ArticleDevelopment (Cambridge, England)2017
Functional characterisation of
Article in Development (Cambridge, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
17 citing papers in PubMed, 39 citations in OpenAlex.
- A degron-based approach to manipulate Eomes functions in the context of the developing mouse embryo.Proceedings of the National Academy of Sciences of the United States of America · 2023Article
- BMP4 triggers regulatory circuits specifying the cardiac mesoderm lineage.Development (Cambridge, England) · 2023Article
- A Mesp1-dependent developmental breakpoint in transcriptional and epigenomic specification of early cardiac precursors.Development (Cambridge, England) · 2023Article
- Capture-C: a modular and flexible approach for high-resolution chromosome conformation capture.Nature protocols · 2022Review
- Organization of the Pluripotent Genome.Cold Spring Harbor perspectives in biology · 2021Review
- High-resolution targeted 3C interrogation of cis-regulatory element organization at genome-wide scale.Nature communications · 2021Article
- Mouse gastrulation: Coordination of tissue patterning, specification and diversification of cell fate.Mechanisms of development · 2020Review
- Dynamic transcriptional and chromatin accessibility landscape of medaka embryogenesis.Genome research · 2020Article
- CytoCensus, mapping cell identity and division in tissues and organs using machine learning.eLife · 2020Article
- Eomes and Brachyury control pluripotency exit and germ-layer segregation by changing the chromatin state.Nature cell biology · 2019Article
- Genetic dissection of Nodal and Bmp signalling requirements during primordial germ cell development in mouse.Nature communications · 2019Article
- Implantation initiation of self-assembled embryo-like structures generated using three types of mouse blastocyst-derived stem cells.Nature communications · 2019Article
- Genome-wide analysis of chromatin accessibility using ATAC-seq.Methods in cell biology · 2019Review
- Combinatorial Smad2/3 Activities Downstream of Nodal Signaling Maintain Embryonic/Extra-Embryonic Cell Identities during Lineage Priming.Cell reports · 2018Article
- Testicular MTHFR deficiency may explain sperm DNA hypomethylation associated with high dose folic acid supplementation.Human molecular genetics · 2018Article
- A transcribed enhancer dictates mesendoderm specification in pluripotency.Nature communications · 2017Article
- Tissue-specific CTCF-cohesin-mediated chromatin architecture delimits enhancer interactions and function in vivo.Nature cell biology · 2017Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors at 2 institutions in 1 country.
Funding
Abstract
The T-box transcription factor (TF) Eomes is a key regulator of cell fate decisions during early mouse development. The
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.