首页/数据集/Distinct specificity and functions of PRC2 subcomplexes in human stem cells and cardiac differentiation. Much et al

Distinct specificity and functions of PRC2 subcomplexes in human stem cells and cardiac differentiation. Much et al

Mendeley Data2026-04-09 收录

细胞表观遗传学

心脏分化调控

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https://data.mendeley.com/datasets/xngr4x532x/1 数据链接链接失效反馈

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Raw imaging and uncropped western blot data published in Much et al. 2025 Mol Cell

应用场景：

细胞表观遗传学

早期胚胎发育

Human embryonic stem cells (hESCs) typically exhibit "primed" pluripotency, analogous to stem cells derived from the mouse post-implantation epiblast. This has led to a search for growth conditions th

NIAID Data Ecosystem50

Role of CxxC-finger Protein 1 in the Establishment of Epigenetic Landscapes in Mouse Oocytes. Role of CxxC-finger Protein 1 in the Establishment of Epigenetic Landscapes in Mouse Oocytes

细胞表观遗传学

组蛋白修饰

During oogenesis, oocytes gain competence to accomplish meiotic maturation and prepare for embryonic development following fertilization. Trimethylated histone H3 on lysine-4 (H3K4me3) mediates a wide

NIAID Data Ecosystem30

SETD2 regulates the maternal epigenome, genomic imprinting and embryonic development [RNA-seq]. SETD2 regulates the maternal epigenome, genomic imprinting and embryonic development [RNA-seq]

细胞表观遗传学

早期胚胎发育

The oocyte epigenome plays critical roles in mammalian gametogenesis and embryogenesis. Yet, how it is established remains elusive. Here, we report that histone-lysine N-methyltransferase SETD2, an H3

NIAID Data Ecosystem30

002-Y0Ab-normRPKM.bwOsteo-mm9 ChIP-seq bw

细胞表观遗传学

ChIP-seq数据分析

oseto mm9 Chip-seq dataset

Figshare2020-01-13 更新50

BP_January_2015_ChIP-Seq_CD14-positive,_CD16-negative_classical_monocyte - samples

细胞表观遗传学

ChIP-seq分析

ChIP-Seq data for 10 CD14-positive, CD16-negative classical monocyte sample(s). 73 run(s), 69 experiment(s), 69 alignment(s). Part of BLUEPRINT release January 2015. Analysis documentation available a

NIAID Data Ecosystem30

Distinct specificity and functions of PRC2 subcomplexes in human stem cells and cardiac differentiation. Much et al

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