Yasunobu Yokoyama

The Partner Gene of AML1 in t(16;21) Myeloid Malignancies Is a Novel Member of the MTG8(ETO) Family

Toshie Gamou, Eiko Kitamura, Fumie Hosoda et al. · Blood · 1998 · 224 citations

Human amnion mesenchyme cells express phenotypes of neuroglial progenitor cells

Norio Sakuragawa, Kenichi Kakinuma, Aiko Kikuchi et al. · Journal of Neuroscience Research · 2004 · 139 citations

Evidence for active acetylcholine metabolism in human amniotic epithelial cells: applicable to intracerebral allografting for neurologic disease

Norio Sakuragawa, H. Misawa, Keiko Ohsugi et al. · Neuroscience Letters · 1997 · 109 citations

Neurodegenerative Diseases, Neurophysiology, Physiology +12

Skewed X-chromosome inactivation causes intra-familial phenotypic variation of an EBP mutation in a family with X-linked dominant chondrodysplasia punctata

Shuya Shirahama, Akira Miyahara, Hiroshi Kitoh et al. · Human Genetics · 2003 · 52 citations

Mendelian Disorder, Cytogenetics, Intra-familial Phenotypic Variation +10

Establishment of a leukaemic cell line from a patient with acquisition of chromosomal abnormalities during disease progression in myelodysplastic syndrome

Toshitaro Nakagawa, Sachiko Matozaki, Tohru Murayama et al. · British Journal of Haematology · 1993 · 50 citations