Masaaki Toshishige
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 9 publications
DNA polymerase β suppresses somatic indels at CpG dinucleotides in developing cortical neurons.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: August 13, 2025
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
Active sites of human MEPE-ASARM regulating bone matrix mineralization.
Journal: Molecular and cellular endocrinology
Published: May 23, 2020
H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promoters.
Journal: Journal of biomedical science
Published: July 17, 2017
Endogenous viral gene ev21 is not responsible for the expression of late feathering in chickens.
Journal: Poultry science
Published: April 03, 2017
Common Variant Near HEY2 Has a Protective Effect on Ventricular Fibrillation Occurrence in Brugada Syndrome by Regulating the Repolarization Current.
Journal: Circulation. Arrhythmia and electrophysiology
Published: January 06, 2016
A nonsynonymous polymorphism in semaphorin 3A as a risk factor for human unexplained cardiac arrest with documented ventricular fibrillation.
Journal: PLoS genetics
Published: May 26, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026