ライフサイエンスコーパス: domestic cat

1 coplasma haemofelis (Mhf) (9.8% guigna, 6.1% domestic cat).

2 than in another member of the Carnivora, the domestic cat.

3 ferent loci control the coat markings of the domestic cat.

4 iple origins for the orange phenotype in the domestic cat.

5 odeficiency in its natural host species, the domestic cat.

6 y in non-T-cell, non-B-cell lymphomas of the domestic cat.

7 ity, greater than has been documented in the domestic cat.

8 safe and durable contraception in the female domestic cat.

9 D volumes of the rod synapse from the female domestic cat.

10 gene produces long-term contraception in the domestic cat.

11 ntially lifetime sterilization in the female domestic cat.

12 human CaSR to that of a model carnivore, the domestic cat.

13 that found, for example, in the well-studied domestic cat.

14 iant causing Chediak-Higashi syndrome in the domestic cat.

15 ce of oviductal EVs on sperm function in the domestic cat.

16 hologically similar to those observed in the domestic cat.

17 re suffering introgression of genes from the domestic cat.

18 chronic renal failure is a common problem in domestic cats.

19 utation event in MLPH gave rise to dilute in domestic cats.

20 d cougar, Puma concolor, during infection of domestic cats.

21 causes AIDS-like immunodeficiency disease in domestic cats.

22 enFeLV-GGAG, respectively, among a survey of domestic cats.

23 FeLVs) are the commonest forms of illness in domestic cats.

24 mia virus (FeLV) is an important pathogen of domestic cats.

25 xogenous FeLV (exFeLV) infection outcomes in domestic cats.

26 nous counterpart and is endemic worldwide in domestic cats.

27 ralizing free heme in the digestive tract of domestic cats.

28 FeLV) is a retrovirus that primarily affects domestic cats.

29 merging cause of spontaneously-arising AE in domestic cats.

30 tudies are available on vitamin B6 status in domestic cats.

31 ildcats possessed little to no ancestry from domestic cats.

32 is growing interest in the facial signals of domestic cats.

33 copy number and exogenous virus infection in domestic cats.

34 not found on guignas and were infrequent on domestic cats.

35 zinc, underpin the high incidence of CIN in domestic cats.

36 ntrogressive hybridization with free-ranging domestic cats.

37 mpetent ERV-DC14 that is commonly present in domestic cats.

38 is a common and important health problem in domestic cats.

39 uctural MRI acquired at 7 T from eight adult domestic cats.

40 previously thought to be uniformly fatal in domestic cats.

41 ognized as a significant cause of colitis in domestic cats.

42 lly transmitted gammaretrovirus that infects domestic cats.

43 as a result of hybridization with introduced domestic cats,(1)(,)(2) though the time frame over which

44 r its euphoric and hallucinogenic effects on domestic cats,(1-3) for its medicinal properties,(4)(,)(

45 ide polymorphisms (SNPs) was analyzed in 139 domestic cats, 130 putative European wildcats and 5 capt

46 ygous compared to the genomes of the outbred domestic cat (24.08 % homozygous), Virunga Mountain Gori

47 To extend this power to the domestic cat, a radiation hybrid (RH) map of the cat was

48 h prevalence of influenza virus infection in domestic cats, a seasonality pattern of influenza virus

49 IV genome sequence from puma, Pallas cat and domestic cat across 5' LTR, gag, pol, vif, orfA, env, re

50 FcaGHV1 was detected in 16% of domestic cats across all study sites.

51 102 wild guignas and 262 co-occurring rural domestic cats across the entire distribution range of gu

52 The dilute phenotype in domestic cats affects both eumelanin and phaeomelanin pi

53 species; the bodies of macaques, humans, and domestic cats all evoked a stronger response when they c

54 e viruses in feline blood and found that the domestic cat and bobcat viruses were widespread across t

55 Three-dimensional shape analysis of domestic cat and dog skulls demonstrated convergence at

56 at reported in other carnivores, such as the domestic cat and dog.

57 for an evolutionary "arms race" between the domestic cat and its cognate lentivirus.

58 us to the clades which have been defined for domestic cat and lion (Panthera leo) FIV.

