Evidence map›Paper›PMID 35606492›Full record

ArticleGene therapy2023

Enzymatically amplified linear dbDNA

Maria Barreira, Claire Kerridge, Sara Jorda, Didrik Olofsson, Alexander Neumann, Helen Horton, Sarah Smith-Moore

Abstract read
In one paragraph

Article in Gene therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Scaling perturbations: beyond genome-scale CRISPR screens.bioRxiv : the preprint server for biology · 2026
    Article
  3. DNA-based delivery of G-CSF as a durable and efficacious approach to treat severe chronic neutropenia.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  4. Article
  5. Manufacturing DNA inMolecular therapy. Methods & clinical development · 2024
    Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. 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

7 authors.

Maria BarreiraTouchlight Genetics Ltd, Hampton, TW12 2ER, United Kingdom.
Claire KerridgeTouchlight Genetics Ltd, Hampton, TW12 2ER, United Kingdom.
Sara JordaTouchlight Genetics Ltd, Hampton, TW12 2ER, United Kingdom.ORCID http://orcid.org/0000-0002-1608-0266
Didrik OlofssonOmiqa Bioinformatics GmbH, Altensteinstraße 40, 14195, Berlin, Germany.
Alexander NeumannOmiqa Bioinformatics GmbH, Altensteinstraße 40, 14195, Berlin, Germany.ORCID http://orcid.org/0000-0002-8512-6643
Helen HortonTouchlight Genetics Ltd, Hampton, TW12 2ER, United Kingdom.
Sarah Smith-MooreTouchlight Genetics Ltd, Hampton, TW12 2ER, United Kingdom. sarah.moore@touchlight.com.ORCID http://orcid.org/0000-0002-0361-5700

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traditional bacterial fermentation techniques used to manufacture plasmid are time-consuming, expensive, and inherently unstable. The production of sufficient GMP grade material thus imposes a major bottleneck on industrial-scale manufacturing of lentiviral vectors (LVV). Touchlight's linear doggybone DNA (dbDNA

Indexed as

Genetic VectorsLentivirusDNAPlasmidsTransfectionDNA

Identifiers

PMID35606492
PMCPMC9935383

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.