Y. Koshiba

Genetic and pharmacological correction of aberrant dopamine synthesis using patient iPSCs with BH 4 metabolism disorders

M. Kinoshita, R. Takahashi, H. Inoue, 2017 .

Genetic and pharmacological correction of aberrant dopamine synthesis using patient iPSCs with BH4 metabolism disorders

M. Kinoshita, R. Takahashi, H. Inoue, 2016, Human molecular genetics.

Pregnancy rates and briths after co-culture of cumulus cells with bovine embryos derived from in vitro fertilization of in-vitro matured follicular oocytes☆

K. Goto, S. Kobayashi, Y. Koshiba, 1990 .

Cytoplasmic aggregates of dynactin in iPSC-derived tyrosine hydroxylase-positive neurons from a patient with Perry syndrome.

R. Takahashi, H. Inoue, A. Watanabe, 2016, Parkinsonism & related disorders.

Molecular insights into Peutz-Jeghers syndrome: two probands with a germline mutation of LKB1

S. Nagayama, H. Okabe, Y. Sakai, 2008, Journal of Gastroenterology.

Novel LGI1 mutation in a Japanese autosomal dominant lateral temporal lobe epilepsy family

A. Ikeda, R. Matsumoto, M. Kinoshita, 2017 .