Results 321 to 330 of about 7,795,985 (403)
Analysis of DNA from brain tissue on stereo-EEG electrodes reveals mosaic epilepsy-related variants. [PDF]
D'Gama AM+16 more
europepmc +1 more source
On the 5-methylcytosine found in the DNA extracted from polyoma virus
Alvin M. Kaye, Ernest Winocour
openalex +1 more source
Osimertinib reduces angiogenesis and PDL1 expression in in ovo tumors, transforming them into ‘cold tumors’ with lower immune activity. Anatomopathological and transcriptomic analyses highlight its therapeutic impact on tumor biology. This study underscores osimertinib's potential to reshape the tumor microenvironment and provides insights into its ...
David Barthélémy+14 more
wiley +1 more source
How do neurons live long and healthy? The mechanism of neuronal genome integrity. [PDF]
Ihara D, Rasli NR, Katsuyama Y.
europepmc +1 more source
A potential tumor suppressor role of PLK2 in glioblastoma
PLK2 was consistently downregulated in GBM tissues. Overexpression of PLK2 in GBM cell lines U87MG and U251 reduced their tumorigenic potential and enhanced cell cycle arrest and apoptosis. Suggesting that PLK2 overexpression could potentially be leveraged as a therapeutic strategy to inhibit tumor progression and enhance apoptosis, providing new ...
Xiangping Xia+5 more
wiley +1 more source
Genome-wide DNA methylation patterns in Daphnia magna are not significantly associated with age. [PDF]
Liu R+4 more
europepmc +1 more source
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
Standards in wildlife forensic science, with a focus on non-human DNA analysis. [PDF]
Frankham GJ+9 more
europepmc +1 more source
This study reports the upregulation of ELMO1 and GPR141 in human Fuchs' endothelial corneal dystrophy (FECD) corneal endothelium and ultraviolet A‐induced FECD mice model. A genetic association of an intergenic single nucleotide polymorphism rs918980 present between both genes is observed with FECD in the Indian population.
Susmita Sharma+3 more
wiley +1 more source