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TABLE 1 from Reprogramming of Tumor-reactive Tumor-infiltrating Lymphocytes to Human-induced Pluripotent Stem Cells

Figshare2023-05-25 更新2026-04-28 收录

实体瘤免疫治疗

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https://figshare.com/articles/dataset/TABLE_1_from_Reprogramming_of_Tumor-reactive_Tumor-infiltrating_Lymphocytes_to_Human-induced_Pluripotent_Stem_Cells/23185862 数据链接链接失效反馈

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The list of antibodies used in the study

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创建时间：

2023-05-25

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染色体不稳定性

The discovery that somatic cells are reprogrammable to pluripotency by ectopic expression of a small subset of transcription factors has created great potential for the development of broadly applicab

NIAID Data Ecosystem90

Analysis of Differential Proteomes of Induced Pluripotent Stem Cells by Protein-Based Reprogramming of Fibroblasts

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蛋白质组学比较分析

The recent generation of induced pluripotent stem (iPS) cells represents a novel opportunity to complement embryonic stem (ES) cell-based approaches. iPS cells can be generated by viral transduction o

Figshare2016-02-23 更新50

Establish a rapid and efficient chemical reprogramming platform (RNA-Seq II)

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表观基因组图谱

Chemically reprogramming somatic cells to iPSCs is time-consuming and low-efficiency. Here, we discribe a rapid chemical reprogramming condition enabling generating iPSCs from MEFs in 12 days. To furt

NIAID Data Ecosystem40

Reprogramming of mouse somatic cells into pluripotent stem cells using a combination of small molecules

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化学生物学

Somatic cells can be reprogrammed to generate induced pluripotent stem cells (iPSCs) by overexpression of four transcription factors, Oct4, Klf4, Sox2, and c-Myc. Bmi1 is responsible for conversion o

NIAID Data Ecosystem60

Epigenetic and transcriptional aberrations in human pluripotent stem cells reflect differences in reprogramming mechanisms [SNP array]

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神经细胞表观遗传学

Human pluripotent stem cells hold great potential for regenerative medicine, but available cell types have important limitations. While embryonic stem cells derived from fertilized embryos (IVF-ESCs)

NIAID Data Ecosystem40

TABLE 1 from Reprogramming of Tumor-reactive Tumor-infiltrating Lymphocytes to Human-induced Pluripotent Stem Cells

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