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

Maxillary mesenchymal chondrosarcoma harboring HEY1::NCOA2 fusion in a 13-year-old girl: a rare case report and literature review

一例13岁女孩上颌间叶性软骨肉瘤伴HEY1::NCOA2融合基因的罕见病例报告及文献复习

Çalışkan Kamış, Şule; Yağcı, Begül; Koç, Ayşe Selcan; Durak, Güliz; Yitik, Ali

HEY1 promotes the development and metastasis of osteosarcoma through CD44/EGFR/FAK pathway

HEY1通过CD44/EGFR/FAK通路促进骨肉瘤的发生发展和转移。

Liu, Yuhang; Zhang, Hao; Yi, Xinzeyu; Wang, Zheng; Yu, Aixi

Orbital mesenchymal chondrosarcoma and its specific fusion gene HEY1-NCOA2

眼眶间叶软骨肉瘤及其特异性融合基因 HEY1-NCOA2

Lin, Jia-Qi; Liu, Xun; Zhao, Jin-Zhi; Wang, Qing; Zhu, Li-Min; Lin, Ting-Ting

SUMOylation Fine-Tunes Endothelial HEY1 in the Regulation of Angiogenesis

SUMO化修饰精细调控内皮细胞HEY1在血管生成中的表达

Ren, Ruizhe; Ding, Sha; Ma, Kefan; Jiang, Yuanqing; Wang, Yiran; Chen, Junbo; Wang, Yunyun; Kou, Yaohui; Fan, Xiao; Zhu, Xiaolong; Qin, Lingfeng; Qiu, Cong; Simons, Michael; Wei, Xiyang; Yu, Luyang

Case report: A mesenchymal chondrosarcoma with alternative HEY1::NCOA2 fusions in the sella turcica

病例报告:蝶鞍中伴有 HEY1::NCOA2 替代融合的间叶性软骨肉瘤

Kishikawa, Satsuki; Kondo, Akihide; Yao, Takashi; Saito, Tsuyoshi

Mesenchymal chondrosarcoma of the head and neck with HEY1::NCOA2 fusion: A clinicopathologic and molecular study of 13 cases with emphasis on diagnostic pitfalls

伴有 HEY1::NCOA2 融合的头颈部间叶软骨肉瘤:13 例临床病理及分子研究,重点关注诊断陷阱

Xu, Bin; Rooper, Lisa M; Dermawan, Josephine K; Zhang, Yanming; Suurmeijer, Albert J H; Dickson, Brendan C; Demicco, Elizabeth G; Antonescu, Cristina R

Cell cycle arrest determines adult neural stem cell ontogeny by an embryonic Notch-nonoscillatory Hey1 module

细胞周期阻滞通过胚胎Notch-非振荡Hey1模块决定成体神经干细胞的发育。

Yujin Harada ,Mayumi Yamada ,Itaru Imayoshi ,Ryoichiro Kageyama ,Yutaka Suzuki ,Takaaki Kuniya ,Shohei Furutachi ,Daichi Kawaguchi ,Yukiko Gotoh

CDX2 enhances natural killer cell-mediated immunotherapy against head and neck squamous cell carcinoma through up-regulating CXCL14

CDX2 通过上调 CXCL14 增强自然杀伤细胞介导的针对头颈部鳞状细胞癌的免疫治疗

Haitao Wang, Shanji Nan, Ying Wang, Chengbi Xu

8q21.11 microdeletion syndrome: Delineation of HEY1 as a candidate gene in neurodevelopmental and cardiac defects

8q21.11微缺失综合征:HEY1基因被确定为神经发育和心脏缺陷的候选基因

Ben Ayed, Ikhlas; Bouzid, Amal; Kammoun, Fatma; Souissi, Amal; Jallouli, Olfa; Mallouli, Salma; Guidara, Souhir; Loukil, Salma; Aloulou, Hajer; Jbeli, Fida; Aouichaoui, Sahar; Abid, Dorra; Abdelhedi, Fatma; Triki, Chahnez; Kamoun, Hassen; Masmoudi, Saber

Over-expression of CDX2 alleviates breast cancer by up-regulating microRNA let-7b and inhibiting COL11A1 expression

CDX2 的过度表达通过上调 microRNA let-7b 和抑制 COL11A1 表达来缓解乳腺癌

Hongbin Wang #, Yanlv Ren #, Cheng Qian, Jiaxin Liu, Ge Li, Zhigao Li