Evidence map›Paper›PMID 33590415›Full record

ReviewMolecular biology reports2021

Toxic milk mice models of Wilson's disease.

Krzysztof Hadrian, Adam Przybyłkowski

Abstract readReview
In one paragraph

Review in Molecular biology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Copper homeostasis and pregnancy complications: a comprehensive review.Journal of assisted reproduction and genetics · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. 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

2 authors.

Krzysztof HadrianDepartment of Gastroenterology and General Medicine, Medical University of Warsaw, Banacha 1a Street, 02-097, Warsaw, Mazovian Voivodeships, Poland.ORCID http://orcid.org/0000-0003-0471-3350
Adam PrzybyłkowskiDepartment of Gastroenterology and General Medicine, Medical University of Warsaw, Banacha 1a Street, 02-097, Warsaw, Mazovian Voivodeships, Poland. aprzybylkowski@wum.edu.pl.ORCID http://orcid.org/0000-0002-5851-2856

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wilson's disease (WD) is a rare genetic disorder inherited as an autosomal recessive trait. The signs and symptoms of this disease are related to dysfunctional ATP7B protein which leads to copper accumulation and cellular damage. The organs that are most commonly affected by WD are the liver and brain. The dysfunctional ATP7B homolog has previously been identified in many different species, including two naturally occurring murine models called toxic milk mice. The aim of this paper was to compare the toxic milk mouse described by Rauch (tx) to that from Jackson Laboratory (txJ) through a review of studies on these two groups of mice. The two mice strains differ in the type of carried mutation and the phenotype of the disease. The data of the studies showed that the tx mice developed mild chronic hepatitis but suffered severe organ destruction with faster progression to full-liver cirrhosis. No changes were noted in the neurological and behavioral status of this strain despite the described toxic accumulation of copper and neuronal destruction in their brain. On the other hand, though the Jackson toxic milk mice (txJ) also presented chronic hepatitis, the condition was a bit milder with slower progression to end-stage disease. Moreover, hepatocyte suitable to perform neurobehavioral research as their phenotype characterized by tremors and locomotor disabilities better corresponds with the cliniconeurological picture of the humans.

Indexed as

AnimalsBrainCopperCopper-Transporting ATPasesDisease Models, AnimalHepatocytesHepatolenticular DegenerationLiverMiceMice, KnockoutMutationPhenotypeAtp7b protein, mouseCopperCopper-Transporting ATPasesAnimal modelsHepatolenticular degenerationToxic milk mouseWDWilson’s disease

Identifiers

PMID33590415
PMCPMC7925478

What OpenQuestion holds

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Registered trials

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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.