Identification of putative target genes of the transcription factor RUNX2

ChEBI2014-02-01 更新2026-07-21 收录

转录因子靶基因

器官发育分子机制

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Identification of putative target genes of the transcription factor RUNX2

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2014-02-01

Smad2 and Smad3 Regulate Chondrocyte Proliferation and Differentiation in the Growth Plate

器官发育分子机制

生长板生物学

TGFβs act through canonical and non-canonical pathways, and canonical signals are transduced via Smad2 and Smad3. However, the contribution of canonical vs. non-canonical pathways in cartilage is unkn

NIAID Data Ecosystem60

ChIP-seq of NGR2

转录因子靶基因

结合基序分析

The ChIP-seq experiment was used to explore the downstream genes and binding motifs of NGR2.

NIAID Data Ecosystem50

Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and POT1a deleted MSPCs Transcriptomes.. Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and POT1a deleted MSPCs Transcriptomes.

转录组学分析

器官发育分子机制

Purpose: Next-generation sequencing (NGS) has revolutionized systems-based analysis of cellular pathways. The goals of this study are to evaluate POT1a deleted MSPCs functions by using NGS-derived MSP

NIAID Data Ecosystem40

Defining the Myb Transcriptional Program Controlled by via Genome-wide Chromatin Occupancy and Expression Analyses. Mus musculus

转录因子靶基因

Myb转录调控

We used the ERMYB cell line (Hogg et al., Oncogene 15, p2885-2898, 1997) as our model system to identify genes regulated by Myb using whole genome microarray expression profiling. ERMYB is a myeloid p

NIAID Data Ecosystem50

Proenkephalin A in bone-derived cells.

器官发育分子机制

骨髓基质细胞基因表达

Enkephalins, a group of small peptides with opiate-like activity, have been defined originally as neuropeptides. Recent reports showed, using in situ hybridization, that the enkephalin-encoding gene,

PubMed Central1991-05-01 更新40

Identification of putative target genes of the transcription factor RUNX2

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