246 research outputs found

    DEVELOPING TRAINING PROGRAMS IN REMOTE SENSING AND GEOSPATIAL APPLICATIONS

    Get PDF
    Capacity building programmes of Indian Space Research Organisation (ISRO) are aimed at transfer of technology in the field of Remote Sensing and Geoinformatics for monitoring and sustainable development. ISRO Carries out its capacity building through IIRS, NRSC, SAC, IIST and CSSTEAP. As part of the ISROs’ programmes, NRSC is engaged in the capacity building by conducting Regular, Thematic and Customized training courses to enable the effective utilization of Remote Sensing, Geospatial Technologies and its Applications. The main focus of NRSC training programmes is to develop skill sets in usage of these technologies to the efficient and effective development of the country. The target participants for NRSC training programmes are decision makers, implementers and working professionals, who attend short duration courses of 1, 2 and 12 weeks. This paper provides information on the training courses conducted by NRSC in the field of Geospatial Applications and also, discuss on the methodology to upgrade these training courses using multi-level approach in meeting user needs/requirements more effectively. The flexibility offered by this method by utilizing the web based and other enabling technologies is discussed

    Crisis in the NICU and the Medley with Midazolam

    Get PDF
    Epidemiologic studies of human patients have revealed a correlation between childhood exposure to general anesthetic and sedative agents and subsequent cognitive deficits. This association is supported by data from animal models, which shows that developmental exposure to both anesthetics and sedatives causes lasting impairments in learning. This study focused on midazolam (MDZ), a common benzodiazepine regularly used as a sedative agent on neonates in the Neonatal Intensive Care Unit (NICU). However, a knowledge gap that remains is how long-term exposure to MDZ during very early stages of life impacts synaptic alterations and neurobiological mechanisms. Elucidation of these mechanisms is of high clinical importance and may develop neuroprotective therapeutic strategies for optimizing outcomes for uniquely vulnerable NICU populations. Using a preclinical rodent model system, we mimicked a dose-escalation regimen from postnatal day 3 (P3) pups until P21 to comprehensively characterize how early-life exposure to MDZ impacts neurodevelopment outcomes at different tiers ─ phenotypic, molecular, behavioral, and high throughput- “omics” levels. Our data demonstrated that repetitive exposure to MDZ at an early age stunts neurodevelopment during the early stages of life disrupts the blood-brain barrier, and alters the synaptic components and neurochemistry, which may be indicative of behavioral deficits at later development. Additionally, our bioinformatics analysis from purified synaptosome identified enrichment of proteins associated with actin-binding and protein depolymerization process. One potential hit identified was alpha adducin (ADD1), belonging to the family of cytoskeleton proteins, upregulated in the MDZ group and whose expression was further validated by western blot. Our study has provided a comprehensive characterization of MDZ effects on development at multiple tiers yielding novel insights on how long-term exposure to MDZ impacts development. Notably, the identification of ADD1 as a potential target and further characterization of its downstream mechanisms can give additional insights into its role as a potential therapeutic for treating neurodevelopmental alterations associated with long-term MDZ use in neonates.https://digitalcommons.unmc.edu/chri_forum/1056/thumbnail.jp

    OmniShare : Encrypted Cloud Storage for the Multi-Device Era

    Get PDF
    Two attractive features of cloud storage services are (1) the automatic synchronization of files between multiple devices and (2) the possibility of sharing files with other users. However, many users are concerned about the security and privacy of data stored in the cloud. Client-side encryption is an effective safeguard, but it requires all client devices to have the decryption key. Current solutions derive these keys from user-chosen passwords, which are easily guessed. We present OmniShare, the first scheme to combine strong client-side encryption with intuitive key distribution mechanisms to enable access from multiple client devices and sharing between users. OmniShare uses a novel combination of out-of-band channels (including QR codes and ultrasonic communication), as well as the cloud storage service itself, to authenticate new devices. We describe the design and implementation of OmniShare and explain how we evaluated its security (using formal methods), its performance (benchmarks), and its usability (cognitive walkthrough).Two attractive features of cloud storage services are (1) the automatic synchronization of files between multiple devices and (2) the possibility of sharing files with other users. However, many users are concerned about the security and privacy of data stored in the cloud. Client-side encryption is an effective safeguard, but it requires all client devices to have the decryption key. Current solutions derive these keys from user-chosen passwords, which are easily guessed. We present OmniShare, the first scheme to combine strong client-side encryption with intuitive key distribution mechanisms to enable access from multiple client devices and sharing between users. OmniShare uses a novel combination of out-of-band channels (including QR codes and ultrasonic communication), as well as the cloud storage service itself, to authenticate new devices. We describe the design and implementation of OmniShare and explain how we evaluated its security (using formal methods), its performance (benchmarks), and its usability (cognitive walkthrough).Peer reviewe

    Integrated Land Use-Transport Model System with Dynamic Time-Dependent Activity-Travel Microsimulation

    Get PDF
    The development of integrated land use-transport model systems has long been of interest because of the complex interrelationships between land use, transport demand, and network supply. This paper describes the design and prototype implementation of an integrated model system that involves the microsimulation of location choices in the land use domain, activity-travel choices in the travel demand domain, and individual vehicles on networks in the network supply modeling domain. Although many previous applications of integrated transport demand-supply models have relied on a sequential coupling of the models, the system presented in this paper involves a dynamic integration of the activity-travel demand model and the dynamic traffic assignment and simulation model with appropriate feedback to the land use model system. The system has been fully implemented, and initial results of model system runs in a case study test application suggest that the proposed model design provides a robust behavioral framework for simulation of human activity-travel behavior in space, time, and networks. The paper provides a detailed description of the design, together with results from initial test runs

