Saburo Sakoda

Age associated axonal features in HNPP with 17p11.2 deletion in Japan

G. Sobue, N. Hattori, K. Nakashima, 2005, Journal of Neurology, Neurosurgery & Psychiatry.

Rapid disease progression correlates with instability of mutant SOD1 in familial ALS

M Nakagawa, A Shimizu, S Sakoda, 2005, Neurology.

A single MEF-2 site is a major positive regulatory element required for transcription of the muscle-specific subunit of the human phosphoglycerate mutase gene in skeletal and cardiac muscle cells

S. Sakoda, Y. Nakatsuji, K. Hidaka, 1992, Molecular and cellular biology.