Rodriguez Alfredo, Chunyu Yang, Elissa Furutani, Benilde García de Teresa, Jessica Filiatrault, Larissa Sambel, Patricia Flores-Guzmán, Silvia Sánchez, Angélica Monsiváis, Héctor Mayani, Ozge Vargel Bolukbasi, Anniina Färkkilä, Michael Epperly, Joel Greenberger, Akiko Shimamura, Frias S, Markus Grompe, Kalindi Parmar, Alan D’Andrea.
Inhibition of TGFbeta1 and TGFbeta3 promotes hematopoiesis in Fanconi anemia.
Exp Hematol. Nov 6:S0301-472X(20)30620-2
2021
Anniina Färkkilä, Alfredo Rodríguez, Jaana Oikkonen, Doga C Gulhan, Huy Nguyen, Julieta Domínguez, Sandra Ramos, Caitlin E Mills, Fernando Perez-Villatoro, Jean-Bernard Lazaro, Jia Zhou, Connor S Clairmont, Lisa A Moreau, Peter J Park, Peter K Sorger, Sampsa Hautaniemi, Sara Frias, Alan D D’Andrea.
Heterogeneity and clonal evolution of acquired PARP inhibitor resistance in TP53- and BRCA1-deficient cells.
Cancer Res. Jan 29;canres.2912.2020
2021
Sevilla-Montoya R, Zavaleta-Abreu MJ, Queipo G, Sanchez S, Frias S, Hidalgo-Bravo A, Grether-González P.
Unravelling complex mosaicism of sex chromosomes in a patient with primary amenorrhea through cytogenetic analysis on urothelial cells.
Taiwan J Obstet Gynecol. May;60(3):526-529
2021
Fiesco- Roa M, Monsivais-Orozco A, Rodríguez A, Frías S, García-de Teresa B.
Síndromes de falla medular hereditarios: etiología, fisiopatología, diagnóstico y tratamiento. Inherited Bone Marrow Failure Syndromes: etiology, pathophysiology, diagnosis, and management.
Acta Pediatr Méx; 42 (4): 192-207
2021
Fiesco-Roa, Moises; Frias, Sara; Garcia-De Teresa, Benilde; Garza-Mayen, Gilda
Microcephaly: diagnostic considerations
Acta Pediatrica De Mexico, Volume 41 Número 5 Páginas 222 a la 230 DOI:
2020
Frias S.; García-De-teresa B.; Rodríguez A.
Chromosome instability in fanconi anemia: From breaks to phenotypic consequences
Genes, Volume 11 Número 12 Páginas 1 a la 35 DOI: 10.3390/genes11121528
2020
Rodríguez A, Kaiyang Zhang, Anniina Farkkila, Jessica Filiatrault, Chunyu Yang, Martha Velázquez, Elissa Furutani, Devorah C. Goldman, Benilde García de Teresa, Gilda Garza-Mayen, Kelsey McQueen, Larissa A. Sambel, Bertha Molina, Leda Torres, Marisol González, Eduardo Vadillo, Rosana Pelayo, William H. Fleming, Markus Grompe, Akiko Shimamura, Sampsa Hautaniemi, Joel Greenberger, Sara Frías, Kalindi Parmar, and Alan D. D’Andrea.
MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia.
Cell Stem Cell, doi: 10.1016/j.stem.2020.09.004
2020
Emiy Yokoyama, Camilo E. Villarroel, Sinhué Diaz, Victoria Del Castillo, Patricia Pérez‐Vera, Consuelo Salas, Samuel Gómez, Reneé Barreda, Bertha Molina and Sara Frias. (autor de correspondencia).
Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review.
Mol Cytogenet,13:42 doi: 10.1186/s13039-020-00510-5
2020
Sandra Ramos, Rebeca Rodríguez, Oscar Castro, Patricia Grether, Bertha Molina and Sara Frias.
Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples.
Int. J. Mol. Sci. 20, 5251; doi:10.3390/ijms20215251
2019
Cristóbal Flores-Castillo, María Luna-Luna, Elizabeth Carreón-Torres,
Victoria López-Olmos, Sara Frías, Marco Antonio Juárez-Oropeza, Martha Franco, José Manuel Fragoso, Gilberto Vargas-Alarcón and Óscar Pérez-Méndez.
