ライフサイエンスコーパス: Rattus

1 escence in non-regenerating mammals (Mus and Rattus).

2 . carinii sp. f. muris and P. carinii sp. f. rattus.

3 tic spillover risk is lower at sites with R. rattus.

4 hypoxic stress among two Spalax species and Rattus.

5 cess gene ontology category in either Mus or Rattus.

6 ent lineage before the separation of Mus and Rattus.

7 revalence of antibody was found in the genus Rattus (59.7%; 166/278).

8 evels were compared with those obtained from Rattus, a primary model for human physiology.

9 As is the case in Mus and Rattus, a very small number of active templates produce

10 articularly due to the competitive nature of Rattus accelerating the rate at which extinction debts a

11 tterns of Flk1 expression between Spalax and Rattus and between muscle and brain.

12 ni-Otomyini-Millardini clade, which excludes Rattus and its relatives.

13 Whereas Rattus and Peromyscus each have three adult alpha-globin

14 nt species revealed that the HBA-T3 genes of Rattus and Peromyscus originated via independent, lineag

15 among the triplicated alpha-globin genes in Rattus and Peromyscus, the red blood cells of both roden

16 mbination with the increasing invasion of R. rattus and perturbations of endemic animal communities b

17 gy, in the skeletal muscle and heart, of the Rattus and two Spalax species.

18 tified using the BLASTX algorithm to Mus and Rattus, and 34 - 54% of all ESTs could be assigned to a

19 diverse murid species of murine genera Mus, Rattus, Apodemus, Diplothrix, Hybomys, Mastomys, and Tok

20 Antibody prevalence was higher among R. rattus brunneusculus and Bandicota bengalensis than in S

21 ion detected four animals (9%; three were R. rattus brunneusculus and one was B. bengalensis) with vi

22 ng L1mlvi2 clade only with its sister taxon, Rattus cf moluccarius.

23 ea and had duodenal cultures positive for E. rattus compared with 0% in the control group.

24 s is more extensive than in either Mus or in Rattus, consistent with the elevated rate of speciation,

25 demonstrate that two rodent species (Mus and Rattus) contain a similar direct repeat structure associ

26 Peromyscus genome organization resembles the Rattus genome more closely than Mus we examined the dist

27 In the Rattus genus, we found one missense mutation Leu90Ile in

28 nterococcus species, designated Enterococcus rattus, has been isolated from the duodenum of these rat

29 ently derived HBA-T3 genes of Peromyscus and Rattus have been attributed to positive selection.

30 tion of cysteine codons, and both Tupaia and Rattus have eliminated an otherwise conserved cysteine c

31 o sustain native biodiversity while averting Rattus hyper-abundance.

32 s on ecosystems, our results suggest that R. rattus invasion has the indirect benefit of decreasing z

33 provide an evolutionary outgroup to the Mus/Rattus lineage and serve as an intermediary between that

34 tion using the extinct Christmas Island rat (Rattus macleari) as a model, an endemic rat species that

35 Within its invasive range in West Africa, R. rattus may compete with the native rodent Mastomys natal

36 These sequences were found in the genomes of Rattus norvegicus (brown rat), Mus spretus (Algerian mou

37 ucleotide position GC (GC3) content for both Rattus norvegicus (r = 0.246, p = 0.01; N = 110) and Mus

38 bing an array of overlapping decapeptides of Rattus norvegicus (Rat) Krp1 with recombinant Lasp-1 rev

39 Homo sapiens (human), Mus musculus (mouse), Rattus norvegicus (rat), Danio rerio (zebrafish), and Ma

40 rats with a rodent hepacivirus isolated from Rattus norvegicus (RHV) is a promising surrogate model d

41 Infection with rodent hepacivirus from Rattus norvegicus (RHV-rn1) in rats shares HCV-defining

42 with rodent hepacivirus isolated from feral Rattus norvegicus (RHV-rn1) mirrors key aspects of HCV i

43 of klotho in the kidney of NMR with that of Rattus Norvegicus (RN) and demonstrated that klotho was

