Showing 1 - 9 results of 9 for search 'Juan C Zenteno', query time: 0.05s Refine Results
  1. 1
    Effectiveness of whole-exome sequencing for the identification of causal mutations in patients with suspected inherited ocular diseases

    Effectiveness of whole-exome sequencing for the identification of causal mutations in patients with suspected inherited ocular diseases by Vianey Ordoñez-Labastida, Luis Montes-Almanza, Froylan García-Martínez, Juan C. Zenteno

    Published 2022-10-01
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  2. 2
    Learning from history in the midst of the COVID-19: epidemics/pandemics of antiquity up to the fall of the Western Roman Empire

    Learning from history in the midst of the COVID-19: epidemics/pandemics of antiquity up to the fall of the Western Roman Empire by Óscar F. Chacón-Camacho, Rocío Arce-González, Juan C. Zenteno, María T. Granillo

    Published 2023-01-01
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  3. 3
    Epidemiological and Molecular Characterization of a Mexican Population Isolate with High Prevalence of Limb-Girdle Muscular Dystrophy Type 2A Due to a Novel Calpain-3 Mutation.

    Epidemiological and Molecular Characterization of a Mexican Population Isolate with High Prevalence of Limb-Girdle Muscular Dystrophy Type 2A Due to a Novel Calpain-3 Mutation. by Carlos A Pantoja-Melendez, Antonio Miranda-Duarte, Bladimir Roque-Ramirez, Juan C Zenteno

    Published 2017-01-01
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  4. 4
    Exogenous CFH Modulates Levels of Pro-Inflammatory Mediators to Prevent Oxidative Damage of Retinal Pigment Epithelial Cells with the At-Risk CFH Y402H Variant

    Exogenous CFH Modulates Levels of Pro-Inflammatory Mediators to Prevent Oxidative Damage of Retinal Pigment Epithelial Cells with the At-Risk CFH Y402H Variant by Henry Velazquez-Soto, Sergio Groman-Lupa, Marisa Cruz-Aguilar, Alberto L. Salazar, Juan C. Zenteno, Maria C. Jimenez-Martinez

    Published 2023-07-01
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  5. 5
    Mutational Profile and Retinal Phenotypes of PCARE-Related Cone-Rod Dystrophies in a Mexican Cohort

    Mutational Profile and Retinal Phenotypes of PCARE-Related Cone-Rod Dystrophies in a Mexican Cohort by Víctor R. López-Rodríguez, Rocío Arce-González, Alan Martínez-Aguilar, Carlos E. Rodríguez-López, Sergio Groman-Lupa, M. Isabel Neria-González, Genaro Rodríguez-Uribe, Juan C. Zenteno

    Published 2024-01-01
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  6. 6
    Molecular and Phenotypic Characterization of Staphylococcus epidermidis Isolates from Healthy Conjunctiva and a Comparative Analysis with Isolates from Ocular Infection.

    Molecular and Phenotypic Characterization of Staphylococcus epidermidis Isolates from Healthy Conjunctiva and a Comparative Analysis with Isolates from Ocular Infection. by Luis A Flores-Páez, Juan C Zenteno, María D Alcántar-Curiel, Carlos F Vargas-Mendoza, Sandra Rodríguez-Martínez, Mario E Cancino-Diaz, Janet Jan-Roblero, Juan C Cancino-Diaz

    Published 2015-01-01
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  7. 7
    Screening Method for 22q11 Deletion Syndrome Involving the Use of TaqMan qPCR for <i>TBX1</i> in Patients with Conotruncal Congenital Heart Disease

    Screening Method for 22q11 Deletion Syndrome Involving the Use of TaqMan qPCR for <i>TBX1</i> in Patients with Conotruncal Congenital Heart Disease by Felix-Julian Campos-Garcia, Addy-Manuela Castillo-Espinola, Carolina-Elizabeth Medina-Escobedo, Juan C. Zenteno, Julio-Cesar Lara-Riegos, Hector Rubio-Zapata, David Cruz-Robles, Ana-Isabel Velazquez-Ibarra

    Published 2022-08-01
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  8. 8
    Characterization of novel GCDH pathogenic variants causing glutaric aciduria type 1 in the southeast of Mexico

    Characterization of novel GCDH pathogenic variants causing glutaric aciduria type 1 in the southeast of Mexico by Felix-Julian Campos-Garcia, Oscar F. Chacon-Camacho, Silvina Contreras-Capetillo, Marisa Cruz-Aguilar, Carolina E. Medina-Escobedo, Claudia M. Moreno-Graciano, Agustín Rodas, Luz del Alba Herrera-Perez, Juan C. Zenteno

    Published 2019-12-01
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  9. 9
    Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next‐generation sequencing

    Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next‐generation sequencing by Juan C. Zenteno, Leopoldo A. García‐Montaño, Marisa Cruz‐Aguilar, Josué Ronquillo, Agustín Rodas‐Serrano, Luis Aguilar‐Castul, Rodrigo Matsui, Carlos I. Vencedor‐Meraz, Rocío Arce‐González, Federico Graue‐Wiechers, Mario Gutiérrez‐Paz, Tatiana Urrea‐Victoria, Ulises deDios Cuadras, Oscar F. Chacón‐Camacho

    Published 2020-01-01
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