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.
Int. J. Mol. Sci. 20, 2521; doi:10.3390/ijms20102521 FI 3.687
2019
Alfredo Rodríguez, J. Jesús Naveja, Leda Torres, Benilde García de Teresa, Ulises Juárez- Figueroa, Cecilia Ayala, Eugenio M. Azpeitia, Luis Mendoza, Sara Frías (autor de correspondencia).
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.
Frontiers in Genetics, 2019 May, 10, 411;1-14. doi: 10.3389/fgene.2019.00411 ISSN: 1664-8021 FI 4.151
2019
García-de Teresa B, Frias S, Molina B, Villarreal MT, Rodríguez A, Carnevale A, López-Hernández G, Vollbrechtshausen L, Olaya-Vargas A, Torres L.
FANCC Dutch Founder Mutation in a Mennonite Family from Mexico.
Mol Genet Genom Med. DOI: 10.1002/mgg3.710. Online ISSN:2324-9269. FI 2.695
2019
Barrientos-Rios R, Frias S, Velázquez-AragónJ, Villarroel C, Sánchez S, Molina B, Martínez A, Carnevale A, García de Teresa B, Bonilla E, Alvarado-Araiza CD, Valderrama Hernández A, Ríos-Gallardo T, Calzada-León R, Altamirano-Bustamante N, Torres L.
Low bone mineral density and renal malformation in Mexican patients with Turner Syndrome are associated with single nucleotide variants in vitamin D-metabolism genes.
Gynecol Endocrinol. ISSN: 0951-3590 DOI: 10.1080/09513590.2019.1582626 FI 1.453
2019
Frias S, Ramos S, Salas C, Molina B, Sánchez S y Rivera-Luna R. (autor de correspondencia)
Nonclonal Chromosome Aberrations and Genome Chaos in Somatic and Germ Cells from Patients and Survivors of Hodgkin Lymphoma.
Genes-Basel, 10(1), 37:1-22 doi:10.3390/genes10010037. FI 3.191, ISSN: 2073-4425
2019
Frias S, Ramos S, Molina B.
Response to Letter to the Editor: Genomic chaos in peripheral blood lymphocytes of Hodgkin’s lymphoma patients one year after ABVD chemotherapy/radiotherapy.
Environ Mol Mutagen. May;60(4):387-388. ISSN:1098-2280 DOI: 10.1002/em.22279
2018
Ramos S, Navarrete-Meneses P, Molina B, Cervantes- Barragán DE, Lozano V, Gallardo E, Marchetti F, Frias S (autor de correspondencia).
Genomic Chaos in Peripheral Blood Lymphocytes of Hodgkin’s Lymphoma Patients One year After ABVD Chemotherapy/ Radiotherapy.
Environmental and Molecular Mutagenesis 59:755-768 (2018). DOI:10.1002/em FI 3.575, ISSN:1098-2280
2018
Yokoyama E, Del Castillo V, Sanchez S, Ramos S, Molina B, Torres L, Navarro MJ, Avila S, Castrillo JL, García-de Teresa B, Asch B, Frias S (autor de correspondencia).
Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics.
Molecular Cytogenetics. 11:30 DOI: 10.1186/s13039-018-0374-4. FI 1.455. ISSN: 1755-8166.
2018
Benilde García-de Teresa, and Sara Frias (autor de correspondencia).
In reference to Fanconi anemia and Laron syndrome.
Am J Med Sci. 355(6):614-615. DOI 10.1016/j.amjms.2018.01.014. PMID: 29891046
F.I. 1.847 ISSN: 0002-9629 ISSN electrónico 1538-2990
2018
Emiy Yokoyama, Dennise Lesley Smith-Pellegrin, Silvia Sánchez, Bertha Molina, Alfredo Rodríguez, Rocío Juárez, Esther Lieberman, Silvia Avila, José Luis Castrillo, Victoria del Castillo, Sara Frías.
7p15 deletion as the cause of hand-foot-genital syndrome: A case report, literature review and proposal of a minimum region for this phenotype.
