Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
292
datasets available to search
ShareScore release 0.9.0
Dataset results
292 results for “rabbits”
Fig. 6 Serum miRNA profile analysis among different groups. a in A combined miRNA-piRNA signature in the serum and urine of rabbits infected with ToxoplaSMa gondii oocysts
Fig. 6 Serum miRNA profile analysis among different groups. a The volcano plot shows the individual statistically significant miRNA between acutely infected group and control group. In this plot, the x-axis is log2 fold-change, which shows the direction of the change (negative scale is decrease and positive scale is increase) in the levels of miRNA expression, while the y-axis is the –log10 FDR, which shows the significance of the change. b The volcano plot shows the individual statistically significant miRNA between chronically infected rabbits and control rabbits. c The volcano plot shows the individual statistically significant miRNA between acutely infected rabbits and chronically infected rabbits. d Venn diagram shows number of differentially expressed miRNA among different comparison pairs. FDR represents false discovery rate
Fig. 7 Serum piRNA profile analysis among different groups. a in A combined miRNA-piRNA signature in the serum and urine of rabbits infected with ToxoplaSMa gondii oocysts
Fig. 7 Serum piRNA profile analysis among different groups. a The volcano plot shows the individual statistically significant piRNA between acutely infected rabbits and control rabbits. In this plot, the x-axis is log2 fold-change, which shows the direction of the change (negative scale is decrease and positive scale is increase) in the levels of piRNA expression, while the y-axis is the –log10 FDR, which shows the significance of the change. b The volcano plot shows the individual statistically significant piRNA between chronically infected rabbits and control rabbits. c The volcano plot shows the individual statistically significant piRNA between acutely infected rabbits and chronically infected rabbits. d Venn diagram shows number of differentially expressed piRNA among different comparison pairs. FDR represents false discovery rate
Fig. 3 in A combined miRNA-piRNA signature in the serum and urine of rabbits infected with ToxoplaSMa gondii oocysts
Fig. 3 Global view of temporal sRNA expression profiles in rabbit serum during T. gondii infection. a The sRNA correlation heatmap of sample clustering. b Principal component analysis of all identified serum sRNA. c Unsupervised hierarchical clustering of sRNA profiling data. sRNA intensity is normalized so that blue represents low intensity and yellow represents high intensity. Columns are hierarchically clustered based on a complete linkage using Pearson correlation coefficients as the distance measure. Sample groups including acutely infected rabbits, chronically infected rabbits and uninfected control rabbits are labeled as AI, CI and Con, respectively
Fig. 2 in A combined miRNA-piRNA signature in the serum and urine of rabbits infected with ToxoplaSMa gondii oocysts
Fig. 2 First nucleotide bias of obtained small RNA in serum samples of rabbits. a First nucleotide bias of known miRNAs in rabbit serum. b First nucleotide bias of predicted miRNAs in rabbit serum. c First nucleotide bias of predicted piRNAs in rabbit serum
Fig. 9 Urine piRNA profile analysis among different groups. a in A combined miRNA-piRNA signature in the serum and urine of rabbits infected with ToxoplaSMa gondii oocysts
Fig. 9 Urine piRNA profile analysis among different groups. a The volcano plot shows the individual statistically significant piRNA between acutely infected group and control group. In this plot, the x-axis is log2 fold-change, which shows the direction of the change (negative scale is decrease and positive scale is increase) in the levels of piRNA expression, while the y-axis is the –log10 FDR, which shows the significance of the change. b The volcano plot shows the individual statistically significant piRNA between chronically infected group and control group. c The volcano plot shows the individual statistically significant piRNA between acutely infected group and chronically infected group. d Venn diagram shows number of differentially expressed piRNA among different comparison pairs
Figure 2 in Expression and immunolocalisation of TpFABP as a candidate antigen for the serodiagnosis of rabbit Taenia pisiformis cysticercosis
Figure 2. Expression of rTpFABP and identification by rabbit antisera in western blotting. Lane (1) molecular weight markers; (2) purified rTpFABP protein; (3) rTpFABP protein reacted with negative rabbit serum (1:100 v/v dilutions) by western blotting analysis; (4) rTpFABP protein reacted with rabbit antisera (1:100 v/v dilutions) by western blotting analysis. Molecular masses (kDa) are indicated on the left.
Figure 1 in Expression and immunolocalisation of TpFABP as a candidate antigen for the serodiagnosis of rabbit Taenia pisiformis cysticercosis
Figure 1. Structural analysis of TpFABP. Alignment of the amino acid residue sequences of Taenia pisiformis FABP with T. solium and Echinococcus granulosus in primary structures. The secondary structure of the TpFABP amino acid residue sequence was predicted and is shown at the top of the alignment. The light-grey shading indicates the identical amino acid sequences, and locations of linear B-cell epitopes are marked with open boxes. TpFABP1, GU205472; TsFABP1, HQ259679; TsFABP2, AFS64570; EgFABP1, 1O8V_A; EgFABP2, AAK12095; H-FABP, NP_004093.
Figure 4 in Expression and immunolocalisation of TpFABP as a candidate antigen for the serodiagnosis of rabbit Taenia pisiformis cysticercosis
Figure 4. Dot-ELISA of naturally infected rabbit experimental sera with rTpFABP. The tan-yellow tint shows the positive reaction: A, negative control sera; B, positive antisera; C, sera at 0 day postinfection; D, sera at 7 days post-infection; E, sera at 14 days post-infection; F, sera at 21 days post-infection; G, sera at 28 days post-infection; H, sera at 35 days post-infection; I, sera at 42 days post-infection; J, sera at 49 days post-infection.
