 re significantly associated with symptoms to cat or dog at age 16 years.

204 gitudinally significantly better than IgE to cat or dog extract.

205 r dog was a better longitudinal predictor of cat or dog symptoms than results of IgE tests with cat o

206 ization to 3 or more allergen molecules from cat or dog was a better longitudinal predictor of cat or

207 urrent asthma did not live in a house with a cat or dog.

208 Vocalizations such as mews and cries in cats or crying and laughter in humans are examples of ex

209 ds that discriminate samples from homes with cats or dogs from those without were calculated using re

210 plaid stimuli differently in mice versus in cats or primates.

211 n prevalence of Salmonella-positive dogs and cats over the last decades and identifies consumption of

212 type were more likely to show no activity on CAT (P < 0.05).

213 more about the underlying mechanism by which Cat-paxillin interactions mediate this effect.

214 ted to a so-called critical period that, for cats, peaks at about one postnatal month and declines th

215 long with the CAR coexpressing catalase (CAR-CAT), performed superior over CAR T cells as they showed

216 interacting factors including invasive rats, cats, pigs, mustelids and mongooses, native species taxo

217 In cat primary visual cortex, where neurons are clustered b

218 pattern motion than are found in area V1 of cats/primates.

219 er of the collective-to-amoeboid transition (CAT), promoting the dissemination of amoeboid-moving sin

220 ls to dust mite, ryegrass, and fungi but not cat, ragweed, or food sources.

221 ocyclic carbene ligand IMes to fac,anti-(ONO(Cat))Re(O)(mu-O)2Re(O)(ONO(Cat)) cleaves the dimer into

222 e dimeric rhenium(VII) complex fac,anti-(ONO(Cat))Re(O)(mu-O)2Re(O)(ONO(Cat)).

223 pid awakening, whereas lesions of the PPT in cats reduce REM sleep.

224 PMe2Ph to give the rhenium(V) compound (ONO(Cat))ReO(IMes), which can be independently prepared by l

225 -tert-butyl-2-phenoxo)amido)rhenium(V), (ONO(Cat))ReO(PPh3), reacts with molecular oxygen to give tri

226 ntly prepared by ligand substitution of (ONO(Cat))ReO(PPh3).

227 e dimer into monomeric C1-symmetric fac-(ONO(Cat))ReO2(IMes).

228 rmore, the ladder treadmill permits to train cats repetitively for weeks and observe whether training

229 owing the assessment of locomotion of intact cats required to place the paws on the rungs of a moving

230 database from 51 domestic cats and a Pallas cat, revealed 50 candidate variants that segregated conc

231 95% CI, 0.71-0.97; P = .022), supporting the cat-rs7216389 genotype interaction (adjusted P = .008).

232 n dry matter and teas from 11 samples of the cat's claw plant.

233 This model is similar to the game "cat's cradle," where the shape of a string is successive

234 These data identify Cat-S as a monocyte/macrophage-derived circulating PAR2

235 treatment of type 2 diabetic db/db mice with Cat-S or PAR2 inhibitors attenuated albuminuria and glom

236 ory symptoms using the COPD Assessment Test (CAT; scores range from 0 to 40, with higher scores indic

237 03[1.63-9.95]), eczema (2.89[1.08-7.76]) and cat sensitization (5.65[1.92-16.6]) among offspring, but

238 allergy; concordance was found for grass and cat sensitization, while venom- and weed pollen-positive

239 ation to the cat lipocalin Fel d 7 among 140 cat-sensitized Swedish patients and elucidated its aller

240 f Ser-552 phosphorylated beta-catenin (pbeta-Cat(Ser-552)) in intestinal epithelial cells (IEC) durin

241 This is the first time a correlation between cat serum levels and household dust has been established

242 Paired samples of cat serum, house dust, and cat food were analyzed for br

243 Thus, the cat shares with the nocturnal rat the feature of having

244 be the causative source of an outbreak in a cat shelter in New York City, which subsequently spread

245 On the other hand, just as with monkeys, cats show segregation of the MIF and SIF medial rectus m

246 nesis by modulating stem-like cells and beta-Cat signaling.

247 R-/- livers had increased beta-catenin (beta-Cat) signaling with overexpression of Axin2, Dkk1 and Cy

248 also report evidence that the mechanism for CAT-SKL inhibition of CSCs may depend on antioxidant-ind

249 Thus, combining the antioxidant CAT-SKL with erlotinib targeted both CSCs and bulk cance

250 Treatment with CAT-SKL-a re-engineered protein form of the antioxidant

251 as 100 muM in a brain tissue mimic through a cat skull.

