Hisahide Nishio

Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center

Yasuhiro Takeshima, Mariko Yagi, Yo Okizuka et al. · Journal of Human Genetics · 2010 · 252 citations

Life Sciences, Genetics, Molecular Genetics +12

Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy.

Naoko Narita, Hisahide Nishio, Yoshihiko Kitoh et al. · Journal of Clinical Investigation · 1993 · 201 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe.

Masafumi Matsuo, Takehiro Masumura, Hisahide Nishio et al. · Journal of Clinical Investigation · 1991 · 155 citations · Full text

Life Sciences, Genetics, Molecular Biology +15

A synthetic peptide derived from p34cdc2 is a specific and efficient substrate of src-family tyrosine kinases.

Heung‐Chin Cheng, Hisahide Nishio, O. Hatase et al. · Journal of Biological Chemistry · 1992 · 150 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +15

Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy: three SMN2 copies fail to rescue some patients from the disease severity

Yosuke Harada, Retno Sutomo, Ahmad Hamim Sadewa et al. · Journal of Neurology · 2002 · 135 citations

Life Sciences, Genetics, Molecular Genetics +13