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Page 1
Identification of genomic copy number variations in lung benign metastasizing leiomyomatosis.
Hernández-Plata E, Velázquez-Wong AC, Jiménez-Ramírez C, Fernández-Ramírez F, Galicia-Sánchez LM, Flores-García CA, Hernández-Hernández JM, Rosas-Vargas H, Huicochea-Montiel JC, Espinosa-Poblano E. Hernández-Plata E, et al. Among authors: velazquez wong ac. Clin Respir J. 2019 Feb;13(2):105-113. doi: 10.1111/crj.12987. Epub 2019 Jan 29. Clin Respir J. 2019. PMID: 30597752
Copy Number Alterations Associated with Acute Lymphoblastic Leukemia in Mexican Children. A report from The Mexican Inter-Institutional Group for the identification of the causes of childhood leukemia.
Rosales-Rodríguez B, Fernández-Ramírez F, Núñez-Enríquez JC, Velázquez-Wong AC, Medina-Sansón A, Jiménez-Hernández E, Flores-Lujano J, Peñaloza-González JG, Espinosa-Elizondo RM, Pérez-Saldívar ML, Torres-Nava JR, Martín-Trejo JA, Martínez-Morales GB, Bekker-Méndez VC, Mejía-Aranguré JM, Rosas-Vargas H. Rosales-Rodríguez B, et al. Among authors: velazquez wong ac. Arch Med Res. 2016 Nov;47(8):706-711. doi: 10.1016/j.arcmed.2016.12.002. Arch Med Res. 2016. PMID: 28476198
Copy Number Alterations are Associated with the Risk of Very Early Relapse in Pediatric B-lineage Acute Lymphoblastic Leukemia: A Nested Case-control MIGICCL Study.
Rosales-Rodríguez B, Núñez-Enríquez JC, Velázquez-Wong AC, González-Torres C, Gaytán-Cervantes J, Jiménez-Hernández E, Martín-Trejo JA, Campo-Martínez MLÁD, Medina-Sanson A, Flores-Lujano J, Flores-Villegas LV, Peñaloza-González JG, Torres-Nava JR, Espinosa-Elizondo RM, Amador-Sánchez R, Miranda-Madrazo MR, Santillán-Juárez JD, Pérez-Saldívar ML, Gurrola-Silva A, Orozco-Ruiz D, Solís-Labastida KA, Velázquez-Aviña MM, Duarte-Rodríguez DA, Mata-Rocha M, Sepúlveda-Robles OA, Ortiz-Maganda M, Bekker-Méndez VC, Jiménez-Morales S, Mejía-Aranguré JM, Rosas-Vargas H. Rosales-Rodríguez B, et al. Among authors: velazquez wong ac. Arch Med Res. 2021 May;52(4):414-422. doi: 10.1016/j.arcmed.2020.12.013. Epub 2021 Feb 1. Arch Med Res. 2021. PMID: 33541741
Clinical and molecular characterization of a patient with 15q21.2q22.2 deletion syndrome.
Velázquez-Wong AC, Ruiz Esparza-Garrido R, Velázquez-Flores MÁ, Huicochea-Montiel JC, Cárdenas-Conejo A, Miguez-Muñoz CP, Araujo-Solís MA, Salamanca-Gómez F, Arenas-Aranda DJ. Velázquez-Wong AC, et al. Cytogenet Genome Res. 2014;144(3):183-9. doi: 10.1159/000370081. Epub 2015 Feb 6. Cytogenet Genome Res. 2014. PMID: 25661042
Duplication of the Miller-Dieker Critical Region in a Patient with a Subtelomeric Unbalanced Translocation t(10;17)(p15.3;p13.3).
Ruiz Esparza-Garrido R, Velázquez-Wong AC, Araujo-Solís MA, Huicochea-Montiel JC, Velázquez-Flores MÁ, Salamanca-Gómez F, Arenas-Aranda DJ. Ruiz Esparza-Garrido R, et al. Among authors: velazquez wong ac. Mol Syndromol. 2012 Aug;3(2):82-8. doi: 10.1159/000339639. Epub 2012 Jul 10. Mol Syndromol. 2012. PMID: 23326253 Free PMC article.
Analysis of polymorphisms in genes (AGT, MTHFR, GPIIIa, and GSTP1) associated with hypertension, thrombophilia and oxidative stress in Mestizo and Amerindian populations of México.
Juárez-Velázquez R, Canto P, Canto-Cetina T, Rangel-Villalobos H, Rosas-Vargas H, Rodríguez M, Canizales-Quinteros S, Velázquez Wong AC, Ordoñez-Razo RM, Vilchis-Dorantes G, Coral-Vázquez RM. Juárez-Velázquez R, et al. Among authors: velazquez wong ac. Dis Markers. 2010;28(5):323-31. doi: 10.3233/DMA-2010-0712. Dis Markers. 2010. PMID: 20592457 Free PMC article.
Differentially Expressed Long Non-Coding RNAs Were Predicted to Be Involved in the Control of Signaling Pathways in Pediatric Astrocytoma.
Ruiz Esparza-Garrido R, Rodríguez-Corona JM, López-Aguilar JE, Rodríguez-Florido MA, Velázquez-Wong AC, Viedma-Rodríguez R, Salamanca-Gómez F, Velázquez-Flores MÁ. Ruiz Esparza-Garrido R, et al. Among authors: velazquez wong ac. Mol Neurobiol. 2017 Oct;54(8):6598-6608. doi: 10.1007/s12035-016-0123-9. Epub 2016 Oct 13. Mol Neurobiol. 2017. PMID: 27738870
12 results