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

[GPSM2 is highly expressed in gastric cancer to affect patient prognosis by promoting tumor cell proliferation]

GPSM2在胃癌中高表达,通过促进肿瘤细胞增殖影响患者预后。

Song, Xue; Chen, Yue; Zhang, Min; Zhang, Nuo; Zuo, Lugen; Li, Jing; Geng, Zhijun; Zhang, Xiaofeng; Wang, Yueyue; Wang, Lian; Hu, Jianguo

Truncated isoforms of GPSM2 containing the GoLoco motif region promote CD4(+) T-cell migration in SLE

含有 GoLoco 基序区域的 GPSM2 截短亚型促进 SLE 中的 CD4(+) T 细胞迁移

Esser, Ruth L; Brück, Carolin; Thiele, Jan; Golumba-Nagy, Viktoria; Meyer, Anja; Steinbach-Knödgen, Eva; Yan, Shuaifeng; Tho Pesch, Carola; Stahl, David; Schiller, Joanna; Kofler, David M

Interaction between Discs large and Pins/LGN/GPSM2: a comparison across species

Discs large 与 Pins/LGN/GPSM2 之间的相互作用:跨物种比较

Schiller, Emily A; Bergstralh, Dan T

Downregulation of GPSM2 is associated with primary resistance to paclitaxel in breast cancer

GPSM2表达下调与乳腺癌对紫杉醇的原发性耐药相关

Zhang, Zhe; Li, Zhi; Deng, Mingming; Liu, Bofang; Xin, Xing; Zhao, Zhenkun; Zhang, Ye; Lv, Qingjie

GPSM2 Serves as an Independent Prognostic Biomarker for Liver Cancer Survival

GPSM2 可作为肝癌生存的独立预后生物标志物

Yang, Dingquan; Ji, Fujian; Li, Yanqing; Jiao, Yan; Fang, Xuedong

MARK2/Par1b kinase present at centrosomes and retraction fibres corrects spindle off-centring induced by actin disassembly

着丝粒和回缩纤维中存在的 MARK2/Par1b 激酶可纠正肌动蛋白分解引起的纺锤体偏心

Madeleine Hart, Ihsan Zulkipli, Roshan Lal Shrestha, David Dang, Duccio Conti, Parveen Gul, Izabela Kujawiak, Viji M Draviam

Dynein-Dynactin-NuMA clusters generate cortical spindle-pulling forces as a multi-arm ensemble

Dynein-Dynactin-NuMA 簇作为多臂整体产生皮质纺锤体拉力

Masako Okumura, Toyoaki Natsume, Masato T Kanemaki, Tomomi Kiyomitsu

GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndrome

GPSM2基因突变会导致丘德利-麦卡洛综合征中的脑畸形和听力丧失。

Doherty, Dan; Chudley, Albert E; Coghlan, Gail; Ishak, Gisele E; Innes, A Micheil; Lemire, Edmond G; Rogers, R Curtis; Mhanni, Aizeddin A; Phelps, Ian G; Jones, Steven J M; Zhan, Shing H; Fejes, Anthony P; Shahin, Hashem; Kanaan, Moien; Akay, Hatice; Tekin, Mustafa; Triggs-Raine, Barbara; Zelinski, Teresa

A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss

GPSM2基因的截断突变与隐性非综合征性听力损失相关。

Yariz, K O; Walsh, T; Akay, H; Duman, D; Akkaynak, A C; King, M-C; Tekin, M

Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82

全外显子组测序和纯合性作图鉴定出细胞极性蛋白GPSM2的突变是导致非综合征性听力损失DFNB82的原因。

Walsh, Tom; Shahin, Hashem; Elkan-Miller, Tal; Lee, Ming K; Thornton, Anne M; Roeb, Wendy; Abu Rayyan, Amal; Loulus, Suheir; Avraham, Karen B; King, Mary-Claire; Kanaan, Moien