Michael V. Zaragoza

Medical Genetics | Pediatrics

Uci Medical Center
101 The City Drive South
Orange, CA 92868

Last Updated: 09/26/2026

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Found 17 publications

Complementary biomolecular coassemblies direct energy transport for cardiac photostimulators.

Complementary biomolecular coassemblies direct energy transport for cardiac photostimulators.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: September 04, 2025

LMNA -Related Dilated Cardiomyopathy: Single-Cell Transcriptomics during Patient-derived iPSC Differentiation Support Cell type and Lineage-specific Dysregulation of Gene Expression and Development for Cardiomyocytes and Epicardium-Derived Cells with Lamin A/C Haploinsufficiency.

LMNA -Related Dilated Cardiomyopathy: Single-Cell Transcriptomics during Patient-derived iPSC Differentiation Support Cell type and Lineage-specific Dysregulation of Gene Expression and Development for Cardiomyocytes and Epicardium-Derived Cells with Lamin A/C Haploinsufficiency.

Journal: bioRxiv : the preprint server for biology

Published: June 25, 2024

LMNA-Related Dilated Cardiomyopathy: Single-Cell Transcriptomics during Patient-Derived iPSC Differentiation Support Cell Type and Lineage-Specific Dysregulation of Gene Expression and Development for Cardiomyocytes and Epicardium-Derived Cells with Lamin A/C Haploinsufficiency.

LMNA-Related Dilated Cardiomyopathy: Single-Cell Transcriptomics during Patient-Derived iPSC Differentiation Support Cell Type and Lineage-Specific Dysregulation of Gene Expression and Development for Cardiomyocytes and Epicardium-Derived Cells with Lamin A/C Haploinsufficiency.

Journal: Cells

Published: June 12, 2024

DNA methylation analysis reveals epimutation hotspots in patients with dilated cardiomyopathy-associated laminopathies.

DNA methylation analysis reveals epimutation hotspots in patients with dilated cardiomyopathy-associated laminopathies.

Journal: Clinical epigenetics

Published: April 03, 2021

A Study of Gene Expression, Structure, and Contractility of iPSC-Derived Cardiac Myocytes from a Family with Heart Disease due to LMNA Mutation.

A Study of Gene Expression, Structure, and Contractility of iPSC-Derived Cardiac Myocytes from a Family with Heart Disease due to LMNA Mutation.

Journal: Annals of biomedical engineering

Published: February 27, 2021

Gene expression profiling of fibroblasts in a family with LMNA-related cardiomyopathy reveals molecular pathways implicated in disease pathogenesis.

Gene expression profiling of fibroblasts in a family with LMNA-related cardiomyopathy reveals molecular pathways implicated in disease pathogenesis.

Journal: BMC medical genetics

Published: March 31, 2020

Databases to Efficiently Manage Medium Sized, Low Velocity, Multidimensional Data in Tissue Engineering.

Databases to Efficiently Manage Medium Sized, Low Velocity, Multidimensional Data in Tissue Engineering.

Journal: Journal of visualized experiments : JoVE

Published: December 10, 2019

The Effect of Cyclic Strain on Human Fibroblasts With Lamin A/C Mutations and Its Relation to Heart Disease.

The Effect of Cyclic Strain on Human Fibroblasts With Lamin A/C Mutations and Its Relation to Heart Disease.

Journal: Journal of biomechanical engineering

Published: January 31, 2019

Age of heart disease presentation and dysmorphic nuclei in patients with LMNA mutations.

Age of heart disease presentation and dysmorphic nuclei in patients with LMNA mutations.

Journal: PloS one

Published: August 17, 2017

Dupuytren's and Ledderhose Diseases in a Family with LMNA-Related Cardiomyopathy and a Novel Variant in the ASTE1 Gene.

Dupuytren's and Ledderhose Diseases in a Family with LMNA-Related Cardiomyopathy and a Novel Variant in the ASTE1 Gene.

Journal: Cells

Published: June 30, 2017

Heart-hand syndrome IV: a second family with LMNA-related cardiomyopathy and brachydactyly.

Heart-hand syndrome IV: a second family with LMNA-related cardiomyopathy and brachydactyly.

Journal: Clinical genetics

Published: August 08, 2016

Exome Sequencing Identifies a Novel LMNA Splice-Site Mutation and Multigenic Heterozygosity of Potential Modifiers in a Family with Sick Sinus Syndrome, Dilated Cardiomyopathy, and Sudden Cardiac Death.

Exome Sequencing Identifies a Novel LMNA Splice-Site Mutation and Multigenic Heterozygosity of Potential Modifiers in a Family with Sick Sinus Syndrome, Dilated Cardiomyopathy, and Sudden Cardiac Death.

Journal: PloS one

Published: April 13, 2016

Showing 1-12 of 17

Last Updated: 09/26/2026