| The eIF3 interactome reveals the translasome, a supercomplex linking protein synthesis and degradation machineries Z Sha, LM Brill, R Cabrera, O Kleifeld, JS Scheliga, MH Glickman, ... Molecular cell 36 (1), 141-152, 2009 | 156 | 2009 |
| Proteasome nuclear import mediated by Arc3 can influence efficient DNA damage repair and mitosis in Schizosaccharomyces pombe R Cabrera, Z Sha, TJ Vadakkan, J Otero, F Kriegenburg, ... Molecular biology of the cell 21 (18), 3125-3136, 2010 | 22 | 2010 |
| Schizosaccharomyces pombe Arc3 is a conserved subunit of the Arp2/3 complex required for polarity, actin organization, and endocytosis R Cabrera, J Suo, E Young, EC Chang Yeast 28 (6), 495-503, 2011 | 19 | 2011 |
| Identification of a New Candidate Locus for Ebstein Anomaly in 1p36. 2 MC Miranda-Fernández, S Ramírez-Oyaga, CM Restrepo, ... Molecular Syndromology, 2018 | 12 | 2018 |
| A Novel Splice-Site Mutation in the ELN Gene Suggests an Alternative Mechanism for Vascular Elastinopathies CA Velandia-Piedrahita, A Morel, DJ Fonseca-Mendoza, ... The application of clinical genetics, 233-240, 2020 | 6 | 2020 |
| Protocol to obtain targeted transcript sequence data from snake venom samples collected in the Colombian field A Fonseca, C Renjifo-Ibáñez, JM Renjifo, R Cabrera Toxicon 148, 1-6, 2018 | 6 | 2018 |
| Identification of clinically relevant phenotypes in patients with Ebstein anomaly R Cabrera, MC Miranda‐Fernández, VM Huertas‐Quiñones, M Carreño, ... Clinical Cardiology 41 (3), 343-348, 2018 | 5 | 2018 |
| Semiconductor whole exome sequencing for the identification of genetic variants in Colombian patients clinically diagnosed with long QT syndrome M Burgos, A Arenas, R Cabrera Molecular diagnosis & therapy 20, 353-362, 2016 | 4 | 2016 |
| Actualidad y proyección del estudio genético de las enfermedades cardiovasculares en Colombia R Cabrera, A Muñoz Revista Colombiana de Cardiología 20 (1), 1-4, 2013 | 3 | 2013 |
| Structural modelling of kcnq1 and kcnh2 double mutant proteins, identified in two severe long qt syndrome cases, reveals new insights into cardiac channelopathies WA Agudelo, SR Gil-Quiñones, A Fonseca, A Arenas, L Castro, ... International Journal of Molecular Sciences 22 (23), 12861, 2021 | 1 | 2021 |
| Proteasome Mobility Mediated by Arc3 Can Influence Efficient DNA Damage Repair and Mitosis in Schizosaccharomyces pombe R Cabrera, Z Sha, TJ Vadakkan, J Otero, F Kriegenburg, ... American Society for Cell Biology, 2010 | 1 | 2010 |
| P‐IG‐45| The RHAG* 01N. 26 Variant Does Not Lead to Rh‐Null but to Rh‐Mod Phenotype: The Importance of Absorption and Elusion Assays A Urbina, Y Flórez, M Hernández, A Rodriguez, N Contreras‐Bravo, ... Transfusion 63, 199A-199A, 2023 | | 2023 |
| Performance Comparison of a Duplex Implementation of the CDC EUA 2019-nCoV Assay with the Seegene Allplex-SARS-CoV-2 Assay for the Detection of SARS-CoV-2 in Nasopharyngeal … KM Jiménez, DJ Fonseca-Mendoza, A Morel, O Ortega-Recalde, ... Methods and Protocols 5 (5), 73, 2022 | | 2022 |
| Abstract P3-07-05: Genetic profile of germline mutations in unselected women with breast cancer in a Colombian population DC Sierra-Díaz, A Morel, DJ Fonseca, N Contreras, M Angulo-Aguado, ... Cancer Research 82 (4_Supplement), P3-07-05-P3-07-05, 2022 | | 2022 |
| Frecuencia de alteraciones germinales en genes de riesgo alto/moderado para riesgo de cáncer de mama hereditario: estudio multicéntrico en población no seleccionada WAM Durán, DCS Díaz, A Morel, N Contreras, MA Aguado, V Balaguera, ... Revista Colombiana de Hematología y Oncología 9 (Supl), 182-183, 2022 | | 2022 |
| Multivariate analysis of comorbidities in congenital heart disease: Making sense of phenotypic heterogeneity R Cabrera, M Miranda-Fernandez, V Huertas-Quinones, G Alberto, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 139-140, 2019 | | 2019 |
| Novel LVNC genetic aetiology discovered by an original whole-exome sequencing data combinatory filtering method S Gallo Bernal, C Carlosama, H Medina, J Contreras, R Cabrera, ... Cambridge University Press, 2019 | | 2019 |
| Influencia del polimorfismo rs11549465 de HIF-1α en los niveles de hemoglobina y lactato en pacientes de cirugía cardiovascular M Burgos, R Cabrera Revista de la Facultad de Medicina 65 (2), 253-260, 2017 | | 2017 |
| Identification of genetic variants and chromosomal abnormalities associated with Ebstein anomaly R Cabrera, MC Miranda, CM Restrepo Fernández, VM Huertas-quiñones, ... Cambridge University Press, 2017 | | 2017 |
| Entendiendo las bases genéticas de la enfermedad coronaria-Polimorfismos en la enzima convertidora de angiotensina R Cabrera Revista Colombiana de Cardiología 20 (5), 285-286, 2013 | | 2013 |
