Evidence map›Paper›PMID 28971611›Full record

ArticlePharmacology research & perspectives2017

Nerve growth factor inhibitor with novel-binding domain demonstrates nanomolar efficacy in both cell-based and cell-free assay systems.

Allison E Kennedy, Corey A Laamanen, Mitchell S Ross, Rahul Vohra, Douglas R Boreham, John A Scott, Gregory M Ross

Open access · goldAbstract read
In one paragraph

Article in Pharmacology research & perspectives, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 46% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

7 authors at 2 institutions in 1 country.

Allison E KennedyNorthern Ontario School of Medicine, Sudbury, Ontario, Canada.ORCID 0000-0002-0247-0626
Corey A LaamanenNorthern Ontario School of Medicine, Sudbury, Ontario, Canada.
Mitchell S RossNorthern Ontario School of Medicine, Sudbury, Ontario, Canada.
Rahul VohraNorthern Ontario School of Medicine, Sudbury, Ontario, Canada.
Douglas R BorehamNorthern Ontario School of Medicine, Sudbury, Ontario, Canada.
John A ScottNorthern Ontario School of Medicine, Sudbury, Ontario, Canada.
Gregory M RossNorthern Ontario School of Medicine, Sudbury, Ontario, Canada.ORCID 0000-0002-7653-6851
NOSM University · CALaurentian University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nerve growth factor (NGF), a member of the neurotrophin family, is known to regulate the development and survival of a select population of neurons through the binding and activation of the TrkA receptor. Elevated levels of NGF have been associated with painful pathologies such as diabetic neuropathy and fibromyalgia. However, completely inhibiting the NGF signal could hold significant side effects, such as those observed in a genetic condition called congenital insensitivity to pain and anhidrosis (CIPA). Previous methods of screening for NGF-inhibitors used labeling techniques which have the potential to alter molecular interactions. SPR spectroscopy and NGF-dependent cellular assays were utilized to identify a novel NGF-inhibitor, BVNP-0197 (IC

Indexed as

AnimalsBinding SitesCell DifferentiationCell-Free SystemCell LineMiceModels, MolecularMolecular Docking SimulationMolecular StructureNaphthalimidesNerve Growth FactorPhosphorylationRatsReceptor, trkANaphthalimidesNerve Growth FactorReceptor, trkANGFpainsmall moleculeSPRTrkA

Identifiers

PMID28971611
PMCPMC5625151
OpenAlexW2748667807

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.