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Page 1
Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease.
Vélez JI, Lopera F, Creagh PK, Piñeros LB, Das D, Cervantes-Henríquez ML, Acosta-López JE, Isaza-Ruget MA, Espinosa LG, Easteal S, Quintero GA, Silva CT, Mastronardi CA, Arcos-Burgos M. Vélez JI, et al. Among authors: isaza ruget ma. Mol Neurobiol. 2019 May;56(5):3235-3243. doi: 10.1007/s12035-018-1298-z. Epub 2018 Aug 15. Mol Neurobiol. 2019. PMID: 30112632 Free PMC article.
Generation of one iPSC line (IMEDEAi006-A) from an early-onset familial Alzheimer's Disease (fAD) patient carrying the E280A mutation in the PSEN1 gene.
Vallejo-Diez S, Fleischer A, Martín-Fernández JM, Sánchez-Gilabert A, Castresana M, Aguillón D, Villegas A, Mastronardi CA, Espinosa LG, Arcos-Burgos M, Del Pozo Á, Herrán E, Gainza E, Isaza-Ruget M, Lopera F, Bachiller D. Vallejo-Diez S, et al. Stem Cell Res. 2019 May;37:101440. doi: 10.1016/j.scr.2019.101440. Epub 2019 Apr 15. Stem Cell Res. 2019. PMID: 31026686 Free article.
Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings.
Aguillon D, Vasquez D, Madrigal L, Moreno S, Hernández D, Isaza-Ruget M, Lopez JJ, Landires I, Nuñez-Samudio V, Restrepo CM, Vidal OM, Vélez JI, Arcos-Holzinger M, Lopera F, Arcos-Burgos M. Aguillon D, et al. Mol Neurobiol. 2022 Jun;59(6):3845-3858. doi: 10.1007/s12035-022-02821-7. Epub 2022 Apr 14. Mol Neurobiol. 2022. PMID: 35420381
Correction to: Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings.
Aguillon D, Vasquez D, Madrigal L, Moreno S, Hernández D, Isaza-Ruget M, Lopez JJ, Landires I, Nunez-Samudio V, Restrepo CM, Vidal OM, Vélez JI, Arcos-Holzinger M, Lopera F, Arcos-Burgos M. Aguillon D, et al. Mol Neurobiol. 2022 Jun;59(6):3859. doi: 10.1007/s12035-022-02874-8. Mol Neurobiol. 2022. PMID: 35585447 No abstract available.
Structural Protein Effects Underpinning Cognitive Developmental Delay of the PURA p.Phe233del Mutation Modelled by Artificial Intelligence and the Hybrid Quantum Mechanics-Molecular Mechanics Framework.
López-Rivera JJ, Rodríguez-Salazar L, Soto-Ospina A, Estrada-Serrato C, Serrano D, Chaparro-Solano HM, Londoño O, Rueda PA, Ardila G, Villegas-Lanau A, Godoy-Corredor M, Cuartas M, Vélez JI, Vidal OM, Isaza-Ruget MA, Arcos-Burgos M. López-Rivera JJ, et al. Among authors: isaza ruget ma. Brain Sci. 2022 Jun 30;12(7):871. doi: 10.3390/brainsci12070871. Brain Sci. 2022. PMID: 35884678 Free PMC article.
Diagnostic yield of chromosomal microarray in the largest Latino clinical cohort.
Carrillo YD, Rueda-Gaitán P, Gualdrón O, Estrada-Serrato C, Castro-Cuesta TA, Londoño O, Rodríguez-Salazar L, Isaza-Ruget M, Arcos-Burgos M, López Rivera JJ. Carrillo YD, et al. Am J Med Genet A. 2024 Feb;194(2):218-225. doi: 10.1002/ajmg.a.63427. Epub 2023 Oct 5. Am J Med Genet A. 2024. PMID: 37795898
Predicting chronic kidney disease progression with artificial intelligence.
Isaza-Ruget MA, Yomayusa N, González CA, H CA, de Oro V FA, Cely A, Murcia J, Gonzalez-Velez A, Robayo A, Colmenares-Mejía CC, Castillo A, Conde MI. Isaza-Ruget MA, et al. BMC Nephrol. 2024 Apr 26;25(1):148. doi: 10.1186/s12882-024-03545-7. BMC Nephrol. 2024. PMID: 38671349 Free PMC article.
Real-world data lipid profiles in one million colombian adults: The LiPAC million person study.
Colmenares-Mejía CC, Godoy-Corredor M, Morales-Mendoza E, Pinto-Pinzón DA, Rozo-Vanstrahlen JM, Acuña-Olmos J, Hilarión-Gaitán L, Suarez-Ramos MDP, Ruiz-Amaya DA, Salazar-Heredia FR, Vargas-Rodríguez J, Isaza-Ruget MA. Colmenares-Mejía CC, et al. Among authors: isaza ruget ma. Atheroscler Plus. 2024 Nov 16;58:51-58. doi: 10.1016/j.athplu.2024.11.001. eCollection 2024 Dec. Atheroscler Plus. 2024. PMID: 39649027 Free PMC article.
16 results