6 results for author:"Yokoseki A." in Literature citations
Results Customize
› Repeat search in UniProtKB (2)
| Cerebral small-vessel disease protein HTRA1 controls the amount of TGF-beta1 via cleavage of proTGF-beta1. Shiga A., Nozaki H., Yokoseki A., Nihonmatsu M., Kawata H., Kato T., Koyama A., Arima K., Ikeda M., Katada S. et al. Hum. Mol. Genet. 20:1800-1810(2011) · Mapped (13) |
| The implications of TDP-43 mutations in pathogenesis of amyotrophic lateral sclerosis. Ishihara T., Yokoseki A., Nishizawa M., Takahashi H., Onodera O. Brain Nerve 61:1301-1307(2009) · Mapped (5) |
| Selective occurrence of TDP-43-immunoreactive inclusions in the lower motor neurons in Machado-Joseph disease. Tan C.F., Yamada M., Toyoshima Y., Yokoseki A., Miki Y., Hoshi Y., Kaneko H., Ikeuchi T., Onodera O., Kakita A. et al. Acta Neuropathol. 118:553-560(2009) · Mapped (5) |
| Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease. Hara K., Shiga A., Fukutake T., Nozaki H., Miyashita A., Yokoseki A., Kawata H., Koyama A., Arima K., Takahashi T. et al. N. Engl. J. Med. 360:1729-1739(2009) · UniProtKB (1) · Mapped (3) |
| TDP-43 mutation in familial amyotrophic lateral sclerosis. Yokoseki A., Shiga A., Tan C.F., Tagawa A., Kaneko H., Koyama A., Eguchi H., Tsujino A., Ikeuchi T., Kakita A. et al. |
| Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3'-phosphate and 3'-phosphoglycolate ends. Takahashi T., Tada M., Igarashi S., Koyama A., Date H., Yokoseki A., Shiga A., Yoshida Y., Tsuji S., Nishizawa M. et al. Nucleic Acids Res. 35:3797-3809(2007) |