ライフサイエンスコーパス: cat

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

2 l bank of the ansate sulcus (areas 1-2) in 2 cats while the cats walked on a flat surface or on a hor

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

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

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

6 superposition of coherent states, known as a cat state.

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

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

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

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

11 rectus capitis anterior (RCA), in the adult cat.

12 For adult cats subjected to 10 days of darkness before 7 days of M

13 Four adult cats that recovered stable hindlimb locomotion after spi

14 s and a random sample of those housing adult cats.

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

16 slow progressive pressure overload in adult cats.

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

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

19 Cross-sectionally, IgE to Fel d 1 and cat extract had similar positive predictive values for c

20 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

21 03[1.63-9.95]), eczema (2.89[1.08-7.76]) and cat sensitization (5.65[1.92-16.6]) among offspring, but

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

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

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

25 r odds of sensitization to the cockroach and cat allergens compared to those without glaucoma.

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

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

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

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

30 n on chr22q11.1 encompassing both IL17RA and cat eye critical region 1 (CECR1).

31 ence of sensitization to house dust mite and cat did not differ between year-of-birth cohorts, but se

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

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

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

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

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

37 date the role of MD2 in inducing pollen- and cat dander-induced innate and allergic airway inflammati

38 TLR4 coreceptor, but its role in pollen- and cat dander-induced innate and allergic inflammation has

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

40 ns to AAF were examined in hearing cats, and cats with early- or adult-onset deafness.

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

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

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

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

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

46 or cortex dynamics is comparable in rats and cats.

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

48 We recorded CINs from anesthetized cats.

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

50 ributes, compared with other species such as cat and monkey.

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

52 a single-mode harmonic oscillator, known as "cat states," have been an elegant demonstration of Schro

53 from the posterior lobe hemisphere in awake cats.

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

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

56 Wnt signaling pathway and its effector beta-cat/TCF serve a beneficial role in suppressing hepatic g

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

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

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

60 Comparison of big cat whole-genome sequences revealed a substantial reduct

61 ss limits the population growth of Asian big cats and may determine their survival.

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

63 viewed as an entangled pair of single-cavity cat states.

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

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

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

67 ull quantum state tomography of this complex cat state over a Hilbert space exceeding 100 dimensions

68 ucting cavity resonator using four-component cat states.

69 e sensory deprivation, the congenitally deaf cat.

70 implants in adult hearing controls and deaf cats.

71 r-order auditory fields in congenitally deaf cats (CDCs).

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

73 In early-deaf cats, ipsilateral neuronal labeling in visual and somato

74 In deaf cats, substantially reduced induced responses were obser

75 ent that were not pruned postnatally in deaf cats.

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

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

78 demonstrated that a nonpiliated DeltaempABC::cat derivative of E. faecium TX82 was attenuated in biof

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

80 ents with rhinitis/asthma sensitised to dog, cat, and horse were recruited.

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

82 knowledge about relevant allergens in dogs, cats and horses.

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

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

85 ecializations, focusing on Felidae (domestic cat, tiger, lion, cheetah, and leopard), Hominidae, and

86 s of coastal development and larger domestic cat populations.

87 data from published reports of the domestic cat brain.

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

89 estigations of the neocortex in the domestic cat, little is known about neuronal morphology in larger

90 ly similar to those observed in the domestic cat.

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

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

93 leg cutaneous stimuli can be modified during cat and human walking and turtle scratching.

94 each paired with a characteristic sound (eg, cat-meow).

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

96 Comparing the connectomes of C. elegans, cats, macaques and humans to surrogate networks in which

97 are 0.47 and 0.32 for healthy and euthyroid cats, respectively, which differs significantly from Swe

98 hows that hyperthyroid compared to euthyroid cats have higher serum concentrations for some of the in

99 legant demonstration of Schrodinger's famous cat paradox.

100 across a diverse mammalian family, Felidae (cats).

101 y introduced species, particularly the feral cat, Felis catus, and European red fox, Vulpes vulpes, a

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

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

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

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

106 al network, as has been shown previously for cat walking and turtle scratching.

107 t had similar positive predictive values for cat allergy.

108 hat dust is a significant exposure route for cats.

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

110 1 from birch pollen (16.3%) and Fel d 1 from cat (14.4%).

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

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

113 istics of spikelets measured in neurons from cat primary visual cortex in vivo.

114 s, and compared our findings with those from cat.

115 , Can f 2 and Can f 4 from dog, Fel d 4 from cats, Bos d 5 from cow's milk, Equ c 1 from horses, and

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

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

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

119 Golden cat and leopard had the lowest occurrence rates in the r

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

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

122 In gyrencephalic cat cortices, when administered post-cortical spreading

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

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

125 d cortical projections to the PAF in hearing cats and those with early- and late-onset deafness.

126 projections to AAF were examined in hearing cats, and cats with early- or adult-onset deafness.

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

128 CPs, may still pose health effects for house cats and, possibly, humans.

129 mmation operator19PBDE level in CA household cats (age >/=10 yr) was 3479 ng/g lipid in 2008-2010 (1s

130 escribe such a case and verify two household cats as the source of infection using repetitive-element

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

132 In cat, most retinal cells have center-surround receptive f

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

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

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

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

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

138 animals, which is transmitted via oocysts in cat faeces or tissue cysts in contaminated meat.

139 imaging of vascular and neural responses in cat and rodent primary visual cortex to investigate the

140 h Can f 1, and may contribute to symptoms in cat- but also in dog-allergic patients.

