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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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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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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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A Boolean network model of the FA/BRCA pathway

Bioinformatics (Oxford, England), 2012-03, Vol.28 (6), p.858-866

2012

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

BioMed research international, 2017-01, Vol.2017, p.8193892-14

2017

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Estudio cromosómico de 303 pérdidas gestacionales en México

Gaceta médica de México, 2024-01, Vol.160 (1), p.81-91

2024

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P659: A comprehensive genotyping study in Mexican patients with Fanconi anemia identified reported, novel, and founder pathogenic variants

Genetics in Medicine Open, 2024, Vol.2, p.101564, Article 101564

2024

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P191: Old school and new findings: Expansion and delineation of the dysmorphological phenotype of Fanconi anemia

Genetics in Medicine Open, 2024, Vol.2, p.101088, Article 101088

2024

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P263: Genotype-phenotype associations in CASK disorders: A systematic literature review and report of three cases

Genetics in Medicine Open, 2024, Vol.2, p.101159, Article 101159

2024

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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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Heterogeneous Diagnoses Underlying Radial Ray Anomalies

Indian journal of pediatrics, 2017-03, Vol.84 (3), p.200-205

2017

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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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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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Chromosome Instability in Fanconi Anemia: From Breaks to Phenotypic Consequences

Genes, 2020-12, Vol.11 (12), p.1528

2020

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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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Microtia-atresia: aspectos clínicos, genéticos y genómicos

Boletín médico del Hospital Infantil de México, 2014-11, Vol.71 (6), p.387-395

2014

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Genetic abnormalities in leukemia secondary to treatment in patients with Hodgkin's disease

Revista de investigacion clinica, 2011-01, Vol.63 (1), p.53-63

2011

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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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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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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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TGF[beta] pathway is required for viable gestation of Fanconi anemia embryos

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

2022

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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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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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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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TGFβ pathway is required for viable gestation of Fanconi anemia embryos

MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia

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

A Boolean network model of the FA/BRCA pathway

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

Estudio cromosómico de 303 pérdidas gestacionales en México

P659: A comprehensive genotyping study in Mexican patients with Fanconi anemia identified reported, novel, and founder pathogenic variants

P191: Old school and new findings: Expansion and delineation of the dysmorphological phenotype of Fanconi anemia

P263: Genotype-phenotype associations in CASK disorders: A systematic literature review and report of three cases

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

Heterogeneous Diagnoses Underlying Radial Ray Anomalies

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

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

Chromosome Instability in Fanconi Anemia: From Breaks to Phenotypic Consequences

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

Microtia-atresia: aspectos clínicos, genéticos y genómicos

Genetic abnormalities in leukemia secondary to treatment in patients with Hodgkin's disease

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

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

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

TGF[beta] pathway is required for viable gestation of Fanconi anemia embryos

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

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

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

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