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Tatsuaki Kurosaki
Tatsuaki Kurosaki
University at Buffalo Jacobs School of Medicine & Biomedical Sciences
在 buffalo.edu 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
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
6392019
Nonsense-mediated mRNA decay in humans at a glance
T Kurosaki, LE Maquat
Journal of cell science 129 (3), 461-467, 2016
4652016
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
1842014
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
1442013
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
412018
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
352012
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
282021
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
272014
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
272005
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
182009
Evolutionary scenario for acquisition of CAG repeats in human SCA1 gene
T Kurosaki, A Ninokata, L Wang, S Ueda
Gene 373, 23-27, 2006
172006
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
122018
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
102022
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
92022
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
92021
Defining nonsense-mediated mRNA decay intermediates in human cells
T Kurosaki, JR Myers, LE Maquat
Methods 155, 68-76, 2019
82019
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
52012
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
42013
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
42008
Molecular autopsy provides evidence for widespread ribosome-phased mRNA fragmentation
T Kurosaki, LE Maquat
Nature Structural & Molecular Biology 25 (4), 299-301, 2018
32018
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