Skip to contents Kumari, Asha; Ayala-Ramirez, Raul; Zenteno, Juan Carlos; Huffman, Kristyn; Sasik, Roman; Ayyagari, Radha; Borooah, Shyamanga Single cell RNA sequencing confirms retinal microglia activation associated with early onset retinal degeneration Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Springer Science and Business Media LLC, 2022 Published in: Scientific Reports Ortiz-Ramirez, Grecia Yael; Villanueva-Mendoza, Cristina; Zenteno Ruiz, Juan Carlos; Reyes, Mariana; Cortés-González, Vianney Autofluorescence in female carriers with choroideremia: A familial case with a novel mutation in the CHM gene Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Informa UK Limited, 2020 Published in: Ophthalmic Genetics Ramírez Jerónimo, Luis F.; Zenteno Torres, Jazmín; Saldivar, Belem; Dávila, Jorge; Ávila Vilchis, Juan Carlos Robust stabilisation of linear time‐invariant time‐delay systems via first order and super‐twisting sliding mode controllers Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Institution of Engineering and Technology (IET), 2020 Published in: IET Control Theory & Applications Pérez‐Solórzano, Sofía; Chacón‐Camacho, Oscar F; Astiazarán, Mirena C; Ledesma‐Gil, Gerardo; Zenteno, Juan Carlos PAX6 allelic heterogeneity in Mexican congenital aniridia patients: expanding the mutational spectrum with seven novel pathogenic variants Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2017 Published in: Clinical & Experimental Ophthalmology Pantoja-Melendez, Carlos A.; Miranda-Duarte, Antonio; Roque-Ramirez, Bladimir; Zenteno, Juan C. 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 Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Public Library of Science (PLoS), 2017 Published in: PLOS ONE Chacon‐Camacho, Oscar Francisco; Fuerte‐Flores, Bertha Irene; Zenteno, Juan Carlos TP63 mutation in a patient with acro‐dermo‐ungual‐lacrimal‐tooth syndrome: Additional evidence of molecular overlap of the ADULT and EEC syndromes Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2016 Published in: American Journal of Medical Genetics Part A Chacon‐Camacho, Oscar Francisco; Fuerte‐Flores, Bertha Irene; Ricardez‐Marcial, Edgar F.; Zenteno, Juan Carlos SOX2 anophthalmia syndrome and dental anomalies Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2015 Published in: American Journal of Medical Genetics Part A Estrada, Higinio; Buentello, Beatriz; Zenteno, Juan Carlos; Fiszman, Rachel; Aguinaga, Mónica The p.L750V mutation in the NLRP7 gene is frequent in Mexican patients with recurrent molar pregnancies and is not associated with recurrent pregnancy loss Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2013 Published in: Prenatal Diagnosis Jaimes, Martha; Rivera-Parra, David; Miranda-Duarte, Antonio; Valdés, Gerardo; Zenteno, Juan Carlos Prevalence of high-risk alleles in theLOXL1gene and its association with pseudoexfoliation syndrome and exfoliation glaucoma in a Latin American population Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Informa UK Limited, 2012 Published in: Ophthalmic Genetics Zenteno, Juan Carlos; Buentello‐Volante, Beatriz; Ayala‐Ramirez, Raul; Villanueva‐Mendoza, Cristina Homozygosity mapping identifies the Crumbs homologue 1 (Crb1) gene as responsible for a recessive syndrome of retinitis pigmentosa and nanophthalmos Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2011 Published in: American Journal of Medical Genetics Part A Zenteno, Juan Carlos; Correa-Gomez, Vicente; Santacruz-Valdez, Concepción; Suarez-Sanchez, Raul; Villanueva-Mendoza, Cristina Clinical and genetic features of TGFBI-linked corneal dystrophies in Mexican population: Description of novel mutations and novel genotype–phenotype correlations Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Elsevier BV, 2009 Published in: Experimental Eye Research Matias-Florentino, Margarita; Ayala-Ramirez, Raul; Graue-Wiechers, Federico; Zenteno, Juan Carlos Molecular Screening ofRhodopsinandPeripherin/RDSGenes in Mexican Families with Autosomal Dominant Retinitis Pigmentosa Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Informa UK Limited, 2009 Published in: Current Eye Research Villanueva-Mendoza, Cristina; Martínez-Guzmán, Oswaldo; Rivera-Parra, David; Zenteno, Juan Carlos Triple A or Allgrove Syndrome. A Case Report with Ophthalmic Abnormalities and a Novel Mutation in theAAASGene Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Informa UK Limited, 2009 Published in: Ophthalmic Genetics Jiménez‐Farfán, Dolores; Guevara, Jorge; Zenteno, Edgar; Hernández‐Guerrero, Juan Carlos Alteration of the sialylation pattern of the murine tooth germ after ethanol