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

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

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

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

7 igenesis, embryogenesis, and inflammation in model animals.

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

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

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

11 to prolong lifespan in various experimental model animals.

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

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

14 Model animal and fungal proteins are included in the dat

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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