Evidence map›Paper›PMID 41226418›Full record

ArticleInternational journal of molecular sciences2025

Specific Glutamylation Patterns of the Cytoskeleton Confer Neuroresistance to Lobe X of the Cerebellum in a Model of Childhood-Onset Neurodegeneration with Cerebellar Atrophy.

Carlos Hernández-Pérez, Andrés A Calderón-García, David Pérez-Boyero, Verónica González-Núñez, Eduardo Weruaga, David Díaz

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Carlos Hernández-PérezLaboratory of Neuronal Plasticity and Neurorepair, Institute for Neuroscience of Castilla y León (INCyL), Universidad de Salamanca, C/Pintor Fernando Gallego 1, E-37007 Salamanca, Spain.
Andrés A Calderón-GarcíaDepartment of Anatomy and Radiology, Universidad de Valladolid, Av. Ramón y Cajal 7, E-47005 Valladolid, Spain.ORCID 0000-0002-5993-5973
David Pérez-BoyeroLaboratory of Neuronal Plasticity and Neurorepair, Institute for Neuroscience of Castilla y León (INCyL), Universidad de Salamanca, C/Pintor Fernando Gallego 1, E-37007 Salamanca, Spain.ORCID 0000-0003-2514-3270
Verónica González-NúñezInstitute of Biomedical Research of Salamanca (IBSAL), P.º de San Vicente, 182, E-37007 Salamanca, Spain.ORCID 0000-0002-9410-5510
Eduardo WeruagaLaboratory of Neuronal Plasticity and Neurorepair, Institute for Neuroscience of Castilla y León (INCyL), Universidad de Salamanca, C/Pintor Fernando Gallego 1, E-37007 Salamanca, Spain.ORCID 0000-0003-2887-5506
David DíazLaboratory of Neuronal Plasticity and Neurorepair, Institute for Neuroscience of Castilla y León (INCyL), Universidad de Salamanca, C/Pintor Fernando Gallego 1, E-37007 Salamanca, Spain.ORCID 0000-0003-3705-817X

Funding

Centre for Regenerative Medicine and Cell Therapy of Castile and Leon no numberConsejería de Educación de la Junta de Castilla y León SA030P17Consejería de Educación de la Junta de Castilla y León SA112P24Consejería de Educación de la Junta de Castilla y León SA129P20Ministerio de Ciencia, Innovación y Universidades PID2019-106943RB-I00Ministerio de Ciencia, Innovación y Universidades PID2022-140456NB-I00Ministry of Economy, Industry and Competitiveness SAF2016-79668-RUniversidad de Salamanca no number
6 · The paper itself

Abstract

The cytoskeleton relies heavily on the dynamic nature of microtubules, regulated by post-translational modifications such as polyglutamylation and deglutamylation. Disruption of its internal balance, particularly through the absence of cytosolic carboxypeptidase 1 (CCP1), leads to cytoskeletal collapse and cell death. An example of this occurrence exists in the Purkinje Cell Degeneration (PCD) mouse, a direct animal model for childhood-onset neurodegeneration with cerebellar atrophy (CONDCA) human disease. Both CONDCA patients and PCD mice suffer a dramatic degeneration of Purkinje cells. Intriguingly, lobe X appears less vulnerable to this insult. This study revealed in wild-type mice that lobe X expresses less

Indexed as

Cerebellar DiseasesCerebellumCytoskeletonNeurodegenerative DiseasesAnimalsAtrophyDisease Models, AnimalGTP-Binding ProteinsHumansMicePurkinje CellsSerine-Type D-Ala-D-Ala CarboxypeptidaseAgtpbp1 protein, mouseGTP-Binding ProteinsSerine-Type D-Ala-D-Ala CarboxypeptidaseCCPcerebellumCONDCAglutamylationneuroprotectionPurkinje cell degeneration

Identifiers

PMID41226418
PMCPMC12610737

What OpenQuestion holds

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LicenceCC BY
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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.