Rojas-Martinez A - Search Results

1

Genomic Characterization by Whole-Exome Sequencing of Hypermobility Spectrum Disorder.

Alanis-Funes GJ, Lira-Albarrán S, Hernández-Pérez J, Garza-Elizondo MA, Ortíz-López R, Elizondo CV, Rojas-Martinez A, Chávez-Santoscoy RA, Rangel-Escareño C. Alanis-Funes GJ, et al. Genes (Basel). 2022 Jul 18;13(7):1269. doi: 10.3390/genes13071269. Genes (Basel). 2022. PMID: 35886052 Free PMC article.

2

[Genetics and molecular medicine in cardiology].

Rojas Martínez A, Ortiz López R, Delgado Enciso I. Rojas Martínez A, et al. Rev Esp Cardiol. 2001 Jan;54(1):91-108. doi: 10.1016/s0300-8932(01)76268-9. Rev Esp Cardiol. 2001. PMID: 11141459 Free article. Review. Spanish.

3

Oncolytic virotherapy.

Cervantes-García D, Ortiz-López R, Mayek-Pérez N, Rojas-Martínez A. Cervantes-García D, et al. Ann Hepatol. 2008 Jan-Mar;7(1):34-45. Ann Hepatol. 2008. PMID: 18376364 Free article. Review.

4

Analysis of DNA mismatch repair proteins expression and BRAF V600E mutation in a subset of early- and late-onset colorectal carcinoma patients in Mexico.

Luévano-González A, Guzmán AQ, Ancer Rodríguez J, Ortiz López R, Rojas Martínez A, González Guerrero JF, Flores Gutiérrez JP. Luévano-González A, et al. Arch Med Res. 2011 Aug;42(6):457-62. doi: 10.1016/j.arcmed.2011.09.008. Epub 2011 Sep 22. Arch Med Res. 2011. PMID: 21945875

5

[Determination of molecular genetic markers in acute coronary syndromes and their relationship to cardiovascular adverse events].

Canseco-Ávila LM, Jerjes-Sánchez C, Ortiz-López R, Rojas-Martínez A. Canseco-Ávila LM, et al. Arch Cardiol Mex. 2013 Jan-Mar;83(1):8-17. doi: 10.1016/j.acmx.2013.01.001. Arch Cardiol Mex. 2013. PMID: 23433583 Spanish.

6

De novo MECP2 disomy in a Mexican male carrying a supernumerary marker chromosome and no typical Lubs syndrome features.

Neira VA, Romero-Espinoza P, Rojas-Martínez A, Ortiz-López R, Córdova-Fletes C, Plaja A, Barros-Núñez P. Neira VA, et al. Gene. 2013 Jul 25;524(2):381-5. doi: 10.1016/j.gene.2013.04.029. Epub 2013 Apr 29. Gene. 2013. PMID: 23639959

7

Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma.

Martínez-Jacobo L, Córdova-Fletes C, Ortiz-López R, Rivas F, Saucedo-Carrasco C, Rojas-Martínez A. Martínez-Jacobo L, et al. Mol Syndromol. 2013 Sep;4(6):285-91. doi: 10.1159/000353510. Mol Syndromol. 2013. PMID: 24167464 Free PMC article.

8

Clinical and molecular delineation of duplication 9p24.3q21.11 in a patient with psychotic behavior.

Martínez-Jacobo L, Ortíz-López R, Rizo-Méndez A, García-Molina V, Santuario-Facio SK, Rivas F, Rojas-Martínez A. Martínez-Jacobo L, et al. Gene. 2015 Apr 10;560(1):124-7. doi: 10.1016/j.gene.2015.02.010. Epub 2015 Feb 7. Gene. 2015. PMID: 25667990

9

Identification of differentially expressed genes associated with prognosis of B acute lymphoblastic leukemia.

Garza-Veloz I, Martinez-Fierro ML, Jaime-Perez JC, Carrillo-Sanchez K, Ramos-Del Hoyo MG, Lugo-Trampe A, Rojas-Martinez A, Gutierrez-Aguirre CH, Gonzalez-Llano O, Salazar-Riojas R, Hidalgo-Miranda A, Gomez-Almaguer D, Ortiz-Lopez R. Garza-Veloz I, et al. Dis Markers. 2015;2015:828145. doi: 10.1155/2015/828145. Epub 2015 Feb 24. Dis Markers. 2015. PMID: 25802479 Free PMC article.

10

Ionizing radiation-induced DNA injury and damage detection in patients with breast cancer.

Borrego-Soto G, Ortiz-López R, Rojas-Martínez A. Borrego-Soto G, et al. Genet Mol Biol. 2015 Dec;38(4):420-32. doi: 10.1590/S1415-475738420150019. Epub 2015 Nov 24. Genet Mol Biol. 2015. PMID: 26692152 Free PMC article.

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