Norberto Garcia-Leyva

México Xochimilco No. 289, C.P
Arenal, MEX 14389, Mexico

Last Updated: 09/26/2026

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Found 21 publications

Fifteen Years of Myotonic Dystrophy Type 1 in Mexico: Clinical, Molecular, and Socioeconomic Insights from a National Reference Cohort.

Fifteen Years of Myotonic Dystrophy Type 1 in Mexico: Clinical, Molecular, and Socioeconomic Insights from a National Reference Cohort.

Journal: Genes

Published: November 16, 2025

Enrichment of H3S28p and H3K9me2 Epigenetic Marks on Inflammatory-Associated Gene Promoters in Response to Severe Burn Injury.

Enrichment of H3S28p and H3K9me2 Epigenetic Marks on Inflammatory-Associated Gene Promoters in Response to Severe Burn Injury.

Journal: Life (Basel, Switzerland)

Published: October 30, 2024

Current Overview of Spinocerebellar Ataxia Type 7 in Mexican Population: Challenges in Specialized Care for a Rare Disease.

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

Natural Autophagy Activators to Fight Age-Related Diseases.

Natural Autophagy Activators to Fight Age-Related Diseases.

Journal: Cells

Published: August 24, 2024

The Molecular Role of Polyamines in Age-Related Diseases: An Update.

The Molecular Role of Polyamines in Age-Related Diseases: An Update.

Journal: International journal of molecular sciences

Published: September 28, 2023

RNA Foci Formation in a Retinal Glial Model for Spinocerebellar Ataxia Type 7.

RNA Foci Formation in a Retinal Glial Model for Spinocerebellar Ataxia Type 7.

Journal: Life (Basel, Switzerland)

Published: November 22, 2022

Dp71 Point Mutations Induce Protein Aggregation, Loss of Nuclear Lamina Integrity and Impaired Braf35 and Ibraf Function in Neuronal Cells.

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

Genetic Distribution of Five Spinocerebellar Ataxia Microsatellite Loci in Mexican Native American Populations and Its Impact on Contemporary Mestizo Populations.

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

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

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

Journal: Biomolecules

Published: December 31, 2020

Coexistence of Fragile-X Syndrome, 8p23.1 Deletion, and Balanced Translocation t(7;10)(p10;q24) in a Single Family.

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

Association of TLR4 gene polymorphisms with sepsis after a burn injury: findings of the functional role of rs2737190 SNP.

Association of TLR4 gene polymorphisms with sepsis after a burn injury: findings of the functional role of rs2737190 SNP.

Journal: Genes and immunity

Published: June 16, 2020

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.

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.

Journal: International journal of dermatology

Published: March 30, 2020

Showing 1-12 of 21

Last Updated: 09/26/2026