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A Molecular Characterization of the Allelic Expression of the BRCA1 Founder Δ9-12 Pathogenic Variant and Its Potential Clinical Relevance in Hereditary Cancer.
Dominguez-Ortiz J, Álvarez-Gómez RM, Montiel-Manríquez R, Cedro-Tanda A, Alcaraz N, Castro-Hernández C, Bautista-Hinojosa L, Contreras-Espinosa L, Torres-Maldonado L, Fragoso-Ontiveros V, Sánchez-Contreras Y, González-Barrios R, Fuente-Hernández MA, Mejía-Aguayo ML, Juárez-Figueroa U, Padua-Bracho A, Sosa-León R, Obregon-Serrano G, Vidal-Millán S, Núñez-Martínez PM, Pedroza-Torres A, Nicasio-Arzeta S, Rodríguez A, Luna F, Cisneros-Soberanis F, Frías S, Arriaga-Canon C, Herrera-Montalvo LA. Dominguez-Ortiz J, et al. Among authors: frias s. Int J Mol Sci. 2024 Jun 20;25(12):6773. doi: 10.3390/ijms25126773. Int J Mol Sci. 2024. PMID: 38928478 Free PMC article.
Large-scale topological disruption of chromosome territories 9 and 22 is associated with nonresponse to treatment in CML.
Fabian-Morales E, Vallejo-Escamilla D, Gudiño A, Rodríguez A, González-Barrios R, Rodríguez Torres YL, Castro Hernández C, de la Torre-Luján AH, Oliva-Rico DA, Ornelas Guzmán EC, López Saavedra A, Frias S, Herrera LA. Fabian-Morales E, et al. Among authors: frias s. Int J Cancer. 2022 May 1;150(9):1455-1470. doi: 10.1002/ijc.33903. Epub 2021 Dec 29. Int J Cancer. 2022. PMID: 34913480 Free PMC article.
FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México.
García-de Teresa B, Frias S, Molina B, Villarreal MT, Rodriguez A, Carnevale A, López-Hernández G, Vollbrechtshausen L, Olaya-Vargas A, Torres L. García-de Teresa B, et al. Among authors: frias s. Mol Genet Genomic Med. 2019 Jun;7(6):e710. doi: 10.1002/mgg3.710. Epub 2019 May 1. Mol Genet Genomic Med. 2019. PMID: 31044565 Free PMC article.
WIP1 Contributes to the Adaptation of Fanconi Anemia Cells to DNA Damage as Determined by the Regulatory Network of the Fanconi Anemia and Checkpoint Recovery Pathways.
Rodríguez A, Naveja JJ, Torres L, García de Teresa B, Juárez-Figueroa U, Ayala-Zambrano C, Azpeitia E, Mendoza L, Frías S. Rodríguez A, et al. Among authors: frias s. Front Genet. 2019 May 3;10:411. doi: 10.3389/fgene.2019.00411. eCollection 2019. Front Genet. 2019. PMID: 31130988 Free PMC article.
A Boolean network model of the FA/BRCA pathway.
Rodríguez A, Sosa D, Torres L, Molina B, Frías S, Mendoza L. Rodríguez A, et al. Among authors: frias s. Bioinformatics. 2012 Mar 15;28(6):858-66. doi: 10.1093/bioinformatics/bts036. Epub 2012 Jan 20. Bioinformatics. 2012. PMID: 22267503
7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype.
Yokoyama E, Smith-Pellegrin DL, Sánchez S, Molina B, Rodríguez A, Juárez R, Lieberman E, Avila S, Castrillo JL, Del Castillo V, Frías S. Yokoyama E, et al. Among authors: frias s. Mol Cytogenet. 2017 Nov 15;10:42. doi: 10.1186/s13039-017-0345-1. eCollection 2017. Mol Cytogenet. 2017. PMID: 29177010 Free PMC article.
117 results