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2081
Cancer Accumulation and Anticancer Activity of “CROX (Cluster Regulation of RUNX)” PIP in HER2‐Positive Gastric Cancer Evaluated by Chicken Egg Cancer Model
Published 2025-04-01“…ABSTRACT Background We have focused on pyrrole‐imidazole (PI) polyamide compounds, which preferentially bind to their target DNA sequences. To validate our “CROX (Cluster Regulation of RUNX)” strategy, we have created a novel PI polyamide‐based inhibitor against RUNX termed Chb‐M’. …”
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2082
Role of Magnetic Resonance Spectroscopy and Diffusion-weighted Imaging in the Evaluation of Supratentorial Brain Tumours with Histopathology Correlation at a Tertiary Care Hospital...
Published 2024-12-01“…Thus, the study aimed to evaluate the effectiveness of these non-invasive diagnostic methods in patients with suspected intracranial lesions. …”
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2083
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2084
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2085
Peripheral Blood T‐Cell Receptor Repertoire Diversity as a Potential Biomarker in the Diagnosis and Treatment Evaluation of Colorectal and Lung Cancers: A Prospective Observational...
Published 2025-05-01“…This study aimed to evaluate the potential D50 value in the diagnosis and treatment evaluation of colorectal cancer (CRC) and nonsmall‐cell lung cancer (NSCLC). …”
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2086
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2087
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2088
Microbiome profiling in patients with Bladder Pain Syndrome/Interstitial cystitis
Published 2025-06-01“…The small pilot that was done to evaluate microbiome stability over time in a single BPS/IC patient, showed remarkable stability of microbiome composition during a one-year follow-up.…”
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2089
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2090
Comparative evaluation of push-out bond strength after root perforation repair using recently introduced bioceramic and calcium silicate-based materials – An in vitro study
Published 2025-04-01“…Aim: This study was planned to comparatively evaluate the push-out bond strength (PBS) after perforation (PF) repair using mineral trioxide aggregate (MTA) repair high plasticity (HP), Biodentine, and EndoSequence Bioceramic (BC) root repair material (ERRM). …”
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2091
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2092
A Genome Scaffold Algorithm for Extending Repetitive and Nonrepetitive Contigs
Published 2017-11-01“…The next generation sequencing platform produces massive short reads data. …”
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2093
Identification of multiomics and immune infiltration-associated biomarkers for early gastric cancer: a machine learning-based diagnostic model development study
Published 2025-05-01“…Methods We employed serum proteomics combined with bioinformatics to identify genes differentially expressed in the serum of non-metastatic GC patients. Single-cell RNA sequencing (ScRNA-seq) and immune infiltration analysis were performed to evaluate the relationship between gene expression and immune cell function. …”
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2094
Simulation-Based Hierarchical Heuristic for Printed Circuit Board Assembly Optimization in a Spin-Head Surface Mounter
Published 2024-09-01“…This article proposes a simulation-based hierarchical heuristic (SHH) method to optimize nozzle assignment, feeder assignment, and component sequencing in a single spin-head gantry type surface mounter. …”
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2095
Inherited glycosylphosphatidylinositol deficiency disorders: a new group of inherited metabolic disorders
Published 2024-12-01“…The current state of knowledge connects the highly differentiated course of clinical presentation with the heterogenic molecular background evaluated in the next-generation sequencing methods. …”
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2096
CoPaD-Mark: A Coded Parallelizable Deep Learning-Based Scheme for Robust Image Watermarking
Published 2025-01-01“…This code’s message is constructed by combining a chaotic binary sequence with the original watermark bits. The inclusion of chaotic sequences adds randomness and complexity to the encoding process, enhancing robustness against attempts to alter the watermark. …”
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2097
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2098
Genetic insights into progressive myoclonic epilepsies: A case study of KCTD7 mutation in an Iranian-Azeri-Turkish family
Published 2025-06-01“…A 5-year-old boy and his 8-year-old sister, presenting with PME-related electroclinical features such as myoclonic seizures and progressive cognitive and motor decline, underwent comprehensive clinical evaluations, including pedigree analysis, laboratory tests, and EEG assessments, followed by Whole-Exome Sequencing (WES) to identify potential disease-causing mutations. …”
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2099
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2100
Identification of a novel AGO2 variant causing LESKRES in a Chinese family with intellectual disability
Published 2025-06-01“…BackgroundLessel-Kreienkamp syndrome (LESKRES, MIM #619149), an autosomal dominant genetic disorder caused by variants in AGO2 (MIM*606229), primarily leads to neurodevelopmental symptoms.ObjectiveThis study aims to investigate the genetic etiology of a family with intellectual disability.MethodsWhole-exome sequencing (WES) was used to initially identify the pathogenic variants responsible for the intellectual disability in the family, and Sanger sequencing was employed for confirmation. …”
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