Shahnaz Ibrahim

Fluorescent probes for targeting the Golgi apparatus: design strategies and applications

Small and long non-coding RNAs: Past, present, and future

Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10 , a Manganese Transporter in Man