59 h resemble those of BSE transmitted to mice, domestic cat and macaque, consistent with BSE being the

60 plexity of the subgingival microbiota of the domestic cat and reveal both differences and similaritie

61 nstructed with a hybrid pedigree between the domestic cat and the Asian leopard cat, this map was gen

62 r the mapping of phenotypic variation in the domestic cat and the use of this species as a model syst

63 s were also measured in 6 naturally infected domestic cats and 11 naturally infected Florida panthers

64 g was compared to a variant database from 51 domestic cats and a Pallas cat, revealed 50 candidate va

65 Adult domestic cats and bobcats were at greater risk for infec

66 FIV is a nonprimate lentivirus that infects domestic cats and causes a syndrome that is reminiscent

67 xtremely low compared with that in wild type domestic cats and could be hypoallergenic cats.

68 lites in a large multigeneration pedigree of domestic cats and detected tight linkage for dilute on c

69 ssion, we investigated the susceptibility of domestic cats and dogs to infection and potential for in

70 Urine arsenic was higher in domestic cats and dogs with CIN.

71 felis, is the most important ectoparasite of domestic cats and dogs worldwide.

72 vated C-reactive protein, after contact with domestic cats and dogs, and a fox.

73 tly related to the universal immunization of domestic cats and dogs.

74 to assess disease transmission risks between domestic cats and forest-dwelling wild felids such as gu

75 and the possibility of transmission between domestic cats and guignas by comparing spatial and phylo

76 (FeMV) is a recently discovered pathogen of domestic cats and has been classified as a morbillivirus

77 The organism has been found in some domestic cats and in nonhuman primates, but the opportun

78 is reproductive isolation between introduced domestic cats and local wildcats was likely the result o

79 may have significant health implications for domestic cats and may aid studies of free-ranging felid

80 Feline malignant lymphoma occurs commonly in domestic cats and may serve as a model for non-Hodgkin's

81 Domestic cats and other felids rub their faces and heads

82 in absence of Nef is restricted by SER5 from domestic cats and protected by its Nef protein.

83 ysis, we inferred 3 spillover events between domestic cats and pumas; 3 puma-to-puma transmissions in

84 a major cause of morbidity and mortality in domestic cats and some wild cats despite the availabilit

85 communities associated with periodontitis in domestic cats and suggest that the ATP-synthase and nitr

86 A genetic assessment of 979 domestic cats and their wild progenitors-Felis silvestri

87 orptive lesions (FORL), affects up to 70% of domestic cats and thus provides a valuable model for inv

88 Certain species, such as domestic cats and tigers, are susceptible to SARS-CoV-2

89 entified in transmissions to mice of TSEs of domestic cats and two exotic species of ruminant, provid

90 Domestic cats and white-tailed deer (WTD) are particular

91 dynamics of the transmission of FeLV between domestic cats and wild felids and presents evidence of m

92 Both domestic cats and wild relatives of the Felis genus harb

93 the under-annotated genomes of Felis catus (domestic cat) and Bos taurus (cow).

94 M. haemominutum (CMhm) (15.7% guigna; 10.3% domestic cat) and Mycoplasma haemofelis (Mhf) (9.8% guig

95 total of 318 primer pairs were optimized for domestic cats, and 86% of the sequenced feline PCR produ

96 ats, female mainland leopard cats and female domestic cats, and female marbled cats and male domestic

97 le Asian golden cats, male jungle cats, male domestic cats, and female marbled cats showed considerab

98 from animals (e.g., white-tailed deer, mink, domestic cats, and others) back to humans has been obser

99 the ASIP gene specifies black coloration in domestic cats, and two different "in-frame" deletions in

100 The most common source of these strains was domestic cats, and we show that the molecular types of M

101 In summary, the kidneys of domestic cats appear to have greater levels of pro-oxida

102 In conclusion, a survey assessing how domestic cats are fed, together with an analysis of comm

103 alysis of commercial cat feeds suggests that domestic cats are likely to experience chronically low o

104 Intraspecific social interactions in domestic cats are often categorised as affiliative or ag

105 Over 94 million domestic cats are susceptible to cancers and other commo

106 Domestic cats are the primary reservoir species, but FeL

107 but not in males--have been described in the domestic cat as Orange, and in the Syrian hamster as Sex

108 e responsible for tabby pattern variation in domestic cats as Transmembrane aminopeptidase Q (Taqpep)

109 ort the isolation and sequencing of a 150-kb domestic cat BAC clone containing the feline CCR genes C

110 ization (FISH) data were generated using 129 domestic cat BAC clones as probes, providing independent

111 d cat genes whose expression is reduced in a domestic cat background, consistent with genetic incompa

112 d partial data from published reports of the domestic cat brain.

