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Page 1
Germline mutations in NKX2-5, GATA4, and CRELD1 are rare in a Mexican sample of Down syndrome patients with endocardial cushion and septal heart defects.
Alcántara-Ortigoza MA, De Rubens-Figueroa J, Reyna-Fabian ME, Estandía-Ortega B, González-del Angel A, Molina-Álvarez B, Velázquez-Aragón JA, Villagómez-Martínez S, Pereira-López GI, Martínez-Cruz V, Álvarez-Gómez RM, Díaz-García L. Alcántara-Ortigoza MA, et al. Among authors: martinez cruz v. Pediatr Cardiol. 2015 Apr;36(4):802-8. doi: 10.1007/s00246-014-1091-3. Epub 2014 Dec 19. Pediatr Cardiol. 2015. PMID: 25524324
Erratum to: Germline Mutations in NKX2-5, GATA4, and CRELD1 are Rare in a Mexican Sample of Down Syndrome Patients with Endocardial Cushion and Septal Heart Defects.
Alcántara-Ortigoza MA, De Rubens-Figueroa J, Reyna-Fabian ME, Estandía-Ortega B, González-Del Angel A, Molina-Álvarez B, Velázquez-Aragón JA, Villagómez-Martínez S, Pereira-López GI, Martínez-Cruz V, Álvarez-Gómez RM, Díaz-García L. Alcántara-Ortigoza MA, et al. Among authors: martinez cruz v. Pediatr Cardiol. 2015 Oct;36(7):1551. doi: 10.1007/s00246-015-1226-1. Pediatr Cardiol. 2015. PMID: 26205256 No abstract available.
Gene Variants in NKX2-1 Do Not Represent a Major Etiological Factor of Primary Congenital Hypothyroidism in Mexican Population.
González-Del Angel A, Fernández-Hernández L, Sánchez-Verdiguel I, González-Núñez A, Martínez-Cruz V, Sánchez C, Moreno-Rojas R, Alcántara-Ortigoza MA. González-Del Angel A, et al. Among authors: martinez cruz v. J Pediatr Genet. 2019 Jun;8(2):41-46. doi: 10.1055/s-0038-1676644. Epub 2019 Jan 2. J Pediatr Genet. 2019. PMID: 31061744 Free PMC article.
Low allelic heterogeneity in a sample of Mexican patients with classical galactosaemia.
Velázquez-Aragón J, Alcántara-Ortigoza MA, Vela-Amieva M, Monroy S, Martínez-Cruz V, Todd-Quiñones C, González-del Angel A. Velázquez-Aragón J, et al. Among authors: martinez cruz v. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S333-7. doi: 10.1007/s10545-008-0905-y. Epub 2008 Oct 29. J Inherit Metab Dis. 2008. PMID: 18956253
Molecular analysis of the PAX8 gene in a sample of Mexican patients with primary congenital hypothyroidism: identification of the recurrent p.Arg31His mutation.
Alcántara-Ortigoza MA, González-del Angel A, Martínez-Cruz V, Vela-Amieva M, Sánchez-Pérez C, Moreno-Rojas R, Estandía-Ortega B, Hernández-Martínez N. Alcántara-Ortigoza MA, et al. Among authors: martinez cruz v. Clin Endocrinol (Oxf). 2012 Jan;76(1):148-50. doi: 10.1111/j.1365-2265.2011.04153.x. Clin Endocrinol (Oxf). 2012. PMID: 21689132 No abstract available.
Histone deacetylases modulate resistance to the therapy in lung cancer.
Contreras-Sanzón E, Prado-Garcia H, Romero-Garcia S, Nuñez-Corona D, Ortiz-Quintero B, Luna-Rivero C, Martínez-Cruz V, Carlos-Reyes Á. Contreras-Sanzón E, et al. Among authors: martinez cruz v. Front Genet. 2022 Oct 3;13:960263. doi: 10.3389/fgene.2022.960263. eCollection 2022. Front Genet. 2022. PMID: 36263432 Free PMC article. Review.