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Human dendritic cells (DCs) are derived from distinct circulating precursors that are precommitted to become CD1c+ or CD141+ DCs

机译：人树突细胞（DCS）衍生自中，以成为CD1C +或CD141 + DC的不同循环前体

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Gaëlle Breton; Shiwei Zheng; Renan Valieris; Israel Tojal da Silva; Rahul Satija; Michel C. Nussenzweig;
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1. Human dendritic cells (DCs) are derived from distinct circulating precursors that are precommitted to become CD1c+ or CD141+ DCs [J] . Ga?lle Breton, Shiwei Zheng, Renan Valieris, The Journal of Experomental Medicine . 2016,第13期

机译：人类树突状细胞（DC）源自不同的循环前体，这些前体被预先承诺成为CD1c +或CD141 + DC
2. Circulating precursors of human CD1c+ and CD141+ dendritic cells [J] . Ga?lle Breton, Jaeyop Lee, Yu Jerry Zhou, The Journal of Experomental Medicine . 2015,第3期

机译：人CD1c +和CD141 +树突状细胞的循环前体
3. Human CD141+ (BDCA-3)+ dendritic cells (DCs) represent a unique myeloid DC subset that cross-presents necrotic cell antigens [J] . Sarah L. Jongbloed, Andrew J. Kassianos, Kylie J. McDonald, The Journal of Experomental Medicine . 2010,第6期

机译：人CD141 +（BDCA-3）+树突状细胞（DC）代表独特的髓样DC亚型，可交叉呈递坏死细胞抗原
4. PLGA microparticle combination therapy induces a tolerogenic phenotype in human monocyte-derived dendritic cells [C] . Maigan Hulme, Joshua Stewart, Jamal Lewis, World biomaterials congress . 2016

机译：PLGA微粒联合疗法在人单核细胞衍生的树突状细胞中诱导耐受性表型
5. Distinct roles of the ERK and the NFkappaB signaling pathways in dendritic cell differentiation of human progenitor cell line. [D] . Lindner, Inna. 2005

机译：ERK和NFkappaB信号通路在人类祖细胞系树突状细胞分化中的不同作用。
6. Human dendritic cells (DCs) are derived from distinct circulating precursors that are precommitted to become CD1c+ or CD141+ DCs [O] . Gaëlle Breton, Shiwei Zheng, Renan Valieris, 2016

机译：人类树突状细胞（DC）源自不同的循环前体这些前体已预先承诺成为CD1c +或CD141 + DC
7. Human CD141+ (BDCA-3)+ dendritic cells (DCs) represent a unique myeloid DC subset that cross-presents necrotic cell antigens [O] . Jongbloed, Sarah L., Kassianos, Andrew J., McDonald, Kylie J., 2010

机译：人CD141 +（BDCA-3）+树突状细胞（DC）代表独特的髓样DC亚型，可交叉呈递坏死细胞抗原

Human dendritic cells (DCs) are derived from distinct circulating precursors that are precommitted to become CD1c+ or CD141+ DCs

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