Evidence map›Paper›PMID 27943094›Full record

ArticleJournal of molecular neuroscience : MN2017

Primary Brain Calcification Causal PiT2 Transport-Knockout Variants can Exert Dominant Negative Effects on Wild-Type PiT2 Transport Function in Mammalian Cells.

Frederik Tibert Larsen, Nina Jensen, Jacob Kwasi Autzen, Iben Boutrup Kongsfelt, Lene Pedersen

Open access · hybridAbstract read
In one paragraph

Article in Journal of molecular neuroscience : MN, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. The Genetics of Primary Familial Brain Calcification: A Literature Review.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. A novel SLC20A2 gene mutation causing primary familial brain calcification in an Ukrainian patient.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2019
    Article
  10. Article
  11. Review
  12. Review
  13. 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

5 authors at 1 institution in 1 country.

Frederik Tibert LarsenDepartment of Molecular Biology and Genetics, Aarhus University, C. F. Møllers Allé 3, Building 1130, 8000, Aarhus, Denmark.
Nina JensenDepartment of Molecular Biology and Genetics, Aarhus University, C. F. Møllers Allé 3, Building 1130, 8000, Aarhus, Denmark.
Jacob Kwasi AutzenDepartment of Molecular Biology and Genetics, Aarhus University, C. F. Møllers Allé 3, Building 1130, 8000, Aarhus, Denmark.
Iben Boutrup KongsfeltDepartment of Molecular Biology and Genetics, Aarhus University, C. F. Møllers Allé 3, Building 1130, 8000, Aarhus, Denmark.
Lene PedersenDepartment of Molecular Biology and Genetics, Aarhus University, C. F. Møllers Allé 3, Building 1130, 8000, Aarhus, Denmark. LP@mbg.au.dk.ORCID http://orcid.org/0000-0002-3396-1292
Aarhus University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary brain calcification (PBC) is a neurodegenerative disorder characterized by calcium-phosphate deposits in the basal ganglia and often also other areas of the brain. The prevalent clinical manifestations are cognitive impairment, neuropsychiatric symptoms, and movement disorders. In recent years, monoallelic variants in SLC20A2, which encodes the type III sodium-dependent inorganic phosphate (P

Indexed as

Mutation, MissenseAnimalsBrainCalcinosisCells, CulturedFibroblastsHumansIon TransportMiceMice, Inbred C57BLPhenotypePhosphatesSodium-Phosphate Cotransporter Proteins, Type IIIPhosphatesSLC20A2 protein, humanSodium-Phosphate Cotransporter Proteins, Type IIIOligomerizationPhosphate transporterPiT2Primary familial brain calcificationSLC20A2

Identifiers

PMID27943094
PMCPMC5321689
OpenAlexW2560596251

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.