ライフサイエンスコーパス: Rattus norvegicus

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

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

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

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

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

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

7 iens tRFs and one newly incorporated species Rattus norvegicus.

8 biochemical stress-related profiles of urban Rattus norvegicus.

9 hioredoxin substrates from P. falciparum and Rattus norvegicus.

10 signaling complex in hippocampal neurons of Rattus norvegicus.

11 Golgi in dissociated hippocampal neurons of Rattus norvegicus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

106 Rattus norvegicus shares the young L1mlvi2 clade only wi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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