113 f genomic organization among cats and inbred domestic cat breeds have illuminated our view of domesti

114 ia viruses (enFeLVs) were determined in four domestic cats (Burmese, Egyptian Mau, Persian, and nonbr

115 quence diversity was present across wild and domestic cats but was locus dependent.

116 his study assessed habitual iodine intake in domestic cats by: (1) conducting a dietary survey involv

117 The domestic cat, by virtue of the fact that it is one of th

118 The world's domestic cats carry patterns of sequence variation in th

119 The Sex-linked orange mutation in domestic cats causes variegated patches of reddish/yello

120 We document a strong association between domestic cat cell susceptibility and FeLV long terminal

121 fibroblasts are more permissive to FeLV than domestic cat cells, and domestic cat FeLV restriction wa

122 arable to between-clade differences seen for domestic cat clades, allowing recognition of 15 phylogen

123 The results raise the possibility that the domestic cat could yield an animal model of HIV-1 infect

124 Domestic cats derive from at least five founders from ac

125 radiation hybrid panel is described for the domestic cat, derived from irradiated male feline fibrob

126 ma species and, contrary to our predictions, domestic cats did not appear to be the main driver of he

127 ancient and modern cat genomes suggests that domestic cats did not spread to Europe with Neolithic fa

128 arently unlike the human and mouse MHCs, the domestic cat DRA and DRB genes have undergone multiple d

129 nstrated close association with a particular domestic cat DRB lineage, suggesting that these allelic

130 Although a recent report has shown that domestic cat encodes 7 haplotypes (hap I to hap VII) of

131 Domestic cat enFeLV env and long terminal repeat (LTR) c

132 Endogenous retroviruses (ERVs) of domestic cats (ERV-DCs) are one of the youngest feline E

133 he uncontrolled reproduction of free-roaming domestic cats exacerbates their welfare challenges and t

134 Our analysis suggests that domestic cats exhibit more rapid facial mimicry in affil

135 mestic cat genome, with potential impacts on domestic cat exogenous FeLV susceptibility and pathogene

136 the feline genome, with potential impacts on domestic cat exogenous FeLV susceptibility and pathogene

137 interspecies backcross pedigree between the domestic cat (F. catus) and the Asian leopard cat (Prion

138 and age and being male were risk factors for domestic cat FcaGHV1 infection.

139 Limited variation in the domestic cat Feca-DRA gene was observed, but abundant va

140 Predation by domestic cats Felis catus can be a threat to biodiversit

141 We present the earliest evidence for domestic cat (Felis catus L., 1758) from Kazakhstan, fou

142 auses AIDS-like disease and mortality in the domestic cat (Felis catus) and serves as a natural model

143 It is known that domestic cat (Felis catus) APOBEC3Z3 (A3Z3), the ortholo

144 y accurate computational nasal model for the domestic cat (Felis catus) based on high resolution micr

145 The domestic cat (Felis catus) descends from the African wil

146 cleotide sequence spanning 758,291 bp of the domestic cat (Felis catus) extended and classical class

147 sent study, we characterized the proteome of domestic cat (Felis catus) follicular fluid EVs (ffEV).

148 We show that the domestic cat (Felis catus) laps by a subtle mechanism ba

149 Urban domestic cat (Felis catus) populations can attain exceed

150 CWD), we evaluated the susceptibility of the domestic cat (Felis catus) to CWD infection experimental

151 ssible functional referentiality in a common domestic cat (Felis catus) vocalization, the authors con

152 class II DRA and DRB gene homologues of the domestic cat (Felis catus) were cloned and sequenced to

153 To identify felid GHVs, we screened domestic cat (Felis catus), bobcat (Lynx rufus), and pum

154 cific strains of FIV have been described for domestic cat (Felis catus), puma (Puma concolor), lion (

155 es, including several closely related to the domestic cat (Felis catus).