exposure Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2005 Published in: Birth Defects Research Part A: Clinical and Molecular Teratology Jiménez‐Farfán, Dolores; Guevara, Jorge; Zenteno, Edgar; Malagón, Héctor; Hernández‐Guerrero, Juan Carlos EGF‐R and erbB‐2 in murine tooth development after ethanol exposure Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2005 Published in: Birth Defects Research Part A: Clinical and Molecular Teratology Zenteno, Juan Carlos; Berdón-Zapata, Valeria; Kofman-Alfaro, Susana; Mutchinick, Osvaldo M. Isolated ectrodactyly caused by a heterozygous missense mutation in the transactivation domain of TP63 : TP63 Gene Mutation in Isolated Ectrodactyly : TP63 Gene Mutation in Isolated Ectrodactyly Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2005 Published in: American Journal of Medical Genetics Part A Jiménez, Ana Luisa; Kofman‐Alfaro, Susana; Berumen, Jaime; Hernández, Eloy; Canto, Patricia; Méndez, Juan Pablo; Zenteno, Juan Carlos Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2000 Published in: American Journal of Medical Genetics Maya‐Núñez, Guadalupe; Cuevas‐Covarrubias, Sergio; Carlos Zenteno, Juan; Ulloa‐Aguirre, Alfredo; Kofman‐Alfaro, Susana; Pablo Méndez, Juan Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 1998 Published in: Clinical Endocrinology Arce-Gonzalez, Rocio; Chacon-Camacho, Oscar F.; Navas-Perez, Alejandro; Gonzalez-Gonzalez, María C.; Martinez-Aguilar, Alan; Zenteno, Juan Carlos Novel CHRDL1 mutation causing X-linked megalocornea in a family with mild anterior segment manifestations in carrier females Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Informa UK Limited, 2022 Published in: Ophthalmic Genetics Arce-González, Rocío; Chacon-Camacho, Oscar Francisco; Ordoñez-Labastida, Vianey; Graue-Hernandez, Enrique O.; Navas-Pérez, Alejandro; Zenteno, Juan Carlos A novel homozygous ZNF469 variant causing brittle cornea syndrome is associated with corneal ectasias in heterozygous carriers Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Springer Science and Business Media LLC, 2022 Published in: International Ophthalmology
Kumari, Asha; Ayala-Ramirez, Raul; Zenteno, Juan Carlos; Huffman, Kristyn; Sasik, Roman; Ayyagari, Radha; Borooah, Shyamanga Single cell RNA sequencing confirms retinal microglia activation associated with early onset retinal degeneration Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Springer Science and Business Media LLC, 2022 Published in: Scientific Reports
Ortiz-Ramirez, Grecia Yael; Villanueva-Mendoza, Cristina; Zenteno Ruiz, Juan Carlos; Reyes, Mariana; Cortés-González, Vianney Autofluorescence in female carriers with choroideremia: A familial case with a novel mutation in the CHM gene Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Informa UK Limited, 2020 Published in: Ophthalmic Genetics
Ramírez Jerónimo, Luis F.; Zenteno Torres, Jazmín; Saldivar, Belem; Dávila, Jorge; Ávila Vilchis, Juan Carlos Robust stabilisation of linear time‐invariant time‐delay systems via first order and super‐twisting sliding mode controllers Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Institution of Engineering and Technology (IET), 2020 Published in: IET Control Theory & Applications
Pérez‐Solórzano, Sofía; Chacón‐Camacho, Oscar F; Astiazarán, Mirena C; Ledesma‐Gil, Gerardo; Zenteno, Juan Carlos PAX6 allelic heterogeneity in Mexican congenital aniridia patients: expanding the mutational spectrum with seven novel pathogenic variants Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2017 Published in: Clinical & Experimental Ophthalmology
Pantoja-Melendez, Carlos A.; Miranda-Duarte, Antonio; Roque-Ramirez, Bladimir; Zenteno, Juan C. 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 Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Public Library of Science (PLoS), 2017 Published in: PLOS ONE
Chacon‐Camacho, Oscar Francisco; Fuerte‐Flores, Bertha Irene; Zenteno, Juan Carlos TP63 mutation in a patient with acro‐dermo‐ungual‐lacrimal‐tooth syndrome: Additional evidence of molecular overlap of the ADULT and EEC syndromes Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2016 Published in: American Journal of Medical Genetics Part A
Chacon‐Camacho, Oscar Francisco; Fuerte‐Flores, Bertha Irene; Ricardez‐Marcial, Edgar F.; Zenteno, Juan Carlos SOX2 anophthalmia syndrome and dental anomalies Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2015 Published in: American Journal of Medical Genetics Part A
Estrada, Higinio; Buentello, Beatriz; Zenteno, Juan Carlos; Fiszman, Rachel; Aguinaga, Mónica The p.L750V mutation in the NLRP7 gene is frequent in Mexican patients with recurrent molar pregnancies and is not associated with recurrent pregnancy loss Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2013 Published in: Prenatal Diagnosis
