https://pubmed.ncbi.nlm.nih.gov/26819560/?dopt=Abstract
Fragile X syndrome is a monogenic disorder and a common cause of intellectual disability. Despite nearly 25 years of research on FMR1, the gene underlying the...
singlenucleotidemutationsrevealnovel
https://pubmed.ncbi.nlm.nih.gov/39192374/?dopt=Abstract
Our observations prove that circFKBP8 promotes BC malignant phenotypes through the miR-432-5p/E2F7 cascade, offering a promising therapeutic and prognostic...
novelmircascadefunctions