Evidence map›Paper›PMID 31615786›Full record

ReviewCold Spring Harbor perspectives in biology2020

Specification of the First Mammalian Cell Lineages In Vivo and In Vitro.

Melanie D White, Nicolas Plachta

Abstract readReview
In one paragraph

Review in Cold Spring Harbor perspectives in biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Cytoskeletal control of early mammalian development.Nature reviews. Molecular cell biology · 2021
    Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Epigenetic regulation of mouse preimplantation embryo development.Current opinion in genetics & development · 2020
    Review
  17. Development of Pre-implantation Mammalian Blastocyst.Advances in anatomy, embryology, and cell biology
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Melanie D WhiteInstitute of Molecular and Cell Biology, A*STAR, Singapore 138673.
Nicolas PlachtaInstitute of Molecular and Cell Biology, A*STAR, Singapore 138673.

Funding

Howard Hughes Medical InstituteWellcome Trust
6 · The paper itself

Abstract

Our understanding of how the first mammalian cell lineages arise has been shaped largely by studies of the preimplantation mouse embryo. Painstaking work over many decades has begun to reveal how a single totipotent cell is transformed into a multilayered structure representing the foundations of the body plan. Here, we review how the first lineage decision is initiated by epigenetic regulation but consolidated by the integration of morphological features and transcription factor activity. The establishment of pluripotent and multipotent stem cell lines has enabled deeper analysis of molecular and epigenetic regulation of cell fate decisions. The capability to assemble these stem cells into artificial embryos is an exciting new avenue of research that offers a long-awaited window into cell fate specification in the human embryo. Together, these approaches are poised to profoundly increase our understanding of how the first lineage decisions are made during mammalian embryonic development.

Indexed as

Cell LineageEpigenesis, GeneticAnimalsBlastocystCell DifferentiationCell LineChromatinDNA MethylationEmbryo, MammalianEmbryonic DevelopmentFemaleGene Expression Regulation, DevelopmentalHistonesHumansIn Vitro TechniquesMiceChromatinHistonesRetroelements

Identifiers

PMID31615786
PMCPMC7111246

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.