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[期刊论文] 作者:Lugui Qiu,Weiping Yuan,Gang Huang,Liang Huang, 来源: 年份:2022
[会议论文] 作者:Ping Lu,Sha Hao,Yajie Wang,Weiping Yuan,Tao Cheng, 来源:2014天津国际干细胞论坛 年份:2014
[会议论文] 作者:Yingchi Zhang,Tianyuan Hu,Chunlan Hua,Xiaomin Wang,Weili Wang,Tao Cheng,Weiping Yuan, 来源:2014天津国际干细胞论坛 年份:2014
[会议论文] 作者:Meikuang Lim,Yakun Pang,Shihui Ma,Yawei Zheng,Xin Gu,Fengchun Yang,Weiping Yuan,Tao Cheng, 来源:2014天津国际干细胞论坛 年份:2014
[会议论文] 作者:Tianyuan Hu,Cong Li,Yingchi Zhang,Luyun Peng,Xiaomin Wang,Yingdai Gao,Tao Cheng,Weiping Yuan, 来源:2014天津国际干细胞论坛 年份:2014
[会议论文] 作者:Meikuang Lim,Yakun Pang,Shihui Ma,Yawei Zheng,Xin Gu,Fengchun Yang,Weiping Yuan,Tao Cheng, 来源:2014天津国际干细胞论坛 年份:2014
We have previously showed that normal hematopoietic and progenitor stem cells (HSPC) were progressively suppressed during leukemogenesis (Hu et al.,2009),suggesting hematopoietic niche may play a role...
[会议论文] 作者:Binfeng Song,Haibo Jia,Qian Zhang,Zhaojun Zhang,Xiangdong Fang,Yang Wan,Xiaofan Zhu,Tao Cheng,Weiping Yuan, 来源:2014天津国际干细胞论坛 年份:2014
[会议论文] 作者:Binfeng Song,Qian Zhang,Zhaojun Zhang,Yang Wan,Xiaofan Zhu,Tao Cheng,Xiangdong Fang,Weiping Yuan,Haibo, 来源:2014天津国际干细胞论坛 年份:2014
Diamond-Blackfan anemia (DBA) is a class of human diseases linked to defective ribosome biogenesis that results in clinical phenotypes.Genetic mutations in ribosome protein (RP) genes lead to DBA phen...
[会议论文] 作者:Yingchi Zhang,Weili Wang,Chunlan Hua,Tianyuan Hu,Xiaomin Wang,Tao Cheng,Weiping Yuan,Qianfei Wang,Jianfeng, 来源:2014天津国际干细胞论坛 年份:2014
[会议论文] 作者:Zhang,Weili Wang,Chunlan Hua,Tianyuan Hu,Xiaomin Wang,Qianfei Wang,Jianfeng Zhou,Tao Cheng,Bin Liu,Weiping Yuan, 来源:2014天津国际干细胞论坛 年份:2014
In mammals,mTOR is the key component of two distinct multi-protein complexes,mTOR complex 1 (mTORC1) and 2 (mTORC2).mTORC2 is insensitive to rapamycin and includes mTOR,Rictor,mLST8,mSin1,Protor-1,and...
[会议论文] 作者:Yingchi Zhang,Luyun Peng,Tianyuan Hu,YangWan,Yuanyuan Ren,Jingliao Zhang,Xiaojuan VVang,Weiping Yuan,, 来源:2014天津国际干细胞论坛 年份:2014
[会议论文] 作者:Yingchi Zhang,Luyun Peng,Tianyuan Hu,YangWan,Yuanyuan Ren,Jingliao Zhang,Xiaojuan VVang,Weiping Yuan,, 来源:2014天津国际干细胞论坛 年份:2014
Our recent study identified a nonsense mutation of La-related protein 4B (LARP4B) from whole genome sequencing of a 3-year-old female monozygotic twin pair discordant for MLL-associated acute myeloid...
[会议论文] 作者:Chunlan Hua,Huidong Guo,Hui Cheng,Yingchi Zhang,Xiaomin Wang,Tao Cheng,Weiping Yuan,Jiachen Bu,Fuhong, 来源:2014天津国际干细胞论坛 年份:2014
[会议论文] 作者:Jiachen Bu,Hui Cheng,Yingchi Zhang,Fuhong He,Xiaomin Wang,Qianfei Wang,Jianfeng Zhou,Tao Cheng,Weiping Yuan, 来源:2014天津国际干细胞论坛 年份:2014
T-cell acute lymphoblastic leukemia (T-ALL) is accounted for about 25% of adult ALL and 10-15% of childhood ALL.Hyper-activation of the PI3K/Akt/mTOR pathway sustains Notch1 mutation induced T-ALL via...
[会议论文] 作者:Jie Zhang,Yapeng Qi,Jianhong Zhong,Wenfeng Gong,Bin Chen,Ning Ma,Fei Lu,Liang Ma,Weiping Yuan,Lequn Li, 来源:2019中国肿瘤学大会 年份:2019
[会议论文] 作者:Hu,Libing Wang,Lin Zou,Sheng Xu,Xiaomeng Zhuang,Chuanhe Jiang,Jianmin Wang,Hui Cheng,Yakun Pang,Weiping Yuan, 来源:2014天津国际干细胞论坛 年份:2014
[会议论文] 作者:Lin,Xiaoxia Hu,Hui Cheng,Yakun Pang,Libing Wang,Lin Zou,Sheng Xu,Xiaomeng Zhuang,Chuanhe Jiang,Weiping Yuan, 来源:2014天津国际干细胞论坛 年份:2014
Cytopenia and delayed immune reconstitution with acute graft-versus-host disease (aGvHD) indicate a poor prognosis.However,how donor-derived cell hematopoiesis is impaired in aGvHD is not well underst...
[会议论文] 作者:Linping Hu,Hui Cheng,Yingdai Gao,Ming Shi,Yanfeng Liu,Jing Xu,Lugui Qiu,Weiping Yuan,Tao Cheng,Zheng, 来源:2014天津国际干细胞论坛 年份:2014
[会议论文] 作者:Linping Hu,Hui Cheng,Yingdai Gao,Ming Shi,Yanfeng Liu,Zheng Hu,Jing Xu,Lugui Qiu,Weiping Yuan,Anskar, 来源:2014天津国际干细胞论坛 年份:2014
Immuno-compromised mice,such as the non-obese diabetic/severe combined immune-deficient (NOD/SCID) mice,have been widely used to examine the in vivo self-renewal and differentiation of human hematopoi...
[会议论文] 作者:Yingchi Zhang,Jingliao Zhang,Wenbin An,Yang Wan,Shihui Ma,Jie Yin,Xichuan Li,Jie Gao,Weiping Yuan,Ye, 来源:The 2nd International Symposium on Erythrocyte Biology(2016第 年份:2016
ALAS2 encodes δ-aminolevulinate synthase,which catalyzes the rate-limiting step of heme biosynthesis in erythroid cells.ALAS2 mutations are responsible for X-linked sideroblastic anemia (XLSA),which m...
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