Molecular Cytogenetics 10:42 DOI 10.1186/s13039-017-0345-1 FI 1.455
2017
García-de-Teresa B, Hernández-Gómez M, Frias S (autor de correspondencia).
DNA damage as a driver for growth delay: chromosome instability syndromes with intrauterine growth retardation.
BioMed Research International Vol 2017, Article ID 8193892, 14 pages doi 10.1155/2017/8193892. FI 2.476
2017
Sevilla-Montoya R, Martínez-Juárez A, Quintana-Palma M, Molina-Alvarez B, Frias S, Grether-González P, Aguinaga-Rios M.
Heterogeneous diagnoses underlying radial ray anomalies.
Indian Journal of Pediatrics. DOI:10.1007/s12098-016-2270-4
2017
Torres L, Juárez U, García L, Miranda-Ríos J and Frias S (autor de correspondencia).
External ear microRNA expression profile during development in the mouse.
Int. J. Dev. Biol. 59: 497-503 FI 2.879. doi: 10.1387/ijdb.150124sf
2015
Rios O, Frias S, Rodríguez A, Kofman S, Merchant H, Torres L, Mendoza L
Analysis of Gonadal Sex Determination and Source of Disorders of Sex Development with a Boolean Network Model
Theoretical Biology and Medical Modelling, 12:26. DOI 10.1186/s12976-015-0023-0 FI 1.03
2015
Alfredo Rodríguez, Leda Torres, Ulises Juárez, David Sosa, Eugenio Azpeitia, Benilde García, Edith Cortés, Rocío Ortiz, Ana M. Salazar, Patricia Ostrosky, Luis Mendoza and Sara Frias (autor de correspondencia).
Fanconi Anemia Cells with Unrepaired DNA Damage Activate Components of the Checkpoint Recovery Process.
Theor Biol Med Mod. Theoretical Biology and Medical Modelling, 12:19 DOI 10.1186/s12976-015-0011-4 ISSN: 1742-4682 FI 1.03
2015
Molina B, Marchetti F, Gomez L, Ramos S, Torres L, Ortiz R, Altamirano-Lozano M, Carnevale A, Frias S (autor de correspondencia).
Hydroxyurea applied during G2 induces chromosomal damage and potentiates the clastogenic effect of mitomycin C in Fanconi Anemia cells
Environ Mol Mutagen. 56:457-467 2015 Feb 6. doi: 10.1002/em.21938. Online ISSN: 1098-2280 FI 3.326
2015
Artículos en revistas arbitradas
Yokoyama-Rebollar E, Frías S, Del Castillo-Ruiz V.
Abordaje citogenético y citogenómico de pacientes con discapacidad intelectual y malformaciones congénitas.
Acta Pediatr Mex.;38(6):433-441. Doi 10.18233/APM38No6pp433-4411511
2017
Torres L, Juarez U, Segura L, Miranda J, Frias S (autor de correspondencia).
Microarray analysis of microRNA expression in mouse fetus at 13.5 and 14.5days post-coitum in ear and back skin tissues.
Genomics Data 9 70–77. FI 0.22 doi 10.1016/j.gdata.2016.06.011 ID Pubmed: PMID:27408816
2016
Vazquez-del Campo AR, Torres-Maldonado L, Sanchez-Sandoval S, Frias-Vazquez S, Lieberman-Hernández E, Del Castillo-Ruiz V, Yokoyama-Rebollar E.
Duplicación 5q34q35.3 que involucra el gen NSD1: región delimitada por microarreglos de hibridación genómica comparativa.
A propósito de un caso. Acta Pediatr Mex.;37(5):271-281. doi 10.18233/APM37No5pp271-281
2016
García de Teresa B, Rodríguez A, Frias S (autor de correspondencia).
Estudio multidisciplinario del paciente con anemia de Fanconi.
Acta Pediatr Mex;37:54-59. DOI: doi 10.18233/APM37No1pp54-59
2016
Ramos S, Molina B, Grether P, Mayén DG, Castro O, Angeles M, Rodríguez R y Frias S (autor de correspondencia).
Identificación de translocaciones crípticas polimórficas en cromosomas acrocéntricos de abortos aneuploides.
Acta Pediatr Mex;36:374-382. DOI: doi 10.18233/APM36No5pp374-382
2015
