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A focus on NKT cell subset characterization and developmental stages.
Immunology and Cell Biology ( IF 3.2 ) Pub Date : 2020-08-07 , DOI: 10.1111/imcb.12378
Jihene Klibi 1, 2 , Ludivine Amable 1, 2 , Kamel Benlagha 1, 2
Affiliation  

Immunology & Cell Biology 2020; 98, 607; https://doi.org/10.1111/imcb.12378

Correction to: Immunology & Cell Biology 2020; 98, 358–368; https://doi.org/10.1111/imcb.12322

An error appeared in the original Figure 3 published with this article. It should be replaced with the corrected version below. The authors wish to apologize for this error.

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Figure 3
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Combined model of NKT cell development. The combined model describes the development of NKT cell subsets through transcription factor expression patterns at the CD44low stage 1 and CD44high stage 2 of NKT cell development. CD138, syndecan‐1; DP, double positive; HSA, heat‐stable antigen; IL‐17RB, IL‐25 receptor b; NKT, natural killer T cell; NKTp, natural killer T‐cell precursors; PLZF, SLAM, signaling lymphocytic activation molecule; TCR, T‐cell receptor.


中文翻译:

重点研究NKT细胞亚群的表征和发育阶段。

免疫学与细胞生物学2020年; 98、607;https://doi.org/10.1111/imcb.12378

更正为:《免疫学与细胞生物学2020》;98,358–368; https://doi.org/10.1111/imcb.12322

本文发布的原始图3中出现错误。应该用下面的更正版本替换它。作者对此错误表示歉意。

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图3
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NKT细胞发育的组合模型。组合模型通过NKT细胞发育CD441期和CD442期的转录因子表达模式描述了NKT细胞亚群的发育。CD138,syndecan-1; DP,双正;HSA,热稳定抗原;IL-17RB,IL-25受体b; NKT,天然杀伤性T细胞;NKTp,天然杀伤性T细胞前体;PLZF,SLAM,信号传导淋巴细胞激活分子;TCR,T细胞受体。
更新日期:2020-08-08
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