Quality and quantity control of gene expression by nonsense-mediated mRNA decay T Kurosaki, MW Popp, LE Maquat Nature reviews Molecular cell biology 20 (7), 406-420, 2019 | 639 | 2019 |
Nonsense-mediated mRNA decay in humans at a glance T Kurosaki, LE Maquat Journal of cell science 129 (3), 461-467, 2016 | 465 | 2016 |
A post-translational regulatory switch on UPF1 controls targeted mRNA degradation T Kurosaki, W Li, M Hoque, MWL Popp, DN Ermolenko, B Tian, ... Genes & development 28 (17), 1900-1916, 2014 | 184 | 2014 |
Rules that govern UPF1 binding to mRNA 3′ UTRs T Kurosaki, LE Maquat Proceedings of the National Academy of Sciences 110 (9), 3357-3362, 2013 | 144 | 2013 |
NMD-degradome sequencing reveals ribosome-bound intermediates with 3′-end non-templated nucleotides T Kurosaki, K Miyoshi, JR Myers, LE Maquat Nature structural & molecular biology 25 (10), 940-950, 2018 | 41 | 2018 |
The Unstable CCTG Repeat Responsible for Myotonic Dystrophy Type 2 Originates from an AluSx Element Insertion into an Early Primate Genome T Kurosaki, S Ueda, T Ishida, K Abe, K Ohno, T Matsuura PLoS One 7 (6), e38379, 2012 | 35 | 2012 |
Loss of the fragile X syndrome protein FMRP results in misregulation of nonsense-mediated mRNA decay T Kurosaki, N Imamachi, C Pröschel, S Mitsutomi, R Nagao, N Akimitsu, ... Nature cell biology 23 (1), 40-48, 2021 | 28 | 2021 |
LDB3 splicing abnormalities are specific to skeletal muscles of patients with myotonic dystrophy type 1 and alter its PKC binding affinity Y Yamashita, T Matsuura, T Kurosaki, Y Amakusa, M Kinoshita, T Ibi, ... Neurobiology of disease 69, 200-205, 2014 | 27 | 2014 |
The neuronal POU transcription factor Brn-2 interacts with Jab1, a gene involved in the onset of neurodegenerative diseases YT Huang, K Iwamoto, T Kurosaki, M Nasu, S Ueda Neuroscience letters 382 (1-2), 175-178, 2005 | 27 | 2005 |
Alu-Mediated Acquisition of Unstable ATTCT Pentanucleotide Repeats in the Human ATXN10 Gene T Kurosaki, T Matsuura, K Ohno, S Ueda Molecular biology and evolution 26 (11), 2573-2579, 2009 | 18 | 2009 |
Evolutionary scenario for acquisition of CAG repeats in human SCA1 gene T Kurosaki, A Ninokata, L Wang, S Ueda Gene 373, 23-27, 2006 | 17 | 2006 |
Identifying Cellular Nonsense-Mediated mRNA Decay (NMD) Targets: Immunoprecipitation of Phosphorylated UPF1 Followed by RNA Sequencing (p-UPF1 RIP− Seq) T Kurosaki, M Hoque, LE Maquat Methods in Molecular Biology 1720, 175-186, 2018 | 12 | 2018 |
Integrative omics indicate FMRP sequesters mRNA from translation and deadenylation in human neuronal cells T Kurosaki, S Mitsutomi, A Hewko, N Akimitsu, LE Maquat Molecular cell 82 (23), 4564-4581. e11, 2022 | 10 | 2022 |
The genetic and molecular features of the intronic pentanucleotide repeat expansion in spinocerebellar ataxia type 10 T Kurosaki, T Ashizawa Frontiers in Genetics 13, 936869, 2022 | 9 | 2022 |
NMD abnormalities during brain development in the Fmr1-knockout mouse model of fragile X syndrome T Kurosaki, H Sakano, C Pröschel, J Wheeler, A Hewko, LE Maquat Genome biology 22, 1-13, 2021 | 9 | 2021 |
Defining nonsense-mediated mRNA decay intermediates in human cells T Kurosaki, JR Myers, LE Maquat Methods 155, 68-76, 2019 | 8 | 2019 |
Comparative genetics of the poly-Q tract of ataxin-1 and its binding protein PQBP-1 T Kurosaki, J Gojobori, S Ueda Biochemical genetics 50, 309-317, 2012 | 5 | 2012 |
Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy T Matsuura, T Kurosaki, Y Omote, N Minami, YK Hayashi, I Nishino, K Abe Journal of human genetics 58 (8), 564-565, 2013 | 4 | 2013 |
Long-range PCR for the diagnosis of spinocerebellar ataxia type 10 T Kurosaki, T Matsuura, K Ohno, S Ueda Neurogenetics 9 (2), 151-152, 2008 | 4 | 2008 |
Molecular autopsy provides evidence for widespread ribosome-phased mRNA fragmentation T Kurosaki, LE Maquat Nature Structural & Molecular Biology 25 (4), 299-301, 2018 | 3 | 2018 |