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

Glial reactivity and cognitive decline follow chronic heterochromatin loss in neurons.

神经元异染色质慢性丢失会导致神经胶质反应性增强和认知能力下降

Newman A G, Sharif J, Bessa P, Zaqout S, Brown J P, Richter D, Dannenberg R, Nakayama M, Mueller S, Schaub T, Manickaraj S, Boehm-Sturm P, Ohara O, Koseki H, Singh P B, Tarabykin V

Remarkable improvement of articular pain by biologics in a Multicentric carpotarsal osteolysis patient with a mutation of MAFB gene

生物制剂显著改善了一例携带MAFB基因突变的多中心腕跗骨骨溶解患者的关节疼痛。

Cortes-Telles, Arturo; Pou-Aguilar, Yuri Noemí; Figueroa-Hurtado, Esperanza; Vazquez-Lopez, Saul; Ortiz, Diana L; Nishikomori, R; Kawai, T; Toshiyuki, K; Oda, H; Yasumi, T; Izawa, K; Ohara, O; Heike, T

PW02-022 - Recurrent fever syndromes: multiple gene mutations

PW02-022 - 复发性发热综合征:多基因突变

Sanner, Helga; Schwartz, Thomas; Flatø, Berit; Vistnes, Maria; Christensen, Geir; Sjaastad, Ivar; Piram, M; Koné-Paut, I; Gattorno, M; Ruperto, N; Kawai, T; Nishikomori, R; Awaya, M; Nakagawa, K; Izawa, K; Yasumi, T; Ohara, O; Heike, T; Alberighi, O Della Casa; Accame, L; Frenkel, J; Gattorno, M; Martini, A; Neven, B; Quartier, P; Pierotti, F; Turchetti, G; Caorsi, R; Insalaco, A; Marotto, D; Frenkel, J; Martini, A; De Benedetti, F; Gattorno, M; Bohm, M; Dolezalova, P; Lachmann, H; Modesto, C; Touitou, I; Woo, P; Finetti, M; Hentgen, V; Cantarini, L; De Benedetti, F; Gallizzi, R; Obici, L; Manna, R; Gallo, E; Ruperto, N; Gattorno, M

Diagnosis of NLRP3 somatic mosaicism in CINCA/NOMID patients using next-generation sequencing

利用新一代测序技术诊断CINCA/NOMID患者的NLRP3体细胞嵌合现象

Rinehart, Jesse; Vázquez, Norma; Kahle, Kristopher T; Hodson, Caleb A; Ring, Aaron M; Gulcicek, Erol E; Louvi, Angeliki; Bobadilla, Norma A; Gamba, Gerardo; Lifton, Richard P; Izawa, K; Nishikomori, R; Tanikaze, N; Saito, MK; Goldbach-Mansky, R; Aksentijevich, I; Yasumi, T; Kawai, T; Nakahata, T; Heike, T; Ohara, O

Unique activation status of peripheral blood mononuclear cells at acute phase of Kawasaki disease

川崎病急性期外周血单核细胞的独特激活状态

Ikeda, K; Yamaguchi, K; Tanaka, T; Mizuno, Y; Hijikata, A; Ohara, O; Takada, H; Kusuhara, K; Hara, T

Directional cDNA library construction assisted by the in vitro recombination reaction

体外重组反应辅助的定向cDNA文库构建

Ohara, O; Temple, G

Association of structural polymorphisms in the human period3 gene with delayed sleep phase syndrome

人类周期3基因结构多态性与睡眠相位延迟综合征的关联

Ebisawa, T; Uchiyama, M; Kajimura, N; Mishima, K; Kamei, Y; Katoh, M; Watanabe, T; Sekimoto, M; Shibui, K; Kim, K; Kudo, Y; Ozeki, Y; Sugishita, M; Toyoshima, R; Inoue, Y; Yamada, N; Nagase, T; Ozaki, N; Ohara, O; Ishida, N; Okawa, M; Takahashi, K; Yamauchi, T

HUGE: a database for human large proteins identified by Kazusa cDNA sequencing project

HUGE:一个收录了Kazusa cDNA测序项目鉴定的人类大型蛋白质的数据库

Suyama, M; Nagase, T; Ohara, O

A DNA cycle sequencing reaction that minimizes compressions on automated fluorescent sequencers

一种可最大限度减少自动荧光测序仪压缩的DNA循环测序反应

Yamakawa, H; Ohara, O

Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene

鹌鹑神经丝缺乏症是由神经丝L基因的无义突变引起的。

Ohara, O; Gahara, Y; Miyake, T; Teraoka, H; Kitamura, T