Mohammed M. Idris

This study shows that exosomes from hepatic stellate cells reduce fibrosis in mice livers by delivering metabolic and regenerative signaling molecules.

This study shows that aging impairs zebrafish caudal fin regeneration by disrupting gene networks and cellular metabolism, with mitochondrial dysfunction playing a key role.

This study evaluates the impact of small molecules on zebrafish caudal fin regeneration using proteomic analysis, identifying shared molecular responses across different treatments.

This paper develops a female chronic social defeat stress model to study sex differences in depression, finding depression-like behaviors and neurobiological changes in female mice.

This study maps phosphoproteomic changes during zebrafish caudal fin regeneration, identifying key signaling pathways and highlighting the role of phosphorylation in tissue regeneration.

This study identifies 1408 genes and 661 proteins differentially regulated during zebrafish caudal fin regeneration using transcriptomics and proteomics.

This study uses CRISPR-Cas9 to knock down Annexin 2a and 2b genes in zebrafish caudal fin regeneration, showing slowed regeneration and downregulation of related genes.

This study identifies genes and proteins involved in tail regeneration in Hemidactylus frenatus using transcriptomics and proteomics, finding 36 commonly expressed genes/proteins and associations with several signaling pathways.