Evidence map›Paper›PMID 20201948›Full record

ReviewBritish journal of haematology2010

Advances in the understanding of haemoglobin switching.

Vijay G Sankaran, Jian Xu, Stuart H Orkin

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in British journal of haematology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07177300 (Effectiveness of Nontraditional Hydroxyurea Algorithms), which is not on this map. Cited by 113 papers.

0numbers the graph read from it
0cells of the map it votes in
113citing papers in PubMed
7.5field-weighted citation impact, top 2% 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.

NCT07177300 phase4recruitingnot on this mapstarted 2024, after this paper: background citation

Effectiveness of Nontraditional Hydroxyurea Algorithms: Novel and Clinical Evaluations (ENHANCE)

TypeinterventionalSponsorChildren's Hospital Medical Center, CincinnatiRan2024 to 2028Enrolled50ConditionsSickle Cell Anemia (HbSS), Sickle-β0-thalassemia (HbSβ0)ArmsPK-optimized oral hydroxyurea at MTD until 15 years of age.
3 · Its place in the literature

Who cites it

113 citing papers in PubMed, 207 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Article
  5. Review
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  7. Review
  8. Article
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  12. Development and IND-enabling studies of a novel Cas9 genome-edited autologous CD34Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  13. Article
  14. Association ofMolecular genetics and metabolism reports · 2024
    Article
  15. Review
  16. Transcriptional Repressor BCL11A in Erythroid Cells.Advances in experimental medicine and biology · 2024
    Review
  17. Article
  18. Article
  19. Article
  20. Article

53 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Vijay G SankaranDivision of Hematology/Oncology, Children's Hospital Boston, Harvard Medical School, Boston, MA, USA.
Jian Xu
Stuart H Orkin
Harvard Stem Cell Institute · USHarvard University · US

Funding

TRANSCRIPTION FACTOR GATA-1 IN TERMINAL ERYTHROID DEVELOPMENTP01HL032262 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI ORKIN, STUART H · 1985 to 2021
$38.9M
MOLECULAR ANALYSIS OF NORMAL AND TYHALASSEMIC DNAR01HL032259 · NHLBI · CHILDREN'S HOSPITAL BOSTON · PI ORKIN, STUART H · 1985 to 2022
$8.8M
Howard Hughes Medical InstituteNHLBI NIH HHS P01 HL032262NHLBI NIH HHS R01 HL032259
6 · The paper itself

Abstract

The study of haemoglobin switching has represented a focus in haematology due in large part to the clinical relevance of the fetal to adult haemoglobin switch for developing targeted approaches to ameliorate the severity of the beta-haemoglobinopathies. Additionally, the process by which this switch occurs represents an important paradigm for developmental gene regulation. In this review, we provide an overview of both the embryonic primitive to definitive switch in haemoglobin expression, as well as the fetal to adult switch that is unique to humans and old world monkeys. We discuss the nature of these switches and models of their regulation. The factors that have been suggested to regulate this process are then discussed. With the increased understanding and discovery of molecular regulators of haemoglobin switching, such as BCL11A, new avenues of research may lead ultimately to novel therapeutic, mechanism-based approaches to fetal haemoglobin reactivation in patients.

Indexed as

Animalsbeta-GlobinsCarrier ProteinsFetal HemoglobinGene Expression Regulation, DevelopmentalGenes, SwitchGlobinsHemoglobinsHumansMiceNuclear ProteinsRepressor ProteinsBCL11A protein, humanbeta-GlobinsCarrier ProteinsFetal HemoglobinGlobinsHemoglobinsNuclear ProteinsRepressor Proteins

Identifiers

PMID20201948
PMCPMC4153468
OpenAlexW2040981306

What OpenQuestion holds

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Registered trials

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.