Evidence mapPaperPMID 41008616Full record

ReviewBiomolecules2025

Novel Animal Models for Multiple Sclerosis: R-Ras GTPases in Myelin Pathophysiology.

Gema M Esteban-Ortega, Gonzalo Garcia-Martin, Beatriz Cubelos

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In one paragraph

Review in Biomolecules, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Gema M Esteban-OrtegaCentro de Biología Molecular Severo Ochoa (CBM), Universidad Autónoma de Madrid, 28049 Madrid, Spain.ORCID 0009-0002-2010-1549
Gonzalo Garcia-MartinCentro de Biología Molecular Severo Ochoa (CBM), Universidad Autónoma de Madrid, 28049 Madrid, Spain.ORCID 0000-0003-2179-2521
Beatriz CubelosCentro de Biología Molecular Severo Ochoa (CBM), Universidad Autónoma de Madrid, 28049 Madrid, Spain.ORCID 0000-0002-2280-8233

Funding

This work was supported by the Spanish Ministry of Science, Innovation and Universities JDC2023-052765-IThis work was supported by the Spanish Ministry of Science, Innovation and Universities PDI-2021-1232690B-I00
6 · The paper itself

Abstract

Demyelinating diseases, such as multiple sclerosis, involve oligodendrocyte death, myelin loss, and neuronal death. These processes have been extensively studied, and a causal relationship has been demonstrated between them: destruction of oligodendrocytes results in myelin deficiency, which subsequently leads to neurodegeneration and the consequent loss of sensory, motor, and cognitive functions. Currently, myelinopathies lack fully effective treatments. Available drugs primarily focus on controlling the immune response without directly promoting myelin regeneration or restoring neuronal functionality. Alongside these treatments, pharmaceutical research has increasingly focused on developing therapies that stimulate oligodendroglial lineage differentiation and myelin sheath regeneration. Despite these advances, the lack of suitable preclinical models has been a significant obstacle in evaluating new therapeutic compounds. In this review, we present the main animal models used in the preclinical phase for the study of myelin-related diseases and their role in the development of new therapies. In addition, we highlight the usefulness of R-Ras animal models for assessing the efficacy of compounds that promote oligodendrocyte differentiation.

Indexed as

Multiple SclerosisMyelin Sheathras ProteinsAnimalsCell DifferentiationDisease Models, AnimalHumansOligodendrogliaras Proteinsmolecular targetsmultiple sclerosismyelinationneuroimmunologyneuroinflammationneurological disordersoligodendrocyteoligodendroglial maturationpreclinical trialsR-Ras relatedtherapeutic strategies

Identifiers

PMID41008616
PMCPMC12467086

What Socratic 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 Socratic graph.