Evidence map›Paper›PMID 22036906›Full record

ReviewAdvanced drug delivery reviews2012

Guided delivery of adeno-associated viral vectors into the primate brain.

Ernesto A Salegio, Lluis Samaranch, Adrian P Kells, John Forsayeth, Krystof Bankiewicz

Abstract readReview
In one paragraph

Review in Advanced drug delivery reviews, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Review
  2. Article
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  12. Review
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  15. Review
  16. Article
  17. Article
  18. Article
  19. Transgene expression in target-defined neuron populations mediated by retrograde infection with adeno-associated viral vectors.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  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

5 authors.

Ernesto A SalegioDepartment of Neurological Surgery, University of California San Francisco, San Francisco, CA 94103–0555, USA.
Lluis Samaranch
Adrian P Kells
John Forsayeth
Krystof Bankiewicz

Funding

Preclinical development of a gene therapy for Niemann-Pick disease, type AR01NS056107 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BANKIEWICZ, KRYSTOF S · 2007 to 2011
$2.0M
NINDS NIH HHS R01 NS056107
6 · The paper itself

Abstract

In this review, we discuss recent developments in the delivery of adeno-associated virus-based vectors (AAV), particularly with respect to the role of axonal transport in vector distribution in the brain. The use of MRI-guidance and new stereotactic aiming devices have now established a strong foundation for neurological gene therapy to become an accepted procedure in interventional neurology.

Indexed as

DependovirusGene Transfer TechniquesAnimalsBrainGenetic TherapyGenetic VectorsHumansMagnetic Resonance Imaging

Identifiers

PMID22036906
PMCPMC3279613

What OpenQuestion holds

Textmetadata
LicenceTDM
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.