Publicaciones 2013

Por Año de la Unidad de Investigación
  1. Overexpression of peroxiredoxin 2 in pterygium. A proteomic approach. Bautista-de Lucio VM, López-Espinosa NL, Robles-Contreras A, Pérez-Cano HJ, Mejía-López H, Mendoza G, Jiménez-Martínez MC, Garfias Y. Experimental Eye Research. 2013; 110:70-75.
  2. The T allele of lysyl oxidase-like 1 rs41435250 is a novel risk factor for pseudoexfoliation syndrome and pseudoexfoliation glaucoma independently and through intragenic epistatic interaction. Guadarrama-Vallejo D, Miranda-Duarte A, Zenteno JC. Mol Vis. 2013; 19:1937-44.
  3. An Imbalance Between Frequency of CD4+CD25+FOXP3+ Regulatory T Cells, and CCR4+ and CCR9+ Circulating Helper T cells is Associated with Active Perennial Allergic Conjunctivitis. Galicia-Carreón J, Santacruz C, Ayala-Balboa J, Robles-Contreras A, Perez-Tapia SM, Garfias Y, Hong E, Jiménez-Martínez MC. Clin Dev Immunol. 2013; 919742.
  4. O-Glycosylation of NnTreg Lymphocytes Recognized by the Amaranthus leucocarpus Lectin. Jiménez-Martínez MC, Lascurain R, Méndez-Reguera A, Estrada-Parra S, Estrada-García I, Gorocica P, Martínez-Cairo S, Zenteno E, Chávez R. Clin Dev Immunol 2013; 506807.
  5. An epidemiological investigation of a Forkhead box protein E3 founder mutation underlying the high frequency of sclerocornea, aphakia, and microphthalmia in a Mexican village. Pantoja-Melendez C, Ali M, Zenteno JC. Mol Vis. 2013; 19:1866-70.
  6. Exome sequencing identifies RDH12 compound heterozygous mutations in a family with severe retinitis pigmentosa. Chacon-Camacho OF, Jitskii S, Buentello-Volante B, Quevedo-Martinez J, Zenteno JC. Gene. 2013; 528:178-82.
  7. Staphylococcus epidermidis with the icaA-/icaD-/IS256- genotype and protein or protein/extracellular-DNA biofilm is frequent in ocular infections. Juárez-Verdayes MA, Ramón-Peréz ML, Flores-Páez LA, Camarillo-Márquez O, Zenteno JC, Jan-Roblero J, Cancino-Diaz ME, Cancino-Diaz JC. J Med Microbiol. 2013; 62:1579-87
    Prenatal exclusion of von Hippel-Lindau syndrome in a Mexican family carrying a novel VHL gene mutation. Chacón-Camacho OF, Benitez-Granados J, Zenteno JC. Ginecol Obstet Mex. 2013; 81:206-10.
  8. Nasopalpebral lipoma-coloboma syndrome: clinical, radiological, and histopathological description of a novel sporadic case. Chacon-Camacho OF, Lopez-Martinez MS, Vázquez J, Nava-Castañeda A, Martin-Biasotti F, Piña-Aguilar RE, Iñiguez-Soto M, Acosta-García J, Zenteno JC. Am J Med Genet A. 2013; 161:1470-4.
  9. A Novel De Novo EFNB1 Gene Mutation in a Mexican Patient with Craniofrontonasal Syndrome. Ramirez-Garcia MA, Chacon-Camacho OF, Leyva-Hernandez C, Cardenas-Conejo A, Zenteno JC. Case Rep Genet. 2013; 349725.
  10. Aplasia cutis congenita of the scalp in a female infant with anophthalmia/microphthalmia-esophageal atresia syndrome negative for SOX2 mutation. Corona-Rivera JR, Zenteno JC, Pelcastre-Luna E, Miguel-Jiménez K, Aguirre-Guillén RL, Cabral-Macías J, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A. Am J Med Genet A. 2013;161A:1189-93.
  11. 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. Exp Eye Res. 2013;109:77-82.
  12. Rhodopsin p.N78I dominant mutation causing sectorial retinitis pigmentosa in a pedigree with intrafamilial clinical heterogeneity. Rivera-De la Parra D, Cabral-Macias J, Matias-Florentino M, Rodriguez-Ruiz G, Robredo V, Zenteno JC. Gene. 2013; 519:173-6.
  13. Expansion of the Clinical Ocular Spectrum of Wolfram Syndrome in a Family Carrying a Novel WFS1 Gene Deletion. Chacón-Camacho O, Arce-Gonzalez R, Granillo-Alvarez M, Flores-Limas S, Ramírez M, Zenteno JC. Ophthalmic Genet. 2013; 34:243-248.
  14. 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. Estrada H, Buentello B, Zenteno JC, Fiszman R, Aguinaga M. Prenat Diagn. 2013;33:205-8.
  15. Homozygosity mapping identifies a GALK1 mutation as the cause of autosomal recessive congenital cataracts in 4 adult siblings. Chacon-Camacho OF, Buentello-Volante B, Velázquez-Montoya R, Ayala-Ramirez R, Zenteno JC. s. Gene. 2013; 534:218-221.
  16. Clinical and microbiological profile of infectious keratitis in children. Chirinos-Saldaña P, Bautista-de Lucio VM, Hernández Camarena JC, Navas A, Ramírez-Miranda A, Vizuet García L, Ortiz Casas M, López-Espinosa N, Gaona-Juárez C, Graue-Hernández EO, Bautista-Hernández LA. BMC Ophthalmol, 2013; 13:54.
  17. Defensin Production by Human Limbo-Corneal Fibroblasts Infected with Mycobacteria. Jorge I. Castañeda-Sánchez, Blanca E. García-Pérez, Ana R. Muñoz-Duarte, Shantal L. Baltierra-Uribe, Herlinda Mejia-López, Carlos López-López, Victor M. Bautista-De Lucio, Atzín Robles-Contreras and Julieta Luna-Herrera. Pathogens 2013; 2:13-32.
  18. The ocular surface: from physiology to the ocular allergic diseases. Galicia-Carreón J, Santacruz C, Hong E, Jiménez-Martínez MC. Rev Alerg Mex 2013; 60:172-183.
  19. Queratitis infecciosas: tendencias microbiológicas y sensibilidad a antibióticos. Segundo Reporte Anual del Grupo de Estudio de Microbiología Ocular del Instituto de Oftalmología “Conde de Valenciana”. Julio C. Hernández-Camarena, Victor M.Bautista-de Lucio, Patricia Chirinos-Saldaña, Alejandro Navas, Arturo Ramírez-Miranda, Alejandro Climent-Flores, Mariana Ortiz-Casas, Nadia L. López-Espinosa, Carolina Gaona-Juárez, Luis A. Bautista-Hernández, Enrique O. Graue-Hernández. Revista Mexicana de Oftalmología 2013; 87:100-109.