An epidemiological investigation of a Forkhead box protein E3 founder mutation underlying the high frequency of sclerocornea, aphakia, and microphthalmia in a Mexican village

por Pantoja-Melendez, Carlos, Ali, Manir, Zenteno, Juan C.
Publicado 2013

Membrane frizzled-related protein gene–related ophthalmological syndrome: 30-month follow-up of a sporadic case and review of genotype-phenotype correlation in the literature

por Neri, Alberto, Leaci, Rosachiara, Zenteno, Juan C., Casubolo, Cristina, Delfini, Elisabetta, Macaluso, Claudio
Publicado 2012

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

por Pantoja-Melendez, Carlos A., Miranda-Duarte, Antonio, Roque-Ramirez, Bladimir, Zenteno, Juan C.
Publicado 2017

USH2A mutational spectrum causing syndromic and non-syndromic retinal dystrophies in a large cohort of Mexican patients

por Ordoñez-Labastida, Vianey, Chacon-Camacho, Oscar F., Lopez-Rodriguez, Victor R., Zenteno, Juan C.
Publicado 2023

Retinal phenotypic characterization of patients with ABCA4 retinopathydue to the homozygous p.Ala1773Val mutation

por López-Rubio, Salvador, Chacon-Camacho, Oscar F., Matsui, Rodrigo, Guadarrama-Vallejo, Dalia, Astiazarán, Mirena C., Zenteno, Juan C.
Publicado 2018

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

por Velazquez-Soto, Henry, Groman-Lupa, Sergio, Cruz-Aguilar, Marisa, Salazar, Alberto L., Zenteno, Juan C., Jimenez-Martinez, Maria C.
Publicado 2023

16S rRNA gene-based identification of bacteria in postoperative endophthalmitis by PCR-Denaturing Gradient Gel Electrophoresis (PCR-DGGE) fingerprinting

por Navarro-Noya, Yendi, Hernández-Rodríguez, César, Zenteno, Juan C., Buentello-Volante, Beatriz, Cancino-Díaz, Mario E., Jan-Roblero, Janet, Cancino-Díaz, Juan C.
Publicado 2012

Identification and expression analysis of a novel intragenic EFNB1 mutation causing craniofrontonasal syndrome()

por Chacon-Camacho, Oscar F., Arce-Gonzalez, Rocio, Villegas-Ruiz, Vanessa, Pelcastre-Luna, Erika, Uría-Gómez, Conrado E., Granillo-Alvarez, Mariella, Zenteno, Juan C.
Publicado 2013

Molecular and Phenotypic Characterization of Staphylococcus epidermidis Isolates from Healthy Conjunctiva and a Comparative Analysis with Isolates from Ocular Infection

por Flores-Páez, Luis A., Zenteno, Juan C., Alcántar-Curiel, María D., Vargas-Mendoza, Carlos F., Rodríguez-Martínez, Sandra, Cancino-Diaz, Mario E., Jan-Roblero, Janet, Cancino-Diaz, Juan C.
Publicado 2015

Clinical, histopathological, and in silico pathogenicity analyses in a pedigree with familial amyloidosis of the Finnish type (Meretoja syndrome) caused by a novel gelsolin mutatio...

por Cabral-Macias, Jesus, Garcia-Montaño, Leopoldo A., Pérezpeña-Díazconti, Mario, Aguilar, Marisa-Cruz, Garcia, Guillermo, Vencedor-Meraz, Carlos I., Graue-Hernandez, Enrique O., Chacón-Camacho, Oscar F., Zenteno, Juan C.
Publicado 2020

Susceptibility to advanced age-related macular degeneration and alleles of complement factor H, complement factor B, complement component 2, complement component 3, and age-related...

