Evidence map›Paper›PMID 31383820›Full record

ArticleDisease models & mechanisms2019

Functional loss of

Francesco Chiani, Tiziana Orsini, Alessia Gambadoro, Miriam Pasquini, Sabrina Putti, Maurizio Cirilli, Olga Ermakova, Glauco P Tocchini-Valentini

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.4field-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

21 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Essential role of p21Stem cell research & therapy · 2024
    Article
  7. TheCells · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Syndromic Hydrocephalus.Neurosurgery clinics of North America · 2022
    Review
  12. Ependymal Cilia: Physiology and Role in Hydrocephalus.Frontiers in molecular neuroscience · 2022
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Motile cilia genetics and cell biology: big results from little mice.Cellular and molecular life sciences : CMLS · 2021
    Review
  18. Review
  19. Article
  20. 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

8 authors at 1 institution in 1 country.

Francesco ChianiEuropean Mouse Mutant Archive (EMMA), INFRAFRONTIER, Monterotondo Mouse Clinic, Department of Biomedical Sciences (DSB), Italian National Research Council (CNR), Adriano Buzzati-Traverso Campus, via Ramarini, 32, 00015, Monterotondo, Rome, Italy.
Tiziana OrsiniEuropean Mouse Mutant Archive (EMMA), INFRAFRONTIER, Monterotondo Mouse Clinic, Department of Biomedical Sciences (DSB), Italian National Research Council (CNR), Adriano Buzzati-Traverso Campus, via Ramarini, 32, 00015, Monterotondo, Rome, Italy.
Alessia GambadoroEuropean Mouse Mutant Archive (EMMA), INFRAFRONTIER, Monterotondo Mouse Clinic, Department of Biomedical Sciences (DSB), Italian National Research Council (CNR), Adriano Buzzati-Traverso Campus, via Ramarini, 32, 00015, Monterotondo, Rome, Italy.
Miriam PasquiniEuropean Mouse Mutant Archive (EMMA), INFRAFRONTIER, Monterotondo Mouse Clinic, Department of Biomedical Sciences (DSB), Italian National Research Council (CNR), Adriano Buzzati-Traverso Campus, via Ramarini, 32, 00015, Monterotondo, Rome, Italy.
Sabrina PuttiEuropean Mouse Mutant Archive (EMMA), INFRAFRONTIER, Monterotondo Mouse Clinic, Department of Biomedical Sciences (DSB), Italian National Research Council (CNR), Adriano Buzzati-Traverso Campus, via Ramarini, 32, 00015, Monterotondo, Rome, Italy.
Maurizio CirilliInstitute of Biochemistry and Cell Biology (IBBC), Department of Biomedical Sciences (DSB), Italian National Research Council (CNR), Adriano Buzzati-Traverso Campus, via Ramarini, 32, 00015, Monterotondo, Rome, Italy.
Olga ErmakovaEuropean Mouse Mutant Archive (EMMA), INFRAFRONTIER, Monterotondo Mouse Clinic, Department of Biomedical Sciences (DSB), Italian National Research Council (CNR), Adriano Buzzati-Traverso Campus, via Ramarini, 32, 00015, Monterotondo, Rome, Italy olga.ermakova@cnr.it.ORCID 0000-0001-8365-4904
Glauco P Tocchini-ValentiniEuropean Mouse Mutant Archive (EMMA), INFRAFRONTIER, Monterotondo Mouse Clinic, Department of Biomedical Sciences (DSB), Italian National Research Council (CNR), Adriano Buzzati-Traverso Campus, via Ramarini, 32, 00015, Monterotondo, Rome, Italy.
National Research Council · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder affecting normal structure and function of motile cilia, phenotypically manifested as chronic respiratory infections, laterality defects and infertility. Autosomal recessive mutations in genes encoding for different components of the ciliary axoneme have been associated with PCD in humans and in model organisms. The

Indexed as

AnimalsAnimals, NewbornBody PatterningCarrier ProteinsCiliary Motility DisordersDisease Models, AnimalEpendymaGene Expression RegulationHydrocephalusImaging, Three-DimensionalMaleMice, Inbred C57BLMice, KnockoutSpermatogenesisTestisX-Ray MicrotomographyCarrier ProteinsCiliaCSFGene knockoutIMPCMicroCT brain imagingX-ray gene expression imaging

Identifiers

PMID31383820
PMCPMC6737950
OpenAlexW2965263411

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.