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

Vulnerability of SRSF2-mutated chronic myelomonocytic leukemia to perturbation of the cGAS-STING pathway

SRSF2突变型慢性粒单核细胞白血病对cGAS-STING通路扰动的易感性

Chen, Yanan; Chan, Koon Chuen; Sin, Chun Fung; Zheng, Lichuan; Wang, Dandan; Tu, Lingge; He, Fangfang; Hui, Wan Hei Jeffrey; Leung, Hoi Ki; Chan, Leslie Kar Fai; Tsui, Sze Pui; Chan, Hoi Yi; Ma, Alvin Chun Hang; Leung, Anskar Y H; Sun, Xuan

Magrolimab plus azacitidine vs physician's choice for untreated TP53-mutated acute myeloid leukemia: the ENHANCE-2 study

Magrolimab联合阿扎胞苷与医生选择方案治疗未经治疗的TP53突变型急性髓系白血病:ENHANCE-2研究

Zeidner, Joshua F; Sallman, David A; Récher, Christian; Daver, Naval G; Leung, Anskar Y H; Hiwase, Devendra K; Subklewe, Marion; Pabst, Thomas; Montesinos, Pau; Larson, Richard A; Wilde, Lindsay; Enjeti, Anoop K; Kawashima, Ichiro; Papayannidis, Cristina; O'Nions, Jenny; Johnson, Lisa; Dong, Mei; Huang, Julie; Bagheri, Taravat; Hacohen Kleiman, Gal; Lee, Calvin; Vyas, Paresh

asxl1 C-terminal truncation and SRSF2 mutation drive leukemogenesis via immune reprogramming

asxl1 C 端截短和 SRSF2 突变通过免疫重编程驱动白血病发生

Tu, Lingge; He, Fangfang; Liew, Jun Mun; Sin, Chun-Fung; Zheng, Lichuan; Tsui, Sze-Pui; Miao, Xinyu; Chan, Hoi-Yi; Ma, Alvin Chun Hang; Zhang, Wenqing; Zhang, Yiyue; Leung, Anskar Y H; Sun, Xuan

De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome

DDX39B基因的新生突变和遗传突变会导致一种新的神经发育综合征。

Booth, Kevin T A; Jangam, Sharayu V; Chui, Martin M C; Treat, Kayla; Graziani, Lorenzo; Soldano, Alessia; Ruan, Yao; Wan-Hei Hui, Jeffrey; White, Kerry; Christensen, Celanie K; Lynnes, Ty; Yamamoto, Shinya; Kanca, Oguz; Tsang, Mandy H Y; Lynch, Sally A; Mullegama, Sureni V; Baptista, Julia; Iancu, Daniela; Joss, Shelagh K; Wong, Sandra Y Y; Mak, Christopher C Y; Kwong, Anna K Y; Bellen, Hugo J; Conboy, Erin; Sanges, Remo; Leung, Anskar Yu-Hung; Wangler, Michael F; Chung, Brian H Y; Vetrini, Francesco

The synergistic effect of c-Myb hyperactivation and Pu.1 deficiency induces Pelger-Huët anomaly and promotes sAML.

c-Myb 过度激活和 Pu.1 缺乏的协同作用可诱发 Pelger-Huët 异常并促进 sAML

Xu Song'en, Hong Jiaxin, Dongye Meimei, Lin Jiehao, Xue Rongtao, Huang Zhibin, Xu Jin, Zhang Yiyue, Leung Anskar Yu-Hung, Shen Juan, Zhang Wenqing, Liu Wei

Hypomethylating agent versus venetoclax combination: an electronic health records-based target trial emulation among Asian elderly patients with newly diagnosed acute myeloid leukaemia in Hong Kong

去甲基化药物与维奈托克联合用药:一项基于电子健康记录的香港亚洲老年新诊断急性髓系白血病患者靶向试验模拟研究

Fang, Qiwen; Fung, Chi Yeung; Wang, Jiaqi; Lai, Wing Hei; Wong, Raymond S M; Kho, Bonnie C S; Lau, June S M; Mak, Vivien W M; Ha, Chung Yin; Li, Xue; Leung, Anskar Yu-Hung

Early measurable residual disease detection post-haematopoietic stem cell transplantation in acute myeloid leukaemia

急性髓系白血病造血干细胞移植后早期可测量残留病灶的检测

Tsui, Sze P; Lam, Stephen S Y; Au, Chun H; Fung, Chi Y; Ip, Beca B K; Wong, Anthony T C; Leung, Henry C M; Lai, Wing H; Ip, Ho W; Ma, Edmond S K; Leung, Garret M K; Sim, Joycelyn P Y; Leung, Anskar Y H

Integrated Molecular and Histological Insights for Targeted Therapies in Mesenchymal Sinonasal Tract Tumors

整合分子和组织学信息,为间叶性鼻窦肿瘤的靶向治疗提供依据

Hoch, Cosima C; Knoedler, Leonard; Knoedler, Samuel; Bashiri Dezfouli, Ali; Schmidl, Benedikt; Trill, Anskar; Douglas, Jennifer E; Adappa, Nithin D; Stögbauer, Fabian; Wollenberg, Barbara

Giraffe: A tool for comprehensive processing and visualization of multiple long-read sequencing data

Giraffe:一款用于全面处理和可视化多条长读长测序数据的工具

Liu, Xudong; Shao, Yanwen; Guo, Zhihao; Ni, Ying; Sun, Xuan; Leung, Anskar Yu Hung; Li, Runsheng

Application of droplet digital PCR in minimal residual disease monitoring of rare fusion transcripts and mutations in haematological malignancies

液滴数字PCR在血液系统恶性肿瘤罕见融合转录本和突变的微小残留病灶监测中的应用

Ip, Beca B K; Wong, Anthony T C; Law, Janet Hei Yin; Au, Chun Hang; Ma, Shing Yan; Chim, James C S; Liang, Raymond H S; Leung, Anskar Y H; Wan, Thomas S K; Ma, Edmond S K