156 an autosomal genetic linkage (GL) map of the domestic cat (Felis silvestris catus).

157 tion with Helicobacter pylori (H. pylori) in domestic cats (Felis cattus) less than 2 years of age ha

158 e infected primary fibroblasts isolated from domestic cats (Felis catus) and pumas (Puma concolor) wi

159 Domestic cats (Felis catus) and related felids constitut

160 Domestic cats (Felis catus) are known to develop cogniti

161 Domestic cats (Felis catus) are obligate carnivores and

162 Allergens from domestic cats (Felis catus) cause allergy-related health

163 lobal literature documents that free-roaming domestic cats (Felis catus) have substantial negative ef

164 n meows in domestic felids, vocalizations by domestic cats (Felis catus) were compared with cries by

165 uences of three GHVs present in the blood of domestic cats (Felis catus), bobcats (Lynx rufus), and p

166 tivirus which causes an AIDS-like disease in domestic cats (Felis catus).

167 The co-occurrence of domestic cats (Felis silvestris catus) and wild felids i

168 Worldwide, domestic cats (Felis silvestris catus) outnumber domesti

169 ogenesis and host-virus evolution.IMPORTANCE Domestic cats (Felis silvestris catus) were domesticated

170 fundamental frequency (f(o)) ranges of eight domestic cats (Felis silvestris catus) were investigated

171 are one of the youngest feline ERV groups in domestic cats (Felis silvestris catus); some members are

172 mplete 17,009-bp mitochondrial genome of the domestic cat, Felis catus, has been sequenced and confor

173 opard cat, Prionailurus bengalensis, and the domestic cat, Felis catus, with a last common ancestor a

174 e, the development of paw preferences in the domestic cat, Felis silvestris catus, is explored.

175 missive to FeLV than domestic cat cells, and domestic cat FeLV restriction was highly related to enFe

176 s FeLV, produce more virus more rapidly than domestic cat fibroblasts following cell culture challeng

177 ain of FIV, and the leopard cat, which has a domestic cat FIV strain in one population.

178 wing parenteral exposure but, in contrast to domestic cat FIV, it does not cause T-cell dysregulation

179 concolor), carry a virus closely related to domestic cat FIV.

180 types, with FIVPle subtype E more related to domestic cat FIVFca than to FIVPle subtype B and FIVOma

181 PLV establishes productive infection in domestic cats following parenteral exposure but, in cont

182 atures of natural selection that distinguish domestic cats from their wild congeners are enriched in

183 For example, in contrast to mice, the domestic cat genome encodes essential nonreceptor HIV-1

184 -resolution radiation hybrid (RH) map of the domestic cat genome, which includes 2662 markers, transl

185 n linked to solo LTRs distributed within the domestic cat genome, with potential impacts on domestic

186 .5-Mb-resolution radiation hybrid map of the domestic cat genome.

187 A large-insert domestic cat genomic DNA library was developed using a P

188 sues from FeLV-infected Florida panthers and domestic cats had similar exFeLV proviral copy numbers,

189 Studies of the domestic cat have contributed to many scientific advance

190 Studies with the domestic cat have demonstrated that vaccinal immunity to

191 Free-ranging domestic cats have been introduced globally and have con

192 Domestic cats have several features that make them ideal

193 Ps were variable both in wild (HE=0.107) and domestic cats (HE=0.340).

194 ntually a whole genome sequence (WGS) of the domestic cat holds considerable value for human genome a

195 Only the primary domestic cat host and related small cat species harbor a

196 infect felid species other than the endemic domestic cat host, differences in FeLV susceptibility am

197 seasonal human influenza virus infections in domestic cats in Ohio.

198 ce of anti-AAV neutralizing antibodies among domestic cats in Switzerland.

199 I have used an exercise involving domestic cats in the General Genetics course at the Univ

200 Eighty percent of the estimated 600 million domestic cats in the world are free-roaming.

201 Close interactions with domestic cats, including predation, can lead to the inte

202 ead X Chromosome reference assembly from the domestic cat (incorporating 19.3 Mb of targeted BAC clon

203 to analogous work carried out for Orange in domestic cats indicates, surprisingly, that the cat and

204 udy was to determine whether semen from male domestic cats infected with feline immunodeficiency viru

205 Domestic cats infected with the horizontally transmitted

206 mall felid species, including the introduced domestic cat, inhabit Southeast Asia.

