ライフサイエンスコーパス: Rattus

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

2 hypoxic stress among two Spalax species and Rattus.

3 cess gene ontology category in either Mus or Rattus.

4 ent lineage before the separation of Mus and Rattus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

56 Rattus norvegicus shares the young L1mlvi2 clade only wi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

123 hioredoxin substrates from P. falciparum and Rattus norvegicus.

124 signaling complex in hippocampal neurons of Rattus norvegicus.

125 Golgi in dissociated hippocampal neurons of Rattus norvegicus.

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

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

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

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

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

131 seven organisms (Homo sapiens, Mus musculus, Rattus novegicus, Drosophila melanogaster, Danio rerio,

132 The most commonly trapped species was Rattus rattus brunneusculus.

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

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

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

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

137 tion likely is facilitated by the introduced Rattus rattus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

152 yces cerevisiae, Caenorhabditis elegans, and Rattus species.

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

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

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

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

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