44 crystal structure and reaction mechanism of Rattus norvegicus 3'-phosphoadenosine 5'-phosphate and i

45 Arabidopsis alpha1,4-fucosyltransferase, and Rattus norvegicus alpha2,6-sialyltransferase (a nonplant

46 CALMII and psi alpha-tubulin pseudogenes of Rattus norvegicus among species belonging to Rattus sens

47 es were isolated from the blood of 63 of 325 Rattus norvegicus and 11 of 92 Rattus rattus from 13 sit

48 n in blood by P. leucopus, Mus musculus, and Rattus norvegicus and adjusted for white cell concentrat

49 methods, we show that synaptotagmin-1 (from Rattus norvegicus and expressed in Escherichia coli) bin

50 ), Candida albicans, Caenorhabditis elegans, Rattus norvegicus and Homo sapiens have been identified

51 gans, Drosophila melanogaster, Mus musculus, Rattus norvegicus and Homo sapiens).

52 er, G. gallus, Homo sapiens, Mus musculus or Rattus norvegicus and identifies the specific miRNAs tha

53 tent with this, M3 alpha1alpha2 domains from Rattus norvegicus and Sigmodon hispidus and from the "nu

54 principal rodent hosts Apodemus agrarius and Rattus norvegicus and the hantavirus infection rate of t

55 rame YLR118c encodes an enzyme homologous to Rattus norvegicus APT1.

56 heoretical proteomes of Escherichia coli and Rattus norvegicus are used to evaluate the efficacy of t

57 Here, using Rattus norvegicus as a model, with subtle and specific b

58 We report that Rattus norvegicus can learn simple rules and apply them

59 ns is sufficient to induce neuronal death in Rattus norvegicus cortical neurons in vitro.

60 rt samples were searched against the UniProt Rattus norvegicus database using the Paragon algorithm i

61 against colorectal cancer, an animal model (Rattus norvegicus F344) was used, involving two doses of

62 uce 15N stable isotopes into the proteins of Rattus norvegicus for use as internal standards.

63 length) within the published version of the Rattus norvegicus genome assembly (v.3.1).

64 period of 96-capillary DNA sequencing of the Rattus norvegicus genome at the Baylor College of Medici

65 Completion of the Rattus norvegicus genome sequence enabled a global inven

66 the most commonly used model organisms - the Rattus norvegicus have not been studied.

67 t of 15 endogenously occurring peptides from Rattus norvegicus hypothalamus.

68 of full-length and caspase-treated XKR9 from Rattus norvegicus in complex with a synthetic nanobody d

69 lution of the genus Mus, while the gene from Rattus norvegicus is likely functional.

70 ave expressed and phosphorylated recombinant Rattus norvegicus left ventricular RLC.

71 t cyclin B1 gene translation start site from Rattus norvegicus liver genomic DNA and a commercial rat

72 first genome-scale network reconstruction of Rattus norvegicus metabolism, iRno, and a significantly

73 ve, whereas forced expression of Myc induces Rattus norvegicus neuronal cell death.

74 present the structure at 2.8 A resolution of Rattus norvegicus NTSR1 in an active-like state, bound t

75 Rattus norvegicus shares the young L1mlvi2 clade only wi

76 from Xenopus laevis and the GluN2B ATD from Rattus norvegicus shows a highly distinct pattern of sub

77 ague using the inbred Brown Norway strain of Rattus norvegicus to characterize the progression and ki

78 d nucleotide divergence from Mus famulus and Rattus norvegicus to compare rates of adaptive evolution

79 rrogans serovar Copenhageni transmitted from Rattus norvegicus to humans is the most prevalent cause

80 ity of a diurnal Octodon degus and nocturnal Rattus norvegicus to synchronise to different nocturnal

81 The responses of 2- and 8-day-old rats (Rattus norvegicus) and hamsters (Mesocricetus auratus) t

82 Previous data suggest that rats (Rattus norvegicus) and pigeons (Columba livia) use diffe

83 ted alpha-globin paralogs of the Norway rat (Rattus norvegicus) and the deer mouse (Peromyscus manicu

84 Norway rats (Rattus norvegicus) are hosts for various microbes.

85 sical eyeblink conditioning in the male rat (Rattus norvegicus) by use of a delay paradigm in which t

86 ranes in a critical-sized defect in the rat (Rattus norvegicus) calvaria.

