11 results for author:"Shimozato K." in Literature citations
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| Impact of CRTC1/3-MAML2 fusions on histological classification and prognosis of mucoepidermoid carcinoma. Okumura Y., Miyabe S., Nakayama T., Fujiyoshi Y., Hattori H., Shimozato K., Inagaki H. Histopathology 59:90-97(2011) · Mapped (5) |
| Clinical and functional data implicate the Arg(151)Ser variant of MSX1 in familial hypodontia. Kamamoto M., Machida J., Yamaguchi S., Kimura M., Ono T., Jezewski P.A., Higashi Y., Nakayama A., Shimozato K., Tokita Y. Eur. J. Hum. Genet. 19:844-850(2011) · Mapped (2) |
| Two missense mutations of the IRF6 gene in two Japanese families with popliteal pterygium syndrome. Matsuzawa N., Kondo S., Shimozato K., Nagao T., Nakano M., Tsuda M., Hirano A., Niikawa N., Yoshiura K. Am. J. Med. Genet. A 152:2262-2267(2010) · UniProtKB (1) · Mapped (5) |
| Searching for genes for cleft lip and/or palate based on breakpoint analysis of a balanced translocation t(9;17)(q32;q12). Machida J., Felix T.M., Murray J.C., Yoshiura K., Tanemura M., Kamamoto M., Shimozato K., Sonta S., Ono T. Cleft Palate Craniofac. J. 46:532-540(2009) · Mapped (7) |
| Clinicopathological significance of the CRTC3-MAML2 fusion transcript in mucoepidermoid carcinoma. Nakayama T., Miyabe S., Okabe M., Sakuma H., Ijichi K., Hasegawa Y., Nagatsuka H., Shimozato K., Inagaki H. Mod. Pathol. 22:1575-1581(2009) · Mapped (3) |
| Prognostic significance of p27Kip1, Ki-67, and CRTC1-MAML2 fusion transcript in mucoepidermoid carcinoma: a molecular and clinicopathologic study of 101 cases. Miyabe S., Okabe M., Nagatsuka H., Hasegawa Y., Inagaki A., Ijichi K., Nagai N., Eimoto T., Yokoi M., Shimozato K. et al. J. Oral Maxillofac. Surg. 67:1432-1441(2009) · Mapped (13) |
| Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip. Suzuki S., Marazita M.L., Cooper M.E., Miwa N., Hing A., Jugessur A., Natsume N., Shimozato K., Ohbayashi N., Suzuki Y. et al. Am. J. Hum. Genet. 84:406-411(2009) · UniProtKB (1) · Mapped (1) |
| Characterization of RagA and RagB in Porphyromonas gingivalis: study using gene-deletion mutants. Nagano K., Murakami Y., Nishikawa K., Sakakibara J., Shimozato K., Yoshimura F. J. Med. Microbiol. 56:1536-1548(2007) · UniProtKB (2) |
| A novel missense mutation in Van der Woude syndrome: usefulness of fingernail DNA for genetic analysis. Matsuzawa N., Shimozato K., Natsume N., Niikawa N., Yoshiura K. J. Dent. Res. 85:1143-1146(2006) · UniProtKB (1) |
| MECT1-MAML2 fusion transcript defines a favorable subset of mucoepidermoid carcinoma. Okabe M., Miyabe S., Nagatsuka H., Terada A., Hanai N., Yokoi M., Shimozato K., Eimoto T., Nakamura S., Nagai N. et al. Clin. Cancer Res. 12:3902-3907(2006) · Mapped (3) |
| Identification of specific autoantigens in Sjoegren's syndrome by SEREX. Uchida K., Akita Y., Matsuo K., Fujiwara S., Nakagawa A., Kazaoka Y., Hachiya H., Naganawa Y., Oh-Iwa I., Ohura K. et al. Immunology 116:53-63(2005) · UniProtKB (1) |