Sort   by:  
 Page size 
In order to characterize the differences between second trimester Down syndrome (DS) and euploid fetuses, we compared gene expression in uncultured amniotic fluid supernatant samples. We identified individually differentially expressed genes via paired t-tests in the matched samples, and a set of di...
ORGANISM(S): Homo sapiens 
Mutations in mitochondrial DNA cause severe multisystem disease, frequently associated with muscle weakness. The m.3243A>G mutation is the major cause of Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke Like episodes (MELAS). Experimental models that recapitulate the disease phenotype in v...
ORGANISM(S): Homo sapiens (Human) 
2025-05-26 | PXD058785 | Pride
Sort   by:  
 Page size