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

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

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

144 sting low or no bioavailability for DBDPE in cats.

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

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

147 esions in the PAG lead to complete mutism in cats, monkeys, as well as in humans.

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

149 forms cysts in vitro that induce oocysts in cats, the gold standard criterion for cysts.

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

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

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

153 associated with increased survival rates in cats treated with A&A.

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

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

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

157 Our in vivo experimental studies in cats revealed that the severity of TBI-mediated epilepto

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

159 ion for clients considering A&A treatment in cats with cytauxzoonosis.

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

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

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

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

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

165 Sensitization to individual cat and dog allergen molecules can contribute differentl

166 Onchocerca lupi, a parasite known to infect cats and dogs, that have been identified in the United S

167 feline immunodeficiency virus (FIV) infected cats, daily intranasal insulin treatment (20.0 IU/200 mu

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

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

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

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

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

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

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

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

176 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 =

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

178 chanism, with measured rate accelerations (k(cat)/k(uncat)) up to 1.9 x 10(7) (here k(cat) and k(unca

179 ehyde 3-phosphate [(k(cat)/K(m))(GAP) and (k(cat)/K(m))DHAP] and of the substrate pieces glycolaldehy

180 orrelation [slope = 0.53 +/- 0.16] between k(cat) for isomerization of GAP and K(d)() for phosphite d

181 eces glycolaldehyde and phosphite dianion (k(cat)/K(HPi)K(GA)) are reported.

182 (k(cat)/k(uncat)) up to 1.9 x 10(7) (here k(cat) and k(uncat) are the Michaelis-Menten enzymatic rat

183 osphate and d-glyceraldehyde 3-phosphate [(k(cat)/K(m))(GAP) and (k(cat)/K(m))DHAP] and of the substr

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

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

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

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

188 gE to common aeroallergens (house dust mite, cat, and grass) and total IgE levels were measured in 32

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

190 Here, we realize a two-mode cat state of electromagnetic fields in two microwave cav

191 dance were abundant in the genomes of modern cats, in many cases indicating hybridization as the most

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

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

194 uencing was performed on 12 different normal cat tissues.

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

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

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

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

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

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

201 scratching based on evidence from studies of cat and human walking and turtle scratching.

202 f undercooked infected meat, or by uptake of cat-shed oocysts.

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

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

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

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

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

208 most important fatal infectious diseases of cats worldwide.

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

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

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

212 neurons in the primary visual cortex (V1) of cats with that of their afferents from lateral geniculat

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

214 We found no association between dog or cat exposure in perinatal life and sensitization or rhin

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

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

217 ith RWPE, other pollen allergic extracts, or cat dander extract (CDE), and activation of nuclear fact

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

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

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

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

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

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

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

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

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

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

228 fic IgE antibodies against a highly purified cat allergen (Fel d1).

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

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

231 reflex can alter the timing of (i.e., reset) cat walking and turtle scratching rhythms; in addition,

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

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

234 ased on the Wilcoxon rank sum test, t-score, cat-score, binary discriminant analysis and random fores

235 Cross-sectionally, cat/dog-polysensitized children had higher IgE levels an

236 In positive sera IgE to specific cat and dog allergens was also assayed.

237 Fel d 7 is a common allergen in a Swedish cat-sensitized population that cross-reacts with Can f 1

238 is analysis uses a normalized time scale, t [cat]T (n) , to adjust entire reaction profiles construct

239 After a lateral left hemisection (T10), cats recovered stepping with both hindlimbs within 3 wee

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

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

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

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

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

245 he midbrain periaqueductal gray (PAG) in the cat generates four different types of vocalization, mews

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

247 ive cell proliferation occurs rapidly in the cat vestibular nuclei (VN) after unilateral vestibular n

248 90-1296), the current study investigated the cat allergen-specific antibody responses.

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

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

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

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

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

254 ghout the superficial and deep layers of the cat SC.

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

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

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

258 -unit recordings were made in area 18 of the cat, the neurons of which show responses to CM and LM st

259 95% CI, 0.71-0.97; P = .022), supporting the cat-rs7216389 genotype interaction (adjusted P = .008).

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

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

262 nsate sulcus (areas 1-2) in 2 cats while the cats walked on a flat surface or on a horizontal ladder,

263 to study the relevance of IgE antibodies to cat and dog allergens in an area in which (1) the climat

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

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

266 as likewise decreased in children exposed to cat.

267 is, conjunctivitis, or asthma at exposure to cat or dog.

268 ized subjects, subjects with specific IgE to cat >= 3.5 kU/l presented relative risk ratios of 11.4 (

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

270 eased with increasing sum of specific IgE to cat/grass/mite.

271 IgE levels to cat and dog were determined by using ImmunoCAP, and leve

272 was observed between specific IgE levels to cat/grass/mite and the risk of symptoms on each allergen

273 ssociation between sensitization patterns to cat and dog allergen molecules during childhood and symp

274 le in induction of allergic sensitization to cat dander and common pollens relevant to human allergic

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

276 her IgE levels and more frequent symptoms to cat and dog than monosensitized children.

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

278 Contrary to cats and primates, cortical contribution to hindlimb loc

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

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

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

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

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

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

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

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

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

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

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

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

291 ost for asexually replicating forms, whereas cats serve as the definitive host for sexual development

292 hinoconjunctivitis symptoms in subjects with cat allergy up to 1 year after the start of a short cour

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

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

295 ther 596 species at risk of extinction, with cats, rodents, dogs, and pigs threatening the most speci

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

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

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

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

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