The genetic and molecular features of the intronic pentanucleotide repeat expansion in spinocerebellar ataxia type 10

por Kurosaki, Tatsuaki, Ashizawa, Tetsuo
Publicado 2022

The Unstable CCTG Repeat Responsible for Myotonic Dystrophy Type 2 Originates from an AluSx Element Insertion into an Early Primate Genome

por Kurosaki, Tatsuaki, Ueda, Shintaroh, Ishida, Takafumi, Abe, Koji, Ohno, Kinji, Matsuura, Tohru
Publicado 2012

NMD abnormalities during brain development in the Fmr1-knockout mouse model of fragile X syndrome

por Kurosaki, Tatsuaki, Sakano, Hitomi, Pröschel, Christoph, Wheeler, Jason, Hewko, Alexander, Maquat, Lynne E.
Publicado 2021

A post-translational regulatory switch on UPF1 controls targeted mRNA degradation

por Kurosaki, Tatsuaki, Li, Wencheng, Hoque, Mainul, Popp, Maximilian W.-L., Ermolenko, Dmitri N., Tian, Bin, Maquat, Lynne E.
Publicado 2014