252 ary history of two lineages of saber-toothed cats (Smilodon and Homotherium) in relation to living ca

253 In the auditory brainstem of cats, spatial patterns of sound-evoked Ve can resemble,

254 ed throughout the study, while production of cat-specific IgG1 and IgG3 was not stimulated by MAT-Fel

255 es, were identified, including several novel cat-specific miRNAs.

256 the role of MHCII, we compared B cells from CatS(-/-) , SPPL2a(-/-) , and SPPL2a-MHCII double-defici

257 onic state to a continuous-variable photonic cat state in a cavity mode.

258 is allows us to quickly generate and measure cat states larger than previously achieved in a harmonic

259 Here we create a variety of cat states of a single trapped atom's motion in a harmon

260 the authors succeed in creating a variety of cat states of a single trapped atom, mapping spin superp

261 copic quantum superpositions, or Schrodinger cat states, are widely studied for fundamental investiga

262 ucting cavity resonator using four-component cat states.

263 Analysis of the black-footed cat studbook suggests additional captive cats are at ris

264 We show that {CAT} subset{Mo24 Fe12 } with different CATs gives the co

265 In deaf cats, substantially reduced induced responses were obser

266 By examining multisensory neurons in cat superior colliculus, the present study demonstrated

267 inal, Ala- and Thr-containing extension-the 'CAT tail'.

268 ated Carboxy-terminal Alanine and Threonine (CAT) tail elongation-can be recapitulated in vitro with

269 g a carboxyl-terminal alanine and threonine (CAT) tail through a noncanonical elongation reaction.

270 Our results suggest that aberrant CAT-tailed protein aggregation results from a defect in

271 RQC component Rqc1p, and that the process of CAT tailing enables robust ubiquitination of the nascent

272 Using this approach, we determined that CAT tailing is mechanistically distinct from canonical t

273 substrates without Ltn1p-accessible lysines, CAT-tailing enabled degradation by exposing lysines sequ

274 Here we examined the role of CAT-tailing in nascent-chain degradation in budding yeas

275 Thus, CAT-tails do not serve as a degron, but rather provide a

276 toxicology studies, we show that quantifying CatD target engagement in cells with the probe is predic

277 region, and 5 patients reported contact with cats that had sporotrichosis.

278 Four adult cats that recovered stable hindlimb locomotion after spi

279 how with in vivo intracellular recordings in cats that while excitation is restricted to RF subregion

280 uencing was performed on 12 different normal cat tissues.

281 A family of heterometallic [Cat][Tix MO(x+1 )(O2 C(t) Bu)2x+2 ] rings is reported wh

282 ach case a homometallic by-product is found [Cat][Tix O(x+1 )(O2 C(t) Bu)2x-1 ].

283 nated (chloro)(silyl)nickel(II) complex 3, {[cat((TMS) L)Si](Cl)Ni<--:BH(NHC)2 }, via the cleavage of

284 Yet, the link between plasma CatD to adult NASH was not examined.

285 We describe the first case of cat-to-human transmission of influenza A(H7N2), an avian

286 compartments similar to SPPL2a(-/-) B cells, CatS(-/-) traditional stage 1 B cells show unimpaired de

287 nses to abrupt local changes of luminance in cat V1.

288 ximately 10% vs <1.3%) compared with primate/cat V1.

289 l activity from areas 5b and 7 of the PPC of cats walking on a treadmill and stepping over a moving o

290 did not collapse DeltaPsi until OLIG, BA, or CAT was added.

291 activity for man and chicken versus baby and cat was found in the right pSTS responsive to biological

292 ity), and the threshold level for homes with cats was 46 ng/m(2) Fel d 1 (92% sensitivity, 94.9% spec

293 We then confirmed this prediction by rearing cats wearing orthogonally oriented cylindrical lenses ov

294 d serum from the participating families' pet cats were collected, and cat food was purchased matching

295 for 6 weeks on the LTM, whereas the 3 other cats were hemispinalized and trained solely on the FTM t

296 These 6 cats were then hemispinalized and trained for 6 weeks on

297 ed datasets from conjugate array tomography (cAT), which provides voxel-conjugate FM and EM (annotate

298 ill [LTM]) to study the locomotor ability of cats with an intact spinal cord or after a unilateral he

299 V4/21a,V5/PMLS, area 7, and V1/17, in adult cats with central 10 degrees retinal lesions (both sexes

300 ion and after selective deafferentation from cats with unilateral transection of either the MLF or th