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[会议论文] 作者：Lingfeng Zhao,Ping Meng,Kun Wang,Zili Zhang,Mengchang Xu,Xun Qin,Yiyue Zhang,Wenqing Zhang,
来源：第三届全国斑马鱼研究大会 年份：2013
In vertebrates,hematopoietic stem cells(HSCs)form during embryogenesis and maintain our blood system throughout life.Using a cytochemical staining(Sudan Bla...
Establishment of a congenital amegakaryocytic thrombocytopenia model and a thrombocyte-specific repo
[会议论文] 作者：Qing Lin,Yangping Zhang,Riyang Zhou,Yi Zheng,Lingfeng Zhao,Xuebin Zhang,Anskar YH Leung,Wenqing Zhang,
来源：第九届广州国际干细胞与再生医学论坛暨第五届中国再生细胞生物学年会 年份：2016
Mutations in the human myeloproliferative leukemia protein gene(MPL)are known to cause congenital amegakaryocytic thrombocytopenia(CAMT).The prognosis of this heritable disorder is poor and bone marro...
Establishment of an embryonic congenital amegakaryocytic thrombocytopenia model and a thrombocyte-sp
[会议论文] 作者：Qing Lin,Yangping Zhang,Riyang Zhou,Yi Zheng,Lingfeng Zhao,Min Huang,Xuebin Zhang,Anskar YH Leung,Wenqing,
来源：第三届全国斑马鱼PI大会暨中国动物学会斑马鱼分会成立大会 年份：2016
Mutations in the human myeloproliferative leukemia protein gene(MPL)are known to cause congenital amegakaryocytic thrombocytopenia(CAMT).The prognosis of th...
[会议论文] 作者：Wenqing Zhang,Guangzu Zhu,Ping Wu,Xialin Zuo,Houliang Deng,Jingjing Zhang,Zhuomin Wu,Xiaohui Chen,Lingfeng Zhao,
来源：2015广东省药师周大会 年份：2014
RNAi technology is taking strong position among the key therapeutic modalities,with dozens of siRNA-based programs entering and successfully progressing through clinical stages of drug development.To...
Haploinsufficiency of a novel gene on 3p26.1, SMDD1,cause autosomal-dominant dentin dysplasia type Ⅰ
[会议论文] 作者：Fu Xiong,Zhisong Ji,Yanhui Liu,Yu Zhang,Lingling Hu,Qi Yang,Qinwei Qiu,Lingfeng Zhao,Dong Chen,Zhihui,
来源：第十四次全国医学遗传学学术会议 年份：2015
The hereditary dentin defects, dentinogenesis imperfecta(DGI)and dentin dysplasia (DD) comprise a group of autosomal-dominant genetic conditions and the molecular basis of such dental disorders in all...
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