Publications by authors named "S H Eissa"

SLFN11 is a predictive cancer biomarker essential for identifying tumors that are sensitive to DNA-damaging agents, facilitating more personalized and effective treatment approaches. Detecting this biomarker can guide therapeutic decisions and improve outcomes for cancer patients. However, existing detection methods for SLFN11 are complex and require advanced techniques.

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The realization of brain-scale spiking neural networks (SNNs) is impeded by power constraints and low integration density. To address these challenges, multi-core SNNs are utilized to emulate numerous neurons with high energy efficiency, where spike packets are routed through a network-on-chip (NoC). However, the information can be lost in the NoC under high spike traffic conditions, leading to performance degradation.

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Article Synopsis
  • The study presents a novel GO/Cu-MOF nanocomposite for simultaneous detection of biomarkers linked to lower respiratory infections, marking a new application in electrochemical biosensing.
  • The researchers fabricated an immunosensor using this composite that effectively detected M. pneumoniae and L. pneumophila antigens, showing strong selectivity and sensitivity across a wide concentration range.
  • The enhanced performance is attributed to the superior electrocatalytic properties and interactions of the GO-MOF composite, making it a promising tool for rapid pathogen monitoring in environmental samples.
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Multidrug-resistant pathogens are now thought to be the primary global causes of disease and death. Therefore, it is imperative to develop new effective bioactive compounds from microbial sources, such as Streptomyces species. Nevertheless, the pharmaceutical industry suffered financial losses and low-quality end products as a result of Streptomyces bacteriophage contamination.

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Background: Colorectal cancer (CRC) is ranked as the third most commonly diagnosed cancer and the third cause of cancer related deaths. CRC is greatly attributed to genetic and epigenetic mutations and immune dysregulation. Tumor aberrant expression of Toll-like Receptors (TLRs) can contribute to tumorigenesis.

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