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Expert consensus on the diagnosis and treatment of non-small cell lung cancer with MET alteration
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作者 Huijing Feng Yang Xia +106 位作者 Wenxian Wang Chunwei Xu Qian Wang Zhengbo Song Ziming Li Jinpu Yu Wenzhao Zhong Zhijie Wang Yongchang Zhang Jingjing Liu Shirong Zhang Xiuyu Cai Anwen Liu Wen Li Ping Zhan Hongbing Liu Tangfeng Lyu Liyun Miao lingfeng Min gen lin Long Huang Jingping Yuan Zhansheng Jiang Xingxiang Pu Chuangzhou Rao DongqingLyu Zongyang Yu Xiaoyan Li Chuanhao Tang Chengzhi Zhou Qi Mei Hui Guo Qian Chu Rui Meng Xuewen Liu Jingxun Wu Jin Zhou Zhengfei Zhu Weiwei Pan Fei Pang Meizhen Hu Kai Wang Fan Wu Bingwei Xu ling Xu Liping Wang Youcai Zhu Jisheng Li Yanru Xie Xinqing lin Jing Cai lin Wang Yingying Du Wang Yao Xuefei Shi Xiaomin Niu Dongmei Yuan Yanwen Yao Jing Kang Jiatao Zhang Chao Zhang Wenbin Gao Jianhui Huang Yinbin Zhang Pingli Sun Hong Wang Mingxiang Ye Dong Wang Zhaofeng Wang Yue Hao Zheng Wang Bing Wan Donglai Lyu Xiaodong Jiao lin Shi Gang Lan Shengjie Yang Yanhong Shang Yina Wang Bihui Li Gang Jin Kang Zheng Jun Ma Wenfeng Li Zhang Zhang Zhongwu Li Yuan Li Zhefeng Liu Xuelei Ma Nong Yang lin Wu Qiming Wang Guansong Wang Zhuan Hong Jiandong Wang Meiyu Fang Yong Fang Xixu Zhu Yi Shen Ke Wang Xiubao Ren Yiping Zhang Shenglin Ma Junping Zhang Yong Song Wenfeng Fang Yuanzhi Lu 《Cancer Biology & Medicine》 2025年第3期237-265,共29页
Alterations in the mesenchymal-epithelial transition factor(MET)gene are critical drivers of non-small cell lung cancer(NSCLC).In recent years advances in precision therapies targeting MET alterations have significant... Alterations in the mesenchymal-epithelial transition factor(MET)gene are critical drivers of non-small cell lung cancer(NSCLC).In recent years advances in precision therapies targeting MET alterations have significantly expanded treatment options for NSCLC patients.These alterations include MET exon 14 skipping mutations(MET exon 14 skipping),MET gene amplifications,MET point mutations(primarily kinase domain mutations),and MET protein overexpression.Accurate identification of these alterations and appropriate selection of patient populations and targeted therapies are essential for improving clinical outcomes.The East China Lung Cancer Group,Youth Committee(ECLUNG YOUNG,Yangtze River Delta Lung Cancer Cooperation Group)has synthesized insights from China’s innovative drug development landscape and clinical practice to formulate an expert consensus on the diagnosis and treatment of NSCLC patients with MET alterations.This consensus addresses key areas,such as optimal testing timing,testing methods,testing strategies,quality control measures,and treatment approaches.By offering standardized recommendations,this guidance aims to streamline diagnostic and therapeutic processes and enhance clinical decision-making for NSCLC with MET alterations. 展开更多
