O. Sakai

Enhancement of Guanine-Nucleotide Exchange Activity of C3G for Rap1 by the Expression of Crk, CrkL, and Grb2*

J. Groffen, M. Matsuda, S. Hattori, 1997, The Journal of Biological Chemistry.

Structure-activity relationship study and drug profile of N-(4-fluorophenylsulfonyl)-L-valyl-L-leucinal (SJA6017) as a potent calpain inhibitor.

P. Yuen, Kevin K W Wang, Masayuki Nakamura, 2003, Journal of medicinal chemistry.

Complete Amino Acid Sequence of Crystalline α-Glucosidase from Aspergillus niger

A. Kimura, H. Matsui, S. Chiba, 1992 .

Exploration of cornea permeable calpain inhibitors as anticataract agents.

Masayuki Nakamura, J. Inoue, O. Sakai, 2003, Bioorganic & medicinal chemistry.

Exploration of orally available calpain inhibitors 2: peptidyl hemiacetal derivatives.

Masayuki Nakamura, J. Inoue, H. Miyashita, 2006, Journal of medicinal chemistry.

Identification of essential ionizable groups in active site of Aspergillus niger α-glucosidase

H. Mori, A. Kimura, H. Matsui, 1997 .