Evidence map›Paper›PMID 17655741›Full record

ArticleBrain pathology (Zurich, Switzerland)2007

Role of NF2 haploinsufficiency in NF2-associated polyneuropathy.

Clemens O Hanemann, Ruth Diebold, Dieter Kaufmann

Open access · greenAbstract read
In one paragraph

Article in Brain pathology (Zurich, Switzerland), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Low availability of cholineFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  3. Article
  4. Article
  5. A neuronal function of the tumor suppressor protein merlin.Acta neuropathologica communications · 2014
    Review
  6. Article
  7. Review
  8. Neurofibromatosis type 2.Lancet (London, England) · 2009
    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

3 authors at 2 institutions in 2 countries.

Clemens O HanemannClinical Neurobiology, Inst. Biomedical and Clinical Science, Peninsula Medical School, The John Bull Building, Tamar Science Park, Research Way, Plymouth PL6 8BU, UK. Oliver.Hanemann@pms.ac.uk
Ruth Diebold
Dieter Kaufmann
Helmholtz-Institute Ulm · DEPeninsula College of Medicine and Dentistry · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurofibromatosis 2 (NF2) is a hereditary tumor disease characterized by bilateral vestibular schwannomas. Polyneuropathy seems to occur quite frequently in NF2 and in most cases, the etiology of this neuropathy is unclear, especially when the neuropathy is symmetric. NF2 is believed to follow the two-hit hypothesis. According to this, one allele is mutated in the germline, and the second hit is somatic and results in tumor formation. The second hit most frequently is a loss of the NF2 locus, often the entire chromosome 22. We set out to investigate the underlying genetics in peripheral nerve of NF2 patients with polyneuropathy. We identified NF2 patients with polyneuropathy in which we could detect the germline mutation and analyzed NF2 gene dosage in archived nerve biopsies from these patients using a newly developed method. We observed merlin haploinsufficiency in peripheral nerves of two different patients with NF2-related polyneuropathy. This finding was further supported by showing that approximately 50% merlin expression in a cell line using shRNA results in altered gene expression as previously shown in schwannomas. Thus, we suggest that reduced merlin gene dosage is relevant in NF2-associated polyneuropathy.

Indexed as

Cell Line, TumorChromosomes, Human, Pair 22DNA Mutational AnalysisGene DosageGene Expression RegulationGenetic MarkersGenetic Predisposition to DiseaseGenetic TestingGerm-Line MutationHaplotypesHumansNerve Fibers, MyelinatedNeural ConductionNeurofibromatosis 2Neurofibromin 2Peripheral NervesGenetic MarkersNeurofibromin 2

Identifiers

PMID17655741
PMCPMC8095497
OpenAlexW2069499110

What OpenQuestion holds

Textmetadata
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.