关键词 Mesenchymal-epithelial transition factor MET exon 14 skipping mutation MET amplification non-small cell lung cancer precision medicine targeted therapy tyrosine kinase
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多通道升降沿产生激光驱动器超窄脉冲新方法 被引量:1
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作者 韩翰 耿林 吕伟强 《激光与红外》 CAS CSCD 北大核心 2022年第11期1629-1634,共6页
应用于不同领域的超窄脉冲激光驱动器要求输入脉冲宽度极窄,并且大范围内可调。传统的模拟器件可调性差难以满足要求,数字器件例如专用集成电路(ASIC)尽管脉冲宽度可以实现超窄输出,但是大范围内可调不易满足,并且存在可扩展性差,价格... 应用于不同领域的超窄脉冲激光驱动器要求输入脉冲宽度极窄,并且大范围内可调。传统的模拟器件可调性差难以满足要求,数字器件例如专用集成电路(ASIC)尽管脉冲宽度可以实现超窄输出,但是大范围内可调不易满足,并且存在可扩展性差,价格昂贵等特点,同样不利于推广。现场可编程门阵列(FPGA)程控性好,因此在脉冲激光驱动器中的数字脉冲源得到了很好的应用,但是传统的计数方法只能实现脉宽为时钟周期倍数的脉冲输出,因此只能应用于对窄脉宽要求不高的情形。为解决上述问题,本文基于FPGA设计了一种应用于超窄脉冲激光驱动器,在50 MHz时钟频率下利用锁相环倍频成多个通道的基准时钟,并分别利用上升下降沿计数器进行计数,再经不同逻辑运算输出的数字脉冲产生方法。最终的数字电路可以产生脉宽2~50 ns,步长1 ns可调,重复频率1 Hz~1 MHz的数字脉冲信号。最后分析了在高精度锁相环等硬件条件满足的情况下,该方法可以实现亚纳秒脉宽和步长的数字脉冲信号输出,因此具备了很好的可拓展性和前景。 展开更多
关键词 超窄脉冲激光驱动器 现场可编程门阵列(FPGA) 多通道上升下降沿计数器
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International guidelines on the diagnosis and treatment of NUT carcinoma
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作者 Yu Zhang Qi Zhang +171 位作者 Yue Hao Jia Luo Yingshi Piao Wenxian Wang Zhengbo Song Ziming Li Luka Brcic Aijun Liu Jinpu Yu Yasuhiro Tsutani Wenzhao Zhong Wenfeng Fang Zhijie Wang Shengxiang Ren Athanasios G.Papavassiliou Yongchang Zhang Jingjing Liu Shirong Zhang Xiuyu Cai Ayten Kayi Cangir Anwen Liu Wen Li Filippo Lococo Ping Zhan Hongbing Liu Tangfeng Lv Liyun Miao lingfeng Min Helmut Popper Yu Chen Jingping Yuan Feng Wang Zhansheng Jiang gen lin Long Huang Xingxiang Pu Rongbo lin Kalevi Kairemo Weifeng Liu Chuangzhou Rao Dongqing Lv Zongyang Yu Ashrafian Leanne Xiaoyan Li Chuanhao Tang Hifzur R.Siddique Chengzhi Zhou Junping Zhang Junli Xue Vishal Shelat Hui Guo Qian Chu Rui Meng Fatemeh Ardeshir Jingxun Wu Rui Zhang Jin Zhou Robert A.Kratzke Zhengfei Zhu Yongheng Li Hong Qiu Fan Xia Fiorella Calabrese Yang Xia Alessandro Wasum Mariani Yuanyuan Lu Xiaofeng Chen Mark A.Klein Rui Ge Enyong Dai Axel H.Schönthal Yu Han Zhenying Guo Jian Zhang Yinghua Ji Xianbin Liang Hongmei Zhang Xuelei Ma Marco Chiappetta Xuewen Liu Francoise Galateau Salle Yu Yao Malgorzata Szolkowska Weiwei Pan Fei Pang Fan Wu Stefan B.Watzka Liping Wang Youcai Zhu Li lin Aparna Sharma Jianfei Tu Xinqing lin Jing Cai ling Xu Jisheng Li Xiaodong Jiao Kainan Li Marjorie G.Zauderer Jia Wei Huijing Feng lin Wang Yingying Du Wang Yao Elizabeth Dudnik Xuefei Shi Xiaomin Niu Dongmei Yuan Yanwen Yao Jianhui Huang Yue Feng Yinbin Zhang Binbin