207 e Near Eastern cat (NE cat), the ancestor of domestic cats, into Central Europe.

208 will develop PKD and demonstrating that the domestic cat is an ideal model for human PKD.

209 The domestic cat is an important human companion animal that

210 One of the salient features of the domestic cat is the aesthetics of its fur.

211 Tooth resorption (TR) in domestic cats is a common and painful disease characteri

212 ing virulent protozoan parasite that infects domestic cats, is treated with atovaquone and azithromyc

213 ctively-coupled plasma-mass spectrometry) of domestic cats (kidneys, n = 56; urine, n = 21), domestic

214 We estimate that free-ranging domestic cats kill 1.4-3.7 billion birds and 6.9-20.7 bi

215 of Late Neolithic NE cats with the earliest domestic cats known from the territory of Poland, dating

216 The clusters include (1) ocelot lineage, (2) domestic cat lineage, (3) Panthera genus, (4) puma group

217 is an independent insertion from that of the domestic cat lineage, which has been further supported b

218 nsive investigations of the neocortex in the domestic cat, little is known about neuronal morphology

219 elid species: Felis catus GHV 1 (FcaGHV1) in domestic cats, Lynx rufus GHV 1 (LruGHV1) in bobcats, an

220 This suggests that the domestic cat may serve as a potential model for mechanis

221 oss-species transmission between guignas and domestic cats may occur, but is probably uncommon.

222 ls of experience and affinity for cats rated domestic cat meows as far more pleasant sounding than wi

223 evealed clear species-level differences: The domestic cat meows were significantly shorter in mean du

224 artificial chromosome/PAC contig map of the domestic cat MHC class II region was constructed with a

225 species and researchers often cross-amplify domestic cat microsatellites to study these species.

226 Previously we described a domestic cat model of autosomal recessive, juvenile-onse

227 A domestic cat model was developed in which long-term in v

228 for a relevant animal model we present a new domestic cat model with a loss-of-function missense muta

229 vations of 105 unique dyadic interactions of domestic cats (N = 210) captured on videos collected fro

230 (n = 641) and bobcats (n = 212) and shelter domestic cats (n = 304).

231 Domestic cats (n = 51) sustaining burn injuries from the

232 er of the cytoplasmic mtDNA sequences to the domestic cat nucleus and recapitulates evolutionary rela

233 The primary hosts of FeLV are domestic cats of the Felis genus that also harbor endoge

234 e mainland, and female marbled cats and male domestic cats on Borneo and Sumatra.

235 sary to understand the impacts of introduced domestic cats on indigenous small wild felids in Southea

236 estic cats, and female marbled cats and male domestic cats on the mainland, and female marbled cats a

237 Uncertainty remains regarding whether domestic cats originated in the Levant, Egypt, or elsewh

238 Domestic cat origins are focused in the eastern Mediterr

239 For female domestic cats, ovariohysterectomy is the only method of

240 , (ii) provides a linkage map generated in a domestic cat pedigree which will more accurately reflect

241 n about the genetic changes that distinguish domestic cat populations from their wild progenitors.

242 events following contact with reservoir host domestic cat populations.

243 her levels of coastal development and larger domestic cat populations.

244 uropean mainland and in Britain, most modern domestic cats possessed less than 10% of their ancestry

245 The presence of this domestic cat, presented here as an osteobiography using

246 ploy a three-antigen Western blot screening (domestic cat, puma, and lion FIV antigens) and PCR analy

247 Here we describe a high-quality domestic cat reference genome assembly and comparative i

248 redicted to derive ~94% of their genome from domestic cats, regions of the leopard cat genome are tho

249 or creatinine) arsenic content was higher in domestic cats, relative to domestic dogs and wildcats.

250 The subgingival microbial communities of domestic cats remain incompletely characterized and it i

251 ecombination with endogenous retroviruses in domestic cats, resulting in a variety of pathogenic outc

252 of the two spectral types of cone across the domestic cat's retina.