    Oxaliplatin induces drug resistance more rapidly than cisplatin in H69 small cell lung cancer cells

    Get PDF
    Cisplatin produces good responses in solid tumours including small cell lung cancer (SCLC) but this is limited by the development of resistance. Oxaliplatin is reported to show activity against some cisplatin-resistant cancers but there is little known about oxaliplatin in SCLC and there are no reports of oxaliplatin resistant SCLC cell lines. Studies of drug resistance mainly focus on the cellular resistance mechanisms rather than how the cells develop resistance. This study examines the development of cisplatin and oxaliplatin resistance in H69 human SCLC cells in response to repeated treatment with clinically relevant doses of cisplatin or oxaliplatin for either 4 days or 2h. Treatments with 200ng/ml cisplatin or 400ng/ml oxaliplatin for 4 days produced sublines (H69CIS200 and H69OX400 respectively) that showed low level (approximately 2-fold) resistance after 8 treatments. Treatments with 1000ng/ml cisplatin or 2000ng/ml oxaliplatin for 2h also produced sublines, however these were not stably resistant suggesting shorter treatment pulses of drug may be more effective. Cells survived the first five treatments without any increase in resistance, by arresting their growth for a period and then regrowing. The period of growth arrest was reduced after the sixth treatment and the H69CIS200 and H69OX400 sublines showed a reduced growth arrest in response to cisplatin and oxaliplatin treatment suggesting that "regrowth resistance" initially protected against drug treatment and this was further upregulated and became part of the resistance phenotype of these sublines. Oxaliplatin dose escalation produced more surviving sublines than cisplatin dose escalation but neither set of sublines were associated with increased resistance as determined by 5-day cytotoxicity assays, also suggesting the involvement of regrowth resistance. The resistant sublines showed no change in platinum accumulation or glutathione levels even though the H69OX400 subline was more sensitive to buthionine sulfoximine treatment. The H69CIS200 cells were cross-resistant to oxaliplatin demonstrating that oxaliplatin does not have activity against low level cisplatin resistance. Relative to the H69 cells, the H69CIS200 and H69OX400 sublines were more sensitive to paclitaxel and taxotere suggests the taxanes may be useful in the treatment of platinum resistant SCLC. These novel cellular models of cisplatin and oxaliplatin resistant SCLC will be useful in developing strategies to treat platinum-resistant SCLC

    Protective Role for the Disulfide Isomerase PDIA3 in Methamphetamine Neurotoxicity

    Get PDF
    Methamphetamine abuse continues to be a worldwide problem, damaging the individual user as well as society. Only minimal information exists on molecular changes in the brain that result from methamphetamine administered in patterns typical of human abusers. In order to investigate such changes, we examined the effect of methamphetamine on the transcriptional profile in brains of monkeys. Gene expression profiling of caudate and hippocampus identified protein disulfide isomerase family member A3 (PDIA3) to be significantly up-regulated in the animals treated with methamphetamine as compared to saline treated control monkeys. Methamphetamine treatment of mice also increased striatal PDIA3 expression. Treatment of primary striatal neurons with methamphetamine revealed an up-regulation of PDIA3, showing a direct effect of methamphetamine on neurons to increase PDIA3. In vitro studies using a neuroblastoma cell line demonstrated that PDIA3 expression protects against methamphetamine-induced cell toxicity and methamphetamine-induced intracellular reactive oxygen species production, revealing a neuroprotective role for PDIA3. The current study implicates PDIA3 to be an important cellular neuroprotective mechanism against a toxic drug, and as a potential target for therapeutic investigations

    Coronin 1B Regulates S1P-Induced Human Lung Endothelial Cell Chemotaxis: Role of PLD2, Protein Kinase C and Rac1 Signal Transduction

    Get PDF
    Coronins are a highly conserved family of actin binding proteins that regulate actin-dependent processes such as cell motility and endocytosis. We found that treatment of human pulmonary artery endothelial cells (HPAECs) with the bioactive lipid, sphingosine-1-phosphate (S1P) rapidly stimulates coronin 1B translocation to lamellipodia at the cell leading edge, which is required for S1P-induced chemotaxis. Further, S1P-induced chemotaxis of HPAECs was attenuated by pretreatment with small interfering RNA (siRNA) targeting coronin 1B (∼36%), PLD2 (∼45%) or Rac1 (∼50%) compared to scrambled siRNA controls. Down regulation PLD2 expression by siRNA also attenuated S1P-induced coronin 1B translocation to the leading edge of the cell periphery while PLD1 silencing had no effect. Also, S1P-induced coronin 1B redistribution to cell periphery and chemotaxis was attenuated by inhibition of Rac1 and over-expression of dominant negative PKC δ, ε and ζ isoforms in HPAECs. These results demonstrate that S1P activation of PLD2, PKC and Rac1 is part of the signaling cascade that regulates coronin 1B translocation to the cell periphery and the ensuing cell chemotaxis
    corecore