ライフサイエンスコーパス: model animal

1 an ameliorate the disease phenotype in a SCD model animal.

2 ing enables precise genetic modifications in model animals.

3 to prolong lifespan in various experimental model animals.

4 or dual color, whole body imaging studies in model animals.

5 encephalographic (EEG) methods in humans and model animals.

6 ng a mouse model of PTSD in wild-type and AD model animals.

7 ge synchrony is evaluated in both humans and model animals.

8 igenesis, embryogenesis, and inflammation in model animals.

9 n bilaterians, which comprise almost all lab model animals.

10 s are inadequate for MHC typing of these key model animals.

11 of earthworms compared to the well-annotated model animals.

12 DNA do not always correlate with lifespan in model animals.

13 al analysis of amyotrophic lateral sclerosis model animals.

14 down aging and promote healthy longevity in model animals.

15 ious hurdles in studying the genetics of non-model animals.

16 potheses, we used brain slices from AD mouse model animals (5xFAD).

17 ible, and effective alternative to KDEs when modelling animal activity patterns.

18 mic reticulum impairment in retinas of these model animals after light exposure.

19 st of their body surface, as an experimental model animal amenable to genetic manipulation for studyi

20 Using model animal and cell studies, we then show that overexp

21 Model animal and fungal proteins are included in the dat

22 This model animal and its derivatives will be valuable in det

23 Although CNV has been reported in several model animal and plant species, the presence of CNV and

24 ing neural activity on a brain-wide scale in model animals and humans is a major goal of neuroscience

25 creatic islets of several different diabetic model animals and is possibly involved in suppression of

26 ation, which we find is conserved in several model animals and plants, its function remains unclear a

27 luate these hypotheses using cichlid fish as model animals, and although differences in attributes pl

28 When transplanted into PD model animals, aphakia mice, and 6-OHDA-lesioned rats, m

29 Precise genetic modifications in model animals are essential for biomedical research.

30 red that, on the basis of recent findings in model animals, are expected to be polygenic and regulato

31 s has begun to shed light on this problem by modelling animals as random walkers with scent-mediated

32 ment, targeting and manipulation of cells of model animals at single-cell resolution.

33 l symptoms, 2) a lack of equivalency between model animal behavior and human psychiatric symptoms, an

34 investigated the behavioral responses of the model animal Caenorhabditis elegans to food depletion an

35 derivatization-based LC-MS approach and the model animal Caenorhabditis elegans to study microbiome-

36 we are able to program the physiology of the model animal Caenorhabditis elegans with logic gates.

37 riteria, FDA also used in vitro, ex vivo and model animal data to ensure there was no increased immun

38 In these bystander models, animals develop ocular lesions but are unable to

39 that the microminipig could serve as a novel model animal for influenza A virus infection.

40 afish have been utilized for many years as a model animal for pharmacological studies on diabetes and

41 erret is a potentially valuable experimental model animal for understanding the evolution and functio

42 ng that establishes oval squid as laboratory model animals for further research on camouflage.

43 Mice are the most commonly used model animals for itch research and for development of a

44 effective use, and inherent limitations, of model animals for psychiatric research.

45 Model animals had fewer active NMJs, detectable by endpl

46 We argue that model animals have great potential to help us understand

47 logenetic analyses of hundreds of genes from model animals have placed flies closer to vertebrates th

48 wever, recent data, primarily obtained using model animal herpesviruses, suggest that viral miRNAs, w

49 Direct assessment of the vascular lesions of model animals in vivo is important for the development o

50 fied platform of GEMs that covers five major model animals, including Mouse1 (Mus musculus), Rat1 (Ra

51 egulate neural development in all bilaterian model animals indicating that they represent a component

52 When tested in a rabbit model, animals inoculated with PS12 were significantly l

53 In a susceptible mouse model, animals inoculated with SARS-CoV-2 were pre-treat

54 gical response of cardiovascular function on model animals is important especially in the early stage

55 C-1alpha) expression were decreased in ADPKD model animal kidneys, with PGC-1alpha expression inverse

56 The Gunn rat, a Crigler-Najjar syndrome model animal lacking UDP-glucuronosyltransferase (UGT1A1

57 Tissue culture models, animal models and human pathological studies are

58 umerous insults in a variety of cell culture models, animal models and in humans.

59 of spermatogenesis occurring in two pivotal model animals - mouse and Caenorhabditis elegans - and c

60 However, in contrast to classical models, animals must learn to estimate value using only

61 ions allow a reinforcement learning agent to model animals' overall performance during the task.

62 These findings indicate that MmuPV1 is a new model animal papillomavirus with which to study sexually

63 f the computational complexity in real-world model animal pedigrees.

64 In a rat contusion SCI model, animals received direct implantation of galantami

65 In the superantigen-induced shock model, animals received rhTFPI (350 mg/kg) subcutaneousl

66 ties and that viral transmissibility between model animals reflects viral transmissibility between hu

67 Despite these challenges, model animals remain valuable for understanding the basi

68 Apparently inconsistent with the CLASH model, animal research relates predictable environments

69 However, large pedigrees of model animal resources often contain repetitive substruc

70 High-density SNP data of model animal resources provides opportunities for fine-r

71 ndependent of the number of generations, for model animal resources such as the Collaborative Cross (

72 onsiderable evidence in humans and mammalian model animals shows that steroid hormones, which are rel

73 stigated the genome-wide diversity of 76 non-model animal species by sequencing the transcriptome of

74 to those shown for transcription factors in model animal species.

75 e phenomenon is still poorly understood, but model animal studies now show that it is stochastic, wit

76 rformed in simpler organisms or in mammalian model animals supports the feasibility of such multidime

77 targeted disruption of STAT1 were used as a model animal system and infected with the viruses it was

78 ns of aging-related mtDNA mutations in other model animal systems.

79 we take a conceptually different approach to modelling animal telemetry data for making RSF inference

80 kappa light chain antibody repertoires of a model animal, the OmniRat, by high throughput antibody s

81 An unlikely model animal, the planarian Schmidtea mediterranea, is p

82 s, and sebaceous glands) for wound repair in model animals, the present study was designed to assess

83 Here, we used Caenorhabditis elegans as a model animal to elucidate key steps in RQ biosynthesis.

84 st viral dynamics in humans and those in the model animal used (here, ferrets) share quantitative sim

85 However, very few Abs are available for model animals used in tuberculosis research, such as non

86 s induced with Galactosamine-LPS and in both models animals were treated with recAP prior to LPS admi

87 nsity and duration of infection in these two models, animals were given anti-gamma interferon monoclo

88 In both models, animals were randomly assigned to 1 of 4 treatme

89 are not toxic to either eukaryotic cells or model animals when administered orally or topically.

90 mpendium of gene expression profiles for non-model animals, which could be employed to identify poten

91 baseline antibody repertoires of unimmunized model animals will be useful as a benchmark for future i

92 mice, which we previously characterized as a model animal with construct, face, and predictive validi

93 We describe a model animal, with a neural system based loosely on the

94 e utilized the high-contrast features of our model animal, zebrafish larvae, including the eyes and t