FOXL2 and ESR1 binding sites in primary cells from mouse ovarian follicles

ChEBI2015-07-01 更新2026-07-12 收录

卵巢细胞转录调控

转录因子结合位点分析

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FOXL2 and ESR1 binding sites in primary cells from mouse ovarian follicles

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2015-07-01

RFX7 DNA binding landscape in RPE-1

转录因子结合位点分析

ChIP-seq表观遗传学

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Hippo信号通路

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转录因子结合位点分析

胚胎干细胞表观遗传学

Genome binding/occupancy by wild type THAP1 was profiled by high throughput sequencing in wild type mouse ES cells derived from C57Bl/6 blastocysts ChIP Seq was performed by standard methods using a c

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Genome wide STAT3 binding analysis of primary human hepatocytes-derived organoids [ChIP-seq]. Genome wide STAT3 binding analysis of primary human hepatocytes-derived organoids [ChIP-seq]

转录因子结合位点分析

肝细胞类器官

To analyze the primary STAT3 binding sites induced by OSM, chromatin immunoprecipitation sequencing (ChIP-seq) was performed using an anti-human STAT3 antibody. HHOs were cultured in EM for 1 week and

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TF ChIP-seq from K562 (ENCSR017EJY)

转录因子结合位点分析

K562细胞表观遗传学

eGFP-DLX4 ChIP-seq on human K562 For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Research/ENCODE/ENCODE_Data_Use_Policy_for_Externa

NIAID Data Ecosystem60

FOXL2 and ESR1 binding sites in primary cells from mouse ovarian follicles

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