por Buentello-Volante, Beatriz, Rodriguez-Ruiz, Gabriela, Miranda-Duarte, Antonio, Pompa-Mera, Ericka N., Graue-Wiechers, Federico, Bekker-Méndez, Carolina, Ayala-Ramirez, Raul, Quezada, Carlos, Rodríguez-Loaiza, Jose L., Zenteno, Juan C.
Publicado 2012

Giant Ocular Lipodermoid Cyst in Encephalocraniocutaneous Lipomatosis: Surgical Treatment and Genetic Analysis

por Córdoba, Andrea, Graue-Hernández, Enrique O., Navas, Alejandro, Chacon-Camacho, Oscar F., Zenteno, Juan C., Ramirez-Miranda, Arturo, Bermudez-Magner, Jose Antonio, Ordaz-Robles, Thania, Pérez-Solórzano, Sofia, Olivo-Payne, Andrew
Publicado 2019

Characterization of novel GCDH pathogenic variants causing glutaric aciduria type 1 in the southeast of Mexico

por Campos-Garcia, Felix-Julian, Chacon-Camacho, Oscar F., Contreras-Capetillo, Silvina, Cruz-Aguilar, Marisa, Medina-Escobedo, Carolina E., Moreno-Graciano, Claudia M., Rodas, Agustín, Herrera-Perez, Luz del Alba, Zenteno, Juan C.
Publicado 2019

Polymorphism analysis and new JAG1 gene mutations of Alagille syndrome in Mexican population()

por Vázquez-Martínez, Edgar Ricardo, Varela-Fascinetto, Gustavo, García-Delgado, Constanza, Rodríguez-Espino, Benjamín Antonio, Sánchez-Boiso, Adriana, Valencia-Mayoral, Pedro, Heller-Rosseau, Solange, Pelcastre-Luna, Erika Lisselly, Zenteno, Juan C., Cerbón, Marco, Morán-Barroso, Verónica Fabiola
Publicado 2013

Mutations in a novel serine protease PRSS56 in families with nanophthalmos

por Orr, Andrew, Dubé, Marie-Pierre, Zenteno, Juan C., Jiang, Haiyan, Asselin, Geraldine, Evans, Susan C., Caqueret, Aurore, Lakosha, Hesham, Letourneau, Louis, Marcadier, Julien, Matsuoka, Makoto, Macgillivray, Christine, Nightingale, Mathew, Papillon-Cavanagh, Simon, Perry, Scott, Provost, Sylvie, Ludman, Mark, Guernsey, Duane L., Samuels, Mark E.
Publicado 2011

Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next‐generation sequencing

por Zenteno, Juan C., García‐Montaño, Leopoldo A., Cruz‐Aguilar, Marisa, Ronquillo, Josué, Rodas‐Serrano, Agustín, Aguilar‐Castul, Luis, Matsui, Rodrigo, Vencedor‐Meraz, Carlos I., Arce‐González, Rocío, Graue‐Wiechers, Federico, Gutiérrez‐Paz, Mario, Urrea‐Victoria, Tatiana, de Dios Cuadras, Ulises, Chacón‐Camacho, Oscar F.
Publicado 2019

The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome

por Berner, Daniel, Hoja, Ursula, Zenkel, Matthias, Ross, James Julian, Uebe, Steffen, Paoli, Daniela, Frezzotti, Paolo, Rautenbach, Robyn M, Ziskind, Ari, Williams, Susan E, Carmichael, Trevor R, Ramsay, Michele, Topouzis, Fotis, Chatzikyriakidou, Anthi, Lambropoulos, Alexandros, Sundaresan, Periasamy, Ayub, Humaira, Akhtar, Farah, Qamar, Raheel, Zenteno, Juan C, Cruz-Aguilar, Marisa, Astakhov, Yury S, Dubina, Michael, Wiggs, Janey, Ozaki, Mineo, Kruse, Friedrich E, Aung, Tin, Reis, André, Khor, Chiea Chuen, Pasutto, Francesca, Schlötzer-Schrehardt, Ursula
Publicado 2019