Resultados de investigación

This dataset comprises spectral global irradiance on the plane of array (tilted) data (Excel files) measured in Madrid using an EKO MS-700 spectroradiometer during 2016–2017 together with a README file explaining how to interpret the Excel files. These data support part of the experimental analysis presented in the following paper: Marco Antonio Zamalloa-Jara, Miguel Ángel Sevillano-Bendezú, Carolin Ulbrich, Gustavo Nofuentes, Rolf Grieseler, Jan Amaru Töfflinger, Overirradiance conditions and their impact on the spectral distribution at low- and mid-latitude sites, Solar Energy, Volume 259, 2023, Pages 99-106, https://doi.org/10.1016/j.solener.2023.05.010 How to cite: Nofuentes, G. (2026). Dataset for "Overirradiance conditions and their impact on the spectral distribution at low- and mid-latitude sites", Solar Energy, Volume 259, 2023, Pages 99-106, https://doi.org/10.1016/j.solener.2023.05.010 [Data set]. Zenodo. https://doi.org/10.5281/zenodo.18169082, Ministerio de Ciencia, Innovación y Universidades. Proyecto "Estimacion de la energia generada por modulos fotovoltaicos de capa delgada: influencia del espectro". ENE2008-05098/ALT

Processivity or number of nucleotides unwound is expressed in base pairs and velocities in base pairs per second., Data can be processed using Origin, Excel or related software.

Oscilloscope measurements of the time response of a MoS2 microdrum resonator actuated electrically with a burst signal. The videos shows different actuation frequency response graphed as a phase space portrait time-dependent. File list: 15MHz.mp4, 18_2MHz.mp4 and 19_6MHz.mp4 Relationship between files: Different actuation frequencies of the same microdrum called J30-Op.9-T3B, Format MP4

Python 3.11 custom written software.

Datasets associated to the publicaton 10.1021/acs.chemmater.5c01878. The readme files for each dataset are within the corresponding folder., All data can be accessed with any program that reads csv and txt. TAS raw data need processing, but processed data is also given.

STM/STS data acquried at IMDEA laboratories, XAS/XMCD/XLD data acquired at ALBA Synchrotron (BOREAS beamline)., The software to open the STP files is WSxM.

Galectin-1 and -9 (Gal1/9) are essential mediators of immune-inflammatory responses, which makes these proteins potential biomarkers for immune-mediated diseases (IMIDs), such as rheumatoid arthritis (RA), psoriasis (PS), psoriatic arthritis (PsA), inflammatory bowel disease, and systemic lupus erythematosus (SLE). Our aim was to evaluate plasma Gal1/9 differences between IMID patients and healthy donors (HD). We analyzed 980 plasma samples divided into two analytical cohorts (600 discovery group and 380 validation group). Generalized linear models estimated Gal1/9 levels, adjusting for sex, age, storage time, and plate variability. In the overall IMID group, plasma Gal1 levels were comparable to those of HD, while Gal9 levels were significantly elevated. Levels varied across individual diseases: SLE patients consistently showed the highest Gal1/9 levels compared to both HD and other IMIDs, and RA patients had elevated Gal9 levels versus HD. Both Gal1 and Gal9 plasma levels correlated positively with higher disease activity, and Gal1 was higher in patients with longer disease duration. After adjustment for these confounders, SLE and RA patients maintained the highest Gal9 levels compared to HD. Our study demonstrates that Gal1 and Gal9 are differentially expressed across IMIDs, with particularly elevated levels in SLE, and both galectins are associated with disease activity.

This repository contains the anonymised participant-level dataset generated during the GLIAS-III study, a prospective multicentre observational cohort investigating continuous glucose monitoring (CGM), glycaemic variability and clinical outcomes in patients with acute ischaemic stroke. The dataset is made publicly available to promote transparency, reproducibility and secondary research while ensuring compliance with applicable ethical and data protection regulations., The repository contains the following files: -GLIASIII_dataset.csv: Anonymised participant-level dataset. -GLIASIII_Metadata.pdf: Complete metadata describing study design, methodology, variables, anonymisation procedures and data processing. It includes the Data Dictionary (definitions, coding and units) -GLIASIII_README.txt: General information and instructions for dataset reuse.

dataset del artículo Mitochondrial function of peripheral lymphocytes: role on multiple sclerosis clinical subtypes y archivo Readme.txt. asociado, AIMS: Multiple sclerosis (MS) is an immune-mediated neurodegenerative disease of unknown etiology, resulting in unmet therapeutic needs. Symptoms heterogeneity and incomplete mechanistic understanding hinder effective patient stratification. We aimed to evaluate the integrated peripheral immune response in established MS clinical subtypes, focusing on differences in mitochondrial function that might validate this stratification and further clarify MS etiology. MATERIALS AND METHODS: Mitochondrial activity of peripheral blood mononuclear cells (PBMCs) upon PHA-stimulation was analysed in MS patients (58 relapsing-remitting (RRMS), 21 secondary progressive (SPMS), and 35 primary progressive (PPMS)) and 35 healthy controls (HC). KEY FINDINGS: In unstimulated conditions, MS patients presented higher mitochondrial ROS (reactive oxygen species) and decreased coupling than HC. Compared with other progressive MS (PMS) subtypes, PBMCs from RRMS presented significantly higher early/late activation and proliferation after PHA stimulation (P = 0.013/P = 0.002, and P = 0.04, respectively), with increased mitochondrial depolarization (P = 0.017). Compared to HC, PHA-stimulated PBMCs from PMS exhibited marked decreases in basal (P = 0.017), maximal, and ATP-linked respiration, increased coupling (P = 0.009), and lower spare respiratory and glycolytic capacities (basal: P = 0.015, maximal: P = 0.064), with parallel decreased GLUT1 expression (P = 0.025). These changes appeared independent of some treatments. SIGNIFICANCE: Upon PHA-stimulation, PMS patients displayed decreased basal, maximal, ATP-linked respiration, and reduced spare respiratory and glycolytic capacities, compared to RRMS and HC, mirroring opposed trends in unstimulated conditions. These findings suggest a severity gradient across MS clinical forms, supporting a disease continuum rather than strictly defined subtypes. The central role of unresolved mitochondrial dysfunction in MS warrants further investigation and may guide novel therapeutic strategies.