Chromosome 4q;10q translocations; Comparison with different ethnic populations and FSHD patients

Por Matsumura, Tsuyoshi, Goto, Kanako, Yamanaka, Gaku, Lee, Je Hyeon, Zhang, Cheng, Hayashi, Yukiko K, Arahata, Kiichi
Publicado em 2002

MKBP, a Novel Member of the Small Heat Shock Protein Family, Binds and Activates the Myotonic Dystrophy Protein Kinase

Por Suzuki, Atsushi, Sugiyama, Yuki, Hayashi, Yukiko, Nyu-i, Nobuo, Yoshida, Michihiko, Nonaka, Ikuya, Ishiura, Sho-ichi, Arahata, Kiichi, Ohno, Shigeo
Publicado em 1998

Dinucleotide repeat polymorphisms at the SCN4A locus suggest allelic heterogeneity of hyperkalemic periodic paralysis and paramyotonia congenita

Por McClatchey, Andrea I., Trofatter, James, McKenna-Yasek, Diane, Raskind, Wendy, Bird, Thomas, Pericak-Vance, Margaret, Gilchrist, James, Arahata, Kiichi, Radosavljevic, Danica, Worthen, Hilary G., Van den Bergh, Peter, Haines, Jonathan L., Gusella, James F., Brown, Robert H.
Publicado em 1992

Detection of New Paternal Dystrophin Gene Mutations in Isolated Cases of Dystrophinopathy in Females

Por Pegoraro, Elena, Schimke, R. Neil, Arahata, Kiichi, Hayashi, Yukiko, Stern, Harvey, Marks, Harold, Glasberg, Mark R., Carroll, James E., Taber, Joseph W., Wessel, Henry B., Bauserman, Steven C., Marks, Warren A., Toriello, Helga V., Higgins, James V., Appleton, Staci, Schwartz, Lisa, Garcia, Carlos A., Hoffman, Eric P.
Publicado em 1994