Evidence map›Paper›PMID 30076417›Full record

ArticleScientific reports2018

Expression and localization of the polarity protein CRB2 in adult mouse brain: a comparison with the CRB1

Jorge F Dolón, Antonio E Paniagua, Vicente Valle, Alicia Segurado, Rosario Arévalo, Almudena Velasco, Concepción Lillo

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. 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
0.5field-weighted citation impact, top 39% 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, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. LMTK2 and CRB1 are two novel risk genes for Alzheimer's disease in Han Chinese.The journal of prevention of Alzheimer's disease · 2025
    Article
  5. Diverse functions and pathogenetic role of Crumbs in retinopathy.Cell communication and signaling : CCS · 2024
    Review
  6. Article
  7. Review
  8. AAV-Molecular therapy. Methods & clinical development · 2021
    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 1 institution in 2 countries.

Jorge F DolónInstitute of Neurosciences of Castilla y León, IBSAL, Cell Biology and Pathology, University of Salamanca, 37007, Salamanca, Spain.
Antonio E PaniaguaInstitute of Neurosciences of Castilla y León, IBSAL, Cell Biology and Pathology, University of Salamanca, 37007, Salamanca, Spain.
Vicente ValleInstitute of Neurosciences of Castilla y León, IBSAL, Cell Biology and Pathology, University of Salamanca, 37007, Salamanca, Spain.
Alicia SeguradoInstitute of Neurosciences of Castilla y León, IBSAL, Cell Biology and Pathology, University of Salamanca, 37007, Salamanca, Spain.
Rosario ArévaloInstitute of Neurosciences of Castilla y León, IBSAL, Cell Biology and Pathology, University of Salamanca, 37007, Salamanca, Spain.
Almudena VelascoInstitute of Neurosciences of Castilla y León, IBSAL, Cell Biology and Pathology, University of Salamanca, 37007, Salamanca, Spain.
Concepción LilloInstitute of Neurosciences of Castilla y León, IBSAL, Cell Biology and Pathology, University of Salamanca, 37007, Salamanca, Spain. conlillo@usal.es.ORCID 0000-0001-5814-9826
Universidad de Salamanca · ES

Funding

Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) PI15/01240
6 · The paper itself

Abstract

Acquisition of cell polarization is essential for the performance of crucial functions, like a successful secretion and appropriate cell signaling in many tissues, and it depends on the correct functioning of polarity proteins, including the Crumbs complex. The CRB proteins, CRB1, CRB2 and CRB3, identified in mammals, are expressed in epithelial-derived tissues like brain, kidney and retina. CRB2 has a ubiquitous expression and has been detected in embryonic brain tissue; but currently there is no data regarding its localization in the adult brain. In our study, we characterized the presence of CRB2 in adult mice brain, where it is particularly enriched in cortex, hippocampus, hypothalamus and cerebellum. Double immunofluorescence analysis confirmed that CRB2 is a neuron-specific protein, present in both soma and projections where colocalizes with certain populations of exocytic and endocytic vesicles and with other members of the Crumbs complex. Finally, in the cortex of CRB1

Indexed as

AnimalsBrainCell PolarityCerebellumEpithelial CellsGene Expression RegulationHippocampusHypothalamusMembrane ProteinsMiceMutationNeuronsSignal TransductionCrb2 protein, mouseMembrane Proteins

Identifiers

PMID30076417
PMCPMC6076319
OpenAlexW2885269537

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.