Publicaciones 2011

Por Año de la Unidad de Investigación
  1. OCT findings in young asymptomatic subjects carrying familial BEST1 gene mutations. Chacon-Camacho OF, Camarillo-Blancarte L, Zenteno JC. Ophthalmic Genet. 2011; 32:24-30.
  2. Immunophenotyping in peripheral blood mononuclear cells, aqueous humour and vitreous in a Blau syndrome patient caused by a novel NOD2 mutation. Jimenez-Martinez MC, Cruz F, Groman-Lupa S, Zenteno JC. Int J Immunogenet. 2011 ;38:233-42.
  3. Novel Sonic Hedgehog Mutation in a Couple with Variable Expression of Holoprosencephaly. Aguinaga M, Llano I, Zenteno JC, and Kofman Alfaro S. Case Reports in Genetics. 2011, 703497.
  4. Homozygosity mapping identifies the Crumbs homologue 1 (Crb1) gene as responsible for a recessive syndrome of retinitis pigmentosa and nanophthalmos. Zenteno JC, Buentello-Volante B, Ayala-Ramirez R, Villanueva-Mendoza C. Am J Med Genet A. 2011; 155A:1001-6.
  5. Expanding the phenotype of gingival fibromatosis-mental retardation-hypertrichosis (Zimmermann-Laband) syndrome. Chacon-Camacho OF, Vázquez J, Zenteno JC. Am J Med Genet A. 2011; 155A:1716-20.
  6. Down regulation of IL-8 and IL-6 in human limbal epitelial cells cultured with human dialyzable leukocyte extracts. Robles-Contreras A, Vizuet L, Rivera E, Serafin-Lopez J, Estrada-Garcia I, Estrada-Parra S, Chavez R, Garfias Y, Perez-Tapia M, Jimenez-Martinez MC. Rev Alerg Mex 2011; 58:147-154.
  7. Amniotic Membrane is an immunosuppressor of peripheral blood mononuclear cells. Garfias Y, Zaga-Clavellina V, Vadillo-Ortega F, Osorio M, Jiménez-Martinez MC. Immunological Investigations 2011, 40: 1-14