Yukiko Matsuda
5-2 Hijiyama Park
Minami, 7320815, Japan
Minami, 7320815, Japan
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 21 publications
Genomic landscape of radiation-induced somatic mutations in a normal cell.
Journal: Carcinogenesis
Published: April 04, 2025
Monoallelic mutations in MMD2 cause autosomal dominant aggressive periodontitis.
Journal: The Journal of experimental medicine
Published: October 17, 2023
Clinical and Pathological Features of FTDP-17 with MAPT p.K298_H299insQ Mutation.
Journal: Movement disorders clinical practice
Published: September 05, 2023
Spectra and characteristics of somatic mutations induced by ionizing radiation in hematopoietic stem cells.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 05, 2023
CGG repeat expansion in LRP12 in amyotrophic lateral sclerosis.
Journal: American journal of human genetics
Published: March 25, 2023
Kv11 (ether-à-go-go-related gene) voltage-dependent K+ channels promote resonance and oscillation of subthreshold membrane potentials.
Journal: The Journal of physiology
Published: June 16, 2020
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.
Journal: Journal of human genetics
Published: April 09, 2020
Zonisamide can ameliorate the voltage-dependence alteration of the T-type calcium channel CaV3.1 caused by a mutation responsible for spinocerebellar ataxia.
Journal: Molecular brain
Published: February 14, 2020
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.
Journal: Journal of human genetics
Published: October 20, 2019
Last Updated: 09/26/2026