Song Wenfeng Li Jianfei Fu Marina K.Baine Pingli Sun Hong Wang Mingxiang Ye Dong Wang Zhaofeng Wang Jing Wu Yunyun Yang Yuan Fang Zhen Wang Bin Wan Donglai Lv Huafei Chen Shengjie Yang Jing Kang Jiatao Zhang Chao Zhang lin Shi Yina Wang Mohamed Emam Sobeih Bihui Li Bin Lian Lili Mao Zhang Zhang Ke Wang Zhongwu Li Zhefeng Liu Nong Yang lin Wu Xiaobing Chen Gu Jin Miao Li Guansong Wang Thomas U.Marron Jiandong Wang Sanjay Popat Meiyu Fang Yong Fang Daniel Mansilla Yuan Li Xiaojia Wang Jing Chen Yiping Zhang Xixu Zhu Yi Shen Shenglin Ma Aaron S.Mansfield Biyun Wang Lu Si Anja C.Roden Bjørn H.Grønberg Yong Song Geoffrey I.Shapiro Christopher A.French Yuanzhi Lu Qian Wang Chunwei Xu 《The Innovation》 2026年第1期111-126,共16页
1(NUTM1)gene rearrangements(15q14).In 1991,two independent research teams reported NC cases characterized by the t(15;19)translo-cation.1,2 In vitro studies by French et al.3 led to the pivotal discovery of NC in 2003... 1(NUTM1)gene rearrangements(15q14).In 1991,two independent research teams reported NC cases characterized by the t(15;19)translo-cation.1,2 In vitro studies by French et al.3 led to the pivotal discovery of NC in 2003 as a distinct disease entity driven by the fusion of bromodo-main and extraterminal domain(BET)protein 4(BRD4)and NUTM1.In 2004,the World Health Organization(WHO)classified tumors with t(15;19)translocation as a thymic malignancy and designated it“NUT midline carcinoma,”due to its predominant occurrence in midline organs.4 However,subsequent reports revealed NC’s emergence in numerous nonmidline organs,leading to its reclassification as the independent entity“NUT carcinoma of the thorax”by the WHO in 2015.5 NC exhibits rapid progression and profound resistance to conventional radiotherapy and chemotherapy. 展开更多
关键词 t BRD vitro studies translocation nut carcinoma thorax thymic malignancy nut midline carcinoma NUTM
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装配式钢管约束混凝土圆形桥墩地震易损性分析
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作者 付涛 王桂梅 +3 位作者 闫旭 姜润豪 耿琳 贾红玉 《科学技术与工程》 2026年第6期2553-2563,共11页
为研究装配式钢管约束混凝土圆形桥墩在地震作用下的损坏状态和破坏概率,设计了钢管约束混凝土装配式桥墩和装配式钢筋混凝土桥墩,基于拟静力试验现象对两类桥墩的损伤状态进行了划分,采用ABAQUS有限元软件建立了两类桥墩的有限元模型,... 为研究装配式钢管约束混凝土圆形桥墩在地震作用下的损坏状态和破坏概率,设计了钢管约束混凝土装配式桥墩和装配式钢筋混凝土桥墩,基于拟静力试验现象对两类桥墩的损伤状态进行了划分,采用ABAQUS有限元软件建立了两类桥墩的有限元模型,基于拟静力试验结果对桥墩有限元模型进行标定以验证其正确性。采用增量动力分析(incremental dynamic analysis,IDA)方法,以桥墩的墩顶漂移率为损伤指标,对两类桥墩进行了地震易损性分析。研究结果表明:在PGA相同的情况下,装配式钢管约束混凝土桥墩由于钢管的存在,增加了桥墩墩身刚度,且外包钢管对装配式钢管约束混凝土桥墩核心混凝土产生套箍作用,使桥墩发生“轻微、中等、严重、倒塌”损伤状态的超越概率有不同程度的降低,表明外包钢管的存在显著提高了桥墩抵抗地震作用的能力。在高烈度地震下,装配式钢管约束混凝土桥墩与装配式混凝土桥墩在“严重、倒塌”损伤状态下超越概率差值均随地震动峰值加速度的增加而增大,表明在高地震作用下,外包钢管对桥墩抗震性能提升愈发明显。装配式钢管约束混土桥墩在地震作用下具有较大的延性储备,能更好地抵抗地震作用。 展开更多
关键词 装配式钢管约束混凝土桥墩 IDA曲线 时程分析 易损性分析 抗震性能
