Sara Frías

Chromosome Instability in Fanconi Anemia: From Breaks to Phenotypic Consequences.

Authors:

Benilde García-de-Teresa Alfredo Rodríguez Sara Frias

Genes (Basel) 2020 Dec 21;11(12). Epub 2020 Dec 21.

Laboratorio de Citogenética, Instituto Nacional de Pediatría, Ciudad de México 04530, Mexico.

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December 2020

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

Authors:

Sara Frias Paul Van Hummelen Marvin L Meistrich Andrew J Wyrobek

PLoS One 2020 28;15(12):e0242218. Epub 2020 Dec 28.

Health Effects Genetics Division, Lawrence Livermore National Laboratory, Livermore, California, United States of America.

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January 2021

Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia.

Exp Hematol 2020 Nov 7. Epub 2020 Nov 7.

Department of Radiation Oncology and Center for DNA Damage and Repair, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA. Electronic address:

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November 2020

MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia.

Cell Stem Cell 2021 Jan 29;28(1):33-47.e8. Epub 2020 Sep 29.

Department of Radiation Oncology and Center for DNA Damage and Repair, Dana Farber Cancer Institute, Harvard Medical School, Boston, MA 02215, USA. Electronic address:

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January 2021

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

Authors:

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

Mol Cytogenet 2020 7;13:42. Epub 2020 Sep 7.

Laboratorio de Citogenética, Departamento de Genética Humana, Instituto Nacional de Pediatría, Mexico City, Mexico.

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September 2020

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

Authors:

Sandra Ramos Rebeca Rodríguez Oscar Castro Patricia Grether Bertha Molina Sara Frias

Int J Mol Sci 2019 Oct 23;20(21). Epub 2019 Oct 23.

Laboratorio de Citogenética, Instituto Nacional de Pediatría, 04530 Mexico City, Mexico.

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October 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 Pathways.

Authors:

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

Front Genet 2019 3;10:411. Epub 2019 May 3.

Laboratorio de Citogenética, Departamento de Investigación en Genética Humana, Instituto Nacional de Pediatría, Mexico City, Mexico.

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May 2019

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.

Authors:

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 Óscar Pérez-Méndez

Int J Mol Sci 2019 May 22;20(10). Epub 2019 May 22.

Department of Molecular Biology, Instituto Nacional de Cardiología "Ignacio Chávez", 14080 Mexico City, Mexico.

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May 2019

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

Authors:

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

Mol Genet Genomic Med 2019 06 1;7(6):e710. Epub 2019 May 1.

Laboratorio de Citogenética, Instituto Nacional de Pediatría, Ciudad de México, México.

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June 2019

Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes.

Authors:

Rehotbevely Barrientos-Rios Sara Frias José A Velázquez-Aragón Camilo E Villaroel Silvia Sánchez Bertha Molina Angélica Martínez Alessandra Carnevale Benilde García-de-Teresa Edmundo Bonilla Christian David Alvarado-Araiza Alejandro Valderrama-Hernández Paul Tadeo Ríos-Gallardo Raúl Calzada-León Nelly Altamirano-Bustamante Leda Torres

Gynecol Endocrinol 2019 Sep 19;35(9):772-776. Epub 2019 Mar 19.

a Laboratorio de Citogenética, Departamento de Genética Humana, Instituto Nacional de Pediatría , Ciudad de México , Mexico.

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September 2019

Genomic chaos in peripheral blood lymphocytes of hodgkins lymphoma patients 1 year after ABVD chemotherapy/radiotherapy.

Authors:

Sara Frias

Environ Mol Mutagen 2019 05;60(4):387-388

Laboratorio de Citogenética, INP, Insurgentes Sur 3700-C, 6o. piso, Cd. De Mexico, Mexico.

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May 2019

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

Authors:

Sara Frias Sandra Ramos Consuelo Salas Bertha Molina Silvia Sánchez Roberto Rivera-Luna

Genes (Basel) 2019 01 10;10(1). Epub 2019 Jan 10.

Subdirección de Hemato-Oncología, Instituto Nacional de Pediatría, Cd. De Mexico, P.O. Box 04530, Mexico.

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January 2019

Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy.

Authors:

Sandra Ramos Pilar Navarrete-Meneses Bertha Molina David E Cervantes-Barragán Valentn Lozano Emma Gallardo Francesco Marchetti Sara Frias

Environ Mol Mutagen 2018 10 8;59(8):755-768. Epub 2018 Sep 8.

Laboratorio de Citogenética, Instituto Nacional de Pediatría, Ciudad de México, Mexico.

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October 2018

In Reference to Fanconi Anemia and Laron Syndrome.

Authors:

Benilde García-de Teresa Sara Frias

Am J Med Sci 2018 06 7;355(6):614-615. Epub 2018 Feb 7.

Laboratorio de Citogenética, Instituto Nacional de Pediatría, Ciudad de México, México; Departamento de Medicina Genómica y Toxicología Ambiental, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México, México. Electronic address:

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June 2018

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

Authors:

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

Mol Cytogenet 2018 9;11:30. Epub 2018 May 9.

2Laboratorio de Citogenética, Departamento de Genética Humana, Instituto Nacional de Pediatría, Ciudad de México, México.

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May 2018

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

Authors:

Benilde García-de Teresa Mariana Hernández-Gómez Sara Frías

Biomed Res Int 2017 12;2017:8193892. Epub 2017 Nov 12.

Laboratorio de Citogenética, Instituto Nacional de Pediatría, Mexico City, Mexico.

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July 2018

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

Authors:

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

Mol Cytogenet 2017 15;10:42. Epub 2017 Nov 15.

Laboratorio de Citogenética, Departamento de Investigación en Genética Humana. Instituto Nacional de Pediatría, Avenida IMAN no. 1, Torre de Investigación, Colonia Insurgentes Cuicuilco, Coyoacán, Ciudad de México, CDMX, Mexico.

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November 2017

Heterogeneous Diagnoses Underlying Radial Ray Anomalies.

Authors:

Rosalba Sevilla-Montoya Mónica Aguinaga Alejandro Martínez Guadalupe Razo Bertha Molina Sara Frías Patricia Grether

Indian J Pediatr 2017 Mar 17;84(3):200-205. Epub 2016 Dec 17.

Departamento de Genética, Instituto Nacional de Perinatología, Montes Urales 800 Col. Lomas Virreyes, C.P 11000, Torre de investigación 2°, Piso, Ciudad de México, CP 11000, Mexico.

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March 2017

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

Authors:

Leda Torres Ulises Juárez Laura García Juan Miranda-Ríos Sara Frias

Genom Data 2016 Sep 24;9:70-7. Epub 2016 Jun 24.

Laboratorio de Citogenética, Depto. de Investigación en Genética Humana, Instituto Nacional de Pediatría, Ciudad de México, México; Unidad de Genética de la Nutrición, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México e Instituto Nacional de Pediatría, Ciudad de México, México.

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September 2016

External ear microRNA expression profiles during mouse development.

Authors:

Leda Torres Ulises Juárez Laura García Juan Miranda-Ríos Sara Frias

Int J Dev Biol 2015 ;59(10-12):497-503

Laboratorio de Citogenética, Depto. de Investigación en Genética Humana, Instituto Nacional de Pediatría, México DF, México.

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November 2016

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