Chromosome Instability in Fanconi Anemia: From Breaks to Phenotypic Consequences

por García-de-Teresa, Benilde, Rodríguez, Alfredo, Frias, Sara
Publicado 2020

DNA Damage as a Driver for Growth Delay: Chromosome Instability Syndromes with Intrauterine Growth Retardation

por García-de Teresa, Benilde, Hernández-Gómez, Mariana, Frías, Sara
Publicado 2017

Microarray analysis of microRNA expression in mouse fetus at 13.5 and 14.5 days post-coitum in ear and back skin tissues

por Torres, Leda, Juárez, Ulises, García, Laura, Miranda-Ríos, Juan, Frias, Sara
Publicado 2016

Meiotic susceptibility for induction of sperm with chromosomal aberrations in patients receiving combination chemotherapy for Hodgkin lymphoma

por Frias, Sara, Van Hummelen, Paul, Meistrich, Marvin L., Wyrobek, Andrew J.
Publicado 2020

Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples

por Ramos, Sandra, Rodríguez, Rebeca, Castro, Oscar, Grether, Patricia, Molina, Bertha, Frias, Sara
Publicado 2019

Nonclonal Chromosome Aberrations and Genome Chaos in Somatic and Germ Cells from Patients and Survivors of Hodgkin Lymphoma

por Frias, Sara, Ramos, Sandra, Salas, Consuelo, Molina, Bertha, Sánchez, Silvia, Rivera-Luna, Roberto
Publicado 2019

A Boolean network model of human gonadal sex determination

por Ríos, Osiris, Frias, Sara, Rodríguez, Alfredo, Kofman, Susana, Merchant, Horacio, Torres, Leda, Mendoza, Luis
Publicado 2015

Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability

por Fiesco-Roa, Moisés Ó., García-de Teresa, Benilde, Leal-Anaya, Paula, van ‘t Hek, Renée, Wegman-Ostrosky, Talia, Frías, Sara, Rodríguez, Alfredo
Publicado 2022

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

por Rodríguez, Alfredo, Naveja, J. Jesús, Torres, Leda, García de Teresa, Benilde, Juárez-Figueroa, Ulises, Ayala-Zambrano, Cecilia, Azpeitia, Eugenio, Mendoza, Luis, Frías, Sara
Publicado 2019

Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review

por Yokoyama, Emiy, Villarroel, Camilo E., Diaz, Sinhué, Del Castillo, Victoria, Pérez-Vera, Patricia, Salas, Consuelo, Gómez, Samuel, Barreda, Reneé, Molina, Bertha, Frias, Sara
Publicado 2020

FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México

por García‐de Teresa, Benilde, Frias, Sara, Molina, Bertha, Villarreal, María Teresa, Rodriguez, Alfredo, Carnevale, Alessandra, López‐Hernández, Gerardo, Vollbrechtshausen, Lilia, Olaya‐Vargas, Alberto, Torres, Leda
Publicado 2019

7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype

por Yokoyama, Emiy, Smith-Pellegrin, Dennise Lesley, Sánchez, Silvia, Molina, Bertha, Rodríguez, Alfredo, Juárez, Rocío, Lieberman, Esther, Avila, Silvia, Castrillo, José Luis, del Castillo, Victoria, Frías, Sara
Publicado 2017

Fanconi anemia cells with unrepaired DNA damage activate components of the checkpoint recovery process

por Rodríguez, Alfredo, Torres, Leda, Juárez, Ulises, Sosa, David, Azpeitia, Eugenio, Teresa, Benilde García-de, Cortés, Edith, Ortíz, Rocío, Salazar, Ana M., Ostrosky-Wegman, Patricia, Mendoza, Luis, Frías, Sara
Publicado 2015

Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics

por Yokoyama, Emiy, Del Castillo, Victoria, Sánchez, Silvia, Ramos, Sandra, Molina, Bertha, Torres, Leda, Navarro, María José, Avila, Silvia, Castrillo, José Luis, García-De Teresa, Benilde, Asch, Bárbara, Frías, Sara
Publicado 2018

Atorvastatin and Fenofibrate Increase the Content of Unsaturated Acyl Chains in HDL and Modify In Vivo Kinetics of HDL-Cholesteryl Esters in New Zealand White Rabbits

por Flores-Castillo, Cristóbal, Luna-Luna, María, Carreón-Torres, Elizabeth, López-Olmos, Victoria, Frías, Sara, Juárez-Oropeza, Marco Antonio, Franco, Martha, Fragoso, José Manuel, Vargas-Alarcón, Gilberto, Pérez-Méndez, Óscar
Publicado 2019

Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG

por Reyes, Pedro, García-de Teresa, Benilde, Juárez, Ulises, Pérez-Villatoro, Fernando, Fiesco-Roa, Moisés O., Rodríguez, Alfredo, Molina, Bertha, Villarreal-Molina, María Teresa, Meléndez-Zajgla, Jorge, Carnevale, Alessandra, Torres, Leda, Frias, Sara
Publicado 2022

Frequent copy number variants in a cohort of Mexican-Mestizo individuals

por Sánchez, Silvia, Juárez, Ulises, Domínguez, Julieta, Molina, Bertha, Barrientos, Rehotbevely, Martínez-Hernández, Angélica, Carnevale, Alessandra, Grether-González, Patricia, Mayen, Dora Gilda, Villarroel, Camilo, Lieberman, Esther, Yokoyama, Emiy, Del Castillo, Victoria, Torres, Leda, Frias, Sara
Publicado 2023

TGFβ pathway is required for viable gestation of Fanconi anemia embryos

por Rodríguez, Alfredo, Epperly, Michael, Filiatrault, Jessica, Velázquez, Martha, Yang, Chunyu, McQueen, Kelsey, Sambel, Larissa A., Nguyen, Huy, Iyer, Divya Ramalingam, Juárez, Ulises, Ayala-Zambrano, Cecilia, Martignetti, David B., Frías, Sara, Fisher, Renee, Parmar, Kalindi, Greenberger, Joel S., D’Andrea, Alan D.
Publicado 2022

Large‐scale topological disruption of chromosome territories 9 and 22 is associated with nonresponse to treatment in CML

por Fabian‐Morales, Eunice, Vallejo‐Escamilla, David, Gudiño, Adriana, Rodríguez, Alfredo, González‐Barrios, Rodrigo, Rodríguez Torres, Yameli L., Castro Hernández, Clementina, de la Torre‐Luján, Alfredo H., Oliva‐Rico, Diego A., Ornelas Guzmán, Erandhi C., López Saavedra, Alejandro, Frias, Sara, Herrera, Luis A.
Publicado 2021