Evidence map›Paper›PMID 34707296›Full record

ArticleNature2021

The structure of neurofibromin isoform 2 reveals different functional states.

Andreas Naschberger, Rozbeh Baradaran, Bernhard Rupp, Marta Carroni

Open access · hybridAbstract read
In one paragraph

Article in Nature, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
5.4field-weighted citation impact, top 3% 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

29 citing papers in PubMed, 66 citations in OpenAlex.

  1. Review
  2. Article
  3. Apoptotic body-encapsulated zinc-dopedMaterials today. Bio · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Human Disabled-2 regulates thromboxane ANature communications · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. New insights into the molecular basis of spinal neurofibromatosis type 1.European journal of human genetics : EJHG · 2023
    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

4 authors at 2 institutions in 3 countries.

Andreas Naschberger *SciLifeLab, Department of Biochemistry and Biophysics, Stockholm University, Solna, Sweden.
Rozbeh Baradaran *SciLifeLab, Department of Biochemistry and Biophysics, Stockholm University, Solna, Sweden.ORCID http://orcid.org/0000-0002-6096-9169
Bernhard RuppInstitute of Genetic Epidemiology, Medical University Innsbruck, Innsbruck, Austria. br@hofkristallamt.org.ORCID http://orcid.org/0000-0002-3300-6965
Marta CarroniSciLifeLab, Department of Biochemistry and Biophysics, Stockholm University, Solna, Sweden. marta.carroni@scilifelab.se.ORCID http://orcid.org/0000-0002-7697-6427
Innsbruck Medical University · ATStockholm University · SE

Funding

Austrian Science Fund FWF P 28395
6 · The paper itself

Abstract

The autosomal dominant monogenetic disease neurofibromatosis type 1 (NF1) affects approximately one in 3,000 individuals and is caused by mutations in the NF1 tumour suppressor gene, leading to dysfunction in the protein neurofibromin (Nf1)

Indexed as

Cryoelectron MicroscopyAdaptor Proteins, Signal TransducingAlternative SplicingBinding SitesExonsHumansModels, MolecularNeurofibromin 1Neurofibromin 2Protein BindingProtein DomainsProtein IsoformsProtein MultimerizationProtein StabilityZincAdaptor Proteins, Signal TransducingNeurofibromin 1Neurofibromin 2NF1 protein, humanProtein IsoformsSPRED1 protein, humanZinc

Identifiers

PMID34707296
PMCPMC8580823
OpenAlexW3210375384

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.