Jaimes, Martha; Rivera-Parra, David; Miranda-Duarte, Antonio; Valdés, Gerardo; Zenteno, Juan Carlos Prevalence of high-risk alleles in theLOXL1gene and its association with pseudoexfoliation syndrome and exfoliation glaucoma in a Latin American population Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Informa UK Limited, 2012 Published in: Ophthalmic Genetics
Zenteno, Juan Carlos; Buentello‐Volante, Beatriz; Ayala‐Ramirez, Raul; Villanueva‐Mendoza, Cristina Homozygosity mapping identifies the Crumbs homologue 1 (Crb1) gene as responsible for a recessive syndrome of retinitis pigmentosa and nanophthalmos Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2011 Published in: American Journal of Medical Genetics Part A
Zenteno, Juan Carlos; Correa-Gomez, Vicente; Santacruz-Valdez, Concepción; Suarez-Sanchez, Raul; Villanueva-Mendoza, Cristina Clinical and genetic features of TGFBI-linked corneal dystrophies in Mexican population: Description of novel mutations and novel genotype–phenotype correlations Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Elsevier BV, 2009 Published in: Experimental Eye Research
Matias-Florentino, Margarita; Ayala-Ramirez, Raul; Graue-Wiechers, Federico; Zenteno, Juan Carlos Molecular Screening ofRhodopsinandPeripherin/RDSGenes in Mexican Families with Autosomal Dominant Retinitis Pigmentosa Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Informa UK Limited, 2009 Published in: Current Eye Research
Villanueva-Mendoza, Cristina; Martínez-Guzmán, Oswaldo; Rivera-Parra, David; Zenteno, Juan Carlos Triple A or Allgrove Syndrome. A Case Report with Ophthalmic Abnormalities and a Novel Mutation in theAAASGene Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Informa UK Limited, 2009 Published in: Ophthalmic Genetics
Jiménez‐Farfán, Dolores; Guevara, Jorge; Zenteno, Edgar; Hernández‐Guerrero, Juan Carlos Alteration of the sialylation pattern of the murine tooth germ after ethanol exposure Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2005 Published in: Birth Defects Research Part A: Clinical and Molecular Teratology
Jiménez‐Farfán, Dolores; Guevara, Jorge; Zenteno, Edgar; Malagón, Héctor; Hernández‐Guerrero, Juan Carlos EGF‐R and erbB‐2 in murine tooth development after ethanol exposure Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2005 Published in: Birth Defects Research Part A: Clinical and Molecular Teratology
Zenteno, Juan Carlos; Berdón-Zapata, Valeria; Kofman-Alfaro, Susana; Mutchinick, Osvaldo M. Isolated ectrodactyly caused by a heterozygous missense mutation in the transactivation domain of TP63 : TP63 Gene Mutation in Isolated Ectrodactyly : TP63 Gene Mutation in Isolated Ectrodactyly Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2005 Published in: American Journal of Medical Genetics Part A
Jiménez, Ana Luisa; Kofman‐Alfaro, Susana; Berumen, Jaime; Hernández, Eloy; Canto, Patricia; Méndez, Juan Pablo; Zenteno, Juan Carlos Partially deleted SRY gene confined to testicular tissue in a 46,XX true hermaphrodite without SRY in leukocytic DNA Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 2000 Published in: American Journal of Medical Genetics
Maya‐Núñez, Guadalupe; Cuevas‐Covarrubias, Sergio; Carlos Zenteno, Juan; Ulloa‐Aguirre, Alfredo; Kofman‐Alfaro, Susana; Pablo Méndez, Juan Contiguous gene syndrome due to deletion of the first three exons of the Kallmann gene and complete deletion of the steroid sulphatase gene Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Wiley, 1998 Published in: Clinical Endocrinology
Arce-Gonzalez, Rocio; Chacon-Camacho, Oscar F.; Navas-Perez, Alejandro; Gonzalez-Gonzalez, María C.; Martinez-Aguilar, Alan; Zenteno, Juan Carlos Novel CHRDL1 mutation causing X-linked megalocornea in a family with mild anterior segment manifestations in carrier females Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Informa UK Limited, 2022 Published in: Ophthalmic Genetics
Arce-González, Rocío; Chacon-Camacho, Oscar Francisco; Ordoñez-Labastida, Vianey; Graue-Hernandez, Enrique O.; Navas-Pérez, Alejandro; Zenteno, Juan Carlos A novel homozygous ZNF469 variant causing brittle cornea syndrome is associated with corneal ectasias in heterozygous carriers Articles View online Schließen > Access Close > Bookmarks You can manage bookmarks using lists, please log in to your user account for this. Springer Science and Business Media LLC, 2022 Published in: International Ophthalmology
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