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The human nucleoporin Tpr protects cells from RNA-mediated replication stress.
Nat Commun. 2021 Jun 24;12(1):3937. doi: 10.1038/s41467-021-24224-3.
Nat Commun. 2021.
PMID: 34168151
Free PMC article.
POLθ prevents MRE11-NBS1-CtIP-dependent fork breakage in the absence of BRCA2/RAD51 by filling lagging-strand gaps.
Mann A, Ramirez-Otero MA, De Antoni A, Hanthi YW, Sannino V, Baldi G, Falbo L, Schrempf A, Bernardo S, Loizou J, Costanzo V.
Mann A, et al. Among authors: ramirez otero ma.
Mol Cell. 2022 Nov 17;82(22):4218-4231.e8. doi: 10.1016/j.molcel.2022.09.013.
Mol Cell. 2022.
PMID: 36400008
Free article.
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POLθ processes ssDNA gaps and promotes replication fork progression in BRCA1-deficient cells.
Schrempf A, Bernardo S, Arasa Verge EA, Ramirez Otero MA, Wilson J, Kirchhofer D, Timelthaler G, Ambros AM, Kaya A, Wieder M, Ecker GF, Winter GE, Costanzo V, Loizou JI.
Schrempf A, et al. Among authors: ramirez otero ma.
Cell Rep. 2022 Nov 29;41(9):111716. doi: 10.1016/j.celrep.2022.111716. Epub 2022 Nov 17.
Cell Rep. 2022.
PMID: 36400033
Free article.
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A Previously Unrecognized Molecular Landscape of Lynch Syndrome in the Mexican Population.
Padua-Bracho A, Velázquez-Aragón JA, Fragoso-Ontiveros V, Nuñez-Martínez PM, Mejía Aguayo ML, Sánchez-Contreras Y, Ramirez-Otero MA, De la Fuente-Hernández MA, Vidal-Millán S, Wegman-Ostrosky T, Pedroza-Torres A, Arriaga-Canon C, Herrera-Montalvo LA, Alvarez-Gómez RM.
Padua-Bracho A, et al. Among authors: ramirez otero ma.
Int J Mol Sci. 2022 Sep 30;23(19):11549. doi: 10.3390/ijms231911549.
Int J Mol Sci. 2022.
PMID: 36232851
Free PMC article.
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Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient.
Núñez-Martínez PM, Taja-Chayeb L, Ramírez-Otero MA, Fragoso-Ontiveros V, Wegman-Ostrosky T, Cruz-Robles D, Vidal Millán S.
Núñez-Martínez PM, et al. Among authors: ramirez otero ma.
Bol Med Hosp Infant Mex. 2021 May 3;78(4):341-345. doi: 10.24875/BMHIM.20000129.
Bol Med Hosp Infant Mex. 2021.
PMID: 33938902
Free article.
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Mexican BRCA1 founder mutation: Shortening the gap in genetic assessment for hereditary breast and ovarian cancer patients.
Fragoso-Ontiveros V, Velázquez-Aragón JA, Nuñez-Martínez PM, de la Luz Mejía-Aguayo M, Vidal-Millán S, Pedroza-Torres A, Sánchez-Contreras Y, Ramírez-Otero MA, Muñiz-Mendoza R, Domínguez-Ortíz J, Wegman-Ostrosky T, Bargalló-Rocha JE, Gallardo-Rincón D, Reynoso-Noveron N, Arriaga-Canon C, Meneses-García A, Herrera-Montalvo LA, Alvarez-Gomez RM.
Fragoso-Ontiveros V, et al. Among authors: ramirez otero ma.
PLoS One. 2019 Sep 23;14(9):e0222709. doi: 10.1371/journal.pone.0222709. eCollection 2019.
PLoS One. 2019.
PMID: 31545835
Free PMC article.
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