OMIM - Congenital disorder

Homo sapiens

This study contains curated human phenotype data extracted from OMIM. Additional computational processing and curation of the phenotype data was performed to further organize and group data from related phenotypes into unifying disease categories.

Source: NextBio Library/Mutation and Phenotypic data

Total # Biosets: 614

Identifying targets of MeCP2 during neuronal maturational differentiation

Homo sapiens

To control MeCP2 expression and deficiency during neuronal maturation, SH-SY5Y cells were transfected with methylated MeCP2 oligonucleotide decoy to disrupt the binding of MeCP2 to endogenous targets.

Authors: Peddada Sailaja, Yasui H Dag, LaSalle M Janine

Organization: University of California, Davis Medical …

Total # Biosets: 3