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.
91,407
datasets available to search
ShareScore release 0.9.0
Dataset results
91,407 results for “Effectiveness”
Figure 3 in Ameliorative effects of morel mushroom (Morchella esculenta) against Cadmium-induced reproductive toxicity in adult male rats
Figure 3. Photomicrograph of seminiferous tubules. (A) Control; showing compact tubules, filled lumen with spermatid, normal germ cell proliferation along epithelium; (B) Cd treated group; showing tubules with empty lumen and degenerated epithelial layer with increased interstitial space; (C) Cd+10 mg extract treated group & (D) Cd+ 20 mg extract treated group; showing minimal damage to epithelium, lumen filled with spermatid and less interstitial space; (E) 10 mg extract alone group and (F) 20 mg extract alone group; showing narrow lumen, increased epithelial height and compact tubules with less interstitial space. Magnification x40. Spermatogonia (SP), Elongated spermatids (ES), Interstitial space (IS), Epithelium (E).
Figure 5 in Ameliorative effects of morel mushroom (Morchella esculenta) against Cadmium-induced reproductive toxicity in adult male rats
Figure 5. Mean ± SEM of plasma testosterone (ng/ml) concentration in rats of control, Cadmium, Cd + 10 mg of extract, Cd +20 mg extract, 10 mg extract and 20 mg extract group. (All values are expressed as Mean ± SEM) (*= P<0.05, ** P<0.01, *** P <0.001, a=control, b= Cadmium, c= Cd+10 mg extract).
Figure 4 in Ameliorative effects of morel mushroom (Morchella esculenta) against Cadmium-induced reproductive toxicity in adult male rats
Figure 4. photomicrograph of cross section of epididymis (cauda) of rats (H&E, 40X) from: (A) Control group; showing normal morphology of cauda epididymis showing compactly arranged tubules with thick epithelium, lumen filled with sperm; (B) Cadmium group; showing marked changes in structure of tubule with decreased concentration of sperm; (C) Cd+10 mg extract group & (D) Cd+ 20 mg extract group; showing regular arrangement of tubules surrounded by stroma, lumen filled with spermatozoa; (E) 10 mg extract alone group and (F) 20 mg extract alone group; showing increase in epithelium an lumen sperm concentration. Spermatozoa (S), Epithelium (E), Stroma (St). G, H and I summarizes the variations in tubule and lumen diameter and height of epithelium.
Figure 1 in Ameliorative effects of morel mushroom (Morchella esculenta) against Cadmium-induced reproductive toxicity in adult male rats
Figure 1. experimental design showing that the control group is treated with ip dosage of saline, 3 groups are treated with ip dosage of Cd, in which 2 received oral dosage of ME, and final 2 groups received oral gavage of ME alone (ME= Morchella esculenta).
Figure 2 in Ameliorative effects of morel mushroom (Morchella esculenta) against Cadmium-induced reproductive toxicity in adult male rats
Figure 2. Fluorescent photomicrograph of sperm DNA, using comet assay, stained with acridine orange. (A) control with more intact DNA; (B) cadmium group with comets; (C) Cd + 10 mg extract group showing intact DNA with a very short tail length; (D) Cd +20 mg extract group having tail of long length and intact DNA; (E) 10 mg extract alone group in which a tail could be notice but very lesser DNA damage was found; (F) 20 mg extract alone group having short tails and intact DNA.
Figure 3 in Effects of combined treatment of cadmium and oxytetracycline on the terrestrial isopod Porcellio leavis
Figure 3. Concentration of biochemical parameters: Total protein, Lipid peroxidation (LPO), Catalase activity (CAT) and Total free amino acids (TFAA) in P. leavis in different treated groups control, Cd, T1, T2, and T3. Values are the mean of three replicates (n=3) ± SE. The significant difference between the groups were analysed by one-way analysis of variance. Mean values of different subscript letters (a,b,c,d) were significantly different (p<0.001).
Figure 6 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 6. Photomicrographs of hepatocytes in control and experimental treated mice. Liver tissue sections stained with oil red O (×200) (A) and scored (B) by the semi-quantitative percentage of damaged area. (Control) control mice and (AEC) treated with C. gracilis extract (250 mg/kg) alone, showed normal structure. (HFD) high fed diet treated mice, showed a significant increase of lipid content; (AEC + HFD) co-treated with high fed diet and alga extract (250 mg/kg), representative micrograph revealed significantly reduced lipid liver content. Values are expressed as the mean ± SD. **p<0.01; ***p <0.001, indicates a significant difference compared to the control group. ++ p<0.01, indicates a significant difference compared to the HFD alone group.
Figure 3 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 3. Effect of ACE supplementation on plasma levels of inflammatory proteins. Data are given as mean ± SD for group of eight mice each. Values are statistically presented as follows: HFD and AEC-treated groups vs. control group: *p <0.05; **p<0.01. HFD + AEC group vs. HFD group: +p <0.05; ++p<0.01.
Figure 2 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 2. Antioxidant activity of different extracts of C. gracilis. Values are mean ± SD of three experimental tests, mg GAE/g DR: mg gallic acid equivalents per g dry residue. Table 4. Effect of AEC on body weight, liver and adipose tissues relative weight of control and treated mice groups.