87 ual homologous mouse (Mus musculus) and rat (Rattus norvegicus) chromosomal regions are presented as

88 , thresholds in the sham, CTX, and GLX rats (Rattus norvegicus) either improved (lowered) or remained

89 de that cross-reacts with antibodies to rat (Rattus norvegicus) extracellular signal-regulated kinase

90 troglodytes), mouse (Mus musculus) and rat (Rattus norvegicus) for evidence of gene conversion.

91 The present study in rats (Rattus norvegicus) found persistent upregulation after S

92 fied and genetically characterized from rat (Rattus norvegicus) genomic DNA.

93 tic hypercalciuric stone-forming (GHS) rats (Rattus norvegicus) had higher coefficients of variation

94 ies, we examined the impacts of Norway rats (Rattus norvegicus) introduced to the Aleutian Islands on

95 The laboratory rat (Rattus norvegicus) is a key animal model for biomedical

96 The rat (Rattus norvegicus) is an important experimental model fo

97 The laboratory rat (Rattus norvegicus) is an indispensable tool in experimen

98 that mediates human (Homo sapiens) and rat (Rattus norvegicus) movement characteristics on analogous

99 The brown rat (Rattus norvegicus) occupies nearly every terrestrial hab

100 The authors used laboratory rats (Rattus norvegicus) of known relatedness and contrasting

101 tes that the globally distributed brown rat (Rattus norvegicus) originated in northern China and Mong

102 slug (Aplysia californica) central and rat (Rattus norvegicus) peripheral nervous systems.

103 nt experiments investigated whether the rat (Rattus norvegicus) Pf supports flexibility during revers

104 Infant rats (Rattus norvegicus) placed on a shallow incline (2 degree

105 We survey rat (Rattus norvegicus) populations to assess the effect that

106 n(2+) spikes have been recorded in both rat (Rattus norvegicus) primary neuron cultures and organotyp

107 In contrast, infant Norway rats (Rattus norvegicus) produce heat endogenously and are eff

108 nd placed in a cool environment, Norway rat (Rattus norvegicus) pups emit ultrasonic vocalizations th

109 on (USV) responses of 11- to 12-day-old rat (Rattus norvegicus) pups in isolation to the presence or

110 impacts of black (Rattus rattus) and brown (Rattus norvegicus) rats on human society are well docume

111 Female rats (Rattus norvegicus) received 30 paced, 30 nonpaced, or 15

112 We show that small DRG neurons from rats (Rattus norvegicus) receiving thoracic spinal injury 3 d

113 Retrograde tracing in adult male rats (Rattus norvegicus) revealed that the inferior colliculus

114 e trait locus mapping in the laboratory rat (Rattus norvegicus) to gain a broad perspective of gene r

115 expression and sequence analysis in HS rats (Rattus norvegicus) to identify Tpcn2 as a likely causal

116 hemical signaling by female laboratory rats (Rattus norvegicus) to test i) whether females target the

117 after probable percutaneous exposure to rat (Rattus norvegicus) urine in Baltimore alleys.

118 ts we investigated the extent to which rats (Rattus norvegicus) use an egocentric trajectory and land

119 Twenty female rats (Rattus norvegicus) were allocated into two groups: contr

120 Eleven years after invasive Norway rats (Rattus norvegicus) were eradicated from Hawadax Island,

121 ales, adult male and female Long Evans rats (Rattus norvegicus) were inoculated with doses of Seoul v

122 Norway rats (Rattus norvegicus) were introduced to the Falkland Islan

123 ltrasonic vocalization (USV) of infant rats (Rattus norvegicus) were measured on postnatal Day 10.

