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26
results
for author:"Oshima A."
in Literature Citations
| Structure of the connexin 26 gap junction channel at 3.5 A resolution. Maeda S., Nakagawa S., Suga M., Yamashita E., Oshima A., Fujiyoshi Y., Tsukihara T. Nature 458:597-602(2009) · Mapped (2) |
| Projection structure of a N-terminal deletion mutant of connexin 26 channel with decreased central pore density. Oshima A., Tani K., Hiroaki Y., Fujiyoshi Y., Sosinsky G.E. Cell Commun. Adhes. 15:85-93(2008) · Mapped (2) |
| The localization of proteins encoded by CRYM, KIAA1199, UBA52, COL9A3, and COL9A1, genes highly expressed in the cochlea. Usami S., Takumi Y., Suzuki N., Oguchi T., Oshima A., Suzuki H., Kitoh R., Abe S., Sasaki A., Matsubara A. Neuroscience 154:22-28(2008) · Mapped (21) |
| Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type I. Oshima A., Jaijo T., Aller E., Millan J.M., Carney C., Usami S., Moller C., Kimberling W.J. |
| Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutations. Suzuki H., Oshima A., Tsukamoto K., Abe S., Kumakawa K., Nagai K., Satoh H., Kanda Y., Iwasaki S., Usami S. Acta Otolaryngol. 127:1292-1297(2007) · Mapped (5) |
| Three-dimensional structure of a human connexin26 gap junction channel reveals a plug in the vestibule. Oshima A., Tani K., Hiroaki Y., Fujiyoshi Y., Sosinsky G.E. Proc. Natl. Acad. Sci. U.S.A. 104:10034-10039(2007) · Mapped (2) |
| micro-Crystallin as an intracellular 3,5,3'-triiodothyronine holder in vivo. Suzuki S., Suzuki N., Mori J., Oshima A., Usami S., Hashizume K. Mol. Endocrinol. 21:885-894(2007) · Mapped (2) |
| Reciprocal modifications of CLIC4 in tumor epithelium and stroma mark malignant progression of multiple human cancers. Suh K.S., Crutchley J.M., Koochek A., Ryscavage A., Bhat K., Tanaka T., Oshima A., Fitzgerald P., Yuspa S.H. Clin. Cancer Res. 13:121-131(2007) · UniProtKB (1) · Mapped (4) |
| Mutation of a conserved threonine in the third transmembrane helix of alpha- and beta-connexins creates a dominant-negative closed gap junction channel. Beahm D.L., Oshima A., Gaietta G.M., Hand G.M., Smock A.E., Zucker S.N., Toloue M.M., Chandrasekhar A., Nicholson B.J., Sosinsky G.E. J. Biol. Chem. 281:7994-8009(2006) · Mapped (8) |
| Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns. Oguchi T., Ohtsuka A., Hashimoto S., Oshima A., Abe S., Kobayashi Y., Nagai K., Matsunaga T., Iwasaki S., Nakagawa T. et al. J. Hum. Genet. 50:76-83(2005) · Mapped (2) |
| 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 (11,439) · Mapped (2) |
| Roles of Met-34, Cys-64, and Arg-75 in the assembly of human connexin 26. Implication for key amino acid residues for channel formation and function. Oshima A., Doi T., Mitsuoka K., Maeda S., Fujiyoshi Y. J. Biol. Chem. 278:1807-1816(2003) · Mapped (2) |
| Development of lysosomal storage in mice with targeted disruption of the beta-galactosidase gene: a model of human G(M1)-gangliosidosis. Itoh M., Matsuda J., Suzuki O., Ogura A., Oshima A., Tai T., Suzuki Y., Takashima S. Brain Dev. 23:379-384(2001) · Mapped (2) |
| Beta-galactosidase-deficient mouse as an animal model for GM1-gangliosidosis. Matsuda J., Suzuki O., Oshima A., Ogura A., Noguchi Y., Yamamoto Y., Asano T., Takimoto K., Sukegawa K., Suzuki Y. et al. Glycoconj. J. 14:729-736(1997) · Mapped (2) |
| Human IgGFc binding protein (FcgammaBP) in colonic epithelial cells exhibits mucin-like structure. Harada N., Iijima S., Kobayashi K., Yoshida T., Brown W.R., Hibi T., Oshima A., Morikawa M. J. Biol. Chem. 272:15232-15241(1997) · UniProtKB (1) |
| Neurological manifestations of knockout mice with beta-galactosidase deficiency. Matsuda J., Suzuki O., Oshima A., Ogura A., Naiki M., Suzuki Y. Brain Dev. 19:19-20(1997) · Mapped (2) |
| Protective protein gene mutations in galactosialidosis. Shimmoto M., Fukuhara Y., Itoh K., Oshima A., Sakuraba H., Suzuki Y. J. Clin. Invest. 91:2393-2398(1993) · UniProtKB (1) |
| Clinical and molecular analysis of a Japanese boy with Morquio B disease. Ishii N., Oohira T., Oshima A., Sakuraba H., Endo F., Matsuda I., Sukegawa K., Orii T., Suzuki Y. Clin. Genet. 48:103-108(1995) · UniProtKB (1) |
| Regulation of phosphatidylethanolamine methyltransferase level by myo-inositol in Saccaromyces cerevisiae. Yamashita S., Oshima A. Eur. J. Biochem. 104:611-616(1980) · Mapped (1) |
| Regulation of the phosphatidylethanolamine methylation pathway in Saccharomyces cerevisiae. Yamashita S., Oshima A., Nikawa J., Hosaka K. Eur. J. Biochem. 128:589-595(1982) · Mapped (2) |
| Cloning, sequencing, and expression of cDNA for human beta-glucuronidase. Oshima A., Kyle J.W., Miller R.D., Hoffmann J.W., Powell P.P., Grubb J.H., Sly W.S., Tropak M., Guise K.S., Gravel R.A. Proc. Natl. Acad. Sci. U.S.A. 84:685-689(1987) · UniProtKB (1) · Mapped (1) |
| Cloning, sequencing, and expression of cDNA for human beta-galactosidase. Oshima A., Tsuji A., Nagao Y., Sakuraba H., Suzuki Y. Biochem. Biophys. Res. Commun. 157:238-244(1988) · UniProtKB (1) |
| The human cation-independent mannose 6-phosphate receptor. Cloning and sequence of the full-length cDNA and expression of functional receptor in COS cells. Oshima A., Nolan C.M., Kyle J.W., Grubb J.H., Sly W.S. J. Biol. Chem. 263:2553-2562(1988) · UniProtKB (2) |
| Identification of point mutations in the alpha-galactosidase A gene in classical and atypical hemizygotes with Fabry disease. Sakuraba H., Oshima A., Fukuhara Y., Shimmoto M., Nagao Y., Bishop D.F., Desnick R.J., Suzuki Y. Am. J. Hum. Genet. 47:784-789(1990) · UniProtKB (1) |
| Human beta-galactosidase gene mutations in morquio B disease. Oshima A., Yoshida K., Shimmoto M., Fukuhara Y., Sakuraba H., Suzuki Y. Am. J. Hum. Genet. 49:1091-1093(1991) · UniProtKB (1) |
