Results 181 to 190 of about 38,270 (217)
The irreplaceable role of pathology for the clinical translation of patient-derived organoids in precision medicine. [PDF]
Liang Z +6 more
europepmc +1 more source
In this study, an efficient screening system is developed for plant metabolites to find a compound, 7‐epi‐10‐deacetyltaxol, inhibits tissue elongation. It suppresses plant growth through brassinosteroid and microtubule pathways. It is later applied to animal cells and human tumor organoids, resulting in similar cell division suppression. These findings
Yan‐Jie Zhang +20 more
wiley +1 more source
Patient-derived organoids as a model to study tubo-ovarian carcinoma: a pathologist's perspective. [PDF]
Alves-Vale C +8 more
europepmc +1 more source
A Gut‐Brain Axis Underlying Succinate‐Associated Compulsive‐Like Behavior
Gut‐derived succinate is associated with an excitatory‐inhibitory imbalance in dmPFC glutamatergic neurons, involving microglial SUCNR1 activation and vagal afferent signaling via upregulated gut 5‐HT4 receptors along the DVC‐CeA‐dmPFC circuit, changes that are linked to excessive compulsive‐like behavior.
Yi Li +12 more
wiley +1 more source
Patient-derived organoids and neurospheres recapitulate salient features of primary tumor heterogeneity. [PDF]
Moore Z +16 more
europepmc +1 more source
Bioactive phenylboronic acid–chitosan nanoparticles enable responsive silymarin delivery for post‐hepatectomy liver protection. The nanoplatform integrates antioxidant and antibacterial functions, improves hepatic recovery, and is associated with coordinated shifts in gut microbiota, metabolites, cytokines, and hepatic proteomic pathways, suggesting a ...
Jinjin Tong +9 more
wiley +1 more source
Genomic fidelity and evolution of cancer patient-derived organoids
Raz L +8 more
europepmc +1 more source
Advances in precision oncology using patient-derived organoids and functional biomaterials. [PDF]
Singh H, Mijakovic I, Singh P.
europepmc +1 more source
TROP2 is identified as a novel tumor‐selective lysosomal‐targeting receptor with established clinical relevance. TROP2‐targeting chimeras (TRTACs) are developed by genetically fusing a TROP2‐binding nanobody to nanobodies against specific target proteins.
Luping Chen +10 more
wiley +1 more source

