Browsing by Author Yoshida, K.

Showing results 1 to 9 of 9
Issue DateTitleAuthor(s)
2000A comparison between two neural network rule extraction techniques for the diagnosis of hepatobiliary disordersHayashi, Y.; Setiono, R. ; Yoshida, K.
Jan-2011A nonsense mutation of IDH1 in myelodysplastic syndromes and related disordersYoshida, K.; Sanada, M.; Kato, M.; Kawahata, R.; Matsubara, A.; Takita, J.; Shih, L.-Y.; Mori, H.; Koeffler, H.P. ; Ogawa, S.
2004Frequent loss of RUNX3 expression by promoter hypermethylation in gastric carcinomaOshimo, Y.; Oue, N.; Mitani, Y.; Nakayama, H.; Yasui, W.; Kitadai, Y.; Chayama, K.; Yoshida, K.; Ito, Y. 
2004Frequent loss of RUNX3 expression by promoter hypermethylation in gastric carcinomaOshimo, Y.; Oue, N.; Mitani, Y.; Nakayama, H.; Kitadai, Y.; Yoshida, K.; Ito, Y. ; Chayama, K.; Yasui, W.
6-Oct-2011Frequent pathway mutations of splicing machinery in myelodysplasiaYoshida, K.; Sanada, M.; Shiraishi, Y.; Nowak, D.; Nagata, Y.; Yamamoto, R.; Sato, Y.; Sato-Otsubo, A.; Kon, A.; Nagasaki, M.; Chalkidis, G.; Suzuki, Y.; Shiosaka, M.; Kawahata, R.; Yamaguchi, T.; Otsu, M.; Obara, N.; Sakata-Yanagimoto, M.; Ishiyama, K.; Mori, H.; Nolte, F.; Hofmann, W.-K.; Miyawaki, S.; Sugano, S.; Haferlach, C.; Koeffler, H.P. ; Shih, L.-Y.; Haferlach, T.; Chiba, S.; Nakauchi, H.; Miyano, S.; Ogawa, S.
2013Good stress management capability is associated with lower body mass index and restful sleep in the elderlyTeraoka, S.; Hayashida, N.; Shinkawa, T.; Taira, Y.; Nagai-Sekitani, Y.; Irie, S.; Kamasaki, T.; Nakashima-Hashiguchi, K.; Yoshida, K.; Orita, M.; Morishita, M.; Clancey, G. ; Takamura, N.
Feb-2014Landscape of genetic lesions in 944 patients with myelodysplastic syndromesHaferlach, T.; Nagata, Y.; Grossmann, V.; Okuno, Y.; Bacher, U.; Nagae, G.; Schnittger, S.; Sanada, M.; Kon, A.; Alpermann, T.; Yoshida, K.; Roller, A.; Nadarajah, N.; Shiraishi, Y.; Shiozawa, Y.; Chiba, K.; Tanaka, H.; Koeffler, H.P. ; Klein, H.-U.; Dugas, M.; Aburatani, H.; Kohlmann, A.; Miyano, S.; Haferlach, C.; Kern, W.; Ogawa, S.
Oct-2013Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasmsKon, A.; Shih, L.-Y.; Minamino, M.; Sanada, M.; Shiraishi, Y.; Nagata, Y.; Yoshida, K.; Okuno, Y.; Bando, M.; Nakato, R.; Ishikawa, S.; Sato-Otsubo, A.; Nagae, G.; Nishimoto, A.; Haferlach, C.; Nowak, D.; Sato, Y.; Alpermann, T.; Nagasaki, M.; Shimamura, T.; Tanaka, H.; Chiba, K.; Yamamoto, R.; Yamaguchi, T.; Otsu, M.; Obara, N.; Sakata-Yanagimoto, M.; Nakamaki, T.; Ishiyama, K.; Nolte, F.; Hofmann, W.-K.; Miyawaki, S.; Chiba, S.; Mori, H.; Nakauchi, H.; Koeffler, H.P. ; Aburatani, H.; Haferlach, T.; Shirahige, K.; Miyano, S.; Ogawa, S.
11-Oct-2012SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML)Meggendorfer, M.; Roller, A.; Haferlach, T.; Eder, C.; Dicker, F.; Grossmann, V.; Kohlmann, A.; Alpermann, T.; Yoshida, K.; Ogawa, S.; Koeffler, H.P. ; Kern, W.; Haferlach, C.; Schnittger, S.