Yui Tada

Hiroshima, 7348551, Japan

Last Updated: 09/26/2026

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Found 12 publications

Optineurin knock-out forms TDP-43 aggregates to regulate TDP-43 protein levels despite autophagic up-regulation and aberrant TDP-43 expression.

Optineurin knock-out forms TDP-43 aggregates to regulate TDP-43 protein levels despite autophagic up-regulation and aberrant TDP-43 expression.

Journal: Neuroscience research
Published: November 27, 2024

CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis.

CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis.

Journal: American journal of human genetics
Published: March 25, 2023

Spinocerebellar ataxia type 17-digenic TBP/STUB1 disease: neuropathologic features of an autopsied patient.

Spinocerebellar ataxia type 17-digenic TBP/STUB1 disease: neuropathologic features of an autopsied patient.

Journal: Acta neuropathologica communications
Published: September 18, 2022

Correction: Comparison of two families with and without ataxia harboring novel variants in PRKCG.

Correction: Comparison of two families with and without ataxia harboring novel variants in PRKCG.

Journal: Journal of human genetics
Published: July 06, 2022

Comparison of two families with and without ataxia harboring novel variants in PRKCG.

Comparison of two families with and without ataxia harboring novel variants in PRKCG.

Journal: Journal of human genetics
Published: April 25, 2022

The first Japanese case of primary familial brain calcification caused by an MYORG variant.

The first Japanese case of primary familial brain calcification caused by an MYORG variant.

Journal: Journal of human genetics
Published: April 20, 2020

Aggressive periodontitis and NOD2 variants.

Aggressive periodontitis and NOD2 variants.

Journal: Journal of human genetics
Published: April 09, 2020

Optineurin regulates osteoblastogenesis through STAT1.

Optineurin regulates osteoblastogenesis through STAT1.

Journal: Biochemical and biophysical research communications
Published: February 05, 2020

Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia.

Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia.

Journal: Journal of human genetics
Published: October 20, 2019

Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report.

Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report.

Journal: BMC medical genetics
Published: October 18, 2019

Biallelic mutation of HSD17B4 induces middle age-onset spinocerebellar ataxia.

Biallelic mutation of HSD17B4 induces middle age-onset spinocerebellar ataxia.

Journal: Neurology. Genetics
Published: May 03, 2019

C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8.

C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8.

Journal: Journal of the neurological sciences
Published: February 20, 2019
Showing 1-12 of 12

Last Updated: 09/26/2026