日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

First observation of (28)O

首次观测到 (28)O

Kondo, Y; Achouri, N L; Falou, H Al; Atar, L; Aumann, T; Baba, H; Boretzky, K; Caesar, C; Calvet, D; Chae, H; Chiga, N; Corsi, A; Delaunay, F; Delbart, A; Deshayes, Q; Dombrádi, Zs; Douma, C A; Ekström, A; Elekes, Z; Forssén, C; Gašparić, I; Gheller, J-M; Gibelin, J; Gillibert, A; Hagen, G; Harakeh, M N; Hirayama, A; Hoffman, C R; Holl, M; Horvat, A; Horváth, Á; Hwang, J W; Isobe, T; Jiang, W G; Kahlbow, J; Kalantar-Nayestanaki, N; Kawase, S; Kim, S; Kisamori, K; Kobayashi, T; Körper, D; Koyama, S; Kuti, I; Lapoux, V; Lindberg, S; Marqués, F M; Masuoka, S; Mayer, J; Miki, K; Murakami, T; Najafi, M; Nakamura, T; Nakano, K; Nakatsuka, N; Nilsson, T; Obertelli, A; Ogata, K; de Oliveira Santos, F; Orr, N A; Otsu, H; Otsuka, T; Ozaki, T; Panin, V; Papenbrock, T; Paschalis, S; Revel, A; Rossi, D; Saito, A T; Saito, T Y; Sasano, M; Sato, H; Satou, Y; Scheit, H; Schindler, F; Schrock, P; Shikata, M; Shimizu, N; Shimizu, Y; Simon, H; Sohler, D; Sorlin, O; Stuhl, L; Sun, Z H; Takeuchi, S; Tanaka, M; Thoennessen, M; Törnqvist, H; Togano, Y; Tomai, T; Tscheuschner, J; Tsubota, J; Tsunoda, N; Uesaka, T; Utsuno, Y; Vernon, I; Wang, H; Yang, Z; Yasuda, M; Yoneda, K; Yoshida, S

Publisher Correction: First observation of (28)O

出版商更正:首次观测到 (28)O

Kondo, Y; Achouri, N L; Falou, H Al; Atar, L; Aumann, T; Baba, H; Boretzky, K; Caesar, C; Calvet, D; Chae, H; Chiga, N; Corsi, A; Delaunay, F; Delbart, A; Deshayes, Q; Dombrádi, Zs; Douma, C A; Ekström, A; Elekes, Z; Forssén, C; Gašparić, I; Gheller, J-M; Gibelin, J; Gillibert, A; Hagen, G; Harakeh, M N; Hirayama, A; Hoffman, C R; Holl, M; Horvat, A; Horváth, Á; Hwang, J W; Isobe, T; Jiang, W G; Kahlbow, J; Kalantar-Nayestanaki, N; Kawase, S; Kim, S; Kisamori, K; Kobayashi, T; Körper, D; Koyama, S; Kuti, I; Lapoux, V; Lindberg, S; Marqués, F M; Masuoka, S; Mayer, J; Miki, K; Murakami, T; Najafi, M; Nakamura, T; Nakano, K; Nakatsuka, N; Nilsson, T; Obertelli, A; Ogata, K; de Oliveira Santos, F; Orr, N A; Otsu, H; Otsuka, T; Ozaki, T; Panin, V; Papenbrock, T; Paschalis, S; Revel, A; Rossi, D; Saito, A T; Saito, T Y; Sasano, M; Sato, H; Satou, Y; Scheit, H; Schindler, F; Schrock, P; Shikata, M; Shimizu, N; Shimizu, Y; Simon, H; Sohler, D; Sorlin, O; Stuhl, L; Sun, Z H; Takeuchi, S; Tanaka, M; Thoennessen, M; Törnqvist, H; Togano, Y; Tomai, T; Tscheuschner, J; Tsubota, J; Tsunoda, N; Uesaka, T; Utsuno, Y; Vernon, I; Wang, H; Yang, Z; Yasuda, M; Yoneda, K; Yoshida, S

Adhesion of Epstein-Barr virus-positive natural killer cell lines to cultured endothelial cells stimulated with inflammatory cytokines

Epstein-Barr病毒阳性自然杀伤细胞系与经炎症细胞因子刺激的培养内皮细胞的粘附

Kanno, H; Watabe, D; Shimizu, N; Sawai, T

Epithelial overexpression of interleukin-32alpha in inflammatory bowel disease

炎症性肠病中上皮细胞白细胞介素-32α的过度表达

Shioya, M; Nishida, A; Yagi, Y; Ogawa, A; Tsujikawa, T; Kim-Mitsuyama, S; Takayanagi, A; Shimizu, N; Fujiyama, Y; Andoh, A

Transcriptional profiling of Epstein-Barr virus (EBV) genes and host cellular genes in nasal NK/T-cell lymphoma and chronic active EBV infection.

鼻腔NK/T细胞淋巴瘤和慢性活动性EBV感染中Epstein-Barr病毒(EBV)基因和宿主细胞基因的转录谱分析

Zhang Y, Ohyashiki J H, Takaku T, Shimizu N, Ohyashiki K

Aberrant promoter methylation in human DAB2 interactive protein (hDAB2IP) gene in gastrointestinal tumour

胃肠道肿瘤中人DAB2相互作用蛋白(hDAB2IP)基因启动子异常甲基化

Dote, H; Toyooka, S; Tsukuda, K; Yano, M; Ota, T; Murakami, M; Naito, M; Toyota, M; Gazdar, A F; Shimizu, N

The KMDB/MutationView: a mutation database for human disease genes

KMDB/MutationView:人类疾病基因突变数据库

Minoshima, S; Mitsuyama, S; Ohtsubo, M; Kawamura, T; Ito, S; Shibamoto, S; Ito, F; Shimizu, N

A new neurological entity manifesting as involuntary movements and dysarthria with possible abnormal copper metabolism

一种新的神经系统疾病,表现为不自主运动和构音障碍,可能伴有铜代谢异常。

Tagawa, A; Ono, S; Shibata, M; Imai, T; Suzuki, M; Shimizu, N

Keio Mutation Database (KMDB) for human disease gene mutations

庆应突变数据库(KMDB)用于收录人类疾病基因突变

Minoshima, S; Mitsuyama, S; Ohno, S; Kawamura, T; Shimizu, N

Detailed deletion mapping of chromosome band 14q32 in human neuroblastoma defines a 1.1-Mb region of common allelic loss

对人类神经母细胞瘤中14q32染色体带的详细缺失定位,确定了一个1.1 Mb的常见等位基因缺失区域。

Hoshi, M; Otagiri, N; Shiwaku, H O; Asakawa, S; Shimizu, N; Kaneko, Y; Ohi, R; Hayashi, Y; Horii, A