124 skunk (Mephitis mephitis) and 1 Norway rat (Rattus norvegicus) were seropositive for antibodies agai

125 research, pigeons (Columba livia) and rats (Rattus norvegicus) were tested with a simultaneous spati

126 ared from Mus musculus, Mus spretus, or rat (Rattus norvegicus), a comparable number of respiring clo

127 ng three rodents, mouse (Mus musculus), rat (Rattus norvegicus), and deer mouse (Peromyscus maniculat

128 ncluding house mouse (Mus musculus) and rat (Rattus norvegicus), did not support entry of these virus

129 nopus laevis), chicken (Gallus gallus), rat (Rattus norvegicus), mouse (Mus musculus), hamster (Mesoc

130 Using chemogenetics in Sprague Dawley rats (Rattus norvegicus), we found support for this hypothesis

131 In adult Norway rats (Rattus norvegicus), which are nocturnal, the RHT also pr

132 Rattus norvegicus), wild-caught Norway rats (Rattus norvegicus), wild-caught California ground squirr

133 rodents: laboratory Norway rats (Long Evans; Rattus norvegicus), wild-caught Norway rats (Rattus norv

134 mals, including Mouse1 (Mus musculus), Rat1 (Rattus norvegicus), Zebrafish1 (Danio rerio), Fruitfly1

135 ion of conspecific odors in laboratory rats (Rattus norvegicus).

136 s rats (Arvicanthis niloticus) and lab rats (Rattus norvegicus).

137 tranded-DNA-binding protein (SSDP) from rat (Rattus norvegicus).

138 of the behavioral repertoire of Norway rats (Rattus norvegicus).

139 l artery ligation in adult male Wistar rats (Rattus norvegicus).

140 pressed in the liver of Sprague-Dawley rats (Rattus norvegicus).

141 miliaris, Macaca mulatta, P. troglodytes and Rattus norvegicus, and combined with previously characte

142 as mammals (Pan troglodytes, Macaca mulatta, Rattus norvegicus, and Mus musculus) showed a human-like

143 yotic organisms: Homo sapiens, Mus musculus, Rattus norvegicus, Arabidopsis thaliana, Drosophila mela

144 : Homo sapiens, Mus musculus, Gallus gallus, Rattus norvegicus, Arabidopsis thaliana, Zea mays, Schiz

145 sms (Homo sapiens, Mus musculus, Bos taurus, Rattus norvegicus, Danio rerio, Gallus gallus and Arabid

146 w commercial microarrays and annotations for Rattus norvegicus, Drosophila melanogaster and Carnorhab

147 orted organisms (Homo sapiens, Mus musculus, Rattus norvegicus, Drosophila melanogaster, Danio rerio,

148 Because the laboratory rat, Rattus norvegicus, has been used as a model for complex

149 related genes preserved in M. tuberculosis, Rattus norvegicus, Homo sapiens, and Mus musculus.

150 oton-coupled peptide transporter, PepT2 from Rattus norvegicus, in complex with the widely used beta-

151 ined three coronavirus genome sequences from Rattus norvegicus, including a Betacoronavirus (rat coro

152 haracterized the youngest known subfamily in Rattus norvegicus, L1mlvi2, and unexpectedly found that

153 lysis of a new reference genome assembly for Rattus norvegicus, the laboratory rat, a widely used exp

154 d to be transmitted by Apodemus agrarius and Rattus norvegicus, the principal animal hosts of Hantaan

155 dissociated cortical neurons from embryonic Rattus norvegicus, we found here that chronic exposure t

156 Using the laboratory rat Rattus norvegicus, we have discovered a narrowly constra

157 It is descended from wild Norway rats, Rattus norvegicus, which despite their name likely origi

158 iens tRFs and one newly incorporated species Rattus norvegicus.

159 biochemical stress-related profiles of urban Rattus norvegicus.

160 in other rodents, including the Norway rat, Rattus norvegicus.

161 hioredoxin substrates from P. falciparum and Rattus norvegicus.

162 signaling complex in hippocampal neurons of Rattus norvegicus.

163 Golgi in dissociated hippocampal neurons of Rattus norvegicus.

164 s by cardiac fibroblasts (CFs) isolated from Rattus norvegicus.

165 nic with that of the murids Mus musculus and Rattus norvegicus.