Figure 5 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 5. Photographs of liver tissues in control and experimental treated mice. Liver tissue sections stained with hematoxylin and eosin (original magnification × 400). (A), in control mice showing normal histoarchitecture and radiating cell arrangement. (B) In mice treated with aqueous extract of C.gracilis (AEC) (250mg/kg) alone showing the normal liver structure. (C) In High fed diet (HFD) mice, representative photograph shows a significant lipid accumulation. (D) In group co-treated with HFD and AEC, was observed the reduction of fat accumulation.
Figure 1 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 1. Phenolic compounds of Cheatomorpha gracilis extract by chemical High Performance Liquid Chromatography (HPLC) analysis (gallic acid, Rutin, quercetin, Apegenin, kaempferol and Naringenin).
Figure 4 in Potential Hepatoprotective Effect of Cheatomorpha gracilis extract against High Fat Diet (HFD)-Induced Liver Damage, and its characterization by HPLC
Figure 4. Effects of C.gracilis aqueous extract (AEC) on TBARS and protein carbonyls products (PCO) in HFD-treated mice. TBARS: thiobarbituric acid reactive substance. Data are presented as mean ± SD, n =8. *P≤ 0.05, **P≤ 0.01 compared with the control group. +P ≤0.05, ++P ≤0.01 as compared with HFD- treated mice.
Figure 6 in Effect of calcium on Pseudomonas aeruginasa and Bacillus cereus metabolites
Figure 6. Pyorubin production of P. aeruginosa (●), grown in NB medium under static conditions at 37 °C.
Figure 4. H O in Effect of calcium on Pseudomonas aeruginasa and Bacillus cereus metabolites
Figure 4. H O diameter of B. cereus (○) and P. aeruginosa (●), 2 2 grown in NB medium under static conditions at 37 °C.
Figure 3. Las B in Effect of calcium on Pseudomonas aeruginasa and Bacillus cereus metabolites
Figure 3. Las B activity of B.cereus (○) andP.aeruginosa (●), grown in NB medium under static conditions at 37 °C.
Figure 2 in Effect of calcium on Pseudomonas aeruginasa and Bacillus cereus metabolites
Figure 2. Biofilm levels ofB.cereus (○) and P.aeruginosa (●), grown in NB medium under static conditions at 37 °C.
Figure 1 in Effect of calcium on Pseudomonas aeruginasa and Bacillus cereus metabolites
Figure 1. Amylase unit activity of B. cereus (○) and P. aeruginosa (●), grown in NB medium under static conditions at 37 °C.
Figure 1 in Effects of nitrogen and phosphorus availability on the early growth of two congeneric pairs of savanna and forest species
Figure 1. On that figure are the logarithms of root-to-shoot ratio square root in two pairs of congeneric species. The forest houses data from two species (E. contortisiliquum and S. grandiflorum), as do the savanna (E. gummiferum and S. lycocarpum). The complete solution is represented by Com; The solution without N by -N; The solution without P by -P; The solution without both nutrients by -NP.
Figure 1 in Effects of Indole-3-Butyric Acid (IBA) and rooting media on rooting and survival of air layered wax apple (Syzygium samarangense) CV Jambu Madu
Figure 1. Effects of different rooting media and various concentrations of IBA on the rooting of wax apple air layers. M C: Sphagnum 1 0 moss (wet) + IBA 0 mg L-1, M C: Vermicompost + IBA 0 mg L-1, M C: Garden soil + IBA 0 mg L-1, M C: Sphagnum moss (wet) + 2 0 3 0 1 1 IBA 1000 mg L-1, M C: Vermicompost + IBA 1000 mg L-1, M C: Garden soil + IBA 1000 mg L-1, M C: Sphagnum moss (wet) + IBA 2 1 3 1 1 2 1500 mg L-1, M C: Vermicompost + IBA 1500 mg L-1, M C: Garden soil + IBA 1500 mg L-1, M C: Sphagnum moss (wet) + IBA 2000 mg 2 2 3 2 1 3 L-1, M C : Vermicompost + IBA 2000 mg L-1 and M C : Garden soil + IBA 2000 mg L-1.
Figure 3 in Effects of Indole-3-Butyric Acid (IBA) and rooting media on rooting and survival of air layered wax apple (Syzygium samarangense) CV Jambu Madu
Figure 3. Survival rate of air layers (%) of wax apple as affected by different concentrations of IBA and growing media after detaching from mother plants. M C: Sphagnum moss (wet) + IBA 1000 mg L-1, M C: Vermicompost + IBA 1000 mg L-1, M C: Garden soil + IBA 1 1 2 1 3 1 1000 mg L-1, M C: Sphagnum moss (wet) + IBA 1500 mg L-1, M C: Vermicompost + IBA 1500 mg L-1, M C: Garden soil + IBA 1500 mg L-1, 1 2 2 2 3 2 M C : Sphagnum moss (wet) + IBA 2000 mg L-1, M C : Vermicompost + IBA 2000 mg L-1 and M C : Garden soil + IBA 2000 mg L-1.
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.