Evidence map›Paper›PMID 32239389›Full record

ArticleCellular and molecular neurobiology2021

NMDA Receptor and L-Type Calcium Channel Modulate Prion Formation.

Marco Zattoni, Chiara Garrovo, Elena Xerxa, Giada Spigolon, Gilberto Fisone, Krister Kristensson, Giuseppe Legname

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular neurobiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 47% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. New Light on Prions: Putative Role of PrPInternational journal of molecular sciences · 2024
    Review
  3. Review
  4. 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

7 authors at 3 institutions in 2 countries.

Marco ZattoniLaboratory of Prion Biology, Department of Neuroscience, Scuola Internazionale Superiore Di Studi Avanzati (SISSA), Trieste, Italy.
Chiara GarrovoLaboratory of Prion Biology, Department of Neuroscience, Scuola Internazionale Superiore Di Studi Avanzati (SISSA), Trieste, Italy.
Elena XerxaLaboratory of Prion Biology, Department of Neuroscience, Scuola Internazionale Superiore Di Studi Avanzati (SISSA), Trieste, Italy.
Giada SpigolonDepartment of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Gilberto FisoneDepartment of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Krister KristenssonDepartment of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Giuseppe LegnameLaboratory of Prion Biology, Department of Neuroscience, Scuola Internazionale Superiore Di Studi Avanzati (SISSA), Trieste, Italy. legname@sissa.it.
Karolinska Institutet · SEScuola Internazionale Superiore di Studi Avanzati · ITInternational Centre for Genetic Engineering and Biotechnology · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transmissible neurodegenerative prion diseases are characterized by the conversion of the cellular prion protein (PrP

Indexed as

AnimalsCalcium Channels, L-TypeCell LineDizocilpine MaleateExtracellular Signal-Regulated MAP KinasesHumansModels, BiologicalNimodipinePhosphorylationPrionsPrPSc ProteinsReceptors, N-Methyl-D-AspartateCalcium Channels, L-TypeDizocilpine MaleateExtracellular Signal-Regulated MAP KinasesNimodipinePrionsPrPSc ProteinsReceptors, N-Methyl-D-AspartateL-type voltage-dependent calcium channelsMAP kinase pathwaysMEK/ERK-1/2 cascadeNeurodegenerationNMDA receptorsPrionsSynaptic plasticity

Identifiers

PMID32239389
PMCPMC11448565
OpenAlexW3014209496

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.