Zenteno JC - Search Results

1

Significant Association Between Variant in SGCD and Age-Related Macular Degeneration.

Perez-Ortiz AC, Luna-Angulo A, Zenteno JC, Rendon A, Cortes-Ballinas LG, Jimenez-Collado D, Antonio-Aguirre B, Peralta-Ildefonso MJ, Ramírez I, Jacob-Kuttothara S, Estrada-Mena FJ. Perez-Ortiz AC, et al. Among authors: zenteno jc. Genes (Basel). 2018 Sep 25;9(10):467. doi: 10.3390/genes9100467. Genes (Basel). 2018. PMID: 30257524 Free PMC article.

2

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 maculopathy susceptibility 2 genes in a Mexican population.

Buentello-Volante B, Rodriguez-Ruiz G, Miranda-Duarte A, Pompa-Mera EN, Graue-Wiechers F, Bekker-Méndez C, Ayala-Ramirez R, Quezada C, Rodríguez-Loaiza JL, Zenteno JC. Buentello-Volante B, et al. Among authors: zenteno jc. Mol Vis. 2012;18:2518-25. Epub 2012 Oct 11. Mol Vis. 2012. PMID: 23112567 Free PMC article.

3

Assessment of CFH and HTRA1 polymorphisms in age-related macular degeneration using classic and machine-learning approaches.

Martínez-Velasco A, Perez-Ortiz AC, Antonio-Aguirre B, Martínez-Villaseñor L, Lira-Romero E, Palacio-Pastrana C, Zenteno JC, Ramirez I, Zepeda-Palacio C, Mendoza-Velásquez C, Camacho-Ordóñez A, Ortiz Bibriesca DM, Estrada-Mena FJ. Martínez-Velasco A, et al. Among authors: zenteno jc. Ophthalmic Genet. 2020 Dec;41(6):539-547. doi: 10.1080/13816810.2020.1804945. Epub 2020 Aug 24. Ophthalmic Genet. 2020. PMID: 32838591

4

CFH haplotypes and ARMS2, C2, C3, and CFB alleles show association with susceptibility to age-related macular degeneration in Mexicans.

Contreras AV, Zenteno JC, Fernández-López JC, Rodríguez-Corona U, Falfán-Valencia R, Sebastian L, Morales F, Ochoa-Contreras D, Carnevale A, Silva-Zolezzi I. Contreras AV, et al. Among authors: zenteno jc. Mol Vis. 2014 Jan 14;20:105-16. eCollection 2014. Mol Vis. 2014. PMID: 24453474 Free PMC article.

5

Association study of multiple gene polymorphisms with the risk of adult-onset primary open-angle glaucoma in a Mexican population.

Buentello-Volante B, Elizondo-Olascoaga C, Miranda-Duarte A, Guadarrama-Vallejo D, Cabral-Macias J, Zenteno JC. Buentello-Volante B, et al. Among authors: zenteno jc. Exp Eye Res. 2013 Feb;107:59-64. doi: 10.1016/j.exer.2012.11.013. Epub 2012 Nov 30. Exp Eye Res. 2013. PMID: 23206929

6

ABCA4 mutational spectrum in Mexican patients with Stargardt disease: Identification of 12 novel mutations and evidence of a founder effect for the common p.A1773V mutation.

Chacón-Camacho OF, Granillo-Alvarez M, Ayala-Ramírez R, Zenteno JC. Chacón-Camacho OF, et al. Among authors: zenteno jc. Exp Eye Res. 2013 Apr;109:77-82. doi: 10.1016/j.exer.2013.02.006. Epub 2013 Feb 16. Exp Eye Res. 2013. PMID: 23419329

7

ASSOCIATION STUDY BETWEEN POLYMORPHISMS OF THE p53 AND LYMPHOTOXIN ALPHA (LTA) GENES AND THE RISK OF PROLIFERATIVE VITREORETINOPATHY/RETINAL DETACHMENT IN A MEXICAN POPULATION.

Quiroz-Casian N, Lozano-Giral D, Miranda-Duarte A, Garcia-Montalvo I, Rodriguez-Loaiza JL, Zenteno JC. Quiroz-Casian N, et al. Among authors: zenteno jc. Retina. 2018 Jan;38(1):187-191. doi: 10.1097/IAE.0000000000001508. Retina. 2018. PMID: 28106707

8

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

Velazquez-Soto H, Groman-Lupa S, Cruz-Aguilar M, Salazar AL, Zenteno JC, Jimenez-Martinez MC. Velazquez-Soto H, et al. Among authors: zenteno jc. Antioxidants (Basel). 2023 Jul 31;12(8):1540. doi: 10.3390/antiox12081540. Antioxidants (Basel). 2023. PMID: 37627535 Free PMC article.

9

Two different PABPN1 expanded alleles in a Mexican population with oculopharyngeal muscular dystrophy arising from independent founder effects.

Rivera D, Mejia-Lopez H, Pompa-Mera EN, Villanueva-Mendoza C, Nava-Castañeda A, Garnica-Hayashi L, Cuevas-Covarrubias S, Zenteno JC. Rivera D, et al. Among authors: zenteno jc. Br J Ophthalmol. 2008 Jul;92(7):998-1002. doi: 10.1136/bjo.2007.131482. Br J Ophthalmol. 2008. PMID: 18577654

10

Prevalence of high-risk alleles in the LOXL1 gene and its association with pseudoexfoliation syndrome and exfoliation glaucoma in a Latin American population.

Jaimes M, Rivera-Parra D, Miranda-Duarte A, Valdés G, Zenteno JC. Jaimes M, et al. Among authors: zenteno jc. Ophthalmic Genet. 2012 Mar;33(1):12-7. doi: 10.3109/13816810.2011.615078. Epub 2011 Oct 4. Ophthalmic Genet. 2012. PMID: 21970694

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