Figure 3 in Expression and immunolocalisation of TpFABP as a candidate antigen for the serodiagnosis of rabbit Taenia pisiformis cysticercosis
Figure 3. Immunolocalisation of TpFABP in T. pisiformis tapeworm and cysticercus. The yellowish-brown tint shows the TpFABP protein location. (A) negative sera in cysticercus; (B) antisera in cysticercus; (C) negative sera in adult tapeworm; (D) antisera in adult tapeworm. Arrows indicate the areas of the parasite: MT, microthrix; DC, distal cytoplasm; PC, perinuclear cytoplasm; GD, gathering duct; M, microtrichia; ICW, inside the layer of cystic wall; OCW, outer layer of cystic wall; MCW, middle layer of cystic wall. Scale bars: 20 µm.
Figure 5 in Effect of season and housing systems on various physiobehavioral attributes of local breed of rabbits (Oryctolagus cuniculus) in Southern Punjab, Pakistan
Figure 5. Effect of seasons on TSL of male rabbits under cage system. Data is mean (± SE) and different letters on the bars depict statistical difference at (p ≤ 0.05) for seasons.
Figure 4 in Effect of season and housing systems on various physiobehavioral attributes of local breed of rabbits (Oryctolagus cuniculus) in Southern Punjab, Pakistan
Figure 4. Effect of housing system on various physiological attributes of rabbits. Data is mean (± SE). Similar letters on the bars indicate non-significant (p ≥ 0.05) difference within caged and colony reared rabbits for rectal temperature. Different letters on the bars indicate significant (p ≤ 0.05) difference within caged and colony reared rabbits for respiration rate.
Fig. 1 in Variable changes in nematode infection prevalence and intensity after Rabbit Haemorrhagic Disease Virus emerged in wild rabbits in Scotland and New Zealand
Fig. 1. Differences in mean intensity of nematode parasite infection in rabbits sampled seasonally from New Zealand and Scotland before the spread of RHDV (a), rabbits sampled seasonally from Sotland before and after RHDV (b), and rabbits sampled in autumn season from New Zealand and Scotland before and after RHDV (c). Nematode parasites included T. retortaeformis (i) G. strigosum (ii) and P. ambiguus (iii) found in rabbits sampled in spring (Spr), summer (Sum), autumn (Aut) and winter (Win).
A magnetic resonance multi-atlas for the neonatal rabbit brain - Dataset
<p>Dataset related to the Neuroimage paper https://doi.org/10.1016/j.neuroimage.2018.06.029. Download links, documentation and code for the manipulation are available from the software repository https://github.com/gift-surg/SPOT-A-NeonatalRabbit</p>
Dataset including records from the first two generation of selection for feed efficiency in three rabbits lines
<p>This dataset include records from the first two generation of selection of three rabbit lines. The objective was to improve feed efficiency accounting for social interactions within cage. In two lines the feed intake control is done using an electronic feeder, and in the third feed intake is controled at cage level. In the excel book provided, the date from the different lines are recorded in different pages.</p> <p>This dataset has been generated within Feed-a-Gene (H2020) and GENEF (Spanish INIA) projects. It is presented to fullfit the requeriments of Milestone 22 of Feed-a-Gene. This milestone basically aims to show that a selection experiment for feed efficiency on rabbits, accounting for social interactions, can be operationally conducted using an electronic feeder to record individual feed intake of animals raised in groups. This device has also been developed within the frame of these two projects.</p> <p> </p> <p> </p> <p> </p> <p> </p> <p> </p>
Figure 1 in Cardiotoxic effects of enrofloxacin on electrophysiological activity, cardiac markers, oxidative stress, and haematological findings in rabbits
Figure 1. Histological examination of rabbit heart in the negative control (A) shows normal morphology. Histological examination of rabbit heart in group 1 (B) and group 2 (C) shows normal morphology except for some minor abnormalities including hyperaemia in some areas (H&E, 400×).
Figure S1 in mtDNA diversity in a rabbit population from Sicily (Italy)
Figure S1. Multiple sequence alignment of Oryctolagus cuniculus cyt b mtDNA from different individuals. GenBank accession numbers are indicated in Table 1. The single enzyme restriction sites are highlighted in colors/gray.
Figure S2 in mtDNA diversity in a rabbit population from Sicily (Italy)
Figure S2. Shading of the multiple alignment of Oryctolagus cuniculus cyt b mtDNA sequences from different individuals shown in Figure S1. Identical nucleotides are indicated.
Figure 1 in First release of a captured Sumatran striped rabbit Nesolagus netscheri (Schlegel, 1880) into the wild
Figure 1. Two young individuals of N.netscheri received by Nature Conservation Agency of Bengkulu Province from local people, late September 2021, Rejang Lebong District, Bengkulu Province (Photo: Said Jauhari).
Fig. 6 in Three new species of Eimeria (Apicomplexa: Eimeriidae) from the Amami rabbit, Pentalagus furnessi (Mammalia: Leporidae)
Fig. 6. Line drawings of the Eimeria species detected in the Amami rabbit. (a) Eimeria furnessi. (b) Eimeria hilleri. (c) Eimeria sagentae. Scale bar = 10 μ
Fig. 4 in Three new species of Eimeria (Apicomplexa: Eimeriidae) from the Amami rabbit, Pentalagus furnessi (Mammalia: Leporidae)
Fig. 4. Nomarski interference contrast photographs of oocysts of Eimeria hilleri from the Amami rabbit stored in a potassium dichromate solution. M: micropyle; N: nucleus; OWo: outer layer of the wall; OWi: inner layer of the wall; RB: refractile body; SB: Stieda body; SR: sporocyst residuum; SSB: substieda body. Scale bars (all in the same scale) = 10 μm.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.