166 dentity among Homo sapiens, Mus musculus and Rattus norvegicus.

167 of formalin-fixed brain tissue of white rats Rattus norvegicus.

168 Mother rats (Rattus norvegicus; 6 to 8 days postpartum) approach and

169 y, the authors determined that in male rats (Rattus novegicus) tested in a sexually naive or a sexual

170 from Sierra Leone and Guinea to show that R. rattus presence reduces M. natalensis density within the

171 he genomes of the closely related species R. rattus, R. tanezumi, R. exulans, and R. everetti, indica

172 as, as follows: the invasive urban exploiter Rattus rattus (n = 375) and the native urban adapter Sun

173 The most commonly trapped species was Rattus rattus brunneusculus.

174 of 63 of 325 Rattus norvegicus and 11 of 92 Rattus rattus from 13 sites in the United States and Por

175 en considering the co-occurrence of invasive Rattus rattus with M. natalensis in rural settings.

176 networks in the non-native wild black rats (Rattus rattus) across a land-use gradient in Madagascar.

177 While the impacts of black (Rattus rattus) and brown (Rattus norvegicus) rats on hum

178 s, we show that rodents (and, in particular, Rattus rattus) are significant spreaders of UMRVs.

179 a terrestrial invasive species (black rats, Rattus rattus) disrupts a nutrient pathway provided by s

180 The distribution of the black rat (Rattus rattus) has been heavily influenced by its associ

181 The black rat (Rattus rattus) is a globally invasive species that has b

182 wild free-ranging populations of black rats, Rattus rattus, an alien predator of global concern, we t

183 s, Felis catus, and Capra hircus), wildlife (Rattus rattus, Incilius nebulifer, Sciurus carolinensis,

184 llover between rodent species, most probably Rattus rattus, were detected and indicate that these ani

185 e sampled, including 112 Mus musculus and 28 Rattus rattus.

186 tion likely is facilitated by the introduced Rattus rattus.

187 physiological hypoxia, while the response in Rattus reflects the increase of hypoxic stress.

188 LINE-1) elements isolated from 22 species of Rattus sensu lato and Rattus sensu stricto murine rodent

189 th and significantly extend the phylogeny of Rattus sensu lato established by other molecular criteri

190 pecies, we inferred the partial phylogeny of Rattus sensu lato.

191 Rattus norvegicus among species belonging to Rattus sensu stricto is evidence for the common ancestry

192 ted from 22 species of Rattus sensu lato and Rattus sensu stricto murine rodents.

193 group of very closely related rats known as Rattus sensu stricto.

194 contains Berylmys, Sundamys, Bandicota, and Rattus sensu stricto.

195 from both plant (Arabidopsis) and mammalian (Rattus) sources.

196 two partial 3' cDNAs, from Homo sapiens and Rattus sp., also demonstrate homology to the C. elegans

197 These data suggest that Rattus species are a reservoir host for pathogenic Barto

198 origin for Bartonella species recovered from Rattus species introduced into the Americas.

199 Infection in both Rattus species ranged from 0% (e.g., 0/87) to approximat

200 ts (Clethrionomys species, Mus musculus, and Rattus species).

201 yces cerevisiae, Caenorhabditis elegans, and Rattus species.

202 ped it to the reference genomes of different Rattus species.

203 en widely used as the 12 Ma date for the Mus/Rattus split or a more basal split, conclusive paleontol

204 fraction in house mice (Mus spp.) and rats (Rattus spp.).

205 in some highly social species, such as rats (Rattus spp.).

206 potential experiments using a Streptococcus rattus strain, which is sensitive to mutacin 1140, demon

207 ls were gavaged with either 100 microl of E. rattus suspension (1.0 X 10(7) colony forming units, ino

208 minance of the ubiquitous Malayan field rat, Rattus tiomanicus.

209 significantly higher levels under hypoxia in Rattus tissues, with smaller changes in Spalax.

210 c. carinii (prototype) strain and the P. c. rattus (variant) strain, respectively, are single-copy g

211 R. rattus was strongly associated with built infrastructure