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Frontiers in Genetics|May 28, 2019
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 PathwaysAlfredo Rodríguez, J Jesús Naveja, Leda Torres, et al.
Molecular Genetics & Genomic Medicine|May 3, 2019
FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, MéxicoBenilde García-de Teresa, Sara Frias, Bertha Molina, et al.
Theoretical Biology & Medical Modelling|September 20, 2015
Fanconi anemia cells with unrepaired DNA damage activate components of the checkpoint recovery processAlfredo Rodríguez, Leda Torres, Ulises Juárez, et al.
Molecular Cytogenetics|May 16, 2018
Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogeneticsEmiy Yokoyama, Victoria Del Castillo, Silvia Sánchez, et al.
International Journal of Molecular Sciences|February 26, 2022
Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCGPedro Reyes, Benilde García-de Teresa, Ulises Juárez, et al.
Gaceta Medica De Mexico|May 16, 2024
Chromosome analysis of 303 pregnancy losses in MexicoLuz M Garduño-Zarazúa, Dora G Mayén, Ricardo Meléndez-Hernández, et al.
Molecular Cytogenetics|January 11, 2023
Frequent copy number variants in a cohort of Mexican-Mestizo individualsSilvia Sánchez, Ulises Juárez, Julieta Domínguez, et al.
Cancers|June 13, 2025
High Burden of Non-Clonal Chromosome Aberrations Before Onset of Detectable Neoplasia in Fanconi Anemia Bone MarrowSilvia Sánchez, Benilde García-de-Teresa, Marco A Mejía-Barrera, et al.
Frontiers in Aging|March 12, 2026
The tight bond between Fanconi anemia and agingMarco Antonio Mejía-Barrera, Enya Enara Martínez-Torres, Ulises Juárez-Figueroa, et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology|March 20, 2019
Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genesRehotbevely Barrientos-Rios, Sara Frias, José A Velázquez-Aragón, et al.
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