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Page 1
Association of HMOX1 and NQO1 Polymorphisms with Metabolic Syndrome Components.
Martínez-Hernández A, Córdova EJ, Rosillo-Salazar O, García-Ortíz H, Contreras-Cubas C, Islas-Andrade S, Revilla-Monsalve C, Salas-Labadía C, Orozco L. Martínez-Hernández A, et al. PLoS One. 2015 May 1;10(5):e0123313. doi: 10.1371/journal.pone.0123313. eCollection 2015. PLoS One. 2015. PMID: 25933176 Free PMC article.
Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review.
Martínez-Hernández A, Martínez-Anaya D, Durán-McKinster C, Del Castillo-Ruiz V, Navarrete-Meneses P, Córdova EJ, Villegas-Torres BE, Ruiz-Herrera A, Juárez-Velázquez R, Yokoyama-Rebollar E, Cervantes-Barragán D, Pedraza-Meléndez A, Orozco L, Pérez-Vera P, Salas-Labadía C. Martínez-Hernández A, et al. Among authors: salas labadia c. BMC Med Genomics. 2022 Oct 31;15(1):224. doi: 10.1186/s12920-022-01382-x. BMC Med Genomics. 2022. PMID: 36316743 Free PMC article. Review.
Variants in ARID5B gene are associated with the development of acute lymphoblastic leukemia in Mexican children.
Reyes-León A, Ramírez-Martínez M, Fernández-García D, Amaro-Muñoz D, Velázquez-Aragón JA, Salas-Labadía C, Zapata-Tarrés M, Velasco-Hidalgo L, López-Santiago N, López-Ruiz MI, Malavar-Guadarrama MA, Cárdenas-Cardós R, Paredes-Aguilera R, Rivera-Luna R, Dean M, Pérez-Vera P. Reyes-León A, et al. Among authors: salas labadia c. Ann Hematol. 2019 Oct;98(10):2379-2388. doi: 10.1007/s00277-019-03730-x. Epub 2019 Jun 21. Ann Hematol. 2019. PMID: 31227872 Free PMC article. Clinical Trial.
Cytogenomic and phenotypic analysis in low-level monosomy 7 mosaicism with non-supernumerary ring chromosome 7.
Salas-Labadía C, Cervantes-Barragán DE, Cruz-Alcívar R, Daber RD, Conlin LK, Leonard LD, Spinner NB, Durán-McKinster C, Dávila-Ortíz de Montellano DJ, Del Castillo-Ruiz V, Pérez-Vera P. Salas-Labadía C, et al. Am J Med Genet A. 2014 Jul;164A(7):1765-9. doi: 10.1002/ajmg.a.36503. Epub 2014 Mar 26. Am J Med Genet A. 2014. PMID: 24677512 Review.
Significance of CASP8AP2 and H2AFZ expression in survival and risk of relapse in children with acute lymphoblastic leukemia.
Juárez-Velázquez R, Reyes-León A, Salas-Labadía C, Rivera-Luna R, Velasco-Hidalgo L, López-Hernández G, López-Santiago N, Paredes-Aguilera R, Domínguez-López A, Bernáldez R, Pérez-Vera P. Juárez-Velázquez R, et al. Leuk Lymphoma. 2014 Oct;55(10):2305-11. doi: 10.3109/10428194.2013.878458. Epub 2014 Feb 24. Leuk Lymphoma. 2014. PMID: 24397596
Expression of Ik6 and Ik8 Isoforms and Their Association with Relapse and Death in Mexican Children with Acute Lymphoblastic Leukemia.
Reyes-León A, Juárez-Velázquez R, Medrano-Hernández A, Cuenca-Roldán T, Salas-Labadía C, Del Pilar Navarrete-Meneses M, Rivera-Luna R, López-Hernández G, Paredes-Aguilera R, Pérez-Vera P. Reyes-León A, et al. PLoS One. 2015 Jul 1;10(7):e0130756. doi: 10.1371/journal.pone.0130756. eCollection 2015. PLoS One. 2015. PMID: 26131904 Free PMC article.
Genetic and clinical characterization of 73 Pigmentary Mosaicism patients: revealing the genetic basis of clinical manifestations.
Salas-Labadía C, Gómez-Carmona S, Cruz-Alcívar R, Martínez-Anaya D, Del Castillo-Ruiz V, Durán-McKinster C, Ulloa-Avilés V, Yokoyama-Rebollar E, Ruiz-Herrera A, Navarrete-Meneses P, Lieberman-Hernández E, González-Del Angel A, Cervantes-Barragán D, Villarroel-Cortés C, Reyes-León A, Suárez-Pérez D, Pedraza-Meléndez A, González-Orsuna A, Pérez-Vera P. Salas-Labadía C, et al. Orphanet J Rare Dis. 2019 Nov 15;14(1):259. doi: 10.1186/s13023-019-1208-0. Orphanet J Rare Dis. 2019. PMID: 31730496 Free PMC article.
18 results