Publications by authors named "Yui Tada"

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Optineurin knock-out forms TDP-43 aggregates to regulate TDP-43 protein levels despite autophagic up-regulation and aberrant TDP-43 expression.
Yuta Maetani, Takashi Kurashige, Yui Tada, Kodai Kume, Tomoaki Watanabe

Neurosci Res· July 2025

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CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis.
Kodai Kume, Takashi Kurashige, Keiko Muguruma, Hiroyuki Morino, Yui Tada

Am J Hum Genet· July 2023

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Spinocerebellar ataxia type 17-digenic TBP/STUB1 disease: neuropathologic features of an autopsied patient.
Rie Saito, Yui Tada, Daisuke Oikawa, Yusuke Sato, Makiko Seto

Acta Neuropathol Commun· December 2022

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Comparison of two families with and without ataxia harboring novel variants in PRKCG.
Yui Tada, Kodai Kume, Soma Noguchi, Tomoko Sekiya, Kazuto Nishinaka

J Hum Genet· October 2022

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Correction: Comparison of two families with and without ataxia harboring novel variants in PRKCG.
Yui Tada, Kodai Kume, Soma Noguchi, Tomoko Sekiya, Kazuto Nishinaka

J Hum Genet· October 2022

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Aggressive periodontitis and NOD2 variants.
Noriyoshi Mizuno, Kodai Kume, Yukiko Nagatani, Shinji Matsuda, Tomoyuki Iwata, Yui Tada

J Hum Genet· October 2020

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The first Japanese case of primary familial brain calcification caused by an MYORG variant.
Kodai Kume, Tadayuki Takata, Hiroyuki Morino, Yukiko Matsuda, Ryosuke Ohsawa, Yui Tada

J Hum Genet· October 2020

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Optineurin regulates osteoblastogenesis through STAT1.
Noriyoshi Mizuno, Tomoyuki Iwata, Ryosuke Ohsawa, Kazuhisa Ouhara, Shinji Matsuda, Yui Tada

Biochem Biophys Res Commun· May 2020

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Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia.
Yui Tada, Kodai Kume, Yukiko Matsuda, Takashi Kurashige, Yuhei Kanaya

J Hum Genet· April 2020

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Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report.
Kodai Kume, Hiroyuki Morino, Ryosuke Miyamoto, Yukiko Matsuda, Ryosuke Ohsawa, Yui Tada

BMC Med Genet· March 2020

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Biallelic mutation of induces middle age-onset spinocerebellar ataxia.
Yukiko Matsuda, Hiroyuki Morino, Ryosuke Miyamoto, Takashi Kurashige, Kodai Kume, Yui Tada

Neurol Genet· February 2020

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C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8.
Kodai Kume, Hiroyuki Morino, Osamu Komure, Yukiko Matsuda, Ryosuke Ohsawa, Yui Tada

J Neurol Sci· July 2019

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