253 .47% of the bobcat samples, and 6.25% of the domestic cat samples analyzed.

254 V are more permissive to FeLV infection than domestic cat samples, suggesting that endogenization can

255 Four hundred serum samples collected from domestic cats (September 2009 to September 2010) were te

256 mellitus, a common endocrinopathy affecting domestic cats, shares many clinical and pathologic featu

257 us (FIV) is a lentivirus that causes AIDS in domestic cats, similar to human immunodeficiency virus (

258 Our findings indicate that aging domestic cats spontaneously develop both beta-amyloid an

259 at use on that of red foxes and free-ranging domestic cats, suggesting that coyotes function as apex

260 A similar range of patterns in domestic cats suggests a conserved mechanism whose appea

261 st, these viruses efficiently used human and domestic cat TfR1 orthologs.

262 y virus (FIV) induces a disease state in the domestic cat that is similar to AIDS in human immunodefi

263 unodeficiency virus (FIV) is a lentivirus of domestic cats that causes a spectrum of diseases remarka

264 omal recessive lower motor neuron disease in domestic cats that clinically resembles human SMA Type I

265 ommon naturally occurring gammaretrovirus of domestic cats that is associated with degenerative disea

266 omologous DRB exon 2 sequences from 36 feral domestic cats throughout the world plus from three speci

267 at CWD can be transmitted and adapted to the domestic cat, thus raising the issue of potential cervid

268 ietary specializations, focusing on Felidae (domestic cat, tiger, lion, cheetah, and leopard), Homini

269 for cross-species transmission of FIV from a domestic cat to a puma.

270 provide evidence that FeLV transmission from domestic cats to pumas occurs widely across the United S

271 rd cat, this map was generated entirely with domestic cats, using a large multi-generational pedigree

272 ampled population, CIN was more prevalent in domestic cat versus domestic dog (51%, n = 32 of 62 cats

273 (1.9-fold coverage) of an inbred Abyssinian domestic cat was assembled, mapped, and annotated with a

274 A family of domestic cats was found that exhibited clinical and bioc

275 In the common domestic cat, we identified a clinically relevant cardio

276 Male domestic cats were at greater risk for infection than fe

277 mmon feline Mycoplasma species in guigna and domestic cats were Candidatus M. haemominutum (CMhm) (15

278 Domestic cats were derived from the Near Eastern wildcat

279 In total, 44 domestic cats were enrolled, and 139 subgingival samples

280 Retinas from the eyes of domestic cats were examined 1, 3, 7, and 28 days after d

281 Strains isolated from domestic cats were found to exhibit the predominant ribo

282 To develop the model, 8 healthy domestic cats were given a 50% pancreatectomy, which was

283 nucleotide sequence types between guigna and domestic cats were rare, suggesting that cross-species t

284 Here, we show that populations of domestic cats which manifest extra digits, including the

285 eds light on the evolutionary history of the domestic cat, which was likely influenced by lentiviral

286 mune responses are induced upon infection in domestic cats, which curb the progression of clinical di

287 line leukemia virus (FeLV) (clone 33) from a domestic cat with acute myeloid leukemia (AML).

288 Clinical features of 12 domestic cats with ARVC (7 male; 1 to 20 years old, mean

289 We experimentally infected domestic cats with B. koehlerae to establish the microbi

290 the organism was also isolated from several domestic cats with bilateral nasal discharge.

291 n inhabitant of the large intestine in young domestic cats with chronic diarrhea.

292 Infection of domestic cats with feline immunodeficiency virus (FIV) i

293 A3Z3, the relevance of A3Z3 polymorphism in domestic cats with FIV Vif has not yet been addressed.

294 The domestic cat, with its diversity of coat patterns, is an

295 (FIV) causes progressive immunodeficiency in domestic cats, with clinical course dependent on virus s

296 119 participants, interacting with sociable domestic cats within a rehoming context.

297 tion affecting the hip joints of millions of domestic cats worldwide.

298 A comprehensive genetic linkage map of the domestic cat X chromosome was generated with the goal of

299 Our results indicate the domestic cat Y chromosome has retained most X-degenerate

300 pertoire and transcriptional analysis of the domestic cat Y chromosome, and their potential roles in