Yessica S. Guerrero-Tapia
Mexico City, DIF 14389, Mexico
Last Updated: 09/26/2026
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Found 14 publications
Nuclear Lamina Dysfunction and DNA Damage as Drivers of Premature Senescence in a Human Müller Glial Cell Model of Spinocerebellar Ataxia Type 7.
Journal: International journal of molecular sciences
Published: May 12, 2026
Current Overview of Spinocerebellar Ataxia Type 7 in Mexican Population: Challenges in Specialized Care for a Rare Disease.
Journal: International journal of molecular sciences
Published: August 31, 2024
The Molecular Role of Polyamines in Age-Related Diseases: An Update.
Journal: International journal of molecular sciences
Published: September 28, 2023
Dp71 Point Mutations Induce Protein Aggregation, Loss of Nuclear Lamina Integrity and Impaired Braf35 and Ibraf Function in Neuronal Cells.
Journal: International journal of molecular sciences
Published: August 17, 2022
Cross-linked polyvinyl alcohol-xanthan gum hydrogel fabricated by freeze/thaw technique for potential application in soft tissue engineering.
Journal: RSC advances
Published: April 08, 2022
Genetic Distribution of Five Spinocerebellar Ataxia Microsatellite Loci in Mexican Native American Populations and Its Impact on Contemporary Mestizo Populations.
Journal: Genes
Published: November 30, 2021
Coexistence of Fragile-X Syndrome, 8p23.1 Deletion, and Balanced Translocation t(7;10)(p10;q24) in a Single Family.
Journal: Genetic testing and molecular biomarkers
Published: July 28, 2020
Effect of UV and Gamma Irradiation Sterilization Processes in the Properties of Different Polymeric Nanoparticles for Biomedical Applications.
Journal: Materials (Basel, Switzerland)
Published: December 31, 2019
Wide Profiling of Circulating MicroRNAs in Spinocerebellar Ataxia Type 7.
Journal: Molecular neurobiology
Published: October 05, 2018
Origin of the myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution.
Journal: Neuromuscular disorders : NMD
Published: November 10, 2016
Clinical and molecular effect on offspring of a marriage of consanguineous spinocerebellar ataxia type 7 mutation carriers: a family case report.
Journal: International journal of clinical and experimental medicine
Published: September 24, 2014
Last Updated: 09/26/2026