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Gaceta Medica De Mexico
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June 18, 2025
Genomics of cardiometabolic disease: contributions of Mexican research groups
Mayra Domínguez-Pérez, Leonor Jacobo-Albavera, Samuel Canizales-Quinteros, et al.
International Journal of Molecular Sciences
|
February 10, 2021
The Role of the ATP-Binding Cassette A1 (ABCA1) in Human Disease
Leonor Jacobo-Albavera, Mayra Domínguez-Pérez, Diana Jhoseline Medina-Leyte, et al.
International Journal of Molecular Sciences
|
April 30, 2021
Endothelial Dysfunction, Inflammation and Coronary Artery Disease: Potential Biomarkers and Promising Therapeutical Approaches
Diana Jhoseline Medina-Leyte, Oscar Zepeda-García, Mayra Domínguez-Pérez, et al.
Gene
|
June 11, 2017
Compound heterozygous KCNQ1 mutations (A300T/P535T) in a child with sudden unexplained death: Insights into possible molecular mechanisms based on protein modeling
Erika Antúnez-Argüelles, Arturo Rojo-Domínguez, Ana Leticia Arregui-Mena, et al.
Genes
|
January 21, 2022
Clinical Spectrum of <i>SCN5A</i> Channelopathy in Children with Primary Electrical Disease and Structurally Normal Hearts
Teresa Villarreal-Molina, Gabriela Paola García-Ordóñez, Álvaro E Reyes-Quintero, et al.
Frontiers in Cardiovascular Medicine
|
March 11, 2021
Compound Heterozygous <i>KCNQ1</i> Mutations Causing Recessive Romano-Ward Syndrome: Functional Characterization by Mutant Co-expression
Antonia González-Garrido, Mayra Domínguez-Pérez, Leonor Jacobo-Albavera, et al.
Peerj
|
December 13, 2017
A novel approach for human whole transcriptome analysis based on absolute gene expression of microarray data
Shirley Bikel, Leonor Jacobo-Albavera, Fausto Sánchez-Muñoz, et al.
Nutrition & Metabolism
|
November 19, 2015
Dietary fat and carbohydrate modulate the effect of the ATP-binding cassette A1 (ABCA1) R230C variant on metabolic risk parameters in premenopausal women from the Genetics of Atherosclerotic Disease (GEA) Study
Leonor Jacobo-Albavera, Carlos Posadas-Romero, Gilberto Vargas-Alarcón, et al.
International Journal of Molecular Sciences
|
January 23, 2024
<i>KCNQ1</i> p.D446E Variant as a Risk Allele for Arrhythmogenic Phenotypes: Electrophysiological Characterization Reveals a Complex Phenotype Affecting the Slow Delayed Rectifier Potassium Current (IKs) Voltage Dependence by Causing a Hyperpolarizing Shift and a Lack of Response to Protein Kinase A Activation
Antonia González-Garrido, Omar López-Ramírez, Abel Cerda-Mireles, et al.
Molecular Genetics & Genomic Medicine
|
September 24, 2020
Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing
Alessandra Carnevale, Sandra Rosas-Madrigal, Rigoberto Rosendo-Gutiérrez, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
Gaceta Medica De Mexico
|
June 18, 2025
Genomics of cardiometabolic disease: contributions of Mexican research groups
Mayra Domínguez-Pérez, Leonor Jacobo-Albavera, Samuel Canizales-Quinteros, et al.
International Journal of Molecular Sciences
|
February 10, 2021
The Role of the ATP-Binding Cassette A1 (ABCA1) in Human Disease
Leonor Jacobo-Albavera, Mayra Domínguez-Pérez, Diana Jhoseline Medina-Leyte, et al.
International Journal of Molecular Sciences
|
April 30, 2021
Endothelial Dysfunction, Inflammation and Coronary Artery Disease: Potential Biomarkers and Promising Therapeutical Approaches
Diana Jhoseline Medina-Leyte, Oscar Zepeda-García, Mayra Domínguez-Pérez, et al.
Gene
|
June 11, 2017
Compound heterozygous KCNQ1 mutations (A300T/P535T) in a child with sudden unexplained death: Insights into possible molecular mechanisms based on protein modeling
Erika Antúnez-Argüelles, Arturo Rojo-Domínguez, Ana Leticia Arregui-Mena, et al.
Genes
|
January 21, 2022
Clinical Spectrum of <i>SCN5A</i> Channelopathy in Children with Primary Electrical Disease and Structurally Normal Hearts
Teresa Villarreal-Molina, Gabriela Paola García-Ordóñez, Álvaro E Reyes-Quintero, et al.
Frontiers in Cardiovascular Medicine
|
March 11, 2021
Compound Heterozygous <i>KCNQ1</i> Mutations Causing Recessive Romano-Ward Syndrome: Functional Characterization by Mutant Co-expression
Antonia González-Garrido, Mayra Domínguez-Pérez, Leonor Jacobo-Albavera, et al.
Peerj
|
December 13, 2017
A novel approach for human whole transcriptome analysis based on absolute gene expression of microarray data
Shirley Bikel, Leonor Jacobo-Albavera, Fausto Sánchez-Muñoz, et al.
Nutrition & Metabolism
|
November 19, 2015
Dietary fat and carbohydrate modulate the effect of the ATP-binding cassette A1 (ABCA1) R230C variant on metabolic risk parameters in premenopausal women from the Genetics of Atherosclerotic Disease (GEA) Study
Leonor Jacobo-Albavera, Carlos Posadas-Romero, Gilberto Vargas-Alarcón, et al.
International Journal of Molecular Sciences
|
January 23, 2024
<i>KCNQ1</i> p.D446E Variant as a Risk Allele for Arrhythmogenic Phenotypes: Electrophysiological Characterization Reveals a Complex Phenotype Affecting the Slow Delayed Rectifier Potassium Current (IKs) Voltage Dependence by Causing a Hyperpolarizing Shift and a Lack of Response to Protein Kinase A Activation
Antonia González-Garrido, Omar López-Ramírez, Abel Cerda-Mireles, et al.
Molecular Genetics & Genomic Medicine
|
September 24, 2020
Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing
Alessandra Carnevale, Sandra Rosas-Madrigal, Rigoberto Rosendo-Gutiérrez, et al.
Page
of 3