1,159 research outputs found

    Genomics of lung cancer:tumor evolution, heterogeneity and drug resistance

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    Evaluation of Vaca and Caga Genotypes of Helicobacter Pylori in Iranian Patients with Peptic Ulcer Disease

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    Helicobacter pylori infection occurs all over the world, and more than half of the world population is infected by this microorganism. Research on the variety of H. pylori genes is valuable from two perspectives; first, for predicting the outcome of the infection and second, for better understanding of its distribution in the world and the evolutionary origins of this organism. It has been suggested that Helicobacter pylori strains containing cagA gene and the s1/m1 genotype of vacuolating cytotoxin gene A (vacA) may be associated with peptic ulcer diseases. Some studies have also shown that allele s1 of the vacA gene is associated with gastroduodenal diseases In order to investigate the cagA and vacA genes, biopsies of the antrum and corpus of the stomachs of patients were obtained. To detect H. pylori infection, the phosphoglucosamine mutase gene (glmM) was amplified through the PCR method and observed on 2% (w/v) agarose gel electrophoresis. All the H. pylori-positive samples were subjected to further PCR amplification to determine different alleles of the vacA gene. The PCR products were separated on 2% (w/v) agarose gels electrophoresis. 37, 15 and 32 out of 84 specimens were duodenal ulcer (DU), gastric ulcer (GU) and gastritis (GT), respectively. Seventy-seven (91.7%, χ2= 58.333, p < 0.05) out of 84 samples were H. pylori-positive. cagA gene was detected in 80% (χ2= 12.6, p < 0.001), 76.9% (χ2= 3.769, p > 0.05), and 48.3% (χ2= 0.034 p > 0.05) from DU, GU and GT samples, respectively. It was found that 66% (23/35) of DU samples, 62% (8/13) of GU samples and none of 29 GT samples were s1/m1. 17% (6/35) of DU samples, 15% (2/13) of GU samples and 52% (16/29) of GT samples were s1/m2. 17% (6/35) of DU samples, 23% (3/13) of GU samples and 48% (13/29) of GT samples were s2/m2. This study demonstrates that the presence of the m2 allele of vacA is strongly associated with gastritis and the presence of allele s1 is associated with peptic ulcers. Helicobacter pylori strains with vacA-s1/m2-cagA+ genotype are associated with peptic ulceration diseases

    Utilizing CRISPR as a Novel Tool for the Induction of Cell Reprogramming

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    Researchers can now target specific DNA sequences and easily modify them thanks to recent developments in CRISPR technology, enabling genome manipulation with unmatched precision. Furthermore, cell reprogramming is one of the most fascinating fields in which CRISPR-based techniques are being used. Nowadays, without using embryonic stem cells, scientists can change one type of cell into another by inserting particular genetic alterations. This has significant implications for regenerative medicine since it enables the creation of transplantable cell lines that are patient-specific

    Sensitive and rapid spectrophotometric methods for sertraline monitoring in pharmaceutical formulations

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    Purpose: To develop simple, rapid, and selective spectrophotometric methods for the assay of sertraline in a pharmaceutical formulation. Method: These methods depend on the formation of colored ion-pair complexes between the drug and five different reagents; methyl blue (MB), bromophenol red (BPR), methyl green (MG), phenol red (PR), and methyl orange (MO) in B-R buffer solutions of pH ranging from 2.0 – 8.0. The colored products were measured at 668, 747, 647, 717, and 553 nm, respectively. Results: The calibration graphs were linear over the concentration range of 2 – 18 μg/mL for MB and BPR, and 2 – 16 μg/mL for MG, PR, and MO. In all cases, the reaction stoichiometry was 1:1. The proposed methods were successfully applied to solid-dose pharmaceutical preparations (tablets). Excipients in the commercial formulation did not interfere with the analysis. Conclusion: The investigated methods can be recommended for routine analysis and quality control where cost-effectiveness, high specificity of the analytical technique, and time are of great importance

    Leveraging FAERS and Big Data Analytics with Machine Learning for Advanced Healthcare Solutions

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    This research study explores the potential of leveraging the FDA Adverse Event Reporting System (FAERS), combined with big data analytics and machine learning techniques, to enhance healthcare solutions. FAERS serves as a comprehensive database maintained by the U.S. Food and Drug Administration (FDA), encompassing reports of adverse events, medication errors, and product quality issues associated with diverse drugs and therapeutic interventions.By harnessing the power of big data analytics applied to the vast information within FAERS, healthcare professionals and researchers gain valuable insights into drug safety, discover potential adverse reactions, and uncover patterns that may not have been discernible through traditional methods. Particularly, machine learning plays a pivotal role in processing and analyzing this extensive dataset, enabling the extraction of meaningful patterns and prediction of adverse events.The findings of this study demonstrate various ways in which FAERS, big data analytics, and machine learning can be leveraged to provide advanced healthcare solutions. Machine learning algorithms trained on FAERS data can effectively identify early signals of adverse events associated with specific drugs or treatments, allowing for prompt detection and appropriate actions.Big data analytics applied to FAERS data facilitate pharmacovigilance and drug safety monitoring. Machine learning models automatically classify and analyze adverse event reports, efficiently flagging potential safety concerns and identifying emerging trends.The integration of FAERS data with big data analytics and machine learning enables signal detection and causality assessment. This approach aids in the identification of signals that suggest a causal relationship between drugs and adverse events, thereby enhancing the assessment of drug safety.By analyzing FAERS data in conjunction with patient-specific information, machine learning models can assist in identifying patient subgroups that are more susceptible to adverse events. This information is instrumental in personalizing treatment plans and optimizing medication choices, ultimately leading to improved patient outcomes.The combination of FAERS data with other biomedical information offers insights into potential new uses or indications for existing drugs. Machine learning algorithms analyze the integrated data, identifying patterns and making predictions about the efficacy and safety of repurposing existing drugs for new applications.The implementation of FAERS, big data analytics, and machine learning in advanced healthcare solutions necessitates meticulous consideration of data privacy, security, and ethical implications. Safeguarding patient privacy and ensuring responsible data use through anonymization techniques and appropriate data governance are paramount.The integration of FAERS, big data analytics, and machine learning holds immense potential in advancing healthcare solutions, enhancing patient safety, and optimizing medical interventions. The findings of this study demonstrate the multifaceted benefits that can be derived from leveraging these technologies, paving the way for a more efficient and effective healthcare ecosystem

    Perturbative Analysis of Spectral Singularities and Their Optical Realizations

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    We develop a perturbative method of computing spectral singularities of a Schreodinger operator defined by a general complex potential that vanishes outside a closed interval. These can be realized as zero-width resonances in optical gain media and correspond to a lasing effect that occurs at the threshold gain. Their time-reversed copies yield coherent perfect absorption of light that is also known as an antilaser. We use our general results to establish the exactness of the n-th order perturbation theory for an arbitrary complex potential consisting of n delta-functions, obtain an exact expression for the transfer matrix of these potentials, and examine spectral singularities of complex barrier potentials of arbitrary shape. In the context of optical spectral singularities, these correspond to inhomogeneous gain media.Comment: 13 pages, 2 figures, one table, a reference added, typos correcte
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