ライフサイエンスコーパス: Rattus norvegicus

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

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

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

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

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

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

7 hioredoxin substrates from P. falciparum and Rattus norvegicus.

8 signaling complex in hippocampal neurons of Rattus norvegicus.

9 Golgi in dissociated hippocampal neurons of Rattus norvegicus.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

83 Rattus norvegicus shares the young L1mlvi2 clade only wi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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