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Reversion from basal histone H4 hypoacetylation at the replication fork increases DNA damage in FANCA deficient cells

PloS one, 2024-05, Vol.19 (5), p.e0298032

2024

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

PloS one, 2020-12, Vol.15 (12), p.e0242218

2020

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

Frontiers in oncology, 2022-08, Vol.12, p.949435-949435

2022

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

International journal of molecular sciences, 2019-10, Vol.20 (21), p.5251

2019

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

Genes, 2019-01, Vol.10 (1), p.37

2019

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

International journal of molecular sciences, 2022-02, Vol.23 (4), p.2334

2022

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Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico

Frontiers in genetics, 2024-01, Vol.14, p.1293929-1293929

2024

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

Environmental and molecular mutagenesis, 2019-05, Vol.60 (4), p.387-388

Frias, Sara

2019

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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

International journal of molecular sciences, 2019-05, Vol.20 (10), p.2521

2019

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

Molecular cytogenetics, 2023-01, Vol.16 (1), p.2-14, Article 2

2023

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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, 2019-05, Vol.10, p.411-411

2019

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Unravelling complex mosaicism of sex chromosomes in a patient with primary amenorrhea through cytogenetic analysis on urothelial cells

Taiwanese journal of obstetrics & gynecology, 2021-05, Vol.60 (3), p.526-529

2021

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

Molecular cytogenetics, 2020-09, Vol.13 (1), p.42-7, Article 42

2020

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Characterizing Chemotherapy/Radiotherapy-Induced Genome Chaos in Hodgkin's Lymphoma Patients Using M-FISH

Methods in molecular biology (Clifton, N.J.), 2024, Vol.2825, p.247

2024

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

Molecular cytogenetics, 2018-05, Vol.11 (1), p.30-8, Article 30

2018

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TGFβ pathway is required for viable gestation of Fanconi anemia embryos

PLoS genetics, 2022-11, Vol.18 (11), p.e1010459-e1010459

2022

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A Boolean network model of the double-strand break repair pathway choice

Journal of theoretical biology, 2023-09, Vol.573, p.111608-111608, Article 111608

2023

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MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia

Cell stem cell, 2021-01, Vol.28 (1), p.33-47.e8

2021

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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, 2017-11, Vol.10 (1), p.42-9, Article 42

2017

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RAD50 targeting impairs DNA damage response and sensitizes human breast cancer cells to cisplatin therapy

Cancer biology & therapy, 2014-06, Vol.15 (6), p.777-788

2014

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

Molecular genetics & genomic medicine, 2019-06, Vol.7 (6), p.e710-n/a

2019

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NFE2L2 Gene Variants and Arsenic Susceptibility: A Lymphoblastoid Model

Journal of Toxicology and Environmental Health, Part A, 2015-05, Vol.78 (10), p.628-634

2015

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Anemia de Fanconi, Parte 1. Diagnóstico citogenético

Acta pediátrica de México, 2022-04, Vol.43 (2), p.102

2022

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

Theoretical biology and medical modelling, 2015-09, Vol.12 (1), p.19-19, Article 19

2015

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

Genomics data, 2016-09, Vol.9 (C), p.70-77

2016

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Reversion from basal histone H4 hypoacetylation at the replication fork increases DNA damage in FANCA deficient cells

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

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

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

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

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

Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico

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

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

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

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

Unravelling complex mosaicism of sex chromosomes in a patient with primary amenorrhea through cytogenetic analysis on urothelial cells

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

Characterizing Chemotherapy/Radiotherapy-Induced Genome Chaos in Hodgkin's Lymphoma Patients Using M-FISH

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

TGFβ pathway is required for viable gestation of Fanconi anemia embryos

A Boolean network model of the double-strand break repair pathway choice

MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia

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

RAD50 targeting impairs DNA damage response and sensitizes human breast cancer cells to cisplatin therapy

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

NFE2L2 Gene Variants and Arsenic Susceptibility: A Lymphoblastoid Model

Anemia de Fanconi, Parte 1. Diagnóstico citogenético

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

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

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