Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 423 - 436
Published: Nov. 29, 2024
Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 423 - 436
Published: Nov. 29, 2024
Ageing Research Reviews, Journal Year: 2024, Volume and Issue: 100, P. 102414 - 102414
Published: July 14, 2024
Language: Английский
Citations
14Biomedicines, Journal Year: 2025, Volume and Issue: 13(1), P. 167 - 167
Published: Jan. 12, 2025
Background/Objectives: The dual forces of structured inquiry and serendipitous discovery have long shaped neuropsychiatric research, with groundbreaking treatments such as lithium ketamine resulting from unexpected discoveries. However, relying on chance is becoming increasingly insufficient to address the rising prevalence mental health disorders like depression schizophrenia, which necessitate precise, innovative approaches. Emerging technologies artificial intelligence, induced pluripotent stem cells, multi-omics potential transform this field by allowing for predictive, patient-specific interventions. Despite these advancements, traditional methodologies animal models single-variable analyses continue be used, frequently failing capture complexities human conditions. Summary: This review critically evaluates transition serendipity precision-based in research. It focuses key innovations dynamic systems modeling network-based approaches that use genetic, molecular, environmental data identify new therapeutic targets. Furthermore, it emphasizes importance interdisciplinary collaboration human-specific overcoming limitations Conclusions: We highlight precision psychiatry’s transformative revolutionizing care. paradigm shift, combines cutting-edge systematic frameworks, promises increased diagnostic accuracy, reproducibility, efficiency, paving way tailored better patient outcomes
Language: Английский
Citations
1Biomolecules, Journal Year: 2024, Volume and Issue: 14(6), P. 678 - 678
Published: June 11, 2024
Intracerebral hemorrhage (ICH) is a life-threatening condition associated with significant morbidity and mortality. This study investigates transcriptomic alterations in rodent models of ICH severe to shed light on the genetic pathways involved hemorrhagic brain injury. We performed principal component analysis, revealing distinct segments normal rats compared rats. employed heatmaps volcano plots identify differentially expressed genes utilized bar KEGG pathway analysis elucidate molecular involved. identified multitude both models. Our results revealed 5679 common among normal, ICH, groups upregulated group, 1196 downregulated genes, respectively. A plot comparing these further highlighted including PDPN, TIMP1, SERPINE1, TUBB6, CD44. These findings underscore complex interplay inflammation, oxidative stress, neuronal damage. Furthermore, enrichment uncovered key signaling pathways, TNF pathway, protein processing endoplasmic reticulum, MAPK Fc gamma R-mediated phagocytosis, implicated pathogenesis ICH.
Language: Английский
Citations
4Cancer Letters, Journal Year: 2025, Volume and Issue: unknown, P. 217667 - 217667
Published: March 1, 2025
Language: Английский
Citations
0Applied Spectroscopy Reviews, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 30
Published: April 4, 2025
Language: Английский
Citations
0Journal of Neuroscience Methods, Journal Year: 2025, Volume and Issue: 415, P. 110359 - 110359
Published: Jan. 5, 2025
Language: Английский
Citations
0Elsevier eBooks, Journal Year: 2024, Volume and Issue: unknown, P. 423 - 436
Published: Nov. 29, 2024
Citations
0