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Michiko Miyaki

Hereditary Tumor Research Project

Tokyo Metropolitan Komagome Hospital

Bunkyo-ku

Tokyo

Japan

[email]@*.famille.ne.jp

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Hereditary Tumor Research Project, Tokyo Metropolitan Komagome Hospital, Bunkyo-ku, Tokyo, Japan. 1999 - 2008
  • Hereditary Tumor Research Project, Department of Pathology, Tokyo Metropolitan Komagome Hospital. Institute of Molecular Oncology. Showa University. Sasaki Institute, Tokyo, Japan. 2000 - 2004

References

  1. Difference in characteristics of APC mutations between colonic and extracolonic tumors of FAP patients: variations with phenotype. Miyaki, M., Yamaguchi, T., Iijima, T., Takahashi, K., Matsumoto, H., Yasutome, M., Funata, N., Mori, T. Int. J. Cancer (2008) [Pubmed]
  2. Mutations of the PIK3CA gene in hereditary colorectal cancers. Miyaki, M., Iijima, T., Yamaguchi, T., Takahashi, K., Matsumoto, H., Yasutome, M., Funata, N., Mori, T. Int. J. Cancer (2007) [Pubmed]
  3. Germline mutations of the MYH gene in Japanese patients with multiple colorectal adenomas. Miyaki, M., Iijima, T., Yamaguchi, T., Hishima, T., Tamura, K., Utsunomiya, J., Mori, T. Mutat. Res. (2005) [Pubmed]
  4. Novel germline hMSH2 genomic deletion and somatic hMSH2 mutations in a hereditary nonpolyposis colorectal cancer family. Miyaki, M., Iijima, T., Yamaguchi, T., Shirahama, S., Ito, T., Yasuno, M., Mori, T. Mutat. Res. (2004) [Pubmed]
  5. Both BRAF and KRAS mutations are rare in colorectal carcinomas from patients with hereditary nonpolyposis colorectal cancer. Miyaki, M., Iijima, T., Yamaguchi, T., Kadofuku, T., Funata, N., Mori, T. Cancer Lett. (2004) [Pubmed]
  6. Increased frequency of p53 mutation in sporadic colorectal cancer from cigarette smokers. Miyaki, M., Iijima, T., Ishii, R., Kita, Y., Koike, M., Kuroki, T., Mori, T. Jpn. J. Clin. Oncol. (2002) [Pubmed]
  7. High incidence of protein-truncating mutations of the p53 gene in liver metastases of colorectal carcinomas. Miyaki, M., Iijima, T., Yasuno, M., Kita, Y., Hishima, T., Kuroki, T., Mori, T. Oncogene (2002) [Pubmed]
  8. Alterations of repeated sequences in 5' upstream and coding regions in colorectal tumors from patients with hereditary nonpolyposis colorectal cancer and Turcot syndrome. Miyaki, M., Iijima, T., Shiba, K., Aki, T., Kita, Y., Yasuno, M., Mori, T., Kuroki, T., Iwama, T. Oncogene (2001) [Pubmed]
  9. Malignant transformation and EGFR activation of immortalized mouse liver epithelial cells caused by HBV enhancer-X from a human hepatocellular carcinoma. Miyaki, M., Sato, C., Sakai, K., Konishi, M., Tanaka, K., Muraoka, M., Kikuchi-Yanoshita, R., Nadaoka, Y., Kanda, H., Kitagawa, T. Int. J. Cancer (2000) [Pubmed]
  10. Somatic mutations of LKB1 and beta-catenin genes in gastrointestinal polyps from patients with Peutz-Jeghers syndrome. Miyaki, M., Iijima, T., Hosono, K., Ishii, R., Yasuno, M., Mori, T., Toi, M., Hishima, T., Shitara, N., Tamura, K., Utsunomiya, J., Kobayashi, N., Kuroki, T., Iwama, T. Cancer Res. (2000) [Pubmed]
  11. Molecular evidence for multicentric development of thyroid carcinomas in patients with familial adenomatous polyposis. Miyaki, M., Iijima, T., Ishii, R., Hishima, T., Mori, T., Yoshinaga, K., Takami, H., Kuroki, T., Iwama, T. Am. J. Pathol. (2000) [Pubmed]
  12. Frequent mutation of beta-catenin and APC genes in primary colorectal tumors from patients with hereditary nonpolyposis colorectal cancer. Miyaki, M., Iijima, T., Kimura, J., Yasuno, M., Mori, T., Hayashi, Y., Koike, M., Shitara, N., Iwama, T., Kuroki, T. Cancer Res. (1999) [Pubmed]
 
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