Publicaciones 2018

Por Año de la Unidad de Investigación
  1. Calderon-Ezquerro M.C, Guerrero-Guerra C, Galán C, Serrano-Silva N, Guidos-Fogelbach G, Jiménez-Martínez MC,  Larenas-Linnemann, López Espinosa ED, Ayala-Balboa J. Pollen in the atmosphere of Mexico City and its impact on the health of the pediatric population. Atmospheric Environment. 186; 2018: 198-208.
  2. Navas A, Magaña-Guerrero FS, Domínguez-López A, Chávez-García C, Partido G, Graue-Hernández EO, Sánchez-García FJ, Garfias Y. Anti-Inflammatory and Anti-Fibrotic Effects of Human Amniotic Membrane Mesenchymal Stem Cells and Their Potential in Corneal Repair. Stem Cells Transl Med. 2018;7(12):906-917.
  3. Meza-Cuenca F, Medina-Contreras JML, Mailloux-Salinas P, Bautista-Hernández LA, Buentello-Volante B, Domínguez-López A, Garfias Y, Correa-López PV, Bautista de Lucio VM, Bravo G. Characterization of free fatty acid receptors expression in an obesity rat model with high sucrose diet. J Recept Signal Transduct Res. 2018;38(1):76-82.
  4. Serna-Ojeda JC, Pedro-Aguilar L, Rodriguez-Quintanilla C, Mejía-López H, Ponce-Angulo DG, Navas A, Bautista-de Lucio VM, Graue-Hernandez EO. Post-keratoplasty Endophthalmitis by Multidrug-resistant Pseudomonas Aeruginosa With Positive Culture of the Contralateral Donor Cornea: A Case Report. Transplant Proc. 2018;50(3):964-966
  5. Blackburn PR, Chacon-Camacho OF, Ortiz-González XR, Reyes M, Lopez-Uriarte GA, Zarei S, Bhoj EJ, Perez-Solorzano S, Vaubel RA, Murphree MI, Nava J, Cortes-Gonzalez V, Parisi JE, Villanueva-Mendoza C, Tirado-Torres IG, Li D, Klee EW, Pichurin PN, Zenteno JC. Extension of the mutational and clinical spectrum of SOX2 related disorders: Description of six new cases and a novel association with suprasellar teratoma. Am J Med Genet A. 2018 Dec;176(12):2710-2719.
  6. Astiazarán MC, García-Montaño LA, Sánchez-Moreno F, Matiz-Moreno H, Zenteno JC. Next generation sequencing-based molecular diagnosis in familial congenital cataract expands the mutational spectrum in known congenital cataract genes. Am J Med Genet A. 2018 Dec;176(12):2637-2645.
  7. 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. Significant Association Between Variant in SGCD and Age-Related Macular Degeneration. Genes (Basel). 2018 Sep 25;9(10). pii: E467.
  8. Matías-Pérez D, García-Montaño LA, Cruz-Aguilar M, García-Montalvo IA, Nava-Valdéz J, Barragán-Arevalo T, Villanueva-Mendoza C, Villarroel CE, Guadarrama-Vallejo C, la Cruz RV, Chacón-Camacho O, Zenteno JC. Identification of novel pathogenic variants and novel gene-phenotype correlations in Mexican subjects with microphthalmia and/or anophthalmia by next-generation sequencing. J Hum Genet. 2018 Nov;63(11):1169-1180.
  9. Quiroz-Casian N, Chacon-Camacho OF, Barragan-Arevalo T, Nava-Valdez J, Lieberman E, Salgado-Medina A, Navas A, Graue-Hernandez EO, Zenteno JC. Sclerocornea-Microphthalmia-Aphakia Complex: Description of Two Additional Cases Associated With Novel FOXE3 Mutations and Review of the Literature.Cornea. 2018 Sep;37(9):1178-1181.
  10. López-Hernández B, Méndez JP, Coral-Vázquez RM, Benítez-Granados J, Zenteno JC, Villegas-Ruiz V, Calzada-León R, Soderlund D, Canto P. Duplication of SOX9 associated with 46,XX ovotesticular disorder of sex development. Reprod Biomed Online. 2018 Jul;37(1):107-112.
  11. López-Rubio S, Chacon-Camacho OF, Matsui R, Guadarrama-Vallejo D, Astiazarán MC, Zenteno JC. Retinal phenotypic characterization of patients with ABCA4 retinopathydue to the homozygous p.Ala1773Val mutation. Mol Vis. 2018 Feb 1;24:105-114.
  12. Jiménez-Ávila CE, Villegas-Ruíz V, Zapata-Tarres M, Rubio-Portillo AE, Pérez López EI, Zenteno JC, Juárez-Méndez S. Centromere-associated protein E expresses a novel mRNA isoform in acute lymphoblastic leukemia. Int J Mol Epidemiol Genet. 2018 Oct 20;9(5):43-54
  13. Zuazo F, Astiazaran MC, Rodríguez-Cabrera L, Garcia-Regil P, Chacon-Camacho O, Tovilla-Canales JL, Zenteno JC. Clinical Description, Molecular Analysis of TWIST2 Gene, and Surgical Treatment in a Patient With Barber-Say Syndrome. Ophthalmic Plast Reconstr Surg. 2018 Mar/Apr;34(2):e61-e63.
  14. Bhoj EJ, Haye D, Toutain A, Bonneau D, Nielsen IK, Lund IB, Bogaard P, Leenskjold S, Karaer K, Wild KT, Grand KL, Astiazaran MC, Gonzalez-Nieto LA, Carvalho A, Lehalle D, Amudhavalli SM, Repnikova E, Saunders C, Thiffault I, Saadi I, Li D, Hakonarson H, Vial Y, Zackai E, Callier P, Drunat S, Verloes A. Phenotypic spectrum associated with SPECC1L pathogenic variants: new families and critical review of the nosology of Teebi, Opitz GBBB, and Baraitser-Winter syndromes. Eur J Med Genet. 2018, S1769-7212(18)30464-6.