Evidence map›Paper›PMID 23070775›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2013

Lipopeptide delivery of siRNA to the central nervous system.

Mark D Zabel

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 13% 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

2 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
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

1 author at 1 institution in 1 country.

Mark D ZabelDepartment of Microbiology, Immunology and Pathology, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO, USA. mark.zabel@colostate.edu
Colorado State University · US

Funding

Liposome-siRNA-Peptide Complexes as Therapy to Cure Prion Diseases in Mouse ModelR01NS075214 · NINDS · COLORADO STATE UNIVERSITY · PI ZABEL, MARK D · 2012 to 2016
$1.7M
NINDS NIH HHS R01 NS075214
6 · The paper itself

Abstract

RNA interference is a relatively new tool used to silence specific genes in diverse biological systems. The development of this promising new technique for research and therapeutic use in studying and treating neurological diseases has been hampered by the lack of an efficient way to deliver siRNA transvascularly across the blood-brain barrier (BBB) to the central nervous system (CNS). Here we describe a method for delivering siRNA to the CNS by complexing it to a peptide that acts as a neuronal address by binding to acetylcholine receptors (AchRs). Adding cationic liposomes to the complex protects it from serum nucleases and proteases en route. When injected intravenously, these liposome-siRNA-peptide complexes resist serum degradation, effectively cross the BBB, and deliver siRNA to AchR-expressing cells to suppress protein expression in the CNS.

Indexed as

Gene Transfer TechniquesAmino Acid SequenceAnimalsBlood-Brain BarrierBrainDrug CarriersGene Expression RegulationInjectionsLiposomesMiceMolecular Sequence DataPeptidesPrionsReceptors, CholinergicRNA InterferenceRNA, Small InterferingDrug CarriersLiposomesPeptidesPrionsReceptors, CholinergicRNA, Small Interfering

Identifiers

PMID23070775
PMCPMC6043354
OpenAlexW2474307910

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.