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Expert consensus on the diagnosis and treatment of solid tumors with BRAF mutations 被引量:3
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作者 Wenxian Wang Bin Lian +133 位作者 Chunwei Xu Qian Wang Ziming Li Nan Zheng Aijun Liu Jinpu Yu Wenzhao Zhong Zhijie Wang Yongchang Zhang Jingjing Liu Shirong Zhang Xiuyu Cai Anwen Liu Wen Li Lili Mao Ping Zhan Hongbing Liu Tangfeng Lv Liyun Miao lingfeng Min Yu Chen Jingping Yuan Feng Wang Zhansheng Jiang gen lin Long Huang Xingxiang Pu Rongbo lin Weifeng Liu Chuangzhou Rao Dongqing Lv Zongyang Yu Xiaoyan Li Chuanhao Tang Chengzhi Zhou Junping Zhang Junli Xue Hui Guo Qian Chu Rui Meng Xuewen Liu Jingxun Wu Rui Zhang Jin Zhou Zhengfei Zhu Yongheng Li Hong Qiu Fan Xia Yuanyuan Lu Xiaofeng Chen Jian Feng Rui Ge Enyong Dai Yu Han Weiwei Pan Fei Pang Xin Huang Meizhen Hu Qing Hao Kai Wang Fan Wu Binbin Song Bingwei Xu Liping Wang Youcai Zhu Li lin Yanru Xie Xinqing lin Jing Cai ling Xu Jisheng Li Xiaodong Jiao Kainan Li Jia Wei Huijing Feng lin Wang Yingying Du Wang Yao Xuefei Shi Xiaomin Niu Dongmei Yuan Yanwen Yao Jianhui Huang Yue Feng Yinbin Zhang Pingli Sun Hong Wang Mingxiang Ye Dong Wang Zhaofeng Wang Yue Hao Zhen Wang Bin Wan Donglai Lv Shengjie Yang Jin Kang Jiatao Zhang Chao Zhang Wenfeng Li Jianfei Fu Lizhi Wu Shijie Lan Juanjuan Ou lin Shi Zhanqiang Zhai Yina Wang Bihui Li Zhang Zhang Ke Wang Xuelei Ma Zhongwu Li Zhefeng Liu Nong Yang lin Wu Huijuan Wang Gu Jin Guansong Wang Jiandong Wang Hubing Shi Meiyu Fang Yong Fang Yuan Li Xiaojia Wang Jing Chen Yiping Zhang Xixu Zhu Yi Shen Shenglin Ma Biyun Wang Yong Song Zhengbo Song Wenfeng Fang Yuanzhi Lu Lu Si 《The Innovation》 EI 2024年第6期100-116,共17页
The BRAF gene is an important signaling molecule in human cells that is involved in the regulation of cell growth,differentiation,and survival.When the BRAF gene mutates,it can lead to abnormal activation of the signa... The BRAF gene is an important signaling molecule in human cells that is involved in the regulation of cell growth,differentiation,and survival.When the BRAF gene mutates,it can lead to abnormal activation of the signaling pathway,which promotes cell proliferation,inhibits cell apoptosis,and ultimately contributes to the occurrence and development of cancer.BRAF mutations are widely present in various cancers,including malignant melanoma,thyroid cancer,colorectal cancer,non-small cell lung cancer,and hairy cell leukemia,among others.BRAF is an important target for the treatment of various solid tumors,and targeted combination therapies,represented by BRAF inhibitors,have become one of the main treatment modalities for a variety of BRAF-mutation-positive solid tumors. 展开更多
关键词 BRAF DIAGNOSIS TREATMENT
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