Evidence map›Paper›PMID 34831239›Full record

ArticleCells2021

Comprehensive Analysis of microRNAs in Human Adult Erythropoiesis.

Aneesha Nath, Janakiram Rayabaram, Smitha Ijee, Abhirup Bagchi, Anurag Dutta Chaudhury, Debanjan Roy, Karthik Chambayil, Jyoti Singh, Yukio Nakamura, Shaji R Velayudhan

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Potential Use of MicroRNA Technology in Thalassemia Therapy.Journal of clinical medicine research · 2024
    Review
  3. Article
  4. Nuclear miRNAs: Gene Regulation Activities.International journal of molecular sciences · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. 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

10 authors at 4 institutions in 2 countries.

Aneesha NathCenter for Stem Cell Research (A Unit of InStem, Bengaluru, India), Christian Medical College, Vellore 632002, India.
Janakiram RayabaramDepartment of Haematology, Christian Medical College, Vellore 632004, India.
Smitha IjeeCenter for Stem Cell Research (A Unit of InStem, Bengaluru, India), Christian Medical College, Vellore 632002, India.
Abhirup BagchiCenter for Stem Cell Research (A Unit of InStem, Bengaluru, India), Christian Medical College, Vellore 632002, India.ORCID 0000-0002-1794-6471
Anurag Dutta ChaudhuryDepartment of Haematology, Christian Medical College, Vellore 632004, India.
Debanjan RoyDepartment of Haematology, Christian Medical College, Vellore 632004, India.
Karthik ChambayilCenter for Stem Cell Research (A Unit of InStem, Bengaluru, India), Christian Medical College, Vellore 632002, India.
Jyoti SinghNational Centre for Cell Science, University of Pune Campus, Pune 411007, India.ORCID 0000-0003-1175-2403
Yukio NakamuraCell Engineering Division, RIKEN BioResource Research Center, Ibaraki 305-0074, Japan.
Shaji R VelayudhanCenter for Stem Cell Research (A Unit of InStem, Bengaluru, India), Christian Medical College, Vellore 632002, India.
Christian Medical College, Vellore · INManipal Academy of Higher Education · INNational Centre for Cell Science · INRIKEN BioResource Research Center · JP

Funding

Department of Biotechnology, Govt. of India. BT/PR17316/MED/31/326/2015
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are small non-coding RNAs, which play an important role in various cellular and developmental processes. The study of miRNAs in erythropoiesis is crucial to uncover the cellular pathways that are modulated during the different stages of erythroid differentiation. Using erythroid cells derived from human CD34+ hematopoietic stem and progenitor cells (HSPCs)and small RNA sequencing, our study unravels the various miRNAs involved in critical cellular pathways in erythroid maturation. We analyzed the occupancy of erythroid transcription factors and chromatin accessibility in the promoter and enhancer regions of the differentially expressed miRNAs to integrate miRNAs in the transcriptional circuitry of erythropoiesis. Analysis of the targets of the differentially expressed miRNAs revealed novel pathways in erythroid differentiation. Finally, we described the application of Clustered regularly interspaced short palindromic repeats-Cas9 (CRISPR-Cas9) based editing of miRNAs to study their function in human erythropoiesis.

Indexed as

AdultCell DifferentiationCell LineChromatinCRISPR-Cas SystemsErythroid CellsErythropoiesisGene EditingGene Expression ProfilingGene Expression RegulationHumansMicroRNAsSignal TransductionTranscription FactorsChromatinMicroRNAsTranscription FactorsCD34+ HSPCsCRISPR-Cas9erythropoiesismicroRNAssmall RNA sequencing

Identifiers

PMID34831239
PMCPMC8616439
OpenAlexW3210375158

What Socratic holds

Textmetadata
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 Socratic graph.