Results 41 to 50 of about 10,988,700 (173)

Utilizing rat kidney gene co-expression networks to enhance safety assessment biomarker identification and human translation

open access: yesiScience
Summary: Toxicogenomic data provide key insights into molecular mechanisms underlying drug-induced organ toxicities. To simplify transcriptomic data interpretation, we applied weighted gene co-expression network analysis (WGCNA) to rat kidney ...
Steven J. Kunnen   +16 more
doaj   +1 more source

Robust deep learning model for prognostic stratification of pancreatic ductal adenocarcinoma patients

open access: yesiScience, 2021
Summary: A major challenge for treating patients with pancreatic ductal adenocarcinoma (PDAC) is the unpredictability of their prognoses due to high heterogeneity.
Jie Ju   +6 more
doaj   +1 more source

Electroactive Proteinoid–Quantum Dot Systems

open access: yesSmall Science, Volume 5, Issue 12, December 2025.
Proteinoid‐quantum dot conjugates form toroidal nanostructures (145.2 nm outer diameter, 102.3 nm cavity) via glutamic acid‐phenylalanine‐aspartic acid‐cysteine cross‐linking with sulfo‐SMCC (sulfosuccinimidyl 4‐(N‐maleimidomethyl)cyclohexane‐1‐carboxylate).
Panagiotis Mougkogiannis   +1 more
wiley   +1 more source

Pericyte mediates the infiltration, migration, and polarization of macrophages by CD163/MCAM axis in glioblastoma

open access: yesiScience, 2022
Summary: Microenvironment cells (MCs) play a critical role in tumor proliferation, progression, and metastasis. However, it has not been adequately addressed whether MCs could be used as a reliable prognostic marker in glioblastoma (GBM).
Hao Zhang   +12 more
doaj   +1 more source

The dynamics of prion spreading is governed by the interplay between the non-linearities of tissue response and replication kinetics

open access: yesiScience
Summary: Prion diseases, or transmissible spongiform encephalopathies (TSEs), are neurodegenerative disorders caused by the accumulation of misfolded conformers (PrPSc) of the cellular prion protein (PrPC).
Basile Fornara   +6 more
doaj   +1 more source

Modeling foot sole cutaneous afferents: FootSim

open access: yesiScience, 2023
Summary: While walking and maintaining balance, humans rely on cutaneous feedback from the foot sole. Electrophysiological recordings reveal how this tactile feedback is represented in neural afferent populations, but obtaining them is difficult and ...
Natalija Katic   +6 more
doaj   +1 more source

Synaptic Function in Memristor Devices for Neuromorphic Circuit Applications

open access: yesAdvanced Electronic Materials, Volume 11, Issue 14, September 4, 2025.
Discover how neuromorphic devices mimic brain‐like learning: this article explores how ionic and electronic conduction processes enable artificial synapses to adapt across time scales. Uncover the essential ingredients—state‐variable dynamics, rectification, and memory—and how they can be probed through nonlinear diagnostics to engineer smarter, more ...
Juan Bisquert   +3 more
wiley   +1 more source

A Kmer-based paired-end read de novo assembler and genotyper for canine MHC class I genotyping

open access: yesiScience, 2023
Summary: The major histocompatibility complex class I (MHC-I) genes are highly polymorphic. MHC-I genotyping is required for determining the peptide epitopes available to an individual’s T-cell repertoire.
Yuan Feng   +4 more
doaj   +1 more source

Beyond digital twins: the role of foundation models in enhancing the interpretability of multiomics modalities in precision medicine

open access: yesFEBS Open Bio, Volume 15, Issue 8, Page 1192-1208, August 2025.
This review highlights how foundation models enhance predictive healthcare by integrating advanced digital twin modeling with multiomics and biomedical data. This approach supports disease management, risk assessment, and personalized medicine, with the goal of optimizing health outcomes through adaptive, interpretable digital simulations, accessible ...
Sakhaa Alsaedi   +2 more
wiley   +1 more source

Structural aspects of the Huntingtin protein investigated by biocomputing methods

open access: yes, 2011
Huntington’s disease (HD) is a neurodegenerative disorder which leads to death within a couple of decades. It causes uncontrolled movements, loss of intellectual faculties and emotional disturbance. HD is a familial disease, passed from parent to child through a mutation in a specific gene, the HTT gene. This gene provides the genetic information for a
openaire   +2 more sources

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