Veronica M. Cuadra-Borgonio

Calzada México Xochimilco No. 289, CP 14389
Arenal, MEX 14389, Mexico

Last Updated: 09/26/2026

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Found 24 publications

Integrated Plasma and Glial Cell Evidence Indicates a Functional Role for hsa-miR-342-5p in Spinocerebellar Ataxia Type 7 and Its Potential Use as a Biomarker.

Integrated Plasma and Glial Cell Evidence Indicates a Functional Role for hsa-miR-342-5p in Spinocerebellar Ataxia Type 7 and Its Potential Use as a Biomarker.

Journal: International journal of molecular sciences

Published: November 30, 2025

Genetic Insights into Peripheral Artery Disease: A Narrative Review.

Genetic Insights into Peripheral Artery Disease: A Narrative Review.

Journal: Biomedicines

Published: June 29, 2025

Congenital Heart Diseases: Recent Insights into Epigenetic Mechanisms.

Congenital Heart Diseases: Recent Insights into Epigenetic Mechanisms.

Journal: Cells

Published: April 20, 2025

In Silico Analysis of miRNA-Regulated Pathways in Spinocerebellar Ataxia Type 7.

In Silico Analysis of miRNA-Regulated Pathways in Spinocerebellar Ataxia Type 7.

Journal: Current issues in molecular biology

Published: December 31, 2024

Epigenetic Evaluation of the TBX20 Gene and Environmental Risk Factors in Mexican Paediatric Patients with Congenital Septal Defects.

Epigenetic Evaluation of the TBX20 Gene and Environmental Risk Factors in Mexican Paediatric Patients with Congenital Septal Defects.

Journal: Cells

Published: November 27, 2022

Association between Genetic Variants of CELSR2-PSRC1-SORT1 and Cardiovascular Diseases: A Systematic Review and Meta-Analysis.

Association between Genetic Variants of CELSR2-PSRC1-SORT1 and Cardiovascular Diseases: A Systematic Review and Meta-Analysis.

Journal: Journal of cardiovascular development and disease

Published: October 01, 2022

Osteoprotegerin Gene Polymorphisms Are Associated with Subclinical Atherosclerosis in the Mexican Mestizo Population.

Osteoprotegerin Gene Polymorphisms Are Associated with Subclinical Atherosclerosis in the Mexican Mestizo Population.

Journal: Diagnostics (Basel, Switzerland)

Published: May 12, 2022

DNA Methylation Levels of the TBX5 Gene Promoter Are Associated with Congenital Septal Defects in Mexican Paediatric Patients.

DNA Methylation Levels of the TBX5 Gene Promoter Are Associated with Congenital Septal Defects in Mexican Paediatric Patients.

Journal: Biology

Published: November 30, 2021

Osteopontin Gene Polymorphisms Are Associated with Cardiovascular Risk Factors in Patients with Premature Coronary Artery Disease.

Osteopontin Gene Polymorphisms Are Associated with Cardiovascular Risk Factors in Patients with Premature Coronary Artery Disease.

Journal: Biomedicines

Published: September 23, 2021

Variants of PCSK9 Gene Are Associated with Subclinical Atherosclerosis and Cardiometabolic Parameters in Mexicans. The GEA Project.

Variants of PCSK9 Gene Are Associated with Subclinical Atherosclerosis and Cardiometabolic Parameters in Mexicans. The GEA Project.

Journal: Diagnostics (Basel, Switzerland)

Published: March 21, 2021

Association between congenital heart disease and NKX2.5 gene polymorphisms: systematic review and meta-analysis.

Association between congenital heart disease and NKX2.5 gene polymorphisms: systematic review and meta-analysis.

Journal: Biomarkers in medicine

Published: December 21, 2020

Are functional variants of the microRNA-146a gene associated with primary knee OA? Evidence in Mexican mestizo population.

Are functional variants of the microRNA-146a gene associated with primary knee OA? Evidence in Mexican mestizo population.

Journal: Molecular biology reports

Published: October 01, 2020

Showing 1-12 of 24

Last Updated: 09/26/2026