Evidence map›Paper›PMID 29789357›Full record

ArticleBlood2018

Reactivation of γ-globin in adult β-YAC mice after ex vivo and in vivo hematopoietic stem cell genome editing.

Chang Li, Nikoletta Psatha, Pavel Sova, Sucheol Gil, Hongjie Wang, Jiho Kim, Chandana Kulkarni, Cristina Valensisi, R David Hawkins, George Stamatoyannopoulos and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 6% 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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
  2. Genes & diseases · 2026
    Review
  3. Review
  4. Review
  5. Molecular therapy. Methods & clinical development · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Precision Editing as a Therapeutic Approach for β-Hemoglobinopathies.International journal of molecular sciences · 2023
    Review
  17. Article
  18. Article
  19. Review
  20. Review
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 at 1 institution in 2 countries.

Chang LiDivision of Medical Genetics, Department of Medicine.
Nikoletta PsathaDivision of Hematology, Department of Medicine, and.
Pavel SovaDivision of Medical Genetics, Department of Medicine.
Sucheol GilDivision of Medical Genetics, Department of Medicine.
Hongjie WangDivision of Medical Genetics, Department of Medicine.
Jiho KimDivision of Medical Genetics, Department of Medicine.
Chandana KulkarniDivision of Medical Genetics, Department of Medicine.
Cristina ValensisiDivision of Medical Genetics, Department of Medicine.
R David HawkinsDivision of Medical Genetics, Department of Medicine.
George StamatoyannopoulosDivision of Medical Genetics, Department of Medicine.
André LieberDivision of Medical Genetics, Department of Medicine.
Medical Genetics Center · DE

Funding

Ras-MAPK Regulation of Lymphatic Vessel Valve DevelopmentR01HL120888 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PHILIP D KING · 2015 to 2026
$4.6M
In Vivo Hematopoietic Stem Cell Gene Therapy of Beta-Thalassemia and Sickle Cell DiseaseR01HL130040 · NHLBI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 2016 to 2024
$4.3M
Approach for in vivo gene delivery into hematopoietic stem cells for hemophilia A therapyR01HL141781 · NHLBI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 2018 to 2021
$2.3M
In vivo anti-PD1 gene therapyR21CA204036 · NCI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 2017 to 2018
$371k
Hematopoietic stem cell based gene therapy of breast cancerR21CA193077 · NCI · UNIVERSITY OF WASHINGTON · PI LIEBER, ANDRE MICHAEL · 2015 to 2016
$370k
NCI NIH HHS R21 CA193077NCI NIH HHS R21 CA204036NHLBI NIH HHS R01 HL120888NHLBI NIH HHS R01 HL130040NHLBI NIH HHS R01 HL141781
6 · The paper itself

Abstract

Disorders involving β-globin gene mutations, primarily β-thalassemia and sickle cell disease, represent a major target for hematopoietic stem/progenitor cell (HSPC) gene therapy. This includes CRISPR/Cas9-mediated genome editing approaches in adult CD34

Indexed as

CRISPR-Cas SystemsGene ExpressionAnimalsbeta-GlobinsErythrocytesFemalegamma-GlobinsGene EditingHematopoietic Stem Cell MobilizationHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHumansMiceMice, Inbred C57BLMice, TransgenicPromoter Regions, Geneticbeta-Globinsgamma-Globins

Identifiers

PMID29789357
PMCPMC6024639
OpenAlexW2805004547

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.