Multi-modal contrastive drug synergy prediction model guided by single modality. [PDF]
Luo T, Zhang Z, Chen XG, Li Z.
europepmc +1 more source
Modal Control of Two-Dimensional Bending Vibrations : Its Application to Flat Plane Speakers
Tetsuo Sato, Noboru Tominari
openalex +2 more sources
Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker
ABSTRACT Amyotrophic lateral sclerosis (ALS) is a neuromuscular disease. Super oxide dismutase 1 (SOD1) gene mutations cause ALS, and the D90A mutation is associated with primarily upper motor neuron (UMN) loss. Objective Our goal is to reveal the early cellular events in ALS pathology and identify potential pharmacokinetic biomarkers, using well ...
Mukesh Gautam +6 more
wiley +1 more source
Fault Diagnosis of Wind Turbine Rotating Bearing Based on Multi-Mode Signal Enhancement and Fusion. [PDF]
Ding S, Zhou G, Wang X, Li W.
europepmc +1 more source
SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas +18 more
wiley +1 more source
Cross-modal gated feature enhancement for multimodal emotion recognition in conversations. [PDF]
Zhao S, Ren J, Zhou X.
europepmc +1 more source
Diffusion Tractography Biomarker for Epilepsy Severity in Children With Drug‐Resistant Epilepsy
ABSTRACT Objective To develop a novel deep‐learning model of clinical DWI tractography that can accurately predict the general assessment of epilepsy severity (GASE) in pediatric drug‐resistant epilepsy (DRE) and test if it can screen diverse neurocognitive impairments identified through neuropsychological assessments.
Jeong‐Won Jeong +7 more
wiley +1 more source
Multi-modal characteristics of LncRNA-derived subtypes in colorectal cancer. [PDF]
Xiong M +6 more
europepmc +1 more source
ABSTRACT Background Mitofusin 2 (MFN2) is a major causative gene for axonal Charcot – Marie – Tooth disease type 2A (CMT2A), with a wide phenotypic spectrum. Comprehensive large ‐ scale genotype – phenotype association studies are essential for understanding disease pathogenesis and improved clinical management.
Masahiro Ando +13 more
wiley +1 more source
E-CMCA and LSTM-Enhanced Framework for Cross-Modal MRI-TRUS Registration in Prostate Cancer. [PDF]
Shao C, Xue R, Gu L.
europepmc +1 more source

