Results 181 to 190 of about 67,614 (310)
Strain-engineered Si-doped Cs<sub>3</sub>Bi<sub>2</sub>I<sub>9</sub> perovskite for high-performance MIM capacitors: a DFT study. [PDF]
Itas YS, Khandaker MU, Benabdallah F.
europepmc +1 more source
Quasi‐digital memristor with self‐rectifying and synaptic functions in crossbar array architectures
The text should be different from the abstract text. A self‐rectifying quasi‐digital memristor (QDM) featuring a well‐defined p‐AgI/n‐PbI2 heterojunction is developed. It monolithically integrate diode‐like rectification, digital switching, and analog plasticity.
Tianyu Liu +11 more
wiley +1 more source
Molecular-level interactions governed by temperature and composition in double salt ionic liquid-water systems. [PDF]
Rahman KMG, Hossain M, Susan MABH.
europepmc +1 more source
ABSTRACT Background Sinonasal malignancies (SNM) are rare, heterogeneous tumors with poor prognosis. There is an unmet need to improve treatment outcomes. Despite advances in imaging and molecular classification, optimal curative radiotherapy (RT) strategies remain undefined.
M. de Ridder +11 more
wiley +1 more source
Comprehensive Comparison of Molecular Fragmentation Schemes for Proteins. [PDF]
Rüther K +4 more
europepmc +1 more source
Wide‐Bandgap Semiconductor‐Based Neuromorphic Computing
Wide‐bandgap semiconductors enable robust, low‐power neuromorphic devices for extreme environments. This review outlines material advantages, device physics, integration, and future directions for next‐generation brain‐inspired computing. ABSTRACT Neuromorphic computing has emerged as a promising paradigm to overcome the energy inefficiency and data ...
Hongyu Tang +6 more
wiley +1 more source
Interoperable smart city transformation: Insights from European data space for smart communities. [PDF]
Meszaros S, Puura A, Thoeye T.
europepmc +1 more source
Abstract Lynch syndrome (LS) is the most common hereditary colorectal cancer syndrome, caused by a germline pathogenic variant in one of the mismatch repair (MMR) genes. Among these, MSH6‐associated LS represents a distinct subtype with unique molecular and clinical characteristics.
Salwa Ben Yahia +4 more
wiley +1 more source

