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  • Microcracks accumulate around the inner ear. These data represent intersections of microcracks in the human otic capsule with unbiased stereological line grids. The allow the calculation of the surface density (mm2/mm3) of microcracks.
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  • A virus is a small infectious agent that replicates only inside the living cells of an organism. Viruses can infect all types of life forms, from animals and plants to microorganisms, including bacteria and archaea. In evolution, viruses are an important means of horizontal gene transfer, which increases genetic diversity in a way analogous to sexual reproduction. Influenza (Including (COVID-19), is an infectious disease caused by an influenza virus. Some viruses especially smallpox, throughout history, has killed between 300-500 million people in its 12,000-year existence. As modern humans increased in numbers, new infectious diseases emerged, including SARS-CoV-2. We have two groups of virus, RNA and DNA viruses. The most brutal viruses are RNA ones like COVID-19 (Sars-CoV-2
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  • Dataset for modeling risky driver behaviors based on accelerometer (X,Y,Z axis in meters per second squared (m/s2)) and gyroscope (X,Y, Z axis in degrees per second (°/s) ) data. Sampling Rate: Average 2 samples (rows) per second Cars: Ford Fiesta 1.4, Ford Fiesta 1.25, Hyundai i20 Drivers: 3 different drivers with the ages of 27, 28 and 37 Driver Behaviors: Sudden Acceleration (Class Label: 1), Sudden Right Turn (Class Label: 2), Sudden Left Turn (Class Label: 3), Sudden Break (Class Label: 4) Best Window Size: 14 seconds Sensor: MPU6050 Device: Raspberry Pi 3 Model B Please See Summary Table for summary of the collected data.
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  • How precise is quantitative prediction of drug-drug interactions and genotype from in vitro data: A comprehensive analysis on the example CYP2D6 and CYP2C19 substrates -Supplementary material
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  • Experimental data
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  • Hardware design for build a Step Width System Capture
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  • Different human linker histone (H1) variants are expected to have distinct binding modes to the nucleosome. The position and orientation of a number of different H1 globular domains on the nucleosome were investigated through molecular docking using MGLTools and HADDOCK. The nucleosome core and linker DNA in the GH5-chromatosome structure (PDB: 4QLC) were used as a docking template. GH5 (in PDB: 4QLC) was re-docked to this template to test the docking algorithm. Docked and re-docked GH5 compared well. The docking algorithm was further tested by docking the NMR solution structure of the globular domain of chicken H1 (GH1, PDB: 1GHC) to the nucleosome template. The position of docked GH1 on the nucleosome agreed with literature. 
The N-terminal - and globular domain H1x hybrid (NGH1x) was studied using solution NMR in both low (20 mM sodium phosphate, pH 7.0) and high (20 mM sodium phosphate, 1 M sodium perchlorate, pH 7.0) ionic strength conditions (de Wit, H., Vallet, A., Brutscher, B. et al. Biomol NMR Assign (2019) 13: 249. https://doi.org/10.1007/s12104-019-09886-x). These low and high ionic strength structures were docked to the nucleosome template. 
Homology (MODELLER) and ab initio modeling (CS-ROSETTA) were employed to model structures for other human H1 globular domains: GH1.0, GH1.4, GH1oo, and GH1t. The modeled structures were also docked to the nucleosome template.
 All the docking procedures listed above produced 100 models of different energies. In each case, the lowest energy docked model was chosen. The structures of all the H1 globular domains that were docked to the template are given as PDB files (1GHC_lowest_energy.pdb; 2LSO_lowest_energy.pdb; GH5_re-docked_position.pdb; NGH1x_high_salt_NTD.pdb; NGH1x_low_salt_NTD.pdb; modeled_GH1_0_lowest_energy.pdb; modeled_GH1_4_lowest_energy.pdb; modeled_GH1oo_lowest_energy.pdb; modelled_GH1t_lowest_energy.pdb) in the data file. The nucleosome template structure is also given in PDB file format (4QLC_nucleosome_without_GH5.pdb). Finally, the docked models are also given (GH5-chromatosome.pdb; 1GHC-chromatosome.pdb; 2LSO-chromatosome.pdb; GH1_0-chromatosome.pdb; GH1_4-chromatosome.pdb; GH1oo-chromatosome.pdb; GH1t-chromatosome.pdb; NGH1x_no_salt-chromatosome.pdb; NGH1x_salt-chromatosome.pdb). The files are compatible with most molecular graphics software. The file Dockings_modelling_test_and_results.pdf provides the modeling and docking results in figures and tables. A short description of each figure and table is given within the PDF file.
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  • Supplementary materials for publication JAAD-D-19-02716 (Lim et al. Novel Mutations Identified by Whole Exome Sequencing in Acral Melanoma. J Am Acad Dermatol. 2020) Supplementary Appendix 1: Detailed methods Supplementary Appendix 2: Clinical details of 31 acral melanoma patients including 7 nail apparatus melanoma patients Supplementary Appendix 3: Single nucleotide variations and small indels identified through WES Supplementary Appendix 4: Several genes whose mutations were repeatedly detected in this study and previously reported in the literature in association with melanoma Supplementary Appendix 5: Previous studies on the association of CSMD3 and EHMT1 with malignancies
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  • The descriptive data presented in this article is used to measure the level of student’s satisfaction with university facilities which are provided by the university as well as the government. This study involved 280 respondents comprising diploma, bachelor degree and post graduate student at Malaysian Public University. An open-ended question with 10 Likert Scale was distributed to respondents to identify the level of student’s satisfaction with the facilities provided by the university. The one to 10 scale measurements starting with one is Strongly Dissatisfied to 10 is Strongly Satisfied has been used to measure the level of student’s satisfaction towards 14 facilities at the university.
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  • Explanation and description of the microscopic data of mice tissue histology under concern by the Editor's of Plos One
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