mHeart - mHealthCare Platform Adapted to the Heart Transplant Population - Technical Specifications and Software Source Code
Contributors: Mar Gomis-Pastor, Mª Antonia Mangues, Vicente Pellicer
... The information is provided to increase the data transparency and the scalability of eHealth research and particularly the mHeart studies scalability. This dataset contains relevant information on: - The mHealthCare Platform Technological Description and Specifications. This file aims to describe the general mHealthcare Platform developed by the private firm which has been thereafter adapted to the heart transplant specifications (mHeart System). - The mHeart source code of the 3 applications (website, app Android, app Apple) description and storage location. - A video of the clinical use of the mHeart mobile application. - An apk file with a DEMO (Spain Version 2015). Please, notice that this is a dynamic process. Multiples versions will be uploaded since mHeart was developed. Consult the DEMO access directly on Stores. - User Guidelines (Spain Version 2015) - Scientific Authorship Statement - mHeart trademark - the mHeart System funding and reimbursement model. The mHealthCare Platform is an internet-based system to carry out integral healthcare for disease and therapy management in any population. The first version uploaded in Hospital de la Santa Creu i Sant Pau (HSCSP) was directed at transplant populations and was specifically adapted to the heart transplant population in the ambulatory setting. The mHeart program has been classified by authors as a Behavior Intervention Technology (BIT) to facilitate the following overall clinical goals: (1) health behavior change (i.e. increase patients’ healthy behaviors and prevent the onset of disease); and (2) targeted disease management (i.e. facilitate therapeutic interventions and improve patient’s self-management). The mHeart tool is a mobile phone app connected to a website for use by providers and patients. The tool can be used simultaneously on distinct devices to facilitate caregiver and guardian support. The mobile application can be downloaded for free from the Google and Apple online stores. The website link is salud.trilema.es. The system was developed by Socioemprende SL Technical Team. Scientific advice was provided by the heart transplant interdisciplinary healthcare team and directed by the Pharmacy Department, HSCSP. For further questions about the System, please contact with the scientific coordinator Mar Gomis-Pastor: firstname.lastname@example.org
Morphology and lifestyle of endophytic fungi associated with roots of Gaylussacia brasiliensis (Ericaceae) in southern Brazil sand dunes
Contributors: Kelly Besen
... Gaylussacia brasiliensis hair roots, revealing wide morphological diversity. Pezizomicotina fungi have been found in healthy ericaceous roots, showing several morphological structures of the symbiotic association. Morphological and sequencing analyses of seven isolates revealed that they belong to the genera Penicillium, Paraconiothyrium, Cladophialofora, Knufia, Diaporthe, Chaetomium, and Arcopilus. It appears that there are as many association structures as there are fungi capable of producing them.
Asymmetric centromeres differentially coordinate with mitotic machinery to ensure biased sister chromatid segregation in germline stem cells
Contributors: Rajesh Ranjan
... Many stem cells utilize asymmetric cell division (ACD) to produce a self-renewed stem cell and a differentiating daughter cell. How non-genic information could be inherited differentially to establish distinct cell fates is not well understood. Here, we report a series of spatiotemporally regulated asymmetric components, which ensure biased sister chromatid attachment and segregation during ACD of Drosophila male germline stem cells (GSCs). First, sister centromeres are differentially enriched with proteins involved in centromere specification and kinetochore function. Second, temporally asymmetric microtubule activities and polarized nuclear envelope breakdown allow for the preferential recognition and attachment of microtubules to asymmetric sister kinetochores and sister centromeres. Abolishment of either the asymmetric sister centromeres or the asymmetric microtubule activities results in randomized sister chromatid segregation. Together, these results provide the cellular basis for partitioning epigenetically distinct sister chromatids during stem cell ACDs, which opens new directions to study these mechanisms in other biological contexts.
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DATA: Accommodation of manganese into hydroxyapatite and segregation pathway involved in the formation of Mn3O4 nanoparticles
Contributors: Euler Araujo dos Santos
... Raw data and Rietveld refined data used in the article.
Contributors: Eusebio de la Fuente
... This dataset contain the code, test videos and the results of the developed algorithm. The detection is based on texture analysis using the LBP technique.
Data/Software for "Presynaptic Mitochondria Volumes and Complexity of Subsynaptic Distribution Increase During Development at a High-fidelity Synapse"
Contributors: Connon I. Thomas, Christian Keine, Satoko Okayama, Rachel Satterfield, Morgan Musgrove, Debbie Guerrero-Given, Naomi Kamasawa, Samuel M. Young, Jr.
... Contains data and software from the publication: "Presynaptic Mitochondria Volumes and Complexity of Subsynaptic Distribution Increase During Development at a High-fidelity Synapse" currently under review. The preprint to this data set has been published on bioRxiv (https://doi.org/10.1101/689653). In this study, we created a helper-dependent adenoviral vector (HdAd) to co-express cytoplasmic EGFP and a genetically encoded peroxidase marker (mito-APEX2) at the calyx of Held, an excellent model for deciphering regulatory mechanisms of presynaptic function. ABSTRACT: The calyx of Held, a large glutamatergic presynaptic terminal in the auditory brainstem undergoes developmental changes to support the high action-potential firing rates required for auditory information encoding. In addition, calyx terminals are morphologically diverse which impacts vesicle release properties and synaptic plasticity. Mitochondria influence synaptic plasticity through calcium buffering and are crucial for providing the energy required for synaptic transmission. Therefore, it has been postulated that mitochondrial levels increase during development and contribute to the morphological-functional diversity in the mature calyx. However, the developmental profile of mitochondrial volumes and subsynaptic distribution at the calyx of Held remains unclear. To provide insight on this, we developed a helper-dependent adenoviral vector (HdAd) that expresses the genetically encoded peroxidase marker for mitochondria, mito-APEX, at the mouse calyx of Held. We developed protocols to detect labeled mitochondria for use serial block face SEM (SBF-SEM) to carry out semi-automated segmentation of mitochondria, high-throughput whole terminal reconstruction and presynaptic ultrastructure in mice of either sex. Subsequently, we measured mitochondrial volumes and subsynaptic distributions at the immature postnatal day 7 (P7) and the mature (P21) calyx. We found an increase of mitochondria volumes in terminals and axons from P7 to P21 but did not observe differences between stalk and swelling subcompartments in the mature calyx. Based on these findings, we propose that mitochondrial volumes developmentally increase to support high firing rates but have limited contribution to morphological-functional diversity at the calyx. Data are sorted by the figures they appear in. Media (movies and 3D models) and custom-written software are located in separate folders.
Contributors: Nathaniel Hathaway
... Raw data from Headley et al. 2019.
Evaluation of a virtual basic dermatology curriculum for dermoscopy using the Triage Amalgamated Dermoscopic Algorithm (TADA) for novice dermoscopists.
Contributors: Jason Susong
... Supplemental Diagrams and Video.
Contributors: UnaElsLive Natra, mdgmatest5 live
... RDM - File Type Support 21May2019 ElsCustomer Apart from .u3d all files preview [ .obj / .ply / .vtk / .stl / .ent / .brk / .pdb / .pse / .mol / .mol2 / .cif / .u3d / .dcm / .nii] - .pse is not supported
Contributors: Carlos Palacio
... Raw data for the internal Project 2016210 "Preparation and characterization of magnetic nanoparticles based in ferrites"--> UAN-UdeA.