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Jonathan J. Magaña

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63

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Involvement of the Auditory Pathway in Spinocerebellar Ataxia Type 7.

2021 Neurodegenerative Diseases
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Transcriptome Analysis Reveals Altered Inflammatory Pathway in an Inducible Glial Cell Model of Myotonic Dystrophy Type 1

2021
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New Perspectives of Gene Therapy on Polyglutamine Spinocerebellar Ataxias: From Molecular Targets to Novel Nanovectors

2021 Pharmaceutics
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High prevalence of autosomal recessive congenital ichthyosis in a Mexican population caused by a new mutation in the TGM1 gene: epidemiological evidence of a founder effect.

2020 International Journal of Dermatology
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ALOX5, LPA, MMP9 and TPO gene polymorphisms increase atherothrombosis susceptibility in middle-aged Mexicans

2020 Royal Society Open Science
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The Molecular Basis and Biologic Significance of the β-Dystroglycan-Emerin Interaction.

2020 International Journal of Molecular Sciences
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Cognitive Decline and White Matter Integrity Degradation in Myotonic Dystrophy Type I.

2020 Journal of Neuroimaging
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The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1.

2020 Genes
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Loss of Dystroglycan Drives Cellular Senescence via Defective Mitosis-Mediated Genomic Instability.

2020 International Journal of Molecular Sciences
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Founder Effects of Spinocerebellar Ataxias in the American Continents and the Caribbean

2020 The Cerebellum
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