Evidence map›Paper›PMID 38886504›Full record

ArticleNature biomedical engineering2024

Enhancement of erythropoietic output by Cas9-mediated insertion of a natural variant in haematopoietic stem and progenitor cells.

Sofia E Luna, Joab Camarena, Jessica P Hampton, Kiran R Majeti, Carsten T Charlesworth, Eric Soupene, Sridhar Selvaraj, Kun Jia, Vivien A Sheehan, M Kyle Cromer and 1 more

Abstract read
In one paragraph

Article in Nature biomedical engineering, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Angiogenic Doping: Plausible Yet Difficult to Detect.Sports medicine (Auckland, N.Z.) · 2026
    Review
  5. Article
  6. Mobilization meets antibody conditioning: A path toward safer engraftment.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Introducing a hemoglobin G-Makassar variant in HSCs by in vivo base editing treats sickle cell disease in mice.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    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

11 authors.

Sofia E Luna *Department of Pediatrics, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-9173-9518
Joab Camarena *Department of Pediatrics, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-3102-5820
Jessica P HamptonDepartment of Pediatrics, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-0084-5404
Kiran R MajetiDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Carsten T CharlesworthDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Eric SoupeneDepartment of Pediatrics, University of California, San Francisco, Oakland, CA, USA.
Sridhar SelvarajDepartment of Pediatrics, Stanford University, Stanford, CA, USA.
Kun JiaDepartment of Surgery, University of California San Francisco, San Francisco, CA, USA.
Vivien A SheehanAflac Cancer and Blood Disorders Center, Department of Pediatrics, Emory University School of Medicine, Atlanta, GA, USA.ORCID http://orcid.org/0000-0003-2837-2255
M Kyle CromerDepartment of Surgery, University of California San Francisco, San Francisco, CA, USA. kyle.cromer@ucsf.edu.ORCID http://orcid.org/0000-0002-8198-5010
Matthew H PorteusDepartment of Pediatrics, Stanford University, Stanford, CA, USA. mporteus@stanford.edu.ORCID http://orcid.org/0000-0002-3850-4648

Funding

American Society of Hematology (ASH) Junior Faculty Scholar AwardAmerican Society of Hematology (ASH) Minority Medical Student AwardSU | School of Medicine, Stanford University (Stanford School of Medicine, Stanford University) Medical Scientist Training ProgramSU | School of Medicine, Stanford University (Stanford School of Medicine, Stanford University) Stanford Medical Scholars Research Program
6 · The paper itself

Abstract

Some gene polymorphisms can lead to monogenic diseases, whereas other polymorphisms may confer beneficial traits. A well-characterized example is congenital erythrocytosis-the non-pathogenic hyper-production of red blood cells-that is caused by a truncated erythropoietin receptor. Here we show that Cas9-mediated genome editing in CD34

Indexed as

CRISPR-Cas SystemsErythropoiesisGene EditingHematopoietic Stem CellsReceptors, ErythropoietinAntigens, CD34beta-ThalassemiaCRISPR-Associated Protein 9HumansAntigens, CD34CRISPR-Associated Protein 9Receptors, Erythropoietin

Identifiers

PMID38886504
PMCPMC11668683

What OpenQuestion 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 OpenQuestion graph.