Evidence map›Paper›PMID 35330735›Full record

ReviewFrontiers in genetics2022

Epigenetic and Transcriptional Control of Erythropoiesis.

Maeve Wells, Laurie Steiner

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 11% of its field
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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. ReducedInternational journal of molecular sciences · 2026
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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 at 1 institution in 1 country.

Maeve WellsDepartment of Pediatrics, University of Rochester, Rochester, NY, United States.
Laurie SteinerDepartment of Pediatrics, University of Rochester, Rochester, NY, United States.
University of Rochester · US

Funding

Elucidation of the Role of Setd8 and H4K20me1 in ErythropoiesisR01DK104920 · NIDDK · UNIVERSITY OF ROCHESTER · PI STEINER, LAURIE A. · 2016 to 2024
$3.1M
Investigation into the function of RNA polymerase II promoter proximal pausing during terminal erythroid maturationR01DK124777 · NIDDK · UNIVERSITY OF ROCHESTER · PI LAURIE A. STEINER · 2020 to 2026
$2.4M
NIDDK NIH HHS R01 DK104920NIDDK NIH HHS R01 DK124777
6 · The paper itself

Abstract

Erythropoiesis is a process of enormous magnitude, with the average person generating two to three million red cells every second. Erythroid progenitors start as large cells with large nuclei, and over the course of three to four cell divisions they undergo a dramatic decrease in cell size accompanied by profound nuclear condensation, which culminates in enucleation. As maturing erythroblasts are undergoing these dramatic phenotypic changes, they accumulate hemoglobin and express high levels of other erythroid-specific genes, while silencing much of the non-erythroid transcriptome. These phenotypic and gene expression changes are associated with distinct changes in the chromatin landscape, and require close coordination between transcription factors and epigenetic regulators, as well as precise regulation of RNA polymerase II activity. Disruption of these processes are associated with inherited anemias and myelodysplastic syndromes. Here, we review the epigenetic mechanisms that govern terminal erythroid maturation, and their role in human disease.

Indexed as

anemiadiseaseepigeneticerythroidtranscription

Identifiers

PMID35330735
PMCPMC8940284
OpenAlexW4220742697

What OpenQuestion holds

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LicenceCC BY
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.