Evidence map›Paper›PMID 26611592›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2016

AAV-Mediated Gene Transfer to Dorsal Root Ganglion.

Hongwei Yu, Gregory Fischer, Quinn H Hogan

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Efficient genetic perturbation of murine sensory neuronsbioRxiv : the preprint server for biology · 2025
    Article
  5. Labeling phrenic afferents with intrapleural AAV-PHP.S.Journal of neuroscience methods · 2025
    Article
  6. Article
  7. Article
  8. AAV-mediated gene transfer to colon-innervating primary afferent neurons.Frontiers in pain research (Lausanne, Switzerland) · 2023
    Article
  9. Precision spinal gene delivery-induced functional switch in nociceptive neurons reverses neuropathic pain.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
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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.

Hongwei YuDepartment of Anesthesiology, Medical College of Wisconsin, Watertown Plank Road, Milwaukee, WI, 53226, USA. hyu@mcw.edu.
Gregory FischerDepartment of Anesthesiology, Medical College of Wisconsin, Watertown Plank Road, Milwaukee, WI, 53226, USA.
Quinn H HoganDepartment of Anesthesiology, Medical College of Wisconsin, Watertown Plank Road, Milwaukee, WI, 53226, USA.

Funding

DRG engraftment of transduced mesenchymal stem cells to treat neuropathic painR01NS079626 · NINDS · MEDICAL COLLEGE OF WISCONSIN · PI HOGAN, QUINN H · 2012 to 2015
$1.1M
AAV-encoded analgesic peptide aptamers for chronic painI01RX001940 · VA · CLEMENT J. ZABLOCKI VA MEDICAL CENTER · PI HOGAN, QUINN H · 2016 to 2019
–
NINDS NIH HHS R01 NS079626NINDS NIH HHS R01NS079626-01RRD VA I01 RX001940
6 · The paper itself

Abstract

Transferring genetic molecules into the peripheral sensory nervous system to manipulate nociceptive pathophysiology is a powerful approach for experimental modulation of sensory signaling and potentially for translation into therapy for chronic pain. This can be efficiently achieved by the use of recombinant adeno-associated virus (rAAV) in conjunction with nociceptor-specific regulatory transgene cassettes. Among different routes of delivery, direct injection into the dorsal root ganglia (DRGs) offers the most efficient AAV-mediated gene transfer selectively into the peripheral sensory nervous system. Here, we briefly discuss the advantages and applications of intraganglionic microinjection, and then provide a detailed approach for DRG injection, including a list of the necessary materials and description of a method for performing DRG microinjection experiments. We also discuss our experience with several adeno-associated virus (AAV) options for in vivo transgene expression in DRG neurons.

Indexed as

AnimalsChronic PainDependovirusGanglia, SpinalGenetic TherapyGenetic VectorsGene Transfer TechniquesMaleMicroinjectionsRatsRats, Sprague-DawleyTransduction, GeneticAdeno-associated virusChronic painDorsal root ganglionGene therapyMicroinjection

Identifiers

PMID26611592
PMCPMC5459312

What OpenQuestion holds

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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.