8 results for author:"Wagatsuma M." in Literature citations
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| The responsible genes in Japanese deafness patients and clinical application using Invader assay. Usami S., Wagatsuma M., Fukuoka H., Suzuki H., Tsukada K., Nishio S., Takumi Y., Abe S. Acta Otolaryngol. 128:446-454(2008) · Mapped (19) |
| Distribution and frequencies of CDH23 mutations in Japanese patients with non-syndromic hearing loss. Wagatsuma M., Kitoh R., Suzuki H., Fukuoka H., Takumi Y., Usami S. |
| A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene. Van Camp G., Snoeckx R.L., Hilgert N., van den Ende J., Fukuoka H., Wagatsuma M., Suzuki H., Smets R.M., Vanhoenacker F., Declau F. et al. Am. J. Hum. Genet. 79:449-457(2006) · UniProtKB (1) · Mapped (1) |
| Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. Kimura K., Wakamatsu A., Suzuki Y., Ota T., Nishikawa T., Yamashita R., Yamamoto J., Sekine M., Tsuritani K., Wakaguri H. et al. Genome Res. 16:55-65(2006) · UniProtKB (18) |
| Complete sequencing and characterization of 21,243 full-length human cDNAs. Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K. et al. Nat. Genet. 36:40-45(2004) · UniProtKB (12,387) |
| Cloning and characterization of a novel subunit of protein serine/threonine phosphatase 4 from mesangial cells. Wada T., Miyata T., Inagi R., Nangaku M., Wagatsuma M., Suzuki D., Wadzinski B.E., Okubo K., Kurokawa K. J. Am. Soc. Nephrol. 12:2601-2608(2001) · UniProtKB (2) · Mapped (1) |
| Sequences of two porcine glutamic acid decarboxylases (65- and 67-kDa GAD). Suzuki R., Asami N., Amann E., Wagatsuma M. Gene 152:257-260(1995) · UniProtKB (2) |
| Antithrombin III Kumamoto II; a single mutation at Arg393-His increased the affinity of antithrombin III for heparin. Okajima K., Abe H., Wagatsuma M., Okabe H., Takatsuki K. Am. J. Hematol. 48:12-18(1995) · UniProtKB (1) |