A spectral acceleration attenuation model for Japan is presented in the present study. The
data set includes a very large number of strong ground-motion records up to the 2003 Off …

A new attenuation relation for peak horizontal acceleration applicable to the near source
region in Japan is developed. The data base consists of 1372 horizontal components of peak …

We isolated NSD1 from the 5q35 breakpoint in an individual with Sotos syndrome harboring
a chromosomal translocation. We identified 1 nonsense, 3 frameshift and 20 …

A previously unrecognized mental retardation malformation syndrome was observed in five
unrelated Japanese children. Consistent clinical features included moderate-to-severe …

Kawasaki disease is a pediatric systemic vasculitis of unknown etiology for which a genetic
influence is suspected. We identified a functional SNP (itpkc_3) in the inositol 1,4,5-…

By exome sequencing, we found de novo SMARCB1 mutations in two of five individuals
with typical Coffin-Siris syndrome (CSS), a rare autosomal dominant anomaly syndrome. As …

Following the 1995 Hyogo-ken Nanbu Kobe. Earthquake, the Japanese government, in an
effort to prevent future earthquake disasters, installed networks consisting of a large number …

These 62 patients with the Kabuki make‐up syndrome (KMS) were collected in a
collaborative study among 33 institutions and analyzed clinically, cytogenetically, and …

cDNA clones encoding a glucose transporter-like protein have been isolated from adult
human liver and kidney cDNA libraries by cross-hybridization with the human HepG2/erythrocyte …

p57 KIP2 is a potent tight-binding inhibitor of several G 1 cyclin/Cdk complexes, and is a
negative regulator of cell proliferation 1 , 2 . The gene encoding p57 KIP2 is located at 11p15.5 (…