Evidence map›Paper›PMID 31694170›Full record

ReviewInternational journal of molecular sciences2019

Mouse Models of Human Claudin-Associated Disorders: Benefits and Limitations.

Murat Seker, Carmen Fernandez-Rodriguez, Luis Alfonso Martinez-Cruz, Dominik Müller

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. The Fate of Epidermal Tight Junctions in theInternational journal of molecular sciences · 2022
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Claudin-1, A Double-Edged Sword in Cancer.International journal of molecular sciences · 2020
    Review
  11. A Novel Claudinopathy Based on Claudin-10 Mutations.International journal of molecular sciences · 2019
    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

4 authors.

Murat SekerDepartment of Pediatric Gastroenterology, Nephrology and Metabolism, Charité-Universitätsmedizin Berlin, Charité, 13353 Berlin, Germany.ORCID 0000-0003-2306-6005
Carmen Fernandez-RodriguezClC BioGUNE, Bizkaia Science and Technology Park, 801A, 48160 Derio, Spain.
Luis Alfonso Martinez-CruzClC BioGUNE, Bizkaia Science and Technology Park, 801A, 48160 Derio, Spain.ORCID 0000-0002-5856-9377
Dominik MüllerDepartment of Pediatric Gastroenterology, Nephrology and Metabolism, Charité-Universitätsmedizin Berlin, Charité, 13353 Berlin, Germany.ORCID 0000-0002-3478-1576

Funding

Deutsche Forschungsgemeinschaft TJ_Train GRK2318
6 · The paper itself

Abstract

In higher organisms, epithelia separate compartments in order to guarantee their proper function. Such structures are able to seal but also to allow substances to pass. Within the paracellular pathway, a supramolecular structure, the tight junction transport is largely controlled by the temporospatial regulation of its major protein family called claudins. Besides the fact that the expression of claudins has been identified in different forms of human diseases like cancer, clearly defined mutations in the corresponding claudin genes have been shown to cause distinct human disorders. Such disorders comprise the skin and its adjacent structures, liver, kidney, the inner ear, and the eye. From the phenotype analysis, it has also become clear that different claudins can cause a complex phenotype when expressed in different organs. To gain deeper insights into the physiology and pathophysiology of claudin-associated disorders, several mouse models have been generated. In order to model human disorders in detail, they have been designed either as full knockouts, knock-downs or knock-ins by a variety of techniques. Here, we review human disorders caused by CLDN mutations and their corresponding mouse models that have been generated thus far and assess their usefulness as a model for the corresponding human disorder.

Indexed as

MutationAmino Acid SequenceAnimalsClaudinsDisease Models, AnimalEye DiseasesHumansKidney DiseasesLiver DiseasesMiceNeoplasmsSkin DiseasesClaudinsclaudindiseasehumankidneylivermicemutationsskintight junction

Identifiers

PMID31694170
PMCPMC6862546

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.