ライフサイエンスコーパス: domestic cat

1 re suffering introgression of genes from the domestic cat.

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

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

4 hologically similar to those observed in the domestic cat.

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

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

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

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

9 causes AIDS-like immunodeficiency disease in domestic cats.

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

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

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

13 previously thought to be uniformly fatal in domestic cats.

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

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

16 lly transmitted gammaretrovirus that infects domestic cats.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

60 Domestic cats derive from at least five founders from ac

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 .5-Mb-resolution radiation hybrid map of the domestic cat genome.

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

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

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

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

99 Domestic cats have several features that make them ideal

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

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

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

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

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

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

106 Domestic cats infected with the horizontally transmitted

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

108 The domestic cat is an important human companion animal that

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

142 (1.9-fold coverage) of an inbred Abyssinian domestic cat